Thierry Kuntzer

Publications | Mémoires et thèses

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237 publications

2019 | 2018 | 2017 | 2016 | 2015 | 2014 | 2013 | 2012 | 2011 | 2010 | 2009 | 2008 | 2007 | 2006 | 2005 | 2004 | 2003 | 2002 | 2001 | 2000 | 1999 | 1998 | 1997 | 1996 | 1995 | ...
Predictive Factors of Swallowing Disorders and Bronchopneumonia in Acute Ischemic Stroke.
Beharry A., Michel P., Faouzi M., Kuntzer T., Schweizer V., Diserens K., 2019/08. Journal of stroke and cerebrovascular diseases, 28 (8) pp. 2148-2154. Peer-reviewed.
Peripheral neuropathy and cognitive impairment associated with a novel monoallelic HARS variant.
Royer-Bertrand B., Tsouni P., Mullen P., Campos Xavier B., Mittaz Crettol L., Lobrinus A.J., Ghika J., Baumgartner M.R., Rivolta C., Superti-Furga A. et al., 2019/06. Annals of clinical and translational neurology, 6 (6) pp. 1072-1080. Peer-reviewed.
Adverse effects of immune-checkpoint inhibitors: epidemiology, management and surveillance.
Martins F., Sofiya L., Sykiotis G.P., Lamine F., Maillard M., Fraga M., Shabafrouz K., Ribi C., Cairoli A., Guex-Crosier Y. et al., 2019/05/15. Nature reviews. Clinical oncology. Peer-reviewed.
New therapeutic perspectives to manage refractory immune checkpoint-related toxicities.
Martins F., Sykiotis G.P., Maillard M., Fraga M., Ribi C., Kuntzer T., Michielin O., Peters S., Coukos G., Spertini F. et al., 2019/01. The Lancet. Oncology, 20 (1) pp. e54-e64. Peer-reviewed.
A severe case of neuro-Sjögren's syndrome induced by pembrolizumab.
Ghosn J., Vicino A., Michielin O., Coukos G., Kuntzer T., Obeid M., 2018/10/22. Journal for immunotherapy of cancer, 6 (1) p. 110. Peer-reviewed.
Axon reflex-mediated vasodilation is reduced in proportion to disease severity in TTR-FAP.
Calero-Romero I., Suter M.R., Waeber B., Feihl F., Kuntzer T., 2018/08. Neurology. Genetics, 4 (4) pp. e251. Peer-reviewed.
Anti-MAG antibodies in 202 patients: clinicopathological and therapeutic features.
Svahn J., Petiot P., Antoine J.C., Vial C., Delmont E., Viala K., Steck A.J., Magot A., Cauquil C., Zarea A. et al., 2018/05. Journal of neurology, neurosurgery, and psychiatry, 89 (5) pp. 499-505. Peer-reviewed.
Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1.
Renaud M., Moreira M.C., Ben Monga B., Rodriguez D., Debs R., Charles P., Chaouch M., Ferrat F., Laurencin C., Vercueil L. et al., 2018/04/01. JAMA neurology, 75 (4) pp. 495-502. Peer-reviewed.
Symptômes musculaires associés aux statines : quelle prise en charge en 2018 ? [Statin-associated muscle symptoms : Current management in 2018]
Kosinski C., Tran C., Kuntzer T., Rodondi N., Collet T.H., 2018/02/28. Revue medicale suisse, 14 (596) pp. 462-469. Peer-reviewed.
Neurologie [Neurology]
Chopard I., Benninger D., Demonet J.F., Du Pasquier R., Hirt L., Kuntzer T., Michel P., Nater B., Novy J., Rossetti A. et al., 2018/01/10. Revue medicale suisse, 14 (588-589) pp. 58-61. Peer-reviewed.
Clinical phenotype and outcome of hepatitis E virus-associated neuralgic amyotrophy.
van Eijk JJJ, Dalton H.R., Ripellino P., Madden R.G., Jones C., Fritz M., Gobbi C., Melli G., Pasi E., Herrod J. et al., 2017/08/29. Neurology, 89 (9) pp. 909-917. Peer-reviewed.
Electrophysiological Study of Femoral Nerve Function After a Continuous Femoral Nerve Block for Anterior Cruciate Ligament Reconstruction.
Stebler K., Martin R., Kirkham K.R., Küntzer T., Bathory I., Albrecht E., 2017/03. The American journal of sports medicine, 45 (3) pp. 578-583. Peer-reviewed.
L’interniste face aux maladies rares: quand y penser? L’exemple des maladies mitochondriales [Raising the internist's know-how in the field of rare diseases: mitochondrial diseases as an illustrative example]
Tran C., Serratrice J., Nuoffer J.M., Schaller A., Favrat B., Barbey F., Lobrinus J.A., Kern I., Kuntzer T., Ballhausen D., 2017/01/18. Revue medicale suisse, 13 (546) pp. 159-163. Peer-reviewed.
Neurologie [Neurology]
Maulucci F., Benninger D., Démonet J.F., Du Pasquier R.A., Hirt L., Hottinger A., Kuntzer T., Michel P., Nater B., Novy J. et al., 2017/01/11. Revue medicale suisse, 13 (544-545) pp. 79-83. Peer-reviewed.
What is new in 2015 in dysimmune neuropathies?
Kuntzer T., 2016/12. Revue neurologique, 172 (12) pp. 779-784. Peer-reviewed.
The wide POLG-related spectrum: An integrated view.
Béreau M., Anheim M., Echaniz-Laguna A., Magot A., Verny C., Goideau-Sevrain M., Barth M., Amati-Bonneau P., Allouche S., Ayrignac X. et al., 2016/09/15. Journal of the neurological sciences, 368 pp. 70-76. Peer-reviewed.
Amyloïdose héréditaire à transthyrétine [Transthyretin-related hereditary amyloidosis]
Vionnet J., Pascual M., Kuntzer T., Yerly P., Moradpour D., 2016/08/31. Revue medicale suisse, 12 (528) pp. 1434-1440. Peer-reviewed.
Hepatitis E virus infection as a direct cause of neuralgic amyotrophy.
Silva M., Wicki B., Tsouni P., Cunningham S., Doerig C., Zanetti G., Aubert V., Sahli R., Moradpour D., Kuntzer T., 2016/08. Muscle & nerve, 54 (2) pp. 325-327. Peer-reviewed.
A semi-automated method to assess intraepidermal nerve fibre density in human skin biopsies.
Seger S., Stritt M., Doppler K., Frank S., Panaite A., Kuntzer T., Steck A., Pagenstecher A., Sommer C., Stalder A.K., 2016/04. Histopathology, 68 (5) pp. 657-665. Peer-reviewed.
Human Endogenous Retrovirus and Neuroinflammation in Chronic Inflammatory Demyelinating Polyradiculoneuropathy.
Faucard R., Madeira A., Gehin N., Authier F.J., Panaite P.A., Lesage C., Burgelin I., Bertel M., Bernard C., Curtin F. et al., 2016/04. EBioMedicine, 6 pp. 190-198. Peer-reviewed.
Corticosteroids for the treatment of Duchenne muscular dystrophy.
Matthews E., Brassington R., Kuntzer T., Jichi F., Manzur A.Y., 2016. Cochrane Database of Systematic Reviews, 13 (5) pp. CD003725. Peer-reviewed.
Identifying a therapeutic window in acute and subacute inflammatory sensory neuronopathies.
Antoine J.C., Robert-Varvat F., Maisonobe T., Créange A., Franques J., Mathis S., Delmont E., Kuntzer T., Lefaucheur J.P., Pouget J. et al., 2016. Journal of the Neurological Sciences, 361 pp. 187-191. Peer-reviewed.
Intravenous Immunoglobulins Lower Inflammatory Gene Expression in Skin Biopsies of Chronic Inflammatory Demyelinating Polyradiculoneuropathy Patients.
Tsouni P., Panaite P.A., Puttini S., Kuntzer T., Steck A.J., 2016. European Neurology, 75 (5-6) pp. 290-291. Peer-reviewed.
Neuroarthropathy of the foot revealing primary systemic amyloidosis: case report and literature review.
Andrei I.A., Kuntzer T., Lobrinus J.A., Jaccard A., Zufferey P., 2016. Clinical Rheumatology, 35 (2) pp. 535-539.
Neurologie [Neurology].
Sokolov A.A., Rossetti A.O., Michel P., Benninger D., Nater B., Wider C., Hirt L., Kuntzer T., Démonet J.F., Du Pasquier R.A. et al., 2016. Revue Médicale Suisse, 12 (500) pp. 62, 64-62, 66.
Update of the Swiss guidelines on post-treatment Lyme disease syndrome.
Nemeth J., Bernasconi E., Heininger U., Abbas M., Nadal D., Strahm C., Erb S., Zimmerli S., Furrer H., Delaloye J. et al., 2016. Swiss medical weekly, 146 pp. w14353. Peer-reviewed.
Acute painful diabetic neuropathy: an uncommon, remittent type of acute distal small fibre neuropathy.
Tran C., Philippe J., Ochsner F., Kuntzer T., Truffert A., 2015. Swiss Medical Weekly, 145 pp. w14131. Peer-reviewed.
Anti-TNF alpha medications and neuropathy.
Tsouni P., Bill O., Truffert A., Liaudat C., Ochsner F., Steck A.J., Kuntzer T., 2015. Journal of the Peripheral Nervous System : Jpns, 20 (4) pp. 397-402. Peer-reviewed.
Dysferlinopathy in Switzerland: clinical phenotypes and potential founder effects.
Petersen J.A., Kuntzer T., Fischer D., von der Hagen M., Huebner A., Kana V., Lobrinus J.A., Kress W., Rushing E.J., Sinnreich M. et al., 2015. Bmc Neurology, 15 (1) p. 182. Peer-reviewed.
Low penetrance in facioscapulohumeral muscular dystrophy type 1 with large pathological D4Z4 alleles: a cross-sectional multicenter study.
Salort-Campana E., Nguyen K., Bernard R., Jouve E., Solé G., Nadaj-Pakleza A., Niederhauser J., Charles E., Ollagnon E., Bouhour F. et al., 2015. Orphanet Journal of Rare Diseases, 10 (1) p. 2. Peer-reviewed.
mTOR is expressed in polymyositis but not in sporadic inclusion body myositis.
Panaite P.A., Stalder A.K., Ipsen S., Kuntzer T., Steck A.J., 2015. Clinical Neuropathology, 34 (6) pp. 371-373. Peer-reviewed.
Neurologie [News in neuroloey 2014].
Tsetsou S., Rossetti A.O., Michel P., Hirt L., Wider C., Benninger D., Kuntzer T., Nater B., Démonet J.F., Schluep M. et al., 2015. Revue Médicale Suisse, 11 (456-457) pp. 91-96.
PTPN11 mutation manifesting as LEOPARD syndrome associated with hypertrophic plexi and neuropathic pain.
Spatola M., Wider C., Kuntzer T., Croquelois A., 2015. Bmc Neurology, 15 p. 55. Peer-reviewed.
Successful long-term ambulatory norepinephrine infusions in a patient with pure autonomic failure.
Zekeridou A., Michel P., Medlin F., Hayoz D., Lalive P.H., Kuntzer T., 2015. Clinical Autonomic Research, 25 (4) pp. 251-253. Peer-reviewed.
Acetylcholinesterase inhibitor treatment for myasthenia gravis.
Mehndiratta M.M., Pandey S., Kuntzer T., 2014. Cochrane Database of Systematic Reviews, 10 pp. CD006986.
Assessing dystrophies and other muscle diseases at the nanometer scale by atomic force microscopy.
van Zwieten R.W., Puttini S., Lekka M., Witz G., Gicquel-Zouida E., Richard I., Lobrinus J.A., Chevalley F., Brune H., Dietler G. et al., 2014. Nanomedicine, 9 (4) pp. 393-406.
Double seronegative myasthenia gravis with antiphospholipid syndrome: a case report.
Dan D., Bart P.A., Novy J., Kuntzer T., Clair C., 2014. Journal of Medical Case Reports, 8 (1) p. 2. Peer-reviewed.
Fatigue et réduction de la performance motrice chez le sportif, syndrome de surentraînement [Fatigue and reduction in motor performance in sportspeople or overtraining syndrome].
Gremion G., Kuntzer T., 2014. Revue Médicale Suisse, 10 (428) pp. 962-965. Peer-reviewed.
Gene expression changes in chronic inflammatory demyelinating polyneuropathy skin biopsies.
Puttini S., Panaite P.A., Mermod N., Renaud S., Steck A.J., Kuntzer T., 2014. Journal of Neuroimmunology, 270 (1-2) pp. 61-66. Peer-reviewed.
Maintien des capacités des myopathes ou l'art de prescrire l'exercice physique [How to maintain the motor capacities in neuromuscular disorders or the art to prescribe physical exercises].
Vuadens P., Kuntzer T., Mühl A., 2014. Revue Médicale Suisse, 10 (428) pp. 958-961. Peer-reviewed.
Manifestations neurologiques des troubles musculosquelettiques [Neurological manifestations in musculoskeletal disorders].
Tsouni P., Kuntzer T., Ochsner F., 2014. Revue Médicale Suisse, 10 (428) pp. 966-969. Peer-reviewed.
Neurologie [News in neurology 2013].
Spatola M., Rossetti A.O., Michel P., Kuntzer T., Benninger D., Nater B., Démonet J.F., Schluep M., Du Pasquier R.A., Vingerhoets F., 2014. Revue Médicale Suisse, 10 (412-413) pp. 78-81. Peer-reviewed.
Neuropathies diabétiques: tableaux cliniques, détection précoce et appel au spécialiste [Diabetic neuropathies: clinical sub-types, early detection and asking help from the specialist].
Kuntzer T., Ruiz J., 2014. Revue Médicale Suisse, 10 (428) pp. 950-953. Peer-reviewed.
Neuropathies périphériques d'origine médicamenteuse [Drug-induced peripheral neuropathy].
Diezi M., Kuntzer T., 2014. Revue Médicale Suisse, 10 (428) pp. 954-957. Peer-reviewed.
Pratiques dans les maladies neuromusculaires [Practices in neuromuscular diseases].
Kuntzer T., 2014. Revue Médicale Suisse, 10 (428) pp. 947-948. Peer-reviewed.
Revue de la littérature 2013--les neuropathies inflammatoires [2013: what's new in inflammatory neuropathies].
Kuntzer T., 2014. Revue Neurologique, 170 (12) pp. 850-853.
Sporadic late-onset nemaline myopathy with MGUS: Long-term follow-up after melphalan and SCT.
Voermans N.C., Benveniste O., Minnema M.C., Lokhorst H., Lammens M., Meersseman W., Delforge M., Kuntzer T., Novy J., Pabst T. et al., 2014. Neurology, 83 (23) pp. 2133-2139. Peer-reviewed.
Sweet taste loss in myasthenia gravis: more than a coincidence?
Chabwine J.N., Tschirren M.V., Zekeridou A., Landis B.N., Kuntzer T., 2014. Orphanet Journal of Rare Diseases, 9 (1) pp. 50-53. Peer-reviewed.
Testing the validity of a set of diagnostic criteria for sensory neuronopathies: a francophone collaborative study.
Antoine J.C., Robert-Varvat F., Maisonobe T., Créange A., Franques J., Mathis S., Delmont E., Kuntzer T., Lefaucheur J.P., Pouget J. et al., 2014. Journal of Neurology, 261 (11) pp. 2093-2100. Peer-reviewed.
Faiblesse musculaire, à quoi faut-il penser [Muscle weakness, what's your diagnosis?].
Kuntzer T., 2013. Revue Médicale Suisse, 9 (371) p. 231. Peer-reviewed.
Favorable outcome of an acute complex regional pain syndrome with immunoglobulin infusions.
Medlin F., Zekeridou A., Renaud S., Kuntzer T., 2013. Clinical Journal of Pain, 29 (11) pp. e33-e34. Peer-reviewed.
Functional and histopathological identification of the respiratory failure in a DMSXL transgenic mouse model of myotonic dystrophy.
Panaite P.A., Kuntzer T., Gourdon G., Lobrinus J.A., Barakat-Walter I., 2013. Disease Models and Mechanisms, 6 (3) pp. 622-631. Peer-reviewed.
Impairment and disability in 20 CIDP patients according to disease activity status.
Panaite P.A., Renaud S., Kraftsik R., Steck A.J., Kuntzer T., 2013. Journal of the Peripheral Nervous System, 18 (3) pp. 241-246. Peer-reviewed.
Maladies auto-immunes neuromusculaires: diagnostic et prise en charge [Dysimmune neuromuscular disorders: diagnostic challenges and new ways of management].
Lalive P.H., Du Pasquier R.A., Chizzolini C., Kuntzer T., 2013. Revue Médicale Suisse, 9 (384) pp. 934-939. Peer-reviewed.
Neuroborréliose, méningo-encéphalite verno-estivale et neurosyphilis [Neuroborreliosis, tick-borne encephalitis and neurosyphilis].
Meylan P., Kuntzer T., Toutous Trellu L., Lalive P.H., 2013. Revue Médicale Suisse, 9 (384) pp. 922-928. Peer-reviewed.
Neurologie [2012: news in neurology].
Alvarez V., Rossetti A.O., Michel P., Kuntzer T., Nater B., Démonet J.F., Schluep M., Du Pasquier R., Vingerhoets F., 2013. Revue Médicale Suisse, 9 (368) pp. 62-65. Peer-reviewed.
Respiratory failure in a mouse model of myotonic dystrophy does not correlate with the CTG repeat length.
Panaite P.A., Kuntzer T., Gourdon G., Barakat-Walter I., 2013. Respiratory Physiology and Neurobiology, 189 (1) pp. 22-26. Peer-reviewed.
The diagnosis of chronic inflammatory demyelinating polyneuropathy: a Delphi-method approach.
Créange A., Careyron A., French CIDP study group, 2013. Journal of Neurology, 260 (12) pp. 3015-3022. Peer-reviewed.
Toxic and drug-induced peripheral neuropathies: updates on causes, mechanisms and management.
Diezi M., Buclin T., Kuntzer T., 2013. Current Opinion in Neurology, 26 (5) pp. 481-488. Peer-reviewed.
Very late-onset Friedreich ataxia: later than life expectancy?
Alvarez V., Arnold P., Kuntzer T., 2013. Journal of Neurology, 260 (5) pp. 1408-1409. Peer-reviewed.
Schwannoma of the palmar cutaneous nerve: electrodiagnosis with radiologic and pathologic correlations.
Zekeridou A., Ochsner F., Medlin F., Lobrinus J.A., Becce F., Kuntzer T., 2012/11. Archives of neurology, 69 (11) p. 1512. Peer-reviewed.
A clinical pattern-based etiological diagnostic strategy for sensory neuronopathies: a French collaborative study.
Camdessanché J.P., Jousserand G., Franques J., Pouget J., Delmont E., Créange A., Kuntzer T., Maisonobe T., Abba K., Antoine J.C. et al., 2012. Journal of the Peripheral Nervous System, 17 (3) pp. 331-340. Peer-reviewed.
Altered distribution of juxtaparanodal kv1.2 subunits mediates peripheral nerve hyperexcitability in type 2 diabetes mellitus.
Zenker J., Poirot O., de Preux Charles A.S., Arnaud E., Médard J.J., Lacroix C., Kuntzer T., Chrast R., 2012. Journal of Neuroscience, 32 (22) pp. 7493-7498. Peer-reviewed.
Diabetische Neuropathien: Klinische Manifestationsformen, Früherkennung und Zuweisung zu einem Neurologen [Diabetic Neuropathies: Clinical sub-Types, Early Detection, and Asking Help from Neurologist].
Kuntzer T., Medlin F., Burnand B., Camain J.Y., 2012. Praxis, 101 (20) pp. 1315-1319. Peer-reviewed.
High cardiovascular morbidity and mortality in myofibrillar myopathies due to DES gene mutations: a 10-year longitudinal study.
Wahbi K., Béhin A., Charron P., Dunand M., Richard P., Meune C., Vicart P., Laforêt P., Stojkovic T., Bécane H.M. et al., 2012. Neuromuscular Disorders : NMD, 22 (3) pp. 211-218. Peer-reviewed.
Late onset tacrolimus-induced life-threatening polyneuropathy in a kidney transplant recipient patient
Renard D., Gauthier T., Venetz J.-P., Buclin T., Kuntzer T., 2012. Clinical Kidney Journal, 5 (4) pp. 323-326. Peer-reviewed.
Les limites du concept de neuropathies à petites fibres
Kuntzer T., 2012. pp. 341-350 dans Pouget J., Attarian S. (eds.) ENMG 2012, XVIIIes Journées Francophones d'Electroneuromyographie, Solal.
Les limites du concept de « neuropathies des petites fibres »
Kuntzer T., Ochsner F., Renaud S., Magy L., 2012. pp. 158-165 dans Pouget J. (eds.) ENMG 2012 : XVIIIes Journées Francophones d'Electroneuromyographie, Solal.
Long-term follow-up of patients with congenital myasthenic syndrome caused by COLQ mutations.
Wargon I., Richard P., Kuntzer T., Sternberg D., Nafissi S., Gaudon K., Lebail A., Bauche S., Hantaï D., Fournier E. et al., 2012. Neuromuscular Disorders, 22 (4) pp. 318-324. Peer-reviewed.
Neurologie [Neurology].
Chabwine J.N., Rossetti A.R., Hirt L., Kuntzer T., Schluep M., Michel P., Démonet J.F., du Pasquier R.A., Vingerhoets F.G., 2012. Revue Médicale Suisse, 8 (323) pp. 46-50. Peer-reviewed.
Revue de la littérature 2011 : neuropathies dysimmunitaires [2011: What's new in dysimmune neuropathies].
Kuntzer T., 2012. Revue Neurologique, 168 (12) pp. 975-978. Peer-reviewed.
Sensory Neuronopathies or Ganglionopathies
Kuntzer T., Steck A.J., 2012. pp. 273-288 dans Donofrio P.D. (eds.) Textbook of Peripheral Neuropathy chap. 20, Demos Medical.
Traitement de la douleur chronique: rôle de la stimulation transcrânienne du cortex moteur [Treatment of chronic pain: transcranial stimulation of the motor cortex?].
Benninger D., Kuntzer T., 2012. Revue Médicale Suisse, 8 (339) pp. 935-936. Peer-reviewed.
Acetylcholinesterase inhibitor treatment for myasthenia gravis.
Mehndiratta M.M., Pandey S., Kuntzer T., 2011. Cochrane Database of Systematic Reviews, 2 (2) pp. CD006986. Peer-reviewed.
Congenital Myasthenic Syndromes with COLQ mutations: Long term follow-up
Wargon I., Richard P., Kuntzer T., Nafissi S., Gaudon K., Sternberg D., Fournier E., Gevin A., Eymard B., Stojkovic T., 2011. pp. 728-729 dans 16th International Congress of the World Muscle Society, Neuromuscular Disorders. Peer-reviewed.
Neurologie [Therapeutic advances in neurology].
Siclari F., Du Pasquier R.A., Schluep M., Michel P., Hirt L., Kuntzer T., Rossetti A.O., Ghika J., Nater B., Vingerhoets F.J., 2011. Revue Médicale Suisse, 7 (277) pp. 50-56. Peer-reviewed.
Pallidal hyperintensities - a coincidental finding of clinical relevance in Miller Fisher syndrome.
Alvarez V., Siclari F., Kuntzer T., 2011. European Journal of Neurology, 18 (8) pp. e94-e95. Peer-reviewed.
Peripheral neuropathy is linked to a severe form of myotonic dystrophy in transgenic mice.
Panaite P.A., Kielar M., Kraftsik R., Gourdon G., Kuntzer T., Barakat-Walter I., 2011. Journal of Neuropathology and Experimental Neurology, 70 (8) pp. 678-685. Peer-reviewed.
Rituximab is successful in an HIV-positive patient with MuSK myasthenia gravis.
Kuntzer T., Carota A., Novy J., Cavassini M., Du Pasquier R.A., 2011. Neurology, 76 (8) pp. 757-758. Peer-reviewed.
Rituximab treatment in Myasthenia gravis: an open-label trial
Di Virgilio G., Zekeridou A., Menetrey A., Kuntzer T., 2011. p. 248 dans 21st Meeting of the European Neurological Society, Journal of Neurology. Peer-reviewed.
Rituximab treatment in non-malignant inflammatory sensory polyganglionopathy
Zekeridou A., Kleeberg J., Menetrey A., Kuntzer T., 2011. p. 115 dans 21st Meeting of the European Neurological Society, Journal of Neurology. Peer-reviewed.
Successful heart and liver transplantation in a Swiss patient with Glu89Lys transthyretin amyloidosis.
Niederhauser J., Lobrinus J.A., Ochsner F., Wider C., Fellmann F., Yerly P., Antonino A.T., Saraiva M.J., Moradpour D., Kuntzer T., 2011. Transplantation, 91 (6) pp. e40-e42. Peer-reviewed.
Transient femoral neuropathy after knee ligament reconstruction and nerve stimulator-guided continuous femoral nerve block: a case series.
Albrecht E., Niederhauser J., Gronchi F., Löcherbach C., Kombot C., Rossat J., Gilliard N., Kuntzer T., 2011. Anaesthesia, 66 (9) pp. 850-851. Peer-reviewed.
Validation of diagnosis criteria for acquired sensory neuronopathy. a francophone multicenter study
Antoine J.-.C., Abba K., Franques J., Pouget J., Delmont E., Kuntzer T., Petiot P., Gervais-Bernard H., Echaniz-Laguna A., Creange A. et al., 2011. pp. S3-S4 dans Meeting of the Peripheral Nerve Society, Journal of the Peripheral Nervous System. Peer-reviewed.
Chemotherapy is successful in sporadic late onset nemaline myopathy (SLONM) with monoclonal gammopathy.
Novy J., Rosselet A., Spertini O., Lobrinus J.A., Pabst T., Kuntzer T., 2010/02. Muscle & nerve, 41 (2) pp. 286-287. Peer-reviewed.
Atrophie scapulaire : explorations et attitude
Kuntzer T., Bonnard C., Ochsner F., 2010. pp. 173-182 dans Vial C. (eds.) ENMG 2010 : XVIIes Journées Francophones d'Electroneuromyographie, Solal.
Atrophie scapulaire : explorations et attitude
Kuntzer T., Bonnard C., Ochsner F., 2010. pp. 88-98 dans Vial C. (eds.) ENMG 2010 : XVIIes Journées Francophones d'Electroneuromyographie, Solal.
Early onset collagen VI myopathies: Genetic and clinical correlations.
Briñas L., Richard P., Quijano-Roy S., Gartioux C., Ledeuil C., Lacène E., Makri S., Ferreiro A., Maugenre S., Topaloglu H. et al., 2010. Annals of Neurology, 68 (4) pp. 511-520. Peer-reviewed.
Global transcriptional programs in peripheral nerve endoneurium and DRG are resistant to the onset of type 1 diabetic neuropathy in Ins2 mice.
de Preux Charles A.S., Verdier V., Zenker J., Peter B., Médard J.J., Kuntzer T., Beckmann J.S., Bergmann S., Chrast R., 2010. Plos One, 5 (5) pp. e10832. Peer-reviewed.
Marked hemiatrophy in carriers of Duchenne muscular dystrophy.
Rajakulendran S., Kuntzer T., Dunand M., Yau S.C., Ashton E.J., Storey H., McCauley J., Abbs S., Thonney F., Leturcq F. et al., 2010. Archives of Neurology, 67 (4) pp. 497-500. Peer-reviewed.
Statines et effets indésirables musculaires [Statins and muscular side-effects]
Brosteaux C., Ruiz J., Buclin T., Kuntzer T., Rodondi N., 2010. Revue Médicale Suisse, 6 (239) pp. 510-517. Peer-reviewed.
Unsatisfactory outcomes in myasthenia gravis: influence by care providers.
Dunand M., Botez S.A., Borruat F.X., Roux-Lombard P., Spertini F., Kuntzer T., 2010. Journal of Neurology, 257 (3) pp. 338-343. Peer-reviewed.
Confirmation that abnormal desmin accumulation and migration are due to a desmin gene mutation in a familial cardiomyopathy and distal myopathy.
Dunand M., Lobrinus J.A., Jeannet P.Y., Behin A., Claeys K.G., Selcen D., Kuntzer T., 2009/11. Neuromuscular disorders : NMD, 19 (11) p. 802. Peer-reviewed.
Diagnostic d'une myopathie à phénotype rétractile : la peau au secours du muscle
Dunand M., Kuntzer T., Cuisset J.-M., 2009/10. Cahiers de Myologie, 1 (1) pp. 15-16. Peer-reviewed.
Diagnosis of muscular dystrophies at the nanometer scale
Puttini S., Lekka M., Kuntzer T., Mermod N., Kulik A., 2009. pp. 544-545 dans 14th International Congress of the World Muscle Society, Neuromuscular Disorders. Peer-reviewed.
Does the physical disector method provide an accurate estimation of sensory neuron number in rat dorsal root ganglia?
Delaloye S., Kraftsik R., Kuntzer T., Barakat-Walter I., 2009. Journal of Neuroscience Methods, 176 (2) pp. 290-297. Peer-reviewed.
Identification of an agrin mutation that causes congenital myasthenia and affects synapse function.
Huzé C., Bauché S., Richard P., Chevessier F., Goillot E., Gaudon K., Ben Ammar A., Chaboud A., Grosjean I., Lecuyer H.A. et al., 2009. American Journal of Human Genetics, 85 (2) pp. 155-167. Peer-reviewed.
Interferon BETA-1A as adjunctive treatment for multifocal motor neuropathy: an open label trial.
Radziwill Alexander J., Botez Stephan A., Novy Jan, Kuntzer Thierry, 2009. Journal of the Peripheral Nervous System, 14 (3) pp. 201-202. Peer-reviewed.
Local delivery of glial cell line-derived neurotrophic factor improves facial nerve regeneration after late repair.
Barras F.M., Kuntzer T., Zurn A.D., Pasche P., 2009. Laryngoscope, 119 (5) pp. 846-855. Peer-reviewed.
Neurologie [Therapeutic advances in neurology].
Morier J., Du Pasquier R., Kuntzer T., Michel P., Nater B., Niederhauser J., Rossetti A.O., Schluep M., Vingerhoets F., 2009. Revue Médicale Suisse, 5 (185) pp. 39-48. Peer-reviewed.
Subclinical femoral neuropathy after anterior cruciate ligament reconstruction
Albrecht E., Gronchi F., Niederhauser J., Kuntzer T., Loecherbach C., Kombot C., Farron A., Kern C., 2009. pp. 12S-12S dans Annual meeting of the Swiss Society of Anaesthesiology and Resuscitation, Swiss Medical Weekly. Peer-reviewed.
Mirtazapine decreases the pain feeling in healthy participants.
Arnold P., Vuadens P., Kuntzer T., Gobelet C., Deriaz O., 2008/02. Clinical Journal of Pain, 24 (2) pp. 116-119. Peer-reviewed.
Dysautonomies et explorations
Kuntzer T., 2008. pp. 29-38 dans Péréon Y. (eds.) ENMG 2008 : XVIes Journées Francophones d'Electroneuromyographie, Solal.
Glucocorticoid corticosteroids for Duchenne muscular dystrophy
Manzur A., Kuntzer T., Pike M., Swan A., 2008/01. Cochrane Database System Review, 1 pp. CD003725. Peer-reviewed.
Isolated facial and bulbar paresis: a persistent manifestation of neonatal myasthenia gravis.
Jeannet P.Y., Marcoz J.P., Kuntzer T., Roulet-Perez E., 2008/01. Neurology, 70 (3) pp. 237-238. Peer-reviewed.
Myotonic dystrophy transgenic mice exhibit pathologic abnormalities in diaphragm neuromuscular junctions and phrenic nerves
Panaite P. A., Gantelet E., Kraftsik R., Gourdon G., Kuntzer T., Barakat-Walter I., 2008. Journal of Neuropathology and Experimental Neurology, 67 (8) pp. 763-772. Peer-reviewed.
Small cortical stroke in the "hand knob" mimics anterior interosseous syndrome.
Granziera C., Kuntzer T., Vingerhoets F., Cereda C., 2008. Journal of Neurology, 255 (9) pp. 1423-1424. Peer-reviewed.
Stimulus-response curve of human motor nerves: multicenter assessment of various indexes.
Boërio D., Hogrel J.Y., Lefaucheur J.P., Wang F.C., Verschueren A., Pouget J., Carrera E., Kuntzer T., 2008. Neurophysiologie Clinique = Clinical Neurophysiology, 38 (1) pp. 31-38. Peer-reviewed.
The potential use of ephedrine in Lambert-Eaton myasthenic syndrome : clinical and electrophysiological evaluation.
Cereda C., Kuntzer T., 2008. Journal of Neurology, 255 (8) pp. 1259-60. Peer-reviewed.
Le role du pathologiste dans la prise en charge des maladies neuromusculaires. [The role of pathology in neuromuscular diseases]
Lobrinus J. A., Jeannet P. Y., Kohler A., Dunand M., Kuntzer T., 2007/07. Revue Médicale Suisse, 3 (119) pp. 1733-6. Peer-reviewed.
Myasthenie grave, traitements et remissions. [Myasthenia gravis: treatments and remissions]
Dunand M., Lalive P. H., Vokatch N., Kuntzer T., 2007/05. Revue Médicale Suisse, 3 (110) pp. 1185-6, 1188-90. Peer-reviewed.
Prise en charge des polyradiculoneuropathies aigues et chroniques. [Management of the acute and chronic polyradiculoneuropathies]
Novy J., Kuntzer T., 2007/05. Revue Médicale Suisse, 3 (110) pp. 1166-1169. Peer-reviewed.
Autosomal dominant nemaline myopathy: a new phenotype unlinked to previously known genetic loci
Jeannet P. Y., Mittaz L., Dunand M., Lobrinus J. A., Bonafe L., Kuntzer T., 2007/01. Neuromuscular Disorders, 17 (1) pp. 6-12. Peer-reviewed.
Borréliose de Lyme et neuroborréliose
Kuntzer T, Péter O, 2007. pp. 1-9 dans Encyclopédie médico-chirurgicale - Neurologie, Elsevier.
Comparative efficacy of repetitive nerve stimulation, exercise, and cold in differentiating myotonic disorders.
Michel P., Sternberg D., Jeannet P.Y., Dunand M., Thonney F., Kress W., Fontaine B., Fournier E., Kuntzer T., 2007. Muscle & Nerve, 36 (5) pp. 643-650. Peer-reviewed.
Multifocal motor neuropathy: and then, 20 years later ...Editorial (special issue)
Kuntzer T, Ochsner F, Magistris MR. , 2007. Schweiz Archives of Neurololgy & Psychiatry, 2 pp. 51-2. Peer-reviewed.
Multifocal motor neuropathy: clinical background.
Kuntzer T, Radziwill AJ, Botez SA. , 2007. Schweiz Archives of Neurololgy & Psychiatry, 2 pp. 57- 64. Peer-reviewed.
Neurologie [Neurology]
Botez S., Carota A., Dunand M., Du Pasquier R., Kuntzer T., Michel P., Morier J., Schluep M., Rossetti A.O., 2007. Revue Médicale Suisse, 3 (93) pp. 39-47. Peer-reviewed.
Neuropathie d'enclavement: une cause traitable de douleurs musculosquelettiques. [The entrapment neuropathy: a treatable cause of musculoskeletal pain]
Ochsner F., Novy J., Kuntzer T., 2007. Revue Médicale Suisse, 3 (110) pp. 1170-1177. Peer-reviewed.
The expansion of 300 CTG repeats in myotonic dystrophy transgenic mice does not induce sensory or motor neuropathy.
Gantelet E., Kraftsik R., Delaloye S., Gourdon G., Kuntzer T., Barakat-Walter I., 2007. Acta neuropathologica, 114 (2) pp. 175-85. Peer-reviewed.
Thyroid hormone in biodegradable nerve guides stimulates sciatic nerve regeneration: a potential therapeutic approach for human peripheral nerve injuries.
Barakat-Walter I., Kraftsik R., Krafsik R., Schenker M., Kuntzer T., 2007. Journal of neurotrauma, 24 (3) pp. 567-77. Peer-reviewed.
Ganglionopathies: evolution du concept et prise en charge. [Ganglionopathies: evolving concept and ideas on management]
Kuntzer T., 2006/12. Revue Neurologique, 162 (12) pp. 1268-72. Peer-reviewed.
Favourable outcome of progressive multifocal leucoencephalopathy in two patients with dermatomyositis.
Vulliemoz S., Lurati-Ruiz F., Borruat F.X., Delavelle J., Koralnik I.J., Kuntzer T., Bogousslavsky J., Picard F., Landis T., Du Pasquier R.A., 2006/09. Journal of Neurology, 77 (9) pp. 1079-1082. Peer-reviewed.
Dermatomyositis, lobar panniculitis and inflammatory myopathy with abundant macrophages
Carrera E., Lobrinus J. A., Spertini O., Gherardi R. K., Kuntzer T., 2006/07. Neuromuscular Disorders, 16 (7) pp. 468-471. Peer-reviewed.
Degenerescence programmee de maladies musculaires: aspects moleculaires et previsions therapeutiques. [Mechanisms leading to muscle degeneration: molecular mechanisms and therapeutical forecasts]
Kuntzer T., Bader C. R., Sinnreich M., 2006/05. Revue Médicale Suisse, 2 (64) pp. 1174-7. Peer-reviewed.
Mecanismes pathogeniques des maladies neurodegeneratives: l'exemple de la sclerose laterale amyotrophique. [Pathogenic mechanisms of neurodegenerative diseases: amyotrophic lateral sclerosis]
Kato A. C., Vingerhoets F. J., Magistris M. R., Kuntzer T., Burkhard P. R., 2006/05. Revue Médicale Suisse, 2 (64) pp. 1152-4, 1156-7. Peer-reviewed.
Les limites therapeutiques des polyradiculonevrites chroniques. [Treatment options for chronic inflammatory demyelinating polyradiculoneuropathy (CIDP)]
Kuntzer T., 2006/04. Revue Neurologique, 162 (4) pp. 539-43. Peer-reviewed.
Bilateral compressive lumbosacral plexopathy due to internal iliac artery aneurysms.
Wider C., Kuntzer T., Von Segesser L.K., Qanadli S.D., Bogousslavsky J., Vingerhoets F., 2006. Journal of Neurology, 253 (6) pp. 809-810. Peer-reviewed.
Expanding view of phenotype and oxidative stress in Friedreich's ataxia patients with and without idebone.
Arnold P., Boulat O., Maire R., Kuntzer T., 2006. Schweizer Archiv für Neurologie und Psychiatrie, 157 (4) pp. 169-176. Peer-reviewed.
Familial oculoparetic torticolis.
Carrera E., Bogousslavsky J., Kuntzer T., Maeder P., Ghika J., 2006. European Journal of Neurology, 13 (8) pp. e3-e4. Peer-reviewed.
Improved sciatic nerve regeneration by local thyroid hormone treatment in adult rat is accompanied by increased expression of SCG10
Voria I., Hauser J., Axis A., Schenker M., Bichet S., Kuntzer T., Grenningloh G., Barakat-Walter I., 2006/01. Experimental Neurology, 197 (1) pp. 258-267. Peer-reviewed.
Mycophenolate mofetil for chronic inflammatory demyelinating polyradiculoneuropathy: An open-label study
Radziwill A. J., Schweikert K., Kuntzer T., Fuhr P., Steck A. J., 2006. European Neurology, 56 (1) pp. 37-8. Peer-reviewed.
Douleurs neuropathiques: contexte, nouveaux outils, nouveaux medicaments. [Neuropathic pains: background, new tools, new drugs]
Kuntzer T., Decosterd I., 2005/11. Revue Médicale Suisse, 1 (43) pp. 2812-6. Peer-reviewed.
Successful treatment of a postpolio tinnitus with type a botulinum toxin
Scolozzi P., Carrera E., Jaques B., Kuntzer T., 2005/07. Laryngoscope, 115 (7) pp. 1288-90. Peer-reviewed.
Eosinophilic perimyositis as the presenting feature of a monoclonal T-cell expansion
Dunand M., Lobrinus J. A., Spertini O., Kuntzer T., 2005/05. Muscle and Nerve, 31 (5) pp. 646-651. Peer-reviewed.
Hirayama disease associated with a severe rhythmic movement disorder involving neck flexions
Jeannet P. Y., Kuntzer T., Deonna T., Roulet-Perez E., 2005/04. Neurology, 64 (8) pp. 1478-9. Peer-reviewed.
Amyotrophie de type Charcot-Marie-Tooth associée à une ataxie cérébelleuse autosomique récessive révélatrice d'une mutation du gène de l'aprataxine [Mutation of the aprataxin gene presenting with Charcot-Marie-Tooth-like neuropathy and cerebellar ataxia]
Ochsner F., Le Ber I., Said G., Moreira M.C., Michel P., Koenig M., Dürr A., Brice A., Kuntzer T., 2005. Revue neurologique, 161 (3) pp. 331-336. Peer-reviewed.
Beauchemin J.P, Beer J, Bogousslavsky J, Bouchard J.P, Carruzzo A, Clarke S, D'Acremont V, Dehdashti A.R, Du Pasquier R, Favre J et al., 2005. pp. 503-573 dans SURF. Guide thérapeutique de Médecine Interne & Diagnostic différentiel selon INVESTI-MED, D & F Gmbh.
Reichhart M, Beauchemin J.P, Beer J, Bogousslavsky J, Bouchard J.P, Carruzzo A, Clarke S, D'Acremont V, Dehdashti A.R, Du Pasquier R et al., 2005. pp. 247-286 dans SURF Urgences. Urgences médicales en médecine interne, cardiologie, D & F Gmbh.
Traitements immunomodulateurs/ suppresseurs en neurologie. [Immunomodulatory/suppressive treatments in neurology]
Schluep M., Chofflon M., Kuntzer T., Du Pasquier R., 2005. Revue Médicale Suisse, 1 (18) pp. 1229-1232. Peer-reviewed.
New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis
Vicart S., Sternberg D., Fournier E., Ochsner F., Laforet P., Kuntzer T., Eymard B., Hainque B., Fontaine B., 2004/12. Neurology, 63 (11) pp. 2120-7. Peer-reviewed.
Clinical features and pathophysiological basis of sensory neuronopathies (ganglionopathies)
Kuntzer T., Antoine J. C., Steck A. J., 2004/09. Muscle and Nerve, 30 (3) pp. 255-68. Peer-reviewed.
Electrophysiologie clinique des canalopathies musculaires. [Electrophysiological testing in muscle channelopathies]
Kuntzer T., 2004/05. Revue Neurologique, 160 (5 Pt 2) pp. S49-54. Peer-reviewed.
Glucocorticoid corticosteroids for Duchenne muscular dystrophy.
Manzur A.Y., Kuntzer T., Pike M., Swan A., 2004. Cochrane Database of Systematic Reviews 2 pp. CD003725. Peer-reviewed.
Listériose et neurolistériose
Kuntzer T., Radziwill A.J., Bogousslavsky J., Bille J., 2004. dans EMC - Neurologie, Elsevier, Paris.
Muscle membrane polarisation after provocative tests, and after cooling: the normal CMAP changes to be expected.
Kuntzer T., Michel P., 2004. Clinical Neurophysiology, 115 (6) pp. 1457-1463. Peer-reviewed.
Number of Edb motor units estimated using an adapted multiple point stimulation method: normal values and longitudinal studies in ALS and peripheral neuropathies.
Albrecht E., Kuntzer T., 2004. Clinical Neurophysiology, 115 (3) pp. 557-563. Peer-reviewed.
Pathologies nerveuses microtraumatiques du sportif. [Microtraumatic peripheral neuropathies in sports]
Ochsner F., Kuntzer T., 2004. Revue Médicale de Liège, 59 Suppl 1 pp. 49-57. Peer-reviewed.
Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studies
Le Ber I., Moreira M. C., Rivaud-Pechoux S., Chamayou C., Ochsner F., Kuntzer T., Tardieu M., Said G., Habert M. O., Demarquay G. et al., 2003/12. Brain, 126 (Pt 12) pp. 2761-72. Peer-reviewed.
Efficacy of lidocaine patch 5% in the treatment of focal peripheral neuropathic pain syndromes: a randomized, double-blind, placebo-controlled study
Meier T., Wasner G., Faust M., Kuntzer T., Ochsner F., Hueppe M., Bogousslavsky J., Baron R., 2003/11. Pain, 106 (1-2) pp. 151-8. Peer-reviewed.
Phenotypic expression of a Pro 87 to Leu mutation in the connexin 32 gene in a large Swiss family with Charcot-Marie-Tooth neuropathy
Kuntzer T., Dunand M., Schorderet D. F., Vallat J. M., Hahn A. F., Bogousslavsky J., 2003/03. Journal of the Neurological Sciences, 207 (1-2) pp. 77-86. Peer-reviewed.
Principal mutation hotspot for central core disease and related myopathies in the C-terminal transmembrane region of the RYR1 gene
Davis M. R., Haan E., Jungbluth H., Sewry C., North K., Muntoni F., Kuntzer T., Lamont P., Bankier A., Tomlinson P. et al., 2003/02. Neuromuscular Disorders, 13 (2) pp. 151-7. Peer-reviewed.
Complications neurologiques périphériques du diabète
Ghika J., Küntzer T., Waeber G., 2003. Médecine et Hygiène, 61 (2436) pp. 960-964. Peer-reviewed.
Thyroid hormone reduces the loss of axotomized sensory neurons in dorsal root ganglia after sciatic nerve transection in adult rat.
Schenker M., Kraftsik R., Glauser L., Kuntzer T., Bogousslavsky J., Barakat-Walter I., 2003. Experimental neurology, 184 (1) pp. 225-36. Peer-reviewed.
Neuropathies alcooliques et nutritionnelles. [Alcoholic neuropathies and nutrients]
Kuntzer T., 2002/12. Revue Neurologique, 158 (12 Pt 1) pp. 1236-42. Peer-reviewed.
Dysglobulinemies IgM et complications neurologiques. [Neurological manifestations of IgM dysglobulinemia]
Steck A. J., Kuntzer T., 2002/10. Revue Neurologique, 158 (10 Pt 1) pp. 971-8. Peer-reviewed.
Mecanismes immunitaires et traitements du syndrome de Guillain-Barre et des polyradiculonevrites inflammatoires chroniques. [Immunopathology and treatments of Guillain-Barre syndrome and of chronic inflammatory demyelinating polyneuropathy]
Radziwill A. J., Kuntzer T., Steck A. J., 2002/03. Revue Neurologique, 158 (3) pp. 301-10. Peer-reviewed.
Atteintes nerf-muscle de la grossesse et du post-partum
Francini K., Ochsner F., Meyer S., Kuntzer T., 2002. Médecine et Hygiène, 60 (2390) pp. 894-898. Peer-reviewed.
Myéloradiculopathie chronique progressive chez un homme de 61 ans [Chronic progressive myeloradiculopathy in a 61-year-old man]
Kuntzer T., Regli L., Lettry-Trouillat R., Meuli R., Uské A., Bogousslavsky J., 2002. Revue neurologique, 158 (11) pp. 1110-1114. Peer-reviewed.
Thyroid hormones stimulate expression and modification of cytoskeletal protein during rat sciatic nerve regeneration.
Schenker M., Riederer B.M., Kuntzer T., Barakat-Walter I., 2002. Brain Research, 957 (2) pp. 259-270. Peer-reviewed.
Syndrome du canal carpien de cause rare: une tumeur maligne des gaines nerveuses du nerf median. [Carpal tunnel syndrome with an unusual cause: a malignant nerve sheath tumor of the median nerve]
Ochsner F., Baumann R. P., Kuntzer T., 2001/12. Revue Neurologique, 157 (12) pp. 1547-9. Peer-reviewed.
Peripheral axonal motor degeneration after spinal cord infarct.
Michel P., Miklossy J., Kuntzer T., 2001. Journal of Neurology, Neurosurgery, and Psychiatry, 71 (1) p. 128. Peer-reviewed.
Situations d'urgence.
Bogousslavsky J, Carruzzo A, Clarke S, Curty B, Favre J, Ghika J, Kuntzer T, Nater B, Reichhart M, Schwarz U et al., 2001. dans Guide Médical Thérapeutique, Médecine & Hygiène.
Clinicopathological and molecular biological studies in a patient with neurolymphomatosis
Kuntzer T., Lobrinus J. A., Janzer R. C., Ghika J., Bogousslavsky J., 2000/10. Muscle and Nerve, 23 (10) pp. 1604-9. Peer-reviewed.
Differential effect of thyroid hormone deficiency on the growth of calretinin-expressing neurons in rat spinal cord and dorsal root ganglia.
Barakat-Walter I., Kraftsik R., Kuntzer T., Bogousslavsky J., Magistretti P., 2000/10. Journal of Comparative Neurology, 426 (4) pp. 519-533. Peer-reviewed.
Polyneuropathy attributes: a comparison between patients with anti-MAG and anti-sulfatide antibodies
Erb S., Ferracin F., Fuhr P., Rosler K. M., Hess C. W., Kuntzer T., Bogousslavsky J., Sztajzel R., Steck A. J., 2000/10. Journal of Neurology, 247 (10) pp. 767-72. Peer-reviewed.
Epidemiologie des maladies neuromusculaires chez l'adulte. [Epidemiology of adult neuromuscular disorders]
Kuntzer T., Lettry-Trouillat R., Bogousslavsky J., 2000/09. Revue Médicale de la Suisse Romande, 120 (9) pp. 725-31. Peer-reviewed.
Maladies et incapacites, allocations et modes de transports: correlations chez les membres d'une association de patients avec maladies neuromusculaires. Pour l'Association Suisse Romande contre la Myopathie. [Correlation of diseases and disabilities and allocation and modes of transport among the members of an association of patients with neuromuscular diseases. For the Association Suisse Romande contre la Myopathie]
Kuntzer T., Baume F., Bozzio D., Joray Y., Bujard M., Piguet L., Bozzio Y., 2000/09. Revue Médicale de la Suisse Romande, 120 (9) pp. 755-9. Peer-reviewed.
Exercise test in muscle channelopathies and other muscle disorders
Kuntzer T., Flocard F., Vial C., Kohler A., Magistris M., Labarre-Vila A., Gonnaud P. M., Ochsner F., Soichot P., Chan V. et al., 2000/07. Muscle and Nerve, 23 (7) pp. 1089-94. Peer-reviewed.
The mutation of Pro789 to Leu reduces the activity of the fast-twitch skeletal muscle sarco(endo)plasmic reticulum Ca2+ ATPase (SERCA1) and is associated with Brody disease
Odermatt A., Barton K., Khanna V. K., Mathieu J., Escolar D., Kuntzer T., Karpati G., MacLennan D. H., 2000/05. Human Genetics, 106 (5) pp. 482-91. Peer-reviewed.
Scapulalgie et neuropathie sus-scapulaire en pathologie sportive [Scapular pain and supra-scapular neuropathy in sports medicine]
Ochsner F., Bonnard C., Chauplannaz G., Kuntzer T., 2000. Neurophysiologie clinique = Clinical neurophysiology, 30 (1) pp. 21-6. Peer-reviewed.
Troubles neuro-végétatifs ou dysautonomies
Kuntzer T., 2000. 325-350.
Genetic, cytogenetic and physical refinement of the autosomal recessive CMT linked to 5q31-q33: exclusion of candidate genes including EGR1
Guilbot A., Ravise N., Bouhouche A., Coullin P., Birouk N., Maisonobe T., Kuntzer T., Vial C., Grid D., Brice A. et al., 1999/12. European Journal of Human Genetics, 7 (8) pp. 849-59. Peer-reviewed.
Interferon-beta1a in chronic inflammatory demyelinating polyneuropathy
Kuntzer T., Radziwill A. J., Lettry-Trouillat R., Naegeli C., Ochsner F., Erne B., Steck A. J., Bogousslavsky J., 1999/10. Neurology, 53 (6) pp. 1364-5. Peer-reviewed.
Maladies neuromusculaires et vieillissement
Kuntzer T., Lettry-Trouillas R., Leemann B., Bogousslavsky J., 1999. Médecine et Hygiène, 57 (2256) pp. 1082-1089. Peer-reviewed.
Myosite faciale: une forme localisée de myosite généralisée? [Facial myositis: a localized form of generalized myositis?]
Lettry-Trouillat R., Kuntzer T., Janzer R.C., Bogousslavsky J., 1999. Revue Neurologique, 155 (3) pp. 225-228. Peer-reviewed.
Stiffness on exercise: a non progressive disorder of muscle function (Brody-Karpati 's syndrome)
Kuntzer T., Janzer R. C., 1999. 55-61.
Neuropathie peripherique asymetrique des deux membres inferieurs progressive chez un homme de 64 ans. [Progressive asymmetrical peripheral neuropathy of both legs in a 64-year-old man]
Kuntzer T., Talamon C., Said G., 1998/11. Revue Neurologique, 154 (11) pp. 789-94. Peer-reviewed.
Stimulated pressure profile at rest: a noninvasive method for assessing urethral sphincter function
Meyer S., Kuntzer T., De Grandi P., Bachelard O., Schreyer A., 1998/10. Urology, 52 (4) pp. 679-84. Peer-reviewed.
Familial cardiomyopathy and distal myopathy with abnormal desmin accumulation and migration
Lobrinus J. A., Janzer R. C., Kuntzer T., Matthieu J. M., Pfend G., Goy J. J., Bogousslavsky J., 1998/04. Neuromuscular Disorders, 8 (2) pp. 77-86. Peer-reviewed.
Recurrent acute quadriplegic myopathy with myosin deficiency
Kuntzer T., Schaller M. D., Vuadens P., Janzer R. C., 1998/02. Muscle and Nerve, 21 (2) pp. 266-7. Peer-reviewed.
Dysautonomies: contextes et explorations
Kuntzer T., 1998. 164-173.
Maladie de Lyme et neuroborréliose
Kuntzer T., Bogousslavsky J., Péter O., 1998. 1-7.
Maladies neuromusculaires : nouvelles attitudes, nouveaux traitements
Kuntzer T., Lettry-Trouillat R., Bogousslavsky J., 1998. Médecine et Hygiène, 56 (2209) pp. 1045-1053. Peer-reviewed.
Motor neuropathies associated with anti-GM1 ganglioside antibodies
Kuntzer T., Steck A. J., 1998. 190-200.
Neuro-urological and anal sphincter dysfunction
Kuntzer T., 1998. 277-286.
Unilateral femoral neuropathy.
Nogués M.A., Salas E., Martínez A., Romero C., 1998. Muscle &Amp; Nerve, 21 (1) pp. 126-127. Peer-reviewed.
Clinical and prognostic features in unilateral femoral neuropathies
Kuntzer T., van Melle G., Regli F., 1997/02. Muscle and Nerve, 20 (2) pp. 205-11. Peer-reviewed.
Drogues et atteintes neurologiques aiguës
Kuntzer T., Gervasoni J. P., Bogousslavsky J., 1997. Médecine et Hygiène, 55 (2164) pp. 1061-65. Peer-reviewed.
Dystrophie myotonique de Steinert
Kuntzer T., Schorderet D., 1997. 149-164.
Complications neurologiques périphériques et médullaires de la toxicomanie intraveineuse à l'héroïne [Peripheral nerve and spinal cord complication in intravenous heroin addiction].
Bernasconi A., Kuntzer T., Ladbon N., Janzer R.C., Yersin B., Regli F., 1996/11. Revue Neurologique, 152 (11) pp. 688-694. Peer-reviewed.
Atteintes nerf-muscle et accidents cerebrovasculaires. [Neuromuscular involvement and cerebrovascular accidents]
Kuntzer T., Hirt L., Bogousslavsky J., 1996/08. Revue Médicale de la Suisse Romande, 116 (8) pp. 605-9. Peer-reviewed.
Anticorps anti-glycoconjugues et neuropathies peripheriques dysglobulinemiques ou dysimmunitaires. [Anti-glycoconjugate antibodies and dysglobulinemic or dysimmune peripheral neuropathies]
Steck A. J., Kuntzer T., 1996/05. Revue Neurologique, 152 (5) pp. 400-4. Peer-reviewed.
Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study.
Nelis E., Van Broeckhoven C., De Jonghe P., Löfgren A., Vandenberghe A., Latour P., Le Guern E., Brice A., Mostacciuolo M.L., Schiavon F. et al., 1996. European Journal of Human Genetics, 4 (1) pp. 25-33. Peer-reviewed.
Evidence of axonal reinnervation in two arthropod-borne viral encephalomyelitis patients
Kuntzer T., Ochsner F., 1996. European Neurology, 36 (1) pp. 57-9. Peer-reviewed.
Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group.
Lopes J., LeGuern E., Gouider R., Tardieu S., Abbas N., Birouk N., Gugenheim M., Bouche P., Agid Y., Brice A., 1996. American Journal of Human Genetics, 58 (6) pp. 1223-1230. Peer-reviewed.
Stress urinary incontinence due to a low-pressure urethra: a socially invalidizing disease
Meyer S., Kuntzer T., Newsom N., de Grandi P., 1996. Neurourology and Urodynamics, 15 (3) pp. 177-86. Peer-reviewed.
Syndromes myositique: les éléments du diagnostic
Kuntzer T., Marin C., Janzer R. C., 1996. 75-90.
Constant rearrangement of the CMT1A-REP sequences in HNPP patients with a deletion in chromosome 17p11.2: a study of 30 unrelated cases. The French CMT Collaborative Research Group.
LeGuern E., Gouider R., Lopes J., Abbas N., Gugenheim M., Tardieu S., Ravisé N., Léger J.M., Vallat J.M., Bouche P., 1995/09. Human molecular genetics, 4 (9) pp. 1673-1674. Peer-reviewed.
Syndromes myastheniformes: traitements actuels et futurs. [Myasthenia-like syndromes: current and future treatments]
Kuntzer T., Pedrazzi P., 1995/09. Schweizerische Rundschau fur Medizin Praxis, 84 (38) pp. 1042-9. Peer-reviewed.
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