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Psychiatric manifestations revealing inborn errors of metabolism in adolescents and adults

Journal of inherited metabolic disease, 2007-10, Vol.30 (5), p.631-641

2007

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Immunosuppressive therapy is more effective than interferon in neuromyelitis optica

Multiple sclerosis, 2007-03, Vol.13 (2), p.256-259

2007

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The adult form of Niemann–Pick disease type C

Brain (London, England : 1878), 2007-01, Vol.130 (1), p.120-133

2007

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Hereditary spastic paraparesis in adults associated with inborn errors of metabolism: A diagnostic approach

Journal of inherited metabolic disease, 2007-11, Vol.30 (6), p.855-864

2007

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Paroxysmal hypothermia as a clinical feature of multiple sclerosis

Neurology, 2009-01, Vol.72 (2), p.193

2009

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Leukoencephalopathies associated with inborn errors of metabolism in adults

Journal of inherited metabolic disease, 2008-06, Vol.31 (3), p.295-307

2008

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Age at onset determines the occurrence of the progressive phase of multiple sclerosis

Neurology, 2007-03, Vol.68 (10), p.779

2007

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Clinical spectrum of CADASIL: a study of 7 families

The Lancet (British edition), 1995-10, Vol.346 (8980), p.934-939

1995

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Peripheral neuropathy and inborn errors of metabolism in adults

Journal of inherited metabolic disease, 2007-10, Vol.30 (5), p.642-653

2007

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Epilepsy and inborn errors of metabolism in adults: A diagnostic approach

Journal of inherited metabolic disease, 2007-11, Vol.30 (6), p.846-854

2007

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IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations

Genes and immunity, 2008-04, Vol.9 (3), p.259-263

2008

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Quantification of neutralizing antibodies to human type I interferons using division-arrested frozen cells carrying an interferon-regulated reporter-gene

Journal of interferon & cytokine research, 2008-06, Vol.28 (6), p.393

2008

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Paramyotonia congenita : genotype to phenotype correlations in two families and report of a new mutation in the sodium channel gene

Journal of the neurological sciences, 1996-10, Vol.142 (1-2), p.126-133

1996

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Encephalitis after hepatitis B vaccination: recurrent disseminated encephalitis or MS?

Neurology, 1999-07, Vol.53 (2), p.396

1999

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Very early onset AD with a de novo mutation in the presenilin 1 gene (Met 233 Leu)

Neurology, 2003-10, Vol.61 (8), p.1136

2003

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A Second-Generation Genomic Screen for Multiple Sclerosis

American journal of human genetics, 2004-12, Vol.75 (6), p.1070-1078

2004

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Treatable hereditary neuro-metabolic diseases

Revue neurologique, 2007-10, Vol.163 (10), p.884-896

2007

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Guillain-Barré Syndrome, Influenzalike Illnesses, and Influenza Vaccination During Seasons With and Without Circulating A/H1N1 Viruses

American journal of epidemiology, 2011-08, Vol.174 (3), p.326-335

2011

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Localized proton magnetic resonance spectroscopy in relapsing remitting versus secondary progressive multiple sclerosis

Neurology, 1999-09, Vol.53 (5), p.1091

1999

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Prior suggestive symptoms in one-third of patients consulting for a “first” demyelinating event

Journal of neurology, neurosurgery and psychiatry, 2011-03, Vol.82 (3), p.323-325

2011

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Paramedian thalamic and midbrain infarcts: Clinical and neuropathological study

Annals of neurology, 1981-08, Vol.10 (2), p.127-148

1981

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Nitric-oxide triggered neurological disorders in subjects with vitamin B12 deficiency

Revue neurologique, 2007-03, Vol.163 (3), p.362

2007

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Hepatitis B vaccination and central nervous system demyelination: an immunological approach

Journal of autoimmunity, 2005-02, Vol.24 (1), p.33-37

2005

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Myelin and nuclear magnetic resonance

Revue neurologique, 2007-10, Vol.163 (10), p.942

2007

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Troubles neurologiques par carence en vitamine B12 déclenchés par le protoxyde d’azote

Revue neurologique, 2007-03, Vol.163 (3), p.362-364

2007

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Psychiatric manifestations revealing inborn errors of metabolism in adolescents and adults

Immunosuppressive therapy is more effective than interferon in neuromyelitis optica

The adult form of Niemann–Pick disease type C

Hereditary spastic paraparesis in adults associated with inborn errors of metabolism: A diagnostic approach

Paroxysmal hypothermia as a clinical feature of multiple sclerosis

Leukoencephalopathies associated with inborn errors of metabolism in adults

Age at onset determines the occurrence of the progressive phase of multiple sclerosis

Clinical spectrum of CADASIL: a study of 7 families

Peripheral neuropathy and inborn errors of metabolism in adults

Epilepsy and inborn errors of metabolism in adults: A diagnostic approach

IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations

Quantification of neutralizing antibodies to human type I interferons using division-arrested frozen cells carrying an interferon-regulated reporter-gene

Paramyotonia congenita : genotype to phenotype correlations in two families and report of a new mutation in the sodium channel gene

Encephalitis after hepatitis B vaccination: recurrent disseminated encephalitis or MS?

Very early onset AD with a de novo mutation in the presenilin 1 gene (Met 233 Leu)

A Second-Generation Genomic Screen for Multiple Sclerosis

Treatable hereditary neuro-metabolic diseases

Guillain-Barré Syndrome, Influenzalike Illnesses, and Influenza Vaccination During Seasons With and Without Circulating A/H1N1 Viruses

Localized proton magnetic resonance spectroscopy in relapsing remitting versus secondary progressive multiple sclerosis

Prior suggestive symptoms in one-third of patients consulting for a “first” demyelinating event

Paramedian thalamic and midbrain infarcts: Clinical and neuropathological study

Nitric-oxide triggered neurological disorders in subjects with vitamin B12 deficiency

Hepatitis B vaccination and central nervous system demyelination: an immunological approach

Myelin and nuclear magnetic resonance

Troubles neurologiques par carence en vitamine B12 déclenchés par le protoxyde d’azote

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