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Myoclonus-dystonia: clinical and electrophysiologic pattern related to SGCE mutations

Neurology, 2008-03, Vol.70 (13), p.1010-1016

2008

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Herpes simplex encephalitis relapses in children: differentiation of two neurologic entities

Neurology, 2003-07, Vol.61 (2), p.241-243

2003

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Doublecortin Is the Major Gene Causing X-Linked Subcortical Laminar Heterotopia (SCLH)

Human molecular genetics, 1998-07, Vol.7 (7), p.1063-1070

1998

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Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes

Journal of medical genetics, 2006-05, Vol.43 (5), p.394-400

2006

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MRI prognostic factors for relapse after acute CNS inflammatory demyelination in childhood

Brain (London, England : 1878), 2004-09, Vol.127 (9), p.1942-1947

2004

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Recurrence of the T666M Calcium Channel CACNA1A Gene Mutation in Familial Hemiplegic Migraine with Progressive Cerebellar Ataxia

American journal of human genetics, 1999, Vol.64 (1), p.89-98

1999

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First episode of acute CNS inflammatory demyelination in childhood: prognostic factors for multiple sclerosis and disability

The Journal of pediatrics, 2004-02, Vol.144 (2), p.246-252

2004

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Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia

Brain (London, England : 1878), 2009-07, Vol.132 (7), p.1753-1763

2009

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Autism and visual agnosia in a child with right occipital lobectomy

Journal of neurology, neurosurgery and psychiatry, 1998-10, Vol.65 (4), p.555-560

1998

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Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients

Orphanet journal of rare diseases, 2015-09, Vol.10 (1), p.123-123, Article 123

2015

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Infantile spasms with basal ganglia MRI hypersignal may reveal mitochondrial disorder due to T8993G MT DNA mutation

Neuropediatrics, 2003-10, Vol.34 (5), p.265-269

2003

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Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q

Nature (London), 1990-04, Vol.344 (6268), p.767-768

1990

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Increased density of oligodendrocytes in childhood ataxia with diffuse central hypomyelination (CACH) syndrome : neuropathological and biochemical study of two cases

Acta neuropathologica, 1999-05, Vol.97 (5), p.469-480

1999

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DYT1 mutation in French families with idiopathic torsion dystonia

Brain (London, England : 1878), 1999, Vol.122 (1), p.41-45

1999

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Limits of Early Diagnosis of Herpes Simplex Encephalitis in Children: A Retrospective Study of 38 Cases

Clinical infectious diseases, 2003-05, Vol.36 (10), p.1335-1339

2003

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Neurological presentation in pediatric patients with congenital disorders of glycosylation type Ia

Neuropediatrics, 2003-02, Vol.34 (1), p.1-6

2003

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Genetic heterogeneity of familial hemiplegic migraine

American journal of human genetics, 1994-12, Vol.55 (6), p.1166-1172

1994

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Reappraisal of Rasmussen's syndrome with special emphasis on treatment with high doses of steroids

Journal of neurology, neurosurgery and psychiatry, 1994-11, Vol.57 (11), p.1325-1333

1994

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Demyelinating peripheral neuropathy associated with hemophagocytic lymphohistiocytosis. An immuno-electron microscopic study

Acta neuropathologica, 2004-10, Vol.108 (4), p.341-344

2004

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Diffuse cortical dysplasia, or the 'double cortex' syndrome: the clinical and epileptic spectrum in 10 patients

Neurology, 1991-10, Vol.41 (10), p.1656-1656

1991

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Structures d'accueil des enfants handicapés

Journal de pédiatrie et de puériculture, 1999-04, Vol.12 (3), p.169-174

Ponsot, G.

1999

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Hyperglycinémie sans cétose et dysfonctionnement des récepteurs NMDA

Archives de pédiatrie (Paris), 1996, Vol.3, p.S172-S175

Ponsot, G

1996

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Human herpes virus type 6, etiology of an acute encephalitis in childhood: case report

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2007-05, Vol.14 (5), p.472-475

2007

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Fetal neurology: conditions of diagnostic uncertainty

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2006-06, Vol.13 (6), p.825-827

2006

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Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22

Journal of medical genetics, 1997-03, Vol.34 (3), p.177-183

1997

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Myoclonus-dystonia: clinical and electrophysiologic pattern related to SGCE mutations

Herpes simplex encephalitis relapses in children: differentiation of two neurologic entities

Doublecortin Is the Major Gene Causing X-Linked Subcortical Laminar Heterotopia (SCLH)

Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes

MRI prognostic factors for relapse after acute CNS inflammatory demyelination in childhood

Recurrence of the T666M Calcium Channel CACNA1A Gene Mutation in Familial Hemiplegic Migraine with Progressive Cerebellar Ataxia

First episode of acute CNS inflammatory demyelination in childhood: prognostic factors for multiple sclerosis and disability

Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia

Autism and visual agnosia in a child with right occipital lobectomy

Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients

Infantile spasms with basal ganglia MRI hypersignal may reveal mitochondrial disorder due to T8993G MT DNA mutation

Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q

Increased density of oligodendrocytes in childhood ataxia with diffuse central hypomyelination (CACH) syndrome : neuropathological and biochemical study of two cases

DYT1 mutation in French families with idiopathic torsion dystonia

Limits of Early Diagnosis of Herpes Simplex Encephalitis in Children: A Retrospective Study of 38 Cases

Neurological presentation in pediatric patients with congenital disorders of glycosylation type Ia

Genetic heterogeneity of familial hemiplegic migraine

Reappraisal of Rasmussen's syndrome with special emphasis on treatment with high doses of steroids

Demyelinating peripheral neuropathy associated with hemophagocytic lymphohistiocytosis. An immuno-electron microscopic study

Diffuse cortical dysplasia, or the 'double cortex' syndrome: the clinical and epileptic spectrum in 10 patients

Structures d'accueil des enfants handicapés

Hyperglycinémie sans cétose et dysfonctionnement des récepteurs NMDA

Human herpes virus type 6, etiology of an acute encephalitis in childhood: case report

Fetal neurology: conditions of diagnostic uncertainty

Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22

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