Eliane Roulet Perez

Publications | Phd and Masters theses

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114 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 | 1994 | 1993 | 1992 | 1991 | 1990 | 1989 | 1988 |
 
Classification as autonomic versus sensory seizures.
Fisher R.S., Cross H., D'Souza C., French J.A., Haut S., Higurashi N., Hirsch E., Jansen F.E., Peltola J., Moshe S.L. et al., 2019/09. Epilepsia, 60 (9) pp. 2003-2005. Peer-reviewed.
 
Cerebellar lesions in pediatric abusive head trauma
Haas-Lude Karin, Roulet-Perez Eliane, Döbler-Neumann Marion, Groeschel Samuel, Nägele Thomas, Krägeloh-Mann Ingeborg, 2019/07. European journal of paediatric neurology, 23 (4) pp. 604-608. Peer-reviewed.
 
2017 International League Against Epilepsy classifications of seizures and epilepsy are steps in the right direction.
Fisher R.S., Cross H., D'Souza C., French J.A., Haut S., Higurashi N., Hirsch E., Jansen F.E., Peltola J., Moshé S.L. et al., 2019/06. Epilepsia, 60 (6) pp. 1040-1044. Peer-reviewed.
 
Midazolam as a first-line treatment for neonatal seizures: Retrospective study.
Dao K., Giannoni E., Diezi M., Roulet-Perez E., Lebon S., 2018/05. Pediatrics international, 60 (5) pp. 498-500. Peer-reviewed.
 
Childhood epilepsy with centro-temporal spikes (rolandic epilepsy) and written language.
Roulet-Perez E., Mayor C., 2018/03. Developmental medicine and child neurology, 60 (3) p. 219. Peer-reviewed.
 
Periinsular anterior quadrantotomy: technical note.
Cossu G., Lebon S., Seeck M., Pralong E., Messerer M., Roulet-Perez E., Daniel R.T., 2018/02. Journal of neurosurgery. Pediatrics, 21 (2) pp. 124-132. Peer-reviewed.
 
Pédiatrie. Nouvelle classification des crises épileptiques et des épilepsies [Pediatrics - New classification of seizures and epilepsies]
Lebon S., Roulet-Perez É., 2018/01/10. Revue medicale suisse, 14 (588-589) pp. 74-75. Peer-reviewed.
Pediatric stroke related to Lyme neuroborreliosis: Data from the Swiss NeuroPaediatric Stroke Registry and literature review.
Monteventi O., Steinlin M., Regényi M., Roulet-Perez E., Weber P., Fluss J., 2018/01. European journal of paediatric neurology, 22 (1) pp. 113-121. Peer-reviewed.
 
Impact cognitif de la chirurgie de l'épilepsie de l'enfant
Kallay-Zetchi Christine, Roulet-Perez Eliane, 2017/12/01. Epileptologie, 34 pp. 191-195.
 
Prenatal Brainstem Disruptions: Small Lesions-Big Problems.
Boltshauser E., Bauder F., Giarrana M., Hackenberg A., Lebon S., Roulet-Perez E., Schmid R., Schmitt-Mechelke T., Poretti A., 2017/10. Neuropediatrics, 48 (5) pp. 350-355. Peer-reviewed.
 
Response to the numbering of seizure types.
Fisher R.S., Helen Cross J., D'Souza C., French J.A., Haut S., Higurashi N., Hirsch E., Jansen F.E., Lagae L., Moshe S.L. et al., 2017/07. Epilepsia, 58 (7) pp. 1300-1301. Peer-reviewed.
 
Instruction manual for the ILAE 2017 operational classification of seizure types.
Fisher R.S., Cross J.H., D'Souza C., French J.A., Haut S.R., Higurashi N., Hirsch E., Jansen F.E., Lagae L., Moshé S.L. et al., 2017/04. Epilepsia, 58 (4) pp. 531-542. Peer-reviewed.
 
Operational classification of seizure types by the International League Against Epilepsy: Position Paper of the ILAE Commission for Classification and Terminology.
Fisher R.S., Cross J.H., French J.A., Higurashi N., Hirsch E., Jansen F.E., Lagae L., Moshé S.L., Peltola J., Roulet Perez E. et al., 2017/04. Epilepsia, 58 (4) pp. 522-530. Peer-reviewed.
 
Verbal emotional memory in a case with left amygdala damage.
Mayor-Dubois Claire, Deglise Sophie, Poloni Claudia, Maeder Philippe, Roulet-Perez Eliane, 2016. Neurocase, 22 (1) pp. 45-54. Peer-reviewed.
 
Lamotrigine can be beneficial in patients with Dravet syndrome.
Dalic L., Mullen S.A., Roulet Perez E., Scheffer I., 2015. Developmental Medicine and Child Neurology, 57 (2) pp. 200-202. Peer-reviewed.
 
New genes for focal epilepsies with speech and language disorders.
Turner S.J., Morgan A.T., Perez E.R., Scheffer I.E., 2015. Current Neurology and Neuroscience Reports, 15 (6) p. 554. Peer-reviewed.
 
p.L1612P, a novel voltage-gated sodium channel Nav1.7 mutation inducing a cold sensitive paroxysmal extreme pain disorder.
Suter M.R., Bhuiyan Z.A., Laedermann C.J., Kuntzer T., Schaller M., Stauffacher M.W., Roulet E., Abriel H., Decosterd I., Wider C., 2015. Anesthesiology, 122 (2) pp. 414-423. Peer-reviewed.
 
When should clinicians search for GLUT1 deficiency syndrome in childhood generalized epilepsies?
Lebon S., Suarez P., Alija S., Korff C.M., Fluss J., Mercati D., Datta A.N., Poloni C., Marcoz J.P., Campos-Xavier A.B. et al., 2015. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society, 19 (2) pp. 170-175. Peer-reviewed.
 
Congenital ataxia and hemiplegic migraine with cerebral edema associated with a novel gain of function mutation in the calcium channel CACNA1A.
García Segarra N., Gautschi I., Mittaz-Crettol L., Kallay Zetchi C., Al-Qusairi L., Van Bemmelen M.X., Maeder P., Bonafé L., Schild L., Roulet-Perez E., 2014. Journal of the Neurological Sciences, 342 (1-2) pp. 69-78. Peer-reviewed.
 
Nondeclarative learning in children with Specific Language Impairment: Predicting regularities in the visuomotor, phonological, and cognitive domains.
Mayor-Dubois C., Zesiger P., Van der Linden M., Roulet-Perez E., 2014. Child Neuropsychology, 20 (1) pp. 14-22.
 
Pédiatrie 2. Génétique des épilepsies de l'enfant: Pour qui ? Comment? Pourquoi [Genetics of childhood epilepsies: for who? how? why?].
Lebon S., Campos-Xavier B., Bonafé L., Roulet-Perez E., 2014. Revue Médicale Suisse, 10 (412-413) pp. 110-111.
 
Undernutrition in children with profound intellectual and multiple disabilities (PIMD): its prevalence and influence on quality of life.
Holenweg-Gross C., Newman C.J., Faouzi M., Poirot-Hodgkinson I., Bérard C., Roulet-Perez E., 2014. Child, 40 (4) pp. 525-532.
 
When is a child with status epilepticus likely to have Dravet syndrome?
Le Gal F., Lebon S., Ramelli G.P., Datta A.N., Mercati D., Maier O., Combescure C., Rodriguez M.I., Seeck M., Roulet E. et al., 2014. Epilepsy Research, 108 (4) pp. 740-747. Peer-reviewed.
 
Functional independence within the self-memory system: new insights from two cases of developmental amnesia.
Picard L., Mayor-Dubois C., Maeder P., Kalenzaga S., Abram M., Duval C., Eustache F., Roulet-Perez E., Piolino P., 2013. Cortex, 49 (6) pp. 1463-1481. Peer-reviewed.
 
Successful surgical resection in non-lesional operculo-insular epilepsy without intracranial monitoring.
Chiosa V., Granziera C., Spinelli L., Pollo C., Roulet-Perez E., Groppa S., Seeck M., 2013. Epileptic Disorders, 15 (2) pp. 148-157. Peer-reviewed.
 
Anti-N-Methyl-D-Aspartate (NMDA) Receptor Encephalitis Mimicking a Primary Psychiatric Disorder in an Adolescent.
Lebon S., Mayor-Dubois C., Popea I., Poloni C., Selvadoray N., Gumy A., Roulet-Perez E., 2012. Journal of Child Neurology, 27 (12) pp. 1607-1610. Peer-reviewed.
 
Avancées thérapeutiques dans les epilepsies réfractaires de l'enfant [Therapeutic advances in refractory epilepsies in children].
Korff C.M., Lebon S., Roulet-Perez E., 2012. Revue Médicale Suisse, 8 (329) pp. 413-4, 416-7.
 
Brachialgies chez un adolescent [Upper limb pain in an adolescent].
Balomenou S., Roulet-Perez E., Vaudaux B., Lebon S., 2012. Archives de Pédiatrie, 19 (10) pp. 1093-1094.
 
Long-term outcome after cognitive and behavioral regression in non-lesional epilepsy with CSWS
Perez E. Roulet , Deonna T., Mayor-Dubois C., Valenti-Hirsch M. P., Hirsch E., Metz-Lutz M., De Saint-Martin A., Seegmueller C., 2012. p. 76 dans 10th European Congress on Epileptology, Epilepsia.
 
Long-term outcome after cognitive and behavioral regression in nonlesional epilepsy with continuous spike-waves during slow-wave sleep.
Seegmüller C., Deonna T., Dubois C.M., Valenti-Hirsch M.P., Hirsch E., Metz-Lutz M.N., de Saint Martin A., Roulet-Perez E., 2012. Epilepsia, 53 (6) pp. 1067-1076.
 
Acute infantile encephalopathy predominantly affecting the frontal lobe (AIEF): A European case.
Jequier Gygax M., Deonna T., Maeder P., Mayor-Dubois C., Roulet-Perez E., 2011. European Journal of Paediatric Neurology, 15 (2) pp. 158-162.
 
An initial MRI picture of limbic encephalitis in subacute sclerosing panencephalitis.
Lebon S., Maeder P., Maeder-Ingvar M., Poloni C., Mayor-Dubois C., Roulet-Perez E., Jeannet P.Y., 2011. European Journal of Paediatric Neurology, 15 (6) pp. 544-546.
 
Déficit en transporteur cérébral du glucose de type 1 dans les épilepsies généralisées idiopathiques et cryptogéniques de l'enfant
Lebon S, Poloni C, Korff Ch, Bonafé L, Roulet Perez E, 2011. Epileptologie, 28 pp. 107-110.
 
The phenotype of recurrent 10q22q23 deletions and duplications.
van Bon B.W., Balciuniene J., Fruhman G., Nagamani S.C., Broome D.L., Cameron E., Martinet D., Roulet E., Jacquemont S., Beckmann J.S. et al., 2011. European Journal of Human Genetics, 19 (4) pp. 400-408.
 
Recent skin injuries in children with motor disabilities.
Newman C.J., Holenweg-Gross C., Vuillerot C., Jeannet P.Y., Roulet-Perez E., 2010/05. Archives of disease in childhood, 95 (5) pp. 387-390. Peer-reviewed.
 
Correspondence on ''deterioration in cognitive function in children with benign epilepsy of childhood with central temporal spikes treated with sulthiame''.
Deonna T., Roulet-Perez E., Cronel-Ohayon S., Mayor-Dubois C., 2010. Journal of Child Neurology, 25 (1) pp. 127-128.
 
Early-onset acquired epileptic aphasia (Landau-Kleffner syndrome, LKS) and regressive autistic disorders with epileptic EEG abnormalities: the continuing debate.
Deonna T., Roulet-Perez E., 2010. Brain and Development, 32 (9) pp. 746-752.
 
Impact of severe epilepsy on development: Recovery potential after successful early epilepsy surgery.
Roulet-Perez Eliane, Davidoff Veronique, Mayor-Dubois Claire, Maeder-Ingvar Malin, Seeck Margitta, Ruffieux Christiane, Villemure Jean-Guy, Deonna Thierry, 2010. Epilepsia, 51 (7) pp. 1266-1276. Peer-reviewed.
 
Status epilepticus in fragile X syndrome.
Gauthey M., Poloni C.B., Ramelli G.P., Roulet-Perez E., Korff C.M., 2010. Epilepsia, 51 (12) pp. 2470-2473.
 
Visuo-motor and cognitive procedural learning in children with basal ganglia pathology.
Mayor-Dubois C., Maeder P., Zesiger P., Roulet-Perez E., 2010. Neuropsychologia, 48 (7) pp. 2009-2017.
Epilepsie généralisée idiopathique ou épilepsie symptomatique? Similitudes et pièges
Lebon S., Roulet-Perez E., 2009. Epileptologie, 26 (3) pp. 121-130.
 
Outcome of severe unilateral cerebellar hypoplasia.
Poretti Andrea, Limperopoulos Catherine, Roulet-Perez Eliane, Wolf Nicole I., Rauscher Christian, Prayer Daniela, Mueller Anita, Weissert Markus, Kotzaeridou Urania, Du Plessis Adre J. et al., 2009. Developmental Medicine and Child Neurology, 52 (8) pp. 718-724.
 
Perfusion abnormalities in hemimegalencephaly
Wintermark P., Roulet-Perez E., Maeder-Ingvar M., Moessinger A. C., Gudinchet F., Meuli R., 2009. Neuropediatrics, 40 (2) pp. 92-96. Peer-reviewed.
 
Reversible acquired epileptic frontal syndrome and CSWS suppression in a child with congenital hemiparesis treated by hemispherotomy.
Kallay C., Mayor-Dubois C., Maeder-Ingvar M., Seeck M., Debatisse D., Deonna T., Roulet-Perez E., 2009. European Journal of Paediatric Neurology, 13 (5) pp. 430-438.
 
Severe childhood encephalopathy with dyskinesia and prolonged cognitive disturbances: evidence for anti-N-methyl-d-aspartate receptor encephalitis.
Poloni Claudia, Korff Christian M., Ricotti Valeria, King Mary D., Perez Eliane Roulet, Mayor-Dubois Claire, Haenggeli Charles-Antoine, Deonna Thierry, 2009. Developmental Medicine and Child Neurology, 52 (5) pp. 78-82.
 
Sign language in Landau-Kleffner syndrome.
Deonna T., Prelaz-Girod A.C., Mayor-Dubois C., Roulet-Perez E., 2009. Epilepsia, 50 Suppl 7 pp. 77-82.
Sudden unexpected death in an infant with L-2-hydroxyglutaric aciduria.
Gygax Marine Jequier, Roulet-Perez Eliane, Meagher-Villemure Kathleen, Jakobs Cornelis, Salomons Gajja S., Boulat Olivier, Superti-Furga Andrea, Ballhausen Diana, Bonafe Luisa, 2009. European Journal of Pediatrics, 168 (8) pp. 957-962. Peer-reviewed.
Traitements des encéphalopathies épileptiques : revue et actualités
Lebon S., Roulet-Perez E., 2009. Epileptologie, 26 (4) pp. 181-189.
Congenital disorder of glycosylation type Id (CDG Id): phenotypic, biochemical and molecular characterization of a new patient.
Rimella-Le-Huu A., Henry H., Kern I., Hanquinet S., Roulet-Perez E., Newman C.J., Superti-Furga A., Bonafé L., Ballhausen D., 2008. Journal of Inherited Metabolic Disease. Peer-reviewed.
 
Glut-1 deficiency syndrome masquerading as idiopathic generalized epilepsy.
Roulet-Perez E., Ballhausen D., Bonafé L., Cronel-Ohayon S., Maeder-Ingvar M., 2008. Epilepsia, 49 (11) pp. 1955-1958. 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.
 
Retinopathy, progressive intracerebral calcification and epilepsy in a premature new-born: case report of a new entity
Gygax M.J., De Ribeaupierre S., Wolfensberger T.J., Bonafe L., Maeder P., Roulet-Perez E., Jeannet P.Y., 2008. pp. 45S dans Annual Joint Meeting of the Swiss Societies for Paediatrics, Child and Adolescent Psychiatry, Paediatric Surgery, Swiss Medical Weekly. Peer-reviewed.
 
The role of epilepsy in early language development in a child with a congenital lesion in the right hemisphere
Mayor-Dubois C., Maeder-Ingvar M., Deonna T., Roulet-Perez E., 2008. Developmental Medicine and Child Neurology, 50 (11) pp. 870-875. Peer-reviewed.
 
Paroxysmal extreme pain disorder (previously familial rectal pain syndrome)
Fertleman C. R., Ferrie C. D., Aicardi J., Bednarek N. A., Eeg-Olofsson O., Elmslie F. V., Griesemer D. A., Goutieres F., Kirkpatrick M., Malmros I. N. et al., 2007/08. Neurology, 69 (6) pp. 586-95.
 
Autistic regression associated with seizure onset in an infant with tuberous sclerosis
Deonna T., Roulet-Perez E., Chappuis H., Ziegler A.L., 2007/04. Developmental medicine and child neurology, 49 (4) p. 320. Peer-reviewed.
 
Progressive unilateral hemispheric atrophy in an infant with neurofibromatosis
Wintermark P., Meagher-Villemure K., Villemure J. G., Maeder-Ingvar M., Maeder P., Ghariani S., Roulet-Perez E., 2007/04. Neuropediatrics, 38 (2) pp. 100-4. Peer-reviewed.
 
Delayed diagnosis of atypical mild GLUT1 deficiency
Ballhausen D., Kallay C., Cronel-Ohayon S., Maeder-Ingvar M., Roulet-Perez E., Bonafe L., 2007. p. 57 dans 44th Annual Symposium of the Society for the Study of Inborn Errors of Metabolism, Journal of Inherited Metabolic Disease. Peer-reviewed.
 
Glucose transporter type 1 (GLUT-1) deficiency syndrome can be mistaken for primary generalized epilepsy
Maeder-Ingvar M., Cronel-Ohayon S., Kallay C., Ballhausen D., Roulet-Perez E., 2007. p. 87 dans 11th Congress of the European Federation of Neurological Societies, European Journal of Neurology. Peer-reviewed.
 
Multimodality imaging for focus localization in pediatric pharmacoresistant epilepsy
Kurian M., Spinelli L., Delavelle J., Willi J. P., Velazquez M., Chaves V., Habre W., Meagher-Villemure K., Roulet E., Villeneuve J. G. et al., 2007. Epileptic Disorders, 9 (1) pp. 20-31.
 
Neuropsychological problems after paediatric stroke: two year follow-up of Swiss children
Pavlovic J., Kaufmann F., Boltshauser E., Capone Mori A., Gubser Mercati D., Haenggeli C. A., Keller E., Lutschg J., Marcoz J. P., Ramelli G. P. et al., 2006/02. Neuropediatrics, 37 (1) pp. 13-9.
 
Transient dystonic toe-walking: differentiation from cerebral palsy and a rare explanation for some unexplained cases of idiopathic toe-walking
Newman C. J., Ziegler A. L., Jeannet P. Y., Roulet-Perez E., Deonna T. W., 2006/02. Developmental Medicine and Child Neurology, 48 (2) pp. 96-102.
 
Autistic spectrum disorder: evaluating a possible contributing or causal role of epilepsy.
Deonna T., Roulet E., 2006. Epilepsia, 47 Suppl 2 pp. 79-82. Peer-reviewed.
 
Deficit in memory consolidation (abnormal forgetting rate) in childhood temporal lobe epilepsy. Pre and postoperative long-term observation.
Cronel-Ohayon S., Zesiger P., Davidoff V., Boni A., Roulet E., Deonna T., 2006. Neuropediatrics, 37 (6) pp. 317-324. Peer-reviewed.
 
Electrophysiological characteristics of limbic and motor globus pallidus internus (GPI) neurons in two cases of Lesch-Nyhan syndrome
Pralong E., Pollo C., Coubes P., Bloch J., Roulet E., Tetreault M. H., Debatisse D., Villemure J. G., 2005/12. Neurophysiologie Clinique, 35 (5-6) pp. 168-73. Peer-reviewed.
The role of posterior fossa decompression in acute cerebellitis.
de Ribaupierre S., Meagher-Villemure K., Villemure J.G., Cotting J., Jeannet P.Y., Porchet F., Roulet E., Bloch J., 2005/11. Child's Nervous System, 21 (11) pp. 970-974. Peer-reviewed.
 
Anaphylactic reaction and unrelated, subsequent, known side effects during therapy with thiethylperazine.
Rossetti G., Livio F., Roulet E., Hofer M.F., 2005/08. Pediatric allergy and immunology, 16 (5) pp. 453-455. 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.
 
The first three years of the Swiss Neuropaediatric Stroke Registry (SNPSR): a population-based study of incidence, symptoms and risk factors
Steinlin M., Pfister I., Pavlovic J., Everts R., Boltshauser E., Capone Mori A., Gubser Mercati D., Hanggeli C. A., Keller E., Luetschg J. et al., 2005/04. Neuropediatrics, 36 (2) pp. 90-7.
 
Acute brain perfusion disorders in children assessed by quantitative perfusion computed tomography in the emergency setting
Wintermark M., Cotting J., Roulet E., Lepori D., Meuli R., Maeder P., Regli L., Deonna T., Schnyder P., Gudinchet F., 2005. Pediatric Emergency Care, 21 (3) pp. 149-60.
 
Cognitive and behavioural disorders of epileptic origin in children
Deonna T., Roulet Perez E., 2005., Mac Keith Press.
 
Speech delay due to a prelinguistic regression of epileptic origin.
Dubois C.M., Gianella D., Chaves-Vischer V., Haenggeli C.A., Deonna T., Roulet Perez E., 2004/02. Neuropediatrics, 35 (1) pp. 50-53. Peer-reviewed.
 
Brain perfusion in children: evolution with age assessed by quantitative perfusion computed tomography.
Wintermark M., Lepori D., Cotting J., Roulet E., van Melle G., Meuli R., Maeder P., Regli L., Verdun F.R., Deonna T. et al., 2004. Pediatrics, 113 (6) pp. 1642-1652. Peer-reviewed.
 
Les stéréotypies
Roulet Perez E., 2004. Mouvements Neurosciences Cliniques, 5 pp. 21-22.
 
Response to Lena Jacobson’s letter
Deonna T., Roulet Perez E., 2004. DMCN pp. 250 -256.
 
Surgical treatment of temporoparietooccipital cortical dysplasia in infants: report of two cases.
Daniel R.T., Meagher-Villemure K., Roulet E., Villemure J.G., 2004. Epilepsia, 45 (7) pp. 872-6. Peer-reviewed.
 
Isolated absence of optic chiasm revealed by congenital nystagmus, MRI and VEPs.
Korff C.M., Apkarian P., Bour L.J., Meuli R., Verrey J.D., Roulet Perez E., 2003/08. Neuropediatrics, 34 (4) pp. 219-223. Peer-reviewed.
 
Acquired epileptic dysgraphia: a longitudinal study.
Dubois C.M., Zesiger P., Perez E.R., Ingvar M.M., Deonna T., 2003. Developmental medicine and child neurology, 45 (12) pp. 807-12. Peer-reviewed.
 
Acquired epileptic frontal syndrome in children.
Deonnan T., Ziegler A., Roulet Perez E., 2003. dans Frontal lobe seizures and epilepsies in children, John Libbey Eurotext.
 
Ictal bradycardia in a young child with focal cortical dysplasia in the right insular cortex.
Seeck M., Zaim S., Chaves-Vischer V., Blanke O., Maeder-Ingvar M., Weissert M., Roulet E., 2003. European Journal of Paediatric Neurology : EJPN, 7 (4) pp. 177-181. Peer-reviewed.
 
Treatment with Sulthiame (Ospolot) in benign partial epilepsy of childhood and related syndromes: an open clinical and EEG study.
Engler F., Maeder-Ingvar M., Roulet E., Deonna T., 2003. Neuropediatrics, 34 (2) pp. 105-109. Peer-reviewed.
 
Visual impairment due to a dyskinetic eye movement disorder in children with dyskinetic cerebral palsy
Roulet-Perez E., Deonna T., 2002/05. Developmental Medicine and Child Neurology, 44 (5) pp. 356-7; author reply 357.
 
Epileptic falls and gait disturbance in two young children with a sharp wave focus at the vertex: a variant of benign partial epilepsy of childhood?
Vischer V.C., Maeder-Ingvar M., Picard F., Dubois C.M., Davidoff V., Deonna T., Haenggeli C.A., Perez E.R., 2002. European Journal of Paediatric Neurology : EJPN, 6 (3) pp. 169-178. Peer-reviewed.
 
Two brothers with atypical syndactylies, cerebellar atrophy and severe mental retardation.
Schorderet D.F., Addor M.C., Maeder P., Roulet E., Junier L., 2002. Genetic Counseling, 13 (4) pp. 441-447. Peer-reviewed.
 
Langue des signes et langue parlée : compétition ou synergie?
Roulet Perez E, 2001. Paediatrica, 12 (4) pp. 37-40.
 
Primary neonatal thalamic haemorrhage and epilepsy with continuous spike-wave during sleep: a longitudinal follow-up of a possible significant relation.
Monteiro J.P., Roulet-Perez E., Davidoff V., Deonna T., 2001. European Journal of Paediatric Neurology, 5 (1) pp. 41-47.
 
Sign language in childhood epileptic aphasia (Landau-Kleffner syndrome).
Perez E.R., Davidoff V., 2001. Developmental Medicine and Child Neurology, 43 (11) pp. 739-744. Peer-reviewed.
 
Acquired hippocampal damage after temporal lobe seizures in 2 infants.
Perez E.R., Maeder P., Villemure K.M., Vischer V.C., Villemure J.G., Deonna T., 2000/09. Annals of Neurology, 48 (3) pp. 384-387. Peer-reviewed.
 
Intoxication par le monoxyde de carbone chez l'enfant: ne jamais banaliser. [Carbon monoxide poisoning in children: never trivialize]
Scalfaro P., Haenggi M.H., Roulet E., Gehri M., Stucki P., Schaller M.D., Cotting J., 2000/03. Revue Médicale de la Suisse Romande, 120 (3) pp. 259-262.
 
Benign partial epilepsy of childhood: a longitudinal neuropsychological and EEG study of cognitive function.
Deonna T., Zesiger P., Davidoff V., Maeder M., Mayor C., Roulet E., 2000. Developmental Medicine and Child Neurology, 42 (9) pp. 595-603. Peer-reviewed.
 
Home and hospital treatment of acute seizures in children with nasal midazolam.
Jeannet P.Y., Roulet E., Maeder-Ingvar M., Gehri M., Jutzi A., Deonna T., 1999. European Journal of Paediatric Neurology, 3 (2) pp. 73-77. Peer-reviewed.
 
Childhood epilepsy with neuropsychological regression and continuous spike waves during sleep: epilepsy surgery in a young adult.
Roulet Perez E., Seeck M., Mayer E., Despland P.A., de Tribolet N., Deonna T., 1998. European Journal of Paediatric Neurology, 2 (6) pp. 303-311. Peer-reviewed.
 
Post-traumatic mutism in children: clinical characteristics, pattern of recovery and clinicopathological correlations.
Dayer A., Roulet E., Maeder P., Deonna T., 1998. European Journal of Paediatric Neurology, 2 (3) pp. 109-116. Peer-reviewed.
 
Dopa-responsive childhood dystonia: a forme fruste with writer's cramp, triggered by exercise
Deonna T., Roulet E., Ghika J., Zesiger P., 1997/01. Developmental Medicine and Child Neurology, 39 (1) pp. 49-53.
 
Transient acquired stuttering in a child.
Roulet Perez Eliane, Gubser-Mercati Danielle, Davidoff Véronique, 1996. Neurocase, 2 (4) pp. 347-352. Peer-reviewed.
 
Syndromes of acquired epileptic aphasia and epilepsy with continuous spike-waves during sleep: models for prolonged cognitive impairment of epileptic origin
Roulet Perez E., 1995/12. Seminars in Pediatric Neurology, 2 (4) pp. 269-77.
 
Reversible behavioural autistic-like regression: A manifestation of a special (new?) epileptic syndrome in a 28-month-old child. A 2-year longitudinal study .
Deonna Thierry, Ziegler Anne-Lise, Maeder Malin-Ingvar, Ansermet François, Roulet Eliane, 1995. Neurocase, 1 (2) pp. 91-99. Peer-reviewed.
 
Follow-up of optic pathway gliomas in children with neurofibromatosis type 1.
Kuenzle C., Weissert M., Roulet E., Bode H., Schefer S., Huisman T., Landau K., Boltshauser E., 1994. Neuropediatrics, 25 (6) pp. 295-300. Peer-reviewed.
 
Acute fatal parainfectious cerebellar swelling in two children. A rare or an overlooked situation?
Roulet Perez E., Maeder P., Cotting J., Eskenazy-Cottier A. C., Deonna T., 1993/12. Neuropediatrics, 24 (6) pp. 346-51. Peer-reviewed.
 
Mental and behavioural deterioration of children with epilepsy and CSWS: acquired epileptic frontal syndrome
Roulet Perez E., Davidoff V., Despland P. A., Deonna T., 1993/08. Developmental Medicine and Child Neurology, 35 (8) pp. 661-74.
 
Dystonie fruste Dopas-sensible, avec fluctuations liées au sommeil et à l'exercice
Deonna Thierry, Roulet Eliane, Nielsen J., Nançoz M., 1993. pp. 585-586 dans Congrès de la Société de Neurologie Pédiatrique Européenne de Langue Française, Revue Neurologique. Peer-reviewed.
 
Isolated disturbance of written language-acquisition as an initial symptom of epileptic aphasia in a 7-year-old child - a 3-year follow-up-study
Deonna T., Roulet Perez E., Davidoff V., 1993. Aphasiology, 7 (5) pp. 441-450. Peer-reviewed.
 
Isolement de Borrelia Burgdorferi du liquide céphalo-rachidien de trois enfants avec une atteinte neurologique
Peter O., Bretz A.G., Zennhäusern R., Roten H., Roulet E., 1993. Schweizerische Medizinische Wochenschrift = Journal Suisse de Médecine, 123 (1-2) pp. 14-19. Peer-reviewed.
 
Maternally inherited Leigh syndrome.
Ciafaloni E., Santorelli F.M., Shanske S., Deonna T., Roulet E., Janzer C., Pescia G., DiMauro S., 1993. Journal of Pediatrics, 122 (3) pp. 419-422. Peer-reviewed.
 
Speech and oromotor deficits of epileptic origin in benign partial epilepsy of childhood with rolandic spikes (BPERS). Relationship to the acquired aphasia-epilepsy syndrome.
Deonna T.W., Roulet E., Fontan D., Marcoz J.P., 1993. Neuropediatrics, 24 (2) pp. 83-7. Peer-reviewed.
 
Toxic leucoencephalopathy after heroin ingestion in a 21/2-year-old child
Roulet Perez E., Maeder P., Rivier L., Deonna T., 1992/09. Lancet, 340 (8821) p. 729. Peer-reviewed.
 
Myélite transverse et neuromyélite optique chez l'enfant. A propos de trois observations [Transverse myelitis and optic neuromyelitis in children. Apropos of 3 case reports]
Ramelli G.P., Deonna T., Roulet E., Zwingli M., 1992. Schweizerische Rundschau für Medizin Praxis = Revue Suisse de Médecine Praxis, 81 (20) pp. 661-663.
 
Vocal cord paralysis as a presenting sign of acute spinal muscular atrophy SMA type 1.
Roulet E., Deonna T., 1992. Archives of Disease in Childhood, 67 (3) p. 352.
 
Acquired aphasia, dementia, and behavior disorder with epilepsy and continuous spike and waves during sleep in a child
Roulet E., Deonna T., Gaillard F., Peter-Favre C., Despland P. A., 1991/08. Epilepsia, 32 (4) pp. 495-503.
 
Treatment of acquired aphasia and epilepsy.
Deonna T., Roulet E., 1991. Developmental Medicine and Child Neurology, 33 (9) pp. 834-835. Peer-reviewed.
 
Benign paroxysmal tonic upgaze of childhood--a new syndrome.
Deonna T., Roulet E., Meyer H.U., 1990. Neuropediatrics, 21 (4) pp. 213-214. Peer-reviewed.
 
Les camps d'enfants : un instrument précieux dans l'éducation des jeunes diabétiques
Dayer-Métroz M., Roulet Perez E., 1990. Schweizerische Medizinische Wochenschrift = Journal Suisse de Médecine 120 pp. 66-71. Peer-reviewed.
 
Prolonged intermittent drooling and oromotor dyspraxia in benign childhood epilepsy with centrotemporal spikes
Roulet E., Deonna T., Despland P. A., 1989/10. Epilepsia, 30 (5) pp. 564-8.
 
Successful treatment of hereditary dominant chorea with carbamazepine.
Roulet E., Deonna T., 1989. Pediatrics, 83 (6) p. 1077. Peer-reviewed.
 
Benign paroxysmal torticollis in infancy.
Roulet E., Deonna T., 1988. Developmental Medicine and Child Neurology, 30 (3) pp. 409-410. Peer-reviewed.
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