Francis Munier

Publications | Mémoires et thèses

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373 publications

Sous presse | 2019 | 2018 | 2017 | 2016 | 2015 | 2014 | 2013 | 2012 | 2011 | 2010 | 2009 | 2008 | 2007 | ...
 
INTRAVITREAL ANTI-VASCULAR ENDOTHELIAL GROWTH FACTOR FOR THE MANAGEMENT OF NEOVASCULARIZATION IN RETINOBLASTOMA AFTER INTRAVENOUS AND/OR INTRAARTERIAL CHEMOTHERAPY: Long-Term Outcomes in a Series of 35 Eyes.
Stathopoulos C., Gaillard M.C., Moulin A., Puccinelli F., Beck-Popovic M., Munier F.L. Retina. Peer-reviewed.
 
Granular type I corneal dystrophy in a large consanguineous Tunisian family with homozygous p.R124S mutation in the TGFBI gene.
Bouyacoub Y., Falfoul Y., Ouederni M., Sayeb M., Chedli A., Chargui M., Sassi H., Chakroun Chenguel I., Munier F.L., El Matri L. et al., 2019/08. Ophthalmic genetics, 40 (4) pp. 329-337. Peer-reviewed.
 
Conservative management of retinoblastoma: Challenging orthodoxy without compromising the state of metastatic grace. "Alive, with good vision and no comorbidity".
Munier F.L., Beck-Popovic M., Chantada G.L., Cobrinik D., Kivelä T.T., Lohmann D., Maeder P., Moll A.C., Carcaboso A.M., Moulin A. et al., 2019/06/05. Progress in retinal and eye research. Peer-reviewed.
 
Conservative treatment of diffuse infiltrating retinoblastoma: optical coherence tomography-assisted diagnosis and follow-up in three consecutive cases.
Stathopoulos C., Moulin A., Gaillard M.C., Beck-Popovic M., Puccinelli F., Munier F.L., 2019/06. The British journal of ophthalmology, 103 (6) pp. 826-830. Peer-reviewed.
 
Middle meningeal artery occlusion for intra-arterial chemotherapy of retinoblastoma.
Bartolini B., Puccinelli F., Hajdu S.D., Stathopoulos C., Beck-Popovic M., Munier F.L., Saliou G., 2019/06. Interventional neuroradiology, 25 (3) pp. 335-337. Peer-reviewed.
 
Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders.
Zeitz C., Michiels C., Neuillé M., Friedburg C., Condroyer C., Boyard F., Antonio A., Bouzidi N., Milicevic D., Veaux R. et al., 2019/06. Human mutation, 40 (6) pp. 765-787. Peer-reviewed.
 
The utility of massively parallel sequencing for posterior polymorphous corneal dystrophy type 3 molecular diagnosis.
Dudakova L., Evans C.J., Pontikos N., Hafford-Tear N.J., Malinka F., Skalicka P., Horinek A., Munier F.L., Voide N., Studeny P. et al., 2019/05. Experimental eye research, 182 pp. 160-166. Peer-reviewed.
 
Therapeutic targeting of the RB1 pathway in retinoblastoma with the oncolytic adenovirus VCN-01.
Pascual-Pasto G., Bazan-Peregrino M., Olaciregui N.G., Restrepo-Perdomo C.A., Mato-Berciano A., Ottaviani D., Weber K., Correa G., Paco S., Vila-Ubach M. et al., 2019/01/23. Science translational medicine, 11 (476). Peer-reviewed.
 
Bilateral vascular anomalies in Coats disease suggest concurrent retinal vascular disease.
Ambresin Aude, Munier Francis, Zola Marta, 2019. dans ARVO.
 
Dysfunctional LAT2 Amino Acid Transporter Is Associated With Cataract in Mouse and Humans.
Knöpfel E.B., Vilches C., Camargo SMR, Errasti-Murugarren E., Stäubli A., Mayayo C., Munier F.L., Miroshnikova N., Poncet N., Junza A. et al., 2019. Frontiers in physiology, 10 p. 688. Peer-reviewed.
 
YOUNGER AGE AT PRESENTATION IN CHILDREN WITH COATS DISEASE IS ASSOCIATED WITH MORE ADVANCED STAGE AND WORSE VISUAL PROGNOSIS: A Retrospective Study.
Daruich A., Matet A., Munier F.L., 2018/11. Retina, 38 (11) pp. 2239-2246. Peer-reviewed.
 
CRX-linked macular dystrophy with intrafamilial variable expressivity.
Romdhane K., Vaclavik V., Schorderet D.F., Munier F.L., Viet Tran H., 2018/10. Ophthalmic genetics, 39 (5) pp. 637-641. Peer-reviewed.
 
OCT-guided management of subclinical recurrent retinoblastoma.
Gaillard M.C., Houghton S., Stathopoulos C., Munier F.L., 2018/06. Ophthalmic genetics, 39 (3) pp. 338-343. Peer-reviewed.
 
Response to Khetan and Maitray's "Comment: Conservative management of massive choroidal relapse in retinoblastoma patients?"
Stathopoulos C., Gaillard M.C., Puccinelli F., Maeder P., Hadjistilianou D., Beck-Popovic M., Munier F., 2018/06. Ophthalmic genetics, 39 (3) p. 417. Peer-reviewed.
 
Anterior Chamber Chemotherapy in Retinoblastoma-Necessary but Not Sufficient for Aqueous Seeding Control.
Munier F.L., Gaillard M.C., Stathopoulos C., 2018/05/01. JAMA ophthalmology, 136 (5) pp. 596-597. Peer-reviewed.
 
12-Jahres-Resultate nach mikrokeratomassistierter anteriorer lamellierender therapeutischer Keratoplastik (ALTK) für Erkrankungen des anterioren Hornhautstromas – Vergleich von Erwachsenen und Kindern [12-Year Outcomes of Microkeratome-Assisted Anterior Lamellar Therapeutic Keratoplasty (ALTK) for Disorders of the Anterior Part of the Corneal Stroma - A Comparative Review of Adult and Children]
Guber I., Bergin C., Othenin-Girard P., Munier F., Majo F., 2018/04. Klinische Monatsblatter fur Augenheilkunde, 235 (4) pp. 404-408. Peer-reviewed.
Intracameral Chemotherapy for Globe Salvage in Retinoblastoma with Secondary Anterior Chamber Invasion.
Munier F.L., Moulin A., Gaillard M.C., Bongiovanni M., Decembrini S., Houghton S., Beck-Popovic M., Stathopoulos C., 2018/04. Ophthalmology, 125 (4) pp. 615-617. Peer-reviewed.
 
Successful conservative treatment of massive choroidal relapse in 2 retinoblastoma patients monitored by ultrasound biomicroscopy and/or spectral domain optic coherence tomography.
Stathopoulos C., Gaillard M.C., Puccinelli F., Maeder P., Hadjistilianou D., Beck-Popovic M., Munier F.L., 2018/04. Ophthalmic genetics, 39 (2) pp. 242-246. Peer-reviewed.
 
Assessment of retinoblastoma RNA reflux after intravitreal injection of melphalan.
Winter U., Nicolas M., Sgroi M., Sampor C., Torbidoni A., Fandiño A., Chantada G.L., Munier F.L., Schaiquevich P., 2018/03. The British journal of ophthalmology, 102 (3) pp. 415-418. Peer-reviewed.
Juvenile xanthogranuloma involving concurrent iris and skin: Clinical, pathological and molecular pathological evaluations.
Meyer P., Graeff E., Kohler C., Munier F., Bruder E., 2018/03. American journal of ophthalmology case reports, 9 pp. 10-13. Peer-reviewed.
 
Cataract development in children with Coats disease: risk factors and outcome.
Daruich A., Matet A., Munier F.L., 2018/02. Journal of AAPOS, 22 (1) pp. 44-49. Peer-reviewed.
 
Variability in clinical phenotypes of PRPF8-linked autosomal dominant retinitis pigmentosa correlates with differential PRPF8/SNRNP200 interactions.
Escher P., Passarin O., Munier F.L., Tran V.H., Vaclavik V., 2018. Ophthalmic genetics, 39 (1) pp. 80-86. Peer-reviewed.
 
Maladies vasculaires rares, mise en place d’un centre multidisciplinaire spécialisé au CHUV [Rare vascular diseases, building dedicated multidisciplinary specialized center]
Krieger C., Baud D., Bouchardy J., Christen-Zaech S., De Buys A., Deglise S., El Ezzi O., Fresa M., Hofer M., Hohl D. et al., 2017/12/06. Revue medicale suisse, 13 (586) pp. 2109-2115. Peer-reviewed.
 
Optical coherence tomography morphology and evolution in cblC disease-related maculopathy in a case series of very young patients.
Bacci G.M., Donati M.A., Pasquini E., Munier F., Cavicchi C., Morrone A., Sodi A., Murro V., Garcia Segarra N., Defilippi C. et al., 2017/12. Acta ophthalmologica, 95 (8) pp. e776-e782. Peer-reviewed.
 
Risk of Extraocular Extension in Eyes With Retinoblastoma Receiving Intravitreous Chemotherapy.
Francis J.H., Abramson D.H., Ji X., Shields C.L., Teixeira L.F., Schefler A.C., Cassoux N., Hadjistilianou D., Berry J.L., Frenkel S. et al., 2017/12/01. JAMA ophthalmology, 135 (12) pp. 1426-1429. Peer-reviewed.
 
Abnormal creatine transport of mutations in monocarboxylate transporter 12 (MCT12) found in patients with age-related cataract can be partially rescued by exogenous chaperone CD147.
Stäubli A., Capatina N., Fuhrer Y., Munier F.L., Labs S., Schorderet D.F., Tiwari A., Verrey F., Heon E., Cheng C.Y. et al., 2017/11/01. Human molecular genetics, 26 (21) pp. 4203-4214. Peer-reviewed.
 
Diagnosis and management of secondary epipapillary retinoblastoma.
Fabian I.D., Puccinelli F., Gaillard M.C., Beck-Popovic M., Munier F.L., 2017/10. The British journal of ophthalmology, 101 (10) pp. 1412-1418. Peer-reviewed.
First-line intra-arterial versus intravenous chemotherapy in unilateral sporadic group D retinoblastoma: evidence of better visual outcomes, ocular survival and shorter time to success with intra-arterial delivery from retrospective review of 20 years of treatment.
Munier F.L., Mosimann P., Puccinelli F., Gaillard M.C., Stathopoulos C., Houghton S., Bergin C., Beck-Popovic M., 2017/08. The British journal of ophthalmology, 101 (8) pp. 1086-1093. Peer-reviewed.
SUBFOVEAL NODULE IN COATS' DISEASE: Toward an Updated Classification Predicting Visual Prognosis.
Daruich A.L., Moulin A.P., Tran H.V., Matet A., Munier F.L., 2017/08. Retina, 37 (8) pp. 1591-1598. Peer-reviewed.
 
Intracameral Chemotherapy (Melphalan) for Aqueous Seeding in Retinoblastoma: Bicameral Injection Technique and Related Toxicity in a Pilot Case Study.
Munier F.L., Gaillard M.C., Decembrini S., Bongiovanni M., Beck-Popovic M., 2017/07. Ocular oncology and pathology, 3 (2) pp. 149-155. Peer-reviewed.
 
Acute Hemorrhagic Retinopathy following Intravitreal Melphalan Injection for Retinoblastoma: A Report of Two Cases and Technical Modifications to Enhance the Prevention of Retinal Toxicity.
Aziz H.A., Kim J.W., Munier F.L., Berry J.L., 2017/01. Ocular oncology and pathology, 3 (1) pp. 34-40. Peer-reviewed.
 
An international survey of classification and treatment choices for group D retinoblastoma.
Scelfo C., Francis J.H., Khetan V., Jenkins T., Marr B., Abramson D.H., Shields C.L., Pe'er J., Munier F., Berry J. et al., 2017. International journal of ophthalmology, 10 (6) pp. 961-967. Peer-reviewed.
Metastatic deaths in retinoblastoma patients treated with intraarterial chemotherapy (ophthalmic artery chemosurgery) worldwide.
Abramson D.H., Shields C.L., Jabbour P., Teixeira L.F., Fonseca JRF, Marques MCP, Munier F.L., Puccinelli F., Hadjistilianou T., Bracco S. et al., 2017. International journal of retina and vitreous, 3 p. 40. Peer-reviewed.
Multi-channel MRI segmentation of eye structures and tumors using patient-specific features.
Ciller C., De Zanet S., Kamnitsas K., Maeder P., Glocker B., Munier F.L., Rueckert D., Thiran J.P., Bach Cuadra M., Sznitman R., 2017. PloS one, 12 (3) pp. e0173900. Peer-reviewed.
Mutations in the polyglutamylase gene TTLL5, expressed in photoreceptor cells and spermatozoa, are associated with cone-rod degeneration and reduced male fertility.
Bedoni N., Haer-Wigman L., Vaclavik V., Tran V.H., Farinelli P., Balzano S., Royer-Bertrand B., El-Asrag M.E., Bonny O., Ikonomidis C. et al., 2016/10/15. Human molecular genetics, 25 (20) pp. 4546-4555. Peer-reviewed.
 
EXTRAMACULAR FIBROSIS IN COATS' DISEASE.
Daruich A., Matet A., Tran H.V., Gaillard M.C., Munier F.L., 2016/04. Retina (Philadelphia, Pa.), 36 (10) pp. 2022-2028. Peer-reviewed.
Multimodale Bildgebung eines retinalen Astrozyten-Hamartoms assoziert mit angeborener Hypertrophie des retinalen Pigmentepithels [Multimodal Imaging of Retinal Astrocytic Hamartoma Associated with Congenital Hypertrophy of Retinal Pigment Epithelium]
Trojman C., Zografos L., Dirani A., Munier F., De Ancos E., Guex-Crosier Y., 2016/04. Klinische Monatsblatter fur Augenheilkunde, 233 (4) pp. 530-533. Peer-reviewed.
 
Rekurrente ELOVL4 Genmutation verursacht dominante Stargardt-Krankheit in einer Schweizer Familie [Swiss Family with Dominant Stargardt Disease Caused by a Recurrent Mutation in the ELOVL4 Gene]
Tran H.V., Moret E., Vaclavik V., Marcelli F., Abitbol M.M., Munier F.L., Schorderet D.F., 2016/04. Klinische Monatsblatter fur Augenheilkunde, 233 (4) pp. 475-477. Peer-reviewed.
 
Corrélations phénotype-génotype de la rétinopathie pigmentaire non syndromique : à propos de dix familles tunisiennes [Genotype-phenotype correlation in ten Tunisian families with non-syndromic retinitis pigmentosa]
Chebil A., Falfoul Y., Habibi I., Munier F., Schorderet D., El Matri L., 2016/03. Journal francais d'ophtalmologie, 39 (3) pp. 277-286. Peer-reviewed.
Congenital Nystagmus Gene FRMD7 Is Necessary for Establishing a Neuronal Circuit Asymmetry for Direction Selectivity.
Yonehara K., Fiscella M., Drinnenberg A., Esposti F., Trenholm S., Krol J., Franke F., Scherf B.G., Kusnyerik A., Müller J. et al., 2016/01. Neuron, 89 (1) pp. 177-193. Peer-reviewed.
 
Potential blindness in children of patients with hereditary bone disease.
Kheir V., Munier F.L., Aubry-Rozier B., Schorderet D.F., 2016. Osteoporosis International : A Journal Established As Result of Cooperation Between the European Foundation For Osteoporosis and the National Osteoporosis Foundation of the Usa, 27 (2) pp. 841-844. Peer-reviewed.
Presence of a Triple Concentric Autofluorescence Ring in NR2E3-p.G56R-Linked Autosomal Dominant Retinitis Pigmentosa (ADRP).
Escher P., Vaclavik V., Munier F.L., Tran H.V., 2016. Investigative Ophthalmology and Visual Science, 57 (4) pp. 2001-2002. Peer-reviewed.
 
Reply.
Francis J.H., Abramson D.H., Gaillard M.C., Marr B.P., Beck-Popovic M., Munier F.L., 2016. Ophthalmology, 123 (2) pp. e10-e11. Peer-reviewed.
Compound Heterozygous VSX2 Mutation Causing Bilateral Anophthalmia in a Consanguineous Egyptian Family
Jakobsson Cecilia, Youssef Mohamed A, Marzouk Iman, ElShakankiri Nihal, Nader Bayoumi, Munier Francis L., Schorderet Daniel F, Abouzeid Hana, 2015/05. Journal of Clinical & Experimental Ophthalmology, 6 (3) p. 441. Peer-reviewed.
 
Hamartome combiné de la rétine et de l'épithélium pigmentaire
C. Stathopoulos , F.L. Munier , 2015/03. Images en Ophtalmologie, 9 (2) pp. 82-83. Peer-reviewed.
 
Ostéome choroïdien unilatéral chez un enfant de 2 ans
Y. Falfoul , M.C. Gaillard , P. Maeder , C. Stathopoulos , F.L. Munier , 2015/02. Images en Ophtalmologie, 9 (1) pp. 19-21. Peer-reviewed.
 
Rétinome révélé par des myodésopsies
C. M. GAILLARD , B. Fleisch , F. Munier , A. Schalenbourg , 2015/02. Images en Ophtalmologie, 9 (1) pp. 24-25.
 
Automatic Segmentation of the Eye in 3D Magnetic Resonance Imaging: A Novel Statistical Shape Model for Treatment Planning of Retinoblastoma.
Ciller C., De Zanet S.I., Rüegsegger M.B., Pica A., Sznitman R., Thiran J.P., Maeder P., Munier F.L., Kowal J.H., Cuadra M.B., 2015. International Journal of Radiation Oncology, Biology, Physics, 92 (4) pp. 794-802. Peer-reviewed.
 
Differential Dimerization of Variants Linked to Enhanced S-Cone Sensitivity Syndrome (ESCS) Located in the NR2E3 Ligand-Binding Domain.
von Alpen D., Tran H.V., Guex N., Venturini G., Munier F.L., Schorderet D.F., Haider N.B., Escher P., 2015. Human Mutation, 36 (6) pp. 599-610.
 
IC3D classification of corneal dystrophies--edition 2.
Weiss J.S., Møller H.U., Aldave A.J., Seitz B., Bredrup C., Kivelä T., Munier F.L., Rapuano C.J., Nischal K.K., Kim E.K. et al., 2015. Cornea, 34 (2) pp. 117-159. Peer-reviewed.
 
Intravitreal injections in oncology
Konstantinidis L., Munier F., Damato B., 2015. pp. 831-837 dans Ichhpujani P., Spaeth G.L., Yanoff M. (eds.) Expert Techniques in Ophthalmic Surgery chap. 99, Jaypee.
 
Landmark detection for fusion of fundus and MRI toward a patient-specific multimodal eye model.
De Zanet S.I., Ciller C., Rudolph T., Maeder P., Munier F., Balmer A., Cuadra M.B., Kowal J.H., 2015. Ieee Transactions on Bio-medical Engineering, 62 (2) pp. 532-540. Peer-reviewed.
 
Molecular Analysis of NOTCH2 in Patients with Primary Open-Angle Glaucoma.
Jakobsson C., Kheir V., Munier F.L., Schorderet D.F., 2015. Klinische Monatsblätter Für Augenheilkunde, 232 (4) pp. 427-431. Peer-reviewed.
 
NBAS mutations cause a multisystem disorder involving bone, connective tissue, liver, immune system, and retina.
Segarra N.G., Ballhausen D., Crawford H., Perreau M., Campos-Xavier B., van Spaendonck-Zwarts K., Vermeer C., Russo M., Zambelli P.Y., Stevenson B. et al., 2015. American Journal of Medical Genetics. Part A, 167A (12) pp. 2902-2912. Peer-reviewed.
 
Retinoblastoma
Dimaras H., Corson T.W., Cobrinik D., White A., Zhao J., Munier F.L., Abramson D.H., Shields C.L., Chantada G.L., Njuguna F. et al., 2015. Nature Reviews. Disease Primers, 1 p. 15021. Peer-reviewed.
 
The Classification of Vitreous Seeds in Retinoblastoma and Response to Intravitreal Melphalan.
Francis J.H., Abramson D.H., Gaillard M.C., Marr B.P., Beck-Popovic M., Munier F.L., 2015. Ophthalmology, 122 (6) pp. 1173-1179. Peer-reviewed.
 
Treatment of Retinoblastoma in 2015: Agreement and Disagreement.
Abramson D.H., Shields C.L., Munier F.L., Chantada G.L., 2015. Jama Ophthalmology, 133 (11) pp. 1341-1347. Peer-reviewed.
 
Ranibizumab in the management of advanced Coats disease Stages 3B and 4: long-term outcomes.
Gaillard M.C., Mataftsi A., Balmer A., Houghton S., Munier F.L., 2014/11. Retina, 34 (11) pp. 2275-2281. Peer-reviewed.
Treatment of Recurrent or Progressive Intraocular Retinoblastoma: Preliminary Results of A National Phase Ii Study of The Swiss Pediatric Oncology Group
Beck Popovic M, Binaghi S, Gaillard MC, Diezi M, Garcia E, Houghton S, Galley MT, Cornu M, Pampallona S, Munier F, 2014/10. pp. S 135 dans 46th Congress of the International Society of Paediatric Oncology, Pediatric Blood & Cancer.
Active Shape Modeling techniques in Ophthalmology: Automatic Segmentation of the eye in magnetic resonance imaging of children
Ciller C., De Zanet S. I., Pica A., Thiran J.P., Maeder P., Munier F.L., Kowal J. H., Bach Cuadra M., 2014/06., Swiss Institute for Computer Assisted Surgery dans 1st Symposium on Statistical Shape Models and Applications, Delémont, Switzerland. Peer-reviewed.
 
Automatic magnetic resonance imaging segmentation of the eye based on 3D active shape modeling
Ciller C., De Zanet S. I., Pica A., Thiran J.P., Maeder P., Munier F.L., Kowal J. H., Bach Cuadra M., 2014/05. dans Annual Meeting of the Association for Research in Vision and Ophtalmology.
Classification and management of seeds in retinoblastoma. Ellsworth Lecture Ghent August 24th 2013.
Munier F.L., 2014. Ophthalmic Genetics, 35 (4) pp. 193-207.
 
Complement Factor B Polymorphism and the Phenotype of Early Age-related Macular Degeneration.
Mantel I., Ambresin A., Moetteli L., Droz I., Roduit R., Munier F.L., Schorderet D.F., 2014. Ophthalmic Genetics, 35 (1) pp. 12-17. Peer-reviewed.
Enrichment of pathogenic alleles in the brittle cornea gene, ZNF469, in keratoconus.
Lechner J., Porter L.F., Rice A., Vitart V., Armstrong D.J., Schorderet D.F., Munier F.L., Wright A.F., Inglehearn C.F., Black G.C. et al., 2014. Human Molecular Genetics, 23 (20) pp. 5527-35. Peer-reviewed.
 
Mutations in ALDH1A3 represent a frequent cause of microphthalmia/anophthalmia in consanguineous families.
Abouzeid H., Favez T., Schmid A., Agosti C., Youssef M., Marzouk I., El Shakankiry N., Bayoumi N., Munier F.L., Schorderet D.F., 2014. Human Mutation, 35 (8) pp. 949-953. Peer-reviewed.
 
Zapfen-Stäbchen-Dystrophie durch eine neue reinerbige RPE65-Mutation in Leberscher kongenitaler Amaurose Cone-Rod Dystrophy Caused by a Novel Homozygous RPE65 Mutation in Leber Congenital Amaurosis.
Jakobsson C., Othman I.S., Munier F.L., Schorderet D.F., Abouzeid H., 2014. Klinische Monatsblatter Fur Augenheilkunde, 231 (4) pp. 405-410. Peer-reviewed.
A novel homozygous R764H mutation in crumbs homolog 1 causes autosomal recessive retinitis pigmentosa.
Tiab L., Largueche L., Chouchane I., Derouiche K., Munier F.L., El Matri L., Schorderet D.F., 2013. Molecular Vision, 19 pp. 829-834. Peer-reviewed.
 
Anterior uveitis and cataract after rubella vaccination: a case report of a 12-month-old girl.
Ferrini W., Aubert V., Balmer A., Munier F.L., Abouzeid H., 2013. Pediatrics, 132 (4) pp. e1035-e1038. Peer-reviewed.
Brittle cornea syndrome: recognition, molecular diagnosis and management.
Burkitt Wright E.M., Porter L.F., Spencer H.L., Clayton-Smith J., Au L., Munier F.L., Smithson S., Suri M., Rohrbach M., Manson F.D. et al., 2013. Orphanet Journal of Rare Diseases, 8 p. 68. Peer-reviewed.
 
Intra-arterial ophthalmic artery chemotherapy for group D retinoblastoma in children: 4-years Lausanne experience
Binaghi S., Zerlauth J.B., Beck Popovic M., Munier F., Meuli R., 2013. dans ECR 2013, European Congress of Radiology.
Intravitreal chemotherapy for vitreous seeding in retinoblastoma: Recent advances and perspectives.
Munier F.L., Gaillard M.C., Balmer A., Beck-Popovic M., 2013. Saudi Journal of Ophthalmology : Official Journal of the Saudi Ophthalmological Society, 27 (3) pp. 147-150. Peer-reviewed.
 
New-Generation Multifocal Intraocular Lens for Pediatric Cataract.
Abouzeid H., Moetteli L., Munier F., 2013. Ophthalmologica. Journal International D'ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde, 230 (2) pp. 100-107. Peer-reviewed.
 
Novel maculopathy in patients with spinocerebellar ataxia type 1 autofluorescence findings and functional characteristics.
Vaclavik V., Borruat F.X., Ambresin A., Munier F.L., 2013. Jama Ophthalmology, 131 (4) pp. 536-538. Peer-reviewed.
 
Persistence of retinal function after intravitreal melphalan injection for retinoblastoma.
Brodie S.E., Munier F.L., Francis J.H., Marr B., Gobin Y.P., Abramson D.H., 2013. Documenta Ophthalmologica. Advances in Ophthalmology, 126 (1) pp. 79-84. Peer-reviewed.
 
Post-chemoreduction cryptic optic nerve relapse in a patient with bilateral retinoblastoma.
Shetye N.G., Mataftsi A., Maeder P., Moulin A.P., Gaillard M.C., Balmer A., Popovic M.B., Munier F.L., 2013. British Journal of Ophthalmology, 97 (2) pp. 233-246. Peer-reviewed.
 
The Bcl-2/Bcl-XL inhibitor ABT-737 promotes death of retinoblastoma cancer cells.
Allaman-Pillet N., Oberson A., Munier F., Schorderet D.F., 2013. Ophthalmic Genetics, 34 (1-2) pp. 1-13.
The cataract and glucosuria associated monocarboxylate transporter MCT12 is a new creatine transporter.
Abplanalp J., Laczko E., Philp N.J., Neidhardt J., Zuercher J., Braun P., Schorderet D.F., Munier F.L., Verrey F., Berger W. et al., 2013. Human Molecular Genetics, 22 (16) pp. 3218-3226. Peer-reviewed.
 
Efficacy of intra-arterial ophtalmic artery chemotherapy for retinoblastoma in children: 3-years Lausanne experience
Binaghi S., Zerlauth J. B., Mosimann P., Beck Popovic M., Munier F., 2012/05. dans SSR 2012, 99th Annual Meeting of the Swiss Society of Radiology.
 
Ultrasound biomicroscopy evaluation of anterior extension in retinoblastoma: a clinicopathological study.
Moulin A.P., Gaillard M.C., Balmer A., Munier F.L., 2012/03. The British journal of ophthalmology, 96 (3) pp. 337-340. Peer-reviewed.
 
. Phenotype/genotype correlation associated with a novel nonsense Glu20stop mutation in the Rp2 gene in a three-generation family with x-linked retinitis pigmentosa
Vaclavik V., Munier F.L., Tran V.H., Schorderet D.F., 2012., Association for Research in Vision and Ophthalmology dans ARVO E-Abstract 4547/A314. Peer-reviewed.
 
13q deletion syndrome and retinoblastoma in identical dichorionic diamniotic monozygotic twins.
De Francesco S., Galluzzi P., Del Longo A., Piozzi E., Renieri A., Menicacci C., Mari F., Munier F., Hadjistilianou T., Mastrangelo D., 2012. European Journal of Ophthalmology, 22 (5) pp. 857-860. Peer-reviewed.
 
Chiasmatic infiltration secondary to late malignant transformation of retinoma.
Mataftsi A., Zografos L., Balmer A., Uffer S., Stupp R., Janzer R.C., Pica A., Schorderet D.F., Munier F.L., 2012. Ophthalmic Genetics, 33 (3) pp. 155-158. Peer-reviewed.
 
Criteria defining the duration of chemoreduction with focal treatment in retinoblastoma: a long-term update
Popovic Maja Beck, Abouzeid Hana, Gaillard Marie-Claire, Faouzi Mohamed, Pica Alessia, Balmer Aubin, Munier Francis, 2012. p. 985 dans 44th Congress of the International Society of Paediatric Oncology (SIOP) 2012, Pediatric Blood & Cancer.
Double Concentric Autofluorescence Ring in NR2E3-p.G56R-linked Autosomal Dominant Retinitis Pigmentosa.
Escher P., Tran H.V., Vaclavik V., Borruat F.X., Schorderet D.F., Munier F.L., 2012. Investigative Ophthalmology and Visual Science, 53 (8) pp. 4754-4764. Peer-reviewed.
 
Epithelial ingrowth cells after LASIK/ALTK (automated lamellar therapeutic keratoplasty): are they corneal epithelial stem cells?
Nicolas M., Abouzeid H., Deprez M., Hafezi F., Munier F.L., Varga Z., Majo F., 2012. British Journal of Ophthalmology, 96 (7) pp. 1043-1046. Peer-reviewed.
 
Franceschetti hereditary recurrent corneal erosion.
Lisch W., Bron A.J., Munier F.L., Schorderet D.F., Tiab L., Lange C., Saikia P., Reinhard T., Weiss J.S., Gundlach E. et al., 2012. American Journal of Ophthalmology, 153 (6) pp. 1073-81.e4. Peer-reviewed.
 
Intravitreal chemotherapy for vitreous disease in retinoblastoma revisited: from prohibition to conditional indications.
Munier F.L., Gaillard M.C., Balmer A., Soliman S., Podilsky G., Moulin A.P., Beck-Popovic M., 2012. British Journal of Ophthalmology, 96 (8) pp. 1078-1083. Peer-reviewed.
 
Les nouvelles chimiothérapies dans le rétinoblastome
Gaillard M., Balmer A., Houghton S., Munier F., 2012., Société Suisse d'Ophtalmologie pp. S67 dans Ophta.
 
Newer radiation therapy methods
Pica A., Munier F.L., 2012. pp. 150-157 dans Ramasubramanian A., Shields C.L. (eds.) Retinoblastoma, Jaypee Brothers Medical Publishers.
 
Para-arterial sparing phenotype in Leber congenital amaurosis associated with homozygous p.R108X SPATA-7 mutation
Kuonen A., Tran H.V., Vaclavik V., Schorderet D.F., Munier F.L., 2012., Association for Research in Vision and Ophthalmology dans ARVO E-Abstract 4590/D1077. Peer-reviewed.
 
Pattern dystrophy with high intrafamilial variability associated with Y141C mutation in the peripherin/RDS gene and successful treatment of subfoveal CNV related to multifocal pattern type with anti-VEGF (ranibizumab) intravitreal injections.
Vaclavik V., Tran H.V., Gaillard M.C., Schorderet D.F., Munier F.L., 2012. Retina, 32 (9) pp. 1942-1949. Peer-reviewed.
 
Phenotypic variability of retinocytomas: preregression and postregression growth patterns.
Abouzeid H., Balmer A., Moulin A.P., Mataftsi A., Zografos L., Munier F.L., 2012. British Journal of Ophthalmology, 96 (6) pp. 884-889. Peer-reviewed.
 
Profiling safety of intravitreal injections for retinoblastoma using an anti-reflux procedure and sterilisation of the needle track.
Munier F.L., Soliman S., Moulin A.P., Gaillard M.C., Balmer A., Beck-Popovic M., 2012. British Journal of Ophthalmology, 96 (8) pp. 1084-1087. Peer-reviewed.
 
Pupillometric quantification of residual rod and cone activity in leber congenital amaurosis.
Kawasaki A., Munier F.L., Leon L., Kardon R.H., 2012. Archives of Ophthalmology, 130 (6) pp. 798-800. Peer-reviewed.
 
Risk assessment of recurrence in sporadic retinoblastoma using a molecular-based algorithm.
Tran H.V., Schorderet D.F., Gaillard M.C., Balmer A., Munier F.L., 2012. Ophthalmic Genetics, 33 (1) pp. 6-11. Peer-reviewed.
 
Rétinopathie proliférative iatrogène dans le rétinoblastome (Rb) : effet du ranibizumab
Gaillard M., Balmer A., Houghton S., Munier F., 2012., Société Suisse d'Ophtalmologie pp. S90 dans Ophta.
 
The characterization of retinal phenotype in a family with C1QTNF5-related late-onset retinal degeneration.
Vincent A., Munier F.L., Vandenhoven C.C., Wright T., Westall C.A., Héon E., 2012. Retina, 32 (8) pp. 1643-1651. Peer-reviewed.
 
The transcription factor c-Maf controls touch receptor development and function.
Wende H., Lechner S.G., Cheret C., Bourane S., Kolanczyk M.E., Pattyn A., Reuter K., Munier F.L., Carroll P., Lewin G.R. et al., 2012. Science (new York, N.y.), 335 (6074) pp. 1373-1376. Peer-reviewed.
Trilateral retinoblastoma: neuroimaging characteristics and value of routine brain screening on admission.
Rodjan F., de Graaf P., Brisse H.J., Göricke S., Maeder P., Galluzzi P., Aerts I., Alapetite C., Desjardins L., Wieland R. et al., 2012. Journal of Neuro-Oncology, 109 (3) pp. 535-544.
 
Uvéite antérieure et cataracte chez une enfant de 12 mois après vaccination pour la rubéole
Ferrini W., Aubert V., Balmer A., Munier F., Abou Zeid H., 2012., Société Suisse d'Ophtalmologie pp. S107 dans Ophta.
 
Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness.
Audo I., Bujakowska K., Orhan E., Poloschek C.M., Defoort-Dhellemmes S., Drumare I., Kohl S., Luu T.D., Lecompte O., Zrenner E. et al., 2012. American Journal of Human Genetics, 90 (2) pp. 321-330. Peer-reviewed.
 
(reply) An occlusive or toxic mechanism affecting the vascular bed of short posterior ciliary arteries possibly underlies the sectoral choroidal atrophy after superselective ophtalmic artery chemotherapy
Munier Francis, Beck-Popovic Maja, Balmer Aubin, Binaghi Stefano, Bovey Etienne, 2011/09/01. Retina, 31 (8) pp. 1747-1748. Peer-reviewed.
 
Nursing management during intra-aterial therapy in children with retinoblastoma
Bergeron Marie-Paule, Binaghi Stefano, Beck-Popovic Maja, Munier Francis L., Ruchat Gillian, 2011/04. International Journal of Ophthalmic Practice, 2 (2) pp. 71-74. Peer-reviewed.
 
Occurrence of sectoral choroidal occlusive vasculopathy and retinal arteriolar embolization after superselective ophthalmic artery chemotherapy for advanced intraocular retinoblastoma.
Munier F.L., Beck-Popovic M., Balmer A., Gaillard M.C., Bovey E., Binaghi S., 2011/03. Retina, 31 (3) pp. 566-573. Peer-reviewed.
 
3D Ultrasound Tumor Segmentation and Fusion with CT for Stereotactic Radiation Therapy Planning of Retinoblastoma
Pica A., Karahanoglu Fikret I., Ciurte A.R., Gorthi S., Balmer A., Munier F., Thiran J.P., Bach Cuadra M., 2011. dans ISRS 2011, 10th Biennial Congress and Exhibition of the International Stereotactic Radio Surgery Society.
 
500 cas de rétinoblastome : les signes d'appel
Balmer A., Gaillard M., Houghton S., Munier F., 2011., Société Suisse d'Ophtalmologie pp. S80 dans Ophta.
 
A Novel Homozygous R764H Mutation in CRB1 Causes Autosomal Recessive Retinitis Pigmentosa in a Consanguineous Family
Bouayed-Tiab L., Largueche L., Chouchane I., Derouiche K., Bajrami H., Favre I., Munier F.L., El Matri L., Schorderet D.F., 2011., Association for Research in Vision and Ophthalmology dans ARVO E-Abstract 2374/D637. Peer-reviewed.
 
An Efficient Segmentation Method for Ultrasound Images based on a Semi-supervised Approach and Patch-based Features
Ciurte A.R., Houhou N., Nedevschi S., Pica A., Munier F., Thiran J.P., Bresson X., Bach Cuadra M., 2011. pp. 969-972 dans Proceedings of the 8th IEEE International Symposium on Biomedical Imaging: From Nano to Macro, ISBI 2011, Biomedical Imaging.
 
Autofluorescence Findings Of A Novel Maculopathy In Patient With Spinocerebellar Ataxia Type 1 And Of A Cone - Rod Type Retinal Dysfunction In Three Generation Family With Spinocerebellar Ataxia Type 7
Vaclavik V., Munier F.L., Schorderet D.F., Borruat F.X., 2011., Association for Research in Vision and Ophthalmology dans ARVO E-Abstract 2993/D1087. Peer-reviewed.
 
Autofluorescence Study In NR2E3 p.G56R-linked Autosomal Dominant Retinitis Pigmentosa In A Single Kindred
Tran H.V., Escher P., Vaclavik V., Favre I., Bajrami H., Borruat F.X., Schorderet D.F., Munier F.L., 2011., Association for Research in Vision and Ophthalmology dans ARVO E-Abstract 6604. Peer-reviewed.
 
Autosomal Recessive Posterior Microphthalmos/Nanophthalmos is Caused by Loss-of-function Mutations in LOC646960, a Novel Gene Encoding a Trypsin-like Serine Protease
Gal A., Rau I., El Matri L., Kreienkamp H.J., Munier F., Fuchs J., Fledelius H.C., Vilhelmsen K., Thompson D.A., Rosenberg T., 2011., Association for Research in Vision and Ophthalmology dans ARVO E-Abstract 1638. Peer-reviewed.
 
Autosomal-Recessive Posterior Microphthalmos Is Caused by Mutations in PRSS56, a Gene Encoding a Trypsin-Like Serine Protease.
Gal A., Rau I., El Matri L., Kreienkamp H.J., Fehr S., Baklouti K., Chouchane I., Li Y., Rehbein M., Fuchs J. et al., 2011. American Journal of Human Genetics, 88 (3) pp. 382-390.
 
BBS genotype-phenotype assessment of a multiethnic patient cohort calls for a revision of the disease definition.
Deveault C., Billingsley G., Duncan J.L., Bin J., Theal R., Vincent A., Fieggen K.J., Gerth C., Noordeh N., Traboulsi E.I. et al., 2011. Human Mutation, 32 (6) pp. 610-619. Peer-reviewed.
 
Chimiothérapie intra-artérielle super-sélective dans l'artère ophtalmique en cas de rétinoblastome avancé chez l'enfant.
Binaghi M., Mosimann P., Beck Popovic M., Munier F., 2011. dans JFR 2011, 59e Journées Françaises de Radiologie, 32e Journées Francophones de Radiologie. Peer-reviewed.
 
Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in GNAT2 gene.
Ouechtati F., Merdassi A., Bouyacoub Y., Largueche L., Derouiche K., Ouragini H., Nouira S., Tiab L., Baklouti K., Rebai A. et al., 2011. Journal of Human Genetics, 56 (1) pp. 22-28. Peer-reviewed.
 
Famille suisse de trois générations avec un diagnostic phénotypique de North Carolina Macular Dystrophy
Vaclavik V., Tran V., Nessi F., Munier F., 2011., Société Suisse d'Ophtalmologie pp. S79 dans Ophta.
 
IC3D-Klassifikation von Hornhautdystrophien
Weiss J.S., Møller H.U., Lisch W., Kinoshita S., Aldave A.J., Belin M.W., Kivelä T., Busin M., Munier F.L., Seitz B. et al., 2011. Klinische Monatsblätter Für Augenheilkunde, 228 Suppl 1 pp. S1-39. Peer-reviewed.
 
Insertion zonulaire antérieure longue dans la dégénérescence rétinienne et maculaire tardive due au gène C1QTNF5
Tran H., Vaclavik V., Favre I., Schorderet D., Munier F., 2011., Société Suisse d'Ophtalmologie pp. S84 dans Ophta.
 
Iridectomie sectorielle dans les kystes stromaux pédiatriques : une étude pilote
Sabani I., Tran H., Balmer A., Vaudaux J., Majo F., Wolfensberger T., Munier F., 2011., Société Suisse d'Ophtalmologie pp. S64 dans Ophta.
 
Le syndrome d'anophtalmie de Waardenburg : une étude clinique
Abouzeid H., Youssef M., Marzouk I., El Shakankiry N., Bayoumy N., Munier F., Schorderet D., 2011., Société Suisse d'Ophtalmologie pp. S78 dans Ophta.
 
Model-based Segmentation and Fusion of 3D Computed Tomography and 3D Ultrasound of the Eye for Radiotherapy Planning
Bach Cuadra Meritxell, Gorthi Subrahmanyam, Karahanoglu Fikret Isik, Paquier Benoît, Pica Alessia, Do Huu Phuoc, Balmer Aubain, Munier Francis, Thiran Jean-Philippe, 2011. pp. 247-263 dans Tavares João Manuel R. S., Jorge R. M. Natal (eds.) Computational Vision and Medical Image Processing, Springer Netherlands.
 
Modern cataract surgery for radiation-induced cataracts in retinoblastoma.
Osman I.M., Abouzeid H., Balmer A., Gaillard M.C., Othenin-Girard P., Pica A., Moeckli R., Schorderet D.F., Munier F.L., 2011. British Journal of Ophthalmology, 95 (2) pp. 227-230. Peer-reviewed.
 
Mutations in the SPARC-Related Modular Calcium-Binding Protein 1 Gene, SMOC1, Cause Waardenburg Anophthalmia Syndrome.
Abouzeid H., Boisset G., Favez T., Youssef M., Marzouk I., Shakankiry N., Bayoumi N., Descombes P., Agosti C., Munier F.L. et al., 2011. American Journal of Human Genetics, 88 (1) pp. 92-98. Peer-reviewed.
 
Novel Cone Transducin Alpha Subunit Mutation In Tunisian Patients And Genotype-phenotype Correlation In Complete Achromatopsia
Ouechtati F., Merdassi A., Bouyacoub Y., Largueche L., Tiab L., Schorderet D.F., Munier F.L., Zografos L., Abdelhak S., El Matri L., 2011., Association for Research in Vision and Ophthalmology dans ARVO E-Abstract 2376/D639. Peer-reviewed.
 
Phenotype in Two Consanguineous Tunisian Families With non Syndromic Autosomic Recessive Retinitis Pigmentosa Caused by an USH2A Mutation
Chebil A., Largueche L., Kort F., Bouraoui R., Derouiche K., Favre I., Bajrami H., Munier F.L., Schorderet D.F., El Matri L., 2011., Association for Research in Vision and Ophthalmology dans ARVO E-Abstract 2395/D658. Peer-reviewed.
 
Phenotype of two Consanguineous Autosomic Recessive Retinitis Pigmentosa Families Caused by PDE6A and PDE6B Mutations
Largueche L., Baklouti K., Merdassi A., Chouchane I., Bouladi M., Favre I., Bajrami H., Schorderet D.F., Munier F.L., El Matri L., 2011., Association for Research in Vision and Ophthalmology dans ARVO E-Abstract 2372/D635. Peer-reviewed.
 
Preliminary Experience in Treatment of Papillary and Macular Retinoblastoma: Evaluation of Local Control and Local Complications After Treatment with Linear Accelerator-Based Stereotactic Radiotherapy with Micromultileaf Collimator as Second-Line or Salvage Treatment after chemotherapy.
Pica A., Moeckli R., Balmer A., Beck-Popovic M., Chollet-Rivier M., Do H.P., Weber D.C., Munier F.L., 2011. International Journal of Radiation Oncology, Biology, Physics, 81 (5) pp. 1380-1386. Peer-reviewed.
 
Présence concomitante d'un rétinoblastome et d'un morning glory syndrome : présentation de cas et revue de la littérature
Moetteli L., Tran H., Balmer A., Bovey E., Munier F., 2011., Société Suisse d'Ophtalmologie pp. S93 dans Ophta.
 
Retinal Dystrophy In The Oculo-auricular Syndrome Due to HMX1 Mutation.
Vaclavik V., Schorderet D.F., Borruat F.X., Munier F.L., 2011. Ophthalmic Genetics, 32 (2) pp. 114-117. Peer-reviewed.
 
Suivi à long terme d'un rétinoblastome trilatéral avec dissémination méningée
Finger M., Balmer A., Munier F., Gaillard M., Pica A., Beck-Popovic M., 2011., Société Suisse d'Ophtalmologie pp. S96 dans Ophta.
 
Traitement de l'amblyopie dans le rétinoblastome unilatéral
Gaillard M.C., Maillard A., Houghton S., Balmer A., Klainguti G., Munier F., 2011., Société Suisse d'Ophtalmologie pp. S83 dans Ophta.
 
(106)Ruthenium brachytherapy for ciliary recurrence with supraciliary effusion in retinoblastoma.
Chhablani J., Romanzo A., Balmer A., Pica A., Gaillard M.C., Cozza R., Moeckli R., Munier F.L., 2010. Ophthalmic Genetics, 31 (4) pp. 190-192. Peer-reviewed.
 
A Novel Homozygous RPE65 Mutation in Leber Congenital Amaurosis Associated With Cone-Rod Dystrophy
Abouzeid H., Othman I.S., Sabry S., Favre I., Herkenne C., Schorderet D.F., Munier F.L., 2010., ARVO E-Abstract 3083/A278 dans Investigative Ophthalmology and Visual Science. Peer-reviewed.
 
Alterations of the 5'untranslated region of SLC16A12 lead to age-related cataract.
Zuercher J., Neidhardt J., Magyar I., Labs S., Moore A.T., Tanner F.C., Waseem N., Schorderet D.F., Munier F.L., Bhattacharya S. et al., 2010. Investigative Ophthalmology and Visual Science, 51 (7) pp. 3354-3361. Peer-reviewed.
 
Amaurose congénitale de Leber (LCA) associée à une lesion unilatérale de Coat's-like chez un enfant de 4 ans
Vaclavik V., Gaillard M., Balmer A., Munier F., 2010., Société Suisse d'Ophtalmologie pp. S88 dans Ophta.
 
Anomalie de Peters bilatérale et glaucome congénital
Tschuor P., Kaeser P., Cachat F., Schorderet D., Mermoud A., Sharkawi E., Munier F., 2010., Société Suisse d'Ophtalmologie pp. S108 dans Ophta.
 
Cas sporadique et familial du syndrome héréditaire d'hyperferritinémie et cataracte (SHHC) à transmission autosomique dominante
Ferrini W., Hamel M., Munier F., 2010., Société Suisse d'Ophtalmologie pp. S114 dans Ophta.
 
Choristome cornéen dans la trisomie 8 en mosaïque : aspect clinique, histologique, génétique et thérapeutique
Gaillard M., Majo F., Moulin A., Martinet D., Niel Bütschi F., Uffer S., Munier F., 2010., Société Suisse d'Ophtalmologie pp. S101 dans Ophta.
 
Cloudy corneas at birth: a case of bilateral Peters anomaly
Rezbach P., Kaiser P., Tschuor P., Addor M.C., Schorderet D., Cachat F., Munier F., 2010. pp. 16S dans Joint Annual Meeting of the Swiss Society for Pediatrics and the Swiss Society of Pediatric Pneumology, Swiss Medical Weekly.
 
Corneal Opacities in Trisomy 8 Mosaic Syndrome : Clinical, Histologic and Genetic Features
Gaillard M.C., Majo F., Moulin A., Uffer S., Marinet D., Niel Bütschi F., Munier f.l.., 2010., ARVO E-Abstract 4654/D849 dans Investigative Ophthalmology and Visual Science. Peer-reviewed.
 
Late Onset Cystoid Macular Oedema Following Surgery for Radiation Induced Cataract in Patient With Retinoblastoma
Tran H.V., Gaillard M.C., Balmer A., Munier F.L., 2010., ARVO E-Abstract 2076/A16 dans Investigative Ophthalmology and Visual Science. Peer-reviewed.
 
Leuco-encéphalopathie avec micro-angiopathie, calcifications et kystes (CRMCC) imitant une rétinopathie de la prématurité (ROP)
Tran H., Gaillard M., Wolfensberger T., Balmer A., Osterheid C., Schorderet F., Munier F., 2010., Société Suisse d'Ophtalmologie pp. S114 dans Ophta.
 
Novel Homozygous Rax Gene Mutation in Patients With Bilateral Anophthalmia
Schorderet D.F., Youssef M.A., Bayoumi N., ElShakankiri N., Marzouk E., Hauser P., Favez T., Munier F.L., Abouzeid H., 2010., ARVO E-Abstract 704/D807 dans Investigative Ophthalmology and Visual Science. Peer-reviewed.
 
Point Mutations in the Monocarboxylate Transporter SLC16A12 Lead to Juvenile and Age-Related Cataract
Kloeckener-Gruissem B, Zuercher J., Neidhardt J., Magyar I., Moore A.T., Bhattacharya S., Heon E., Munier F., Schorderet D.F., Berger W., 2010., ARVO-Abstract 4773 dans Investigative Ophthalmology and Visual Science. Peer-reviewed.
 
Retinoblastoma : diagnosis, treatment, and prognosis
Balmer A., Munier F., Zografos L., 2010. pp. 319-340 dans Hayat M.A. (eds.) Methods of Cancer Diagnosis, Therapy, and Prognosis chap. 22, Springer.
 
Successful treatment of trilateral retinoblastoma with conventional and high-dose chemotherapy plus radiotherapy: a case report.
De Ioris M.A., Fidani P., Munier F.L., Serra A., Ilari I., Popovic M.B., Natali G., Secco D.E., Cozza R., 2010. Journal of Pediatric Hematology/oncology, 32 (8) pp. e343-e345. Peer-reviewed.
The PROM1 mutation p.R373C causes an autosomal dominant bull's eye maculopathy associated with rod, rod-cone, and macular dystrophy.
Michaelides M., Gaillard M.C., Escher P., Tiab L., Bedell M., Borruat F.X., Barthelmes D., Carmona R., Zhang K., White E. et al., 2010. Investigative Ophthalmology and Visual Science, 51 (9) pp. 4771-4780. Peer-reviewed.
 
Three Generation Family With Pattern Dystrophy and a Successful Treatment of Subfoveal Cnv Related to Pattern Dystrophy With Anti-vegf Intravitreal Injections
Vaclavik V., Munier F.L., 2010., ARVO E-Abstract 3092/A287 dans Investigative Ophthalmology and Visual Science. Peer-reviewed.
 
Traitement par ranibizumab (Lucentis®) d'une rétinopathie actinique proliférative dans un cas de rétinoblastome
Gaillard M., Balmer A., Houghton S., Munier F., 2010., Société Suisse d'Ophtalmologie pp. S89 dans Ophta.
 
Ultrasound Biomicroscopy Evaluation of Anterior Extension of Retinoblastomas : A Clinico-Pathological Study
Moulin A.P., Gaillard M.C., Balmer A., Munier F.L., 2010., ARVO E-Abstract 2075/A15 dans Investigative Ophthalmology and Visual Science. Peer-reviewed.
 
Un cas d'hamartome combiné de la rétine et de l'épithélium pigmentaire avec décollement rétinien exsudatif
Richoz O., Salzmann J., Munier F., Pournaras C., de Haller R., 2010., Société Suisse d'Ophtalmologie pp. S92 dans Ophta.
Variable phenotypic expressivity in a Swiss family with autosomal dominant retinitis pigmentosa due to a T494M mutation in the PRPF3 gene.
Vaclavik V., Gaillard M.C., Tiab L., Schorderet D.F., Munier F.L., 2010. Molecular Vision, 16 pp. 467-475. Peer-reviewed.
 
TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness.
Audo I., Kohl S., Leroy B.P., Munier F.L., Guillonneau X., Mohand-Saïd S., Bujakowska K., Nandrot E.F., Lorenz B., Preising M. et al., 2009/11. American journal of human genetics, 85 (5) pp. 720-729. Peer-reviewed.
 
A new locus for congenital cataract, microcornea, microphthalmia, and atypical iris coloboma maps to chromosome 2.
Abouzeid H., Meire F.M., Osman I., ElShakankiri N., Bolay S., Munier F.L., Schorderet D.F., 2009/01. Ophthalmology, 116 (1) pp. 154-162.e1. Peer-reviewed.
 
Awareness of eye tumours in Down syndrome.
Munier F.L., Satgé D., 2009. British Journal of Ophthalmology, 93 (2) p. 276. Peer-reviewed.
 
Brachythérapie au Iode 125 (I125) comme alternative à l'énucléation ou radiothérapie externe dans le rétinoblastome papillaire
Gaillard M., Möckli R., Balmer A., Zografos L., Beck-Popovic M., Houghton S., Munier F., 2009., Société Suisse d'Ophtalmologie pp. S91 dans Ophta.
 
Brachythérapie comme alternative à l'énucléation chez les patients atteints de médulloépithéliomes du corps ciliaire
Moulin A., Moeckli R., Balmer A., Gaillard M., Munier F., 2009., Société Suisse d'Ophtalmologie pp. S90 dans Ophta.
 
Corrélation fonctionnelle des anomalies d'autofluorescence chez des patients atteints de divers[es] dystrophies rétiniennes
Vaclavik V., Gaillard M., Munier F., 2009., Société Suisse d'Ophtalmologie pp. S58 dans Ophta.
 
Genotyping microarray for CSNB-associated genes.
Zeitz C., Labs S., Lorenz B., Forster U., Uksti J., Kroes H.Y., De Baere E., Leroy B.P., Cremers F.P., Wittmer M. et al., 2009. Investigative Ophthalmology and Visual Science, 50 (12) pp. 5919-5926. Peer-reviewed.
Germline mutations in retinoma patients: relevance to low-penetrance and low-expressivity molecular basis.
Abouzeid H., Schorderet D.F., Balmer A., Munier F.L., 2009. Molecular Vision, 15 pp. 771-777.
 
Model-based Segmentation and Image Fusion of 3D Computed Tomography and 3D Ultrasound of the Eye for Radiotherapy Planning
Bach C.M.Gorthi Subrahmanyam , Karahanoglu F.I., Salvador F., Pica A., Do H.P., Balmer A., Munier F., Thiran J.P., 2009. dans VIPIMAGE 2011 - ECCOMAS 2nd Thematic Conference on Computational Vision and Medical Image Processing.
 
Model-based segmentation and image fusion of 3D computed tomography and 3D ultrasound of the eye for radiotherapy planning
Bach Cuadra M., Gorthi S., Karahanoglu F.I., Salvador F., Pica A., Do H.P., Balmer A, Munier F., Thiran J.P., 2009. pp. 1-6 dans Tavares J.M.R.S., Jorge R.M.N. (eds.) Computational vision and medical image processing, CRC Press.
 
Molecular classification of corneal dystrophies
Munier F.L., Schorderet D.F., 2009. pp. 44-61 dans Mohan R. (eds.) Cornea dystrophies & collagen crosslinking of cornea, All India Ophthalmological Society AIOS.
Mutations in CNNM4 cause recessive cone-rod dystrophy with amelogenesis imperfecta.
Polok B., Escher P., Ambresin A., Chouery E., Bolay S., Meunier I., Nan F., Hamel C., Munier F.L., Thilo B. et al., 2009. American journal of human genetics, 84 (2) pp. 259-65. Peer-reviewed.
Mutations in NR2E3 can cause dominant or recessive retinal degenerations in the same family.
Escher P., Gouras P., Roduit R., Tiab L., Bolay S., Delarive T., Chen S., Tsai C.C., Hayashi M., Zernant J. et al., 2009. Human Mutation, 30 (3) pp. 342-351. Peer-reviewed.
Ophtalmologie. Thérapie génique des rétinopathies héréditaires: premiers résultats [Gene therapy for hereditary eye diseases: where are we?]
Viet Tran H., Schorderet D.F., Kostic C., Munier F.L., Arsenijevic Y., 2009. Revue Médicale Suisse, 5 (186) pp. 118-123.
PAX6 aniridia and interhemispheric brain anomalies.
Abouzeid Hana, Youssef Mohamed A., El Shakankiri Nihal, Hauser Philippe, Munier Francis L., Schorderet Daniel F., 2009. Molecular Vision, 15 (222-224) pp. 2074-2083.
 
PAX6 mutations in Egyptian families with aniridia
Munier F.L., Abouzeid H., Youssef M.A., ElShakankiri N., Hauser P., Schorderet D.F., 2009., ARVO E-Abstract 4109 dans Investigative ophthalmology and visual science. Peer-reviewed.
 
Ranibizumab (Lucentis®) dans le traitement de la maladie de Coats
Gaillard M., Balmer A., Munier F., 2009., Société Suisse d'Ophtalmologie pp. S76 dans Ophta.
 
The metal ion binding protein Cnnm4 is mutated in rod-cone dystrophy/amelogenesis imperfecta syndrome
Schorderet D.F: , Polok B., Escher P., Favez T., Voirol N., Bolay S., Ambresin A., Hamel C., Mégarbane A., Munier F.L., 2009., ARVO E-Abstract 2324 dans Investigative ophthalmology and visual science. Peer-reviewed.
 
Unilateral macular oedema in Zermatt and Stargardt macular dystrophies.
Abouzeid H., Wolfensberger T.J., Schorderet D.F., Munier F.L., 2009. British journal of ophthalmology, 93 (10) pp. 1376-7, 1407-8. Peer-reviewed.
 
Variable phenotypic expressivity in a Swiss family with autosomal dominant retinitis pigmentosa due to mutation T494m in the Prpf3 gene
Vaclavik V., Gaillard M., Tiab L., Favre I., Schorderet D.F., Munier F.L., 2009., ARVO E-Abstract 4132 dans Investigative ophthalmology and visual science. Peer-reviewed.
 
Treatment outcome and histopathology of a case of total bilateral sclerocornea
Tryfinopoulou I., Majo F., 2008/05/06. dans Actes du 41ème Congrès panhellénique d’ophtalmologie.
 
(106)Ruthenium brachytherapy for retinoblastoma.
Abouzeid H., Moeckli R., Gaillard M.C., Beck-Popovic M., Pica A., Zografos L., Balmer A., Pampallona S., Munier F.L., 2008. International Journal of Radiation Oncology, Biology, Physics, 71 (3) pp. 821-8. Peer-reviewed.
 
Anomalie du développement de l'oeil et de l'oreille due à une mutation dans le gène NKX5-3/HMX1. Epilogue d'une histoire commencée il y a plus de 60 ans
Schorderet D., Munier F., 2008. Ophta 4 pp. 273-274. Peer-reviewed.
 
Classification of corneal dystrophies on a molecular genetic basis
Munier F.L., Schorderet D.F., 2008. pp. 83-100 dans Reinhard T., Larkin F. (eds.) Cornea and external eye disease, Springer.
 
Dégénérescences et dystrophies rétino-choroïdiennes
Pournaras J.A., Munier F.L., 2008. pp. 735-741 dans Pournaras C.J. (eds.) Pathologies vasculaires oculaires, Masson.
 
Expression and cell compartmentalization of EFEMP1, a protein associated with Malattia Leventinese
Kundzewicz A., Munier F., Matter J. M., 2008. Advances in Experimental Medicine and Biology, 613 pp. 277-281. Peer-reviewed.
 
Genotype-phenotype correlation of age-related macular degeneration: influence of complement factor H polymorphism.
Droz I., Mantel I., Ambresin A., Faouzi M., Schorderet D.F., Munier F.L., 2008. British Journal of Ophthalmology, 92 (4) pp. 513-517. Peer-reviewed.
 
Injection intravitréenne de Ranibizumab dans le traitement de la maladie de Coats avancée. A propos de 4 cas
Balmer A., Gaillard M.C., Munier F., 2008., Société Française d'Ophtalmologie pp. 1S157 dans J Fr Ophtalmol.
 
Macroanévrisme artériel de la rétine chez un enfant de 6 ans
Gaillard M., Zografos L., Munier F., 2008., Société Suisse d'Ophtalmologie pp. S106 dans Ophta.
 
Maladie de Coats
Balmer A., Munier F., Zografos L., 2008. pp. 692-698 dans Pournaras C.J. (eds.) Pathologies vasculaires oculaires, Masson.
 
Microscopie confocale et OCT dans la dystrophie crystalline de Bietti
Abouzeid H., Majo F., Munier F., 2008. Images en ophtalmologie, 2 pp. 129-130.
Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice.
Yang Z., Chen Y., Lillo C., Chien J., Yu Z., Michaelides M., Klein M., Howes K.A., Li Y., Kaminoh Y. et al., 2008. Journal of Clinical Investigation, 118 (8) pp. 2908-29016. Peer-reviewed.
 
Mutation in the human homeobox gene NKX5-3 causes an oculo-auricular syndrome.
Schorderet D.F., Nichini O., Boisset G., Polok B., Tiab L., Mayeur H., Raji B., de la Houssaye G., Abitbol M.M., Munier F.L., 2008. American Journal of Human Genetics, 82 (5) pp. 1178-1184. Peer-reviewed.
 
New developments in external beam radiotherapy for retinoblastoma: from lens to normal tissue-sparing techniques.
Munier F.L., Verwey J., Pica A., Balmer A., Zografos L., Abouzeid H., Timmerman B., Goitein G., Moeckli R., 2008. Clinical and Experimental Ophthalmology, 36 (1) pp. 78-89.
 
Nouvelles stratégies thérapeutiques en oncologie ophtalmo-pédiatrique [New strategies in pediatric ophthalmic oncology]
Balmer A., Munier F., Zografos L., 2008. Revue Médicale Suisse, 4 (140) pp. 139-143.
Overexpression of a mutant form of TGFBI/BIGH3 induces retinal degeneration in transgenic mice.
Bustamante M., Tasinato A., Maurer F., Elkochairi I., Lepore M.G., Arsenijevic Y., Pedrazzini T., Munier F.L., Schorderet D.F., 2008. Molecular Vision, 14 pp. 1129-1137. Peer-reviewed.
 
Prevalence of subfoveal nodules in Coat's disease
Tran H.V., Stathopoulos C., Balmer A., Abouzeid H., Zografos L., Schorderet D.F., Munier F.L., 2008., ARVO E-Abstract 2130 dans Investigative ophthalmology and visual science. Peer-reviewed.
 
Retinomas : a genotype-phenotype correlation : abstract E-3112
Abouzeid H., Balmer A., Schorderet D., Munier F.L., 2008. dans ARVO 2008 Annual Meeting, Eyes on innovation, Investigative Ophthalmology and Visual Science. Peer-reviewed.
The IC3D classification of the corneal dystrophies.
Weiss J.S., Møller H.U., Lisch W., Kinoshita S., Aldave A.J., Belin M.W., Kivelä T., Busin M., Munier F.L., Seitz B. et al., 2008. Cornea, 27 Suppl 2 pp. S1-83. Peer-reviewed.
 
Traitement, résultat clinique et histopathologique d'un cas de sclérocornée bilatérale
Tryfinopoulos I., Munier F., Uffer S., Zografos L., Konstantinidis L., Majo F., 2008., Société Suisse d'Ophtalmologie pp. S83 dans Ophta.
 
De novo mutation in the BIGH3/TGFB1 gene causing granular corneal dystrophy
Hilton E. N., Black G. C., Manson F. D., Schorderet D. F., Munier F. L., 2007/08. British Journal of Ophthalmology, 91 (8) pp. 1083-4.
 
Novel mutations in FRMD7 in X-linked congenital nystagmus. Mutation in brief #963. Online
Schorderet D. F., Tiab L., Gaillard M. C., Lorenz B., Klainguti G., Kerrison J. B., Traboulsi E. I., Munier F. L., 2007/05. Human Mutation, 28 (5) p. 525.
 
New VMD2 gene mutations identified in patients affected by Best vitelliform macular dystrophy
Marchant D., Yu K., Bigot K., Roche O., Germain A., Bonneau D., Drouin-Garraud V., Schorderet D. F., Munier F., Schmidt D. et al., 2007/03. Journal of Medical Genetics, 44 (3) pp. e70.
 
Retinopathy in Danon disease.
Schorderet D.F., Cottet S., Lobrinus J.A., Borruat F.X., Balmer A., Munier F.L., 2007/02. Archives of ophthalmology, 125 (2) pp. 231-6. Peer-reviewed.
Differential diagnosis of leukocoria and strabismus, first presenting signs of retinoblastoma.
Balmer A., Munier F., 2007. Clinical ophthalmology (Auckland, N.Z.), 1 (4) pp. 431-9. Peer-reviewed.
 
Novel TULP1 mutation causing leber congenital amaurosis or early onset retinal degeneration.
Mataftsi A., Schorderet D.F., Chachoua L., Boussalah M., Nouri M.T., Barthelmes D., Borruat F.X., Munier F.L., 2007. Investigative Ophthalmology & Visual Science, 48 (11) pp. 5160-5167. Peer-reviewed.
 
Patient with Fanconi Syndrome (FS) and retinitis pigmentosa (RP) caused by a deletion and duplication of mitochondrial DNA (mtDNA).
Pitchon E.M., Cachat F., Jacquemont S., Hinard C., Borruat F.X., Schorderet D.F., Morris M.A., Munier F.L., 2007. Klinische Monatsblätter für Augenheilkunde, 224 (4) pp. 340-343. Peer-reviewed.
Retinal stem cells transplanted into models of late stages of retinitis pigmentosa preferentially adopt a glial or a retinal ganglion cell fate
Canola K., Angenieux B., Tekaya M., Quiambao A., Naash M. I., Munier F. L., Schorderet D. F., Arsenijevic Y., 2007/01. Investigative Ophthalmology and Visual Science, 48 (1) pp. 446-54. Peer-reviewed.
 
Ten novel RB1 gene mutations in patients with retinoblastoma.
Abouzeid H., Munier F.L., Thonney F., Schorderet D.F., 2007. Molecular Vision, 13 pp. 1740-1745.
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