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Microglia-neuron interaction at nodes of Ranvier depends on neuronal activity through potassium release and contributes to remyelination

Nature communications, 2021-09, Vol.12 (1), p.5219-5219, Article 5219

2021

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Antibody‐ and macrophage‐mediated segmental demyelination in chronic inflammatory demyelinating polyneuropathy: clinical, electrophysiological, immunological and pathological correlates

European journal of neurology, 2020-04, Vol.27 (4), p.692-701

2020

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Intramuscular interferon beta-1a in chronic inflammatory demyelinating polyradiculoneuropathy

Neurology, 2010-02, Vol.74 (8), p.651-657

2010

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Motor neuronopathy in Chediak–Higashi syndrome

Journal of the neurological sciences, 2014-09, Vol.344 (1), p.203-207

2014

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Severe early-onset axonal neuropathy with homozygous and compound heterozygous MFN2 mutations

Neurology, 2008-05, Vol.70 (19), p.1678-1681

2008

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The clinical and laboratory features of chronic sensory ataxic neuropathy with anti-disialosyl IgM antibodies

Brain (London, England : 1878), 2001-10, Vol.124 (10), p.1968-1977

2001

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Nutritional status is a prognostic factor for survival in ALS patients

Neurology, 1999-09, Vol.53 (5), p.1059-1059

1999

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POEMS syndrome with prominent acute axonal lesions

Journal of the neurological sciences, 2012-02, Vol.313 (1), p.185-188

2012

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Peripheral nervous system neuroimmunology seen by a neuro-pathologist

Revue neurologique, 2014-10, Vol.170 (10), p.564-569

Vallat, J.-M.

2014

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Pain as the presenting symptom of chronic inflammatory demyelinating polyradiculoneuropathy (CIDP)

Journal of the neurological sciences, 2007-03, Vol.254 (1), p.33-38

2007

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Classifications of neurogenetic diseases: An increasingly complex problem

Revue neurologique, 2016-06, Vol.172 (6-7), p.339-349

2016

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Ataxia with oculomotor apraxia type 2: A clinical and genetic study of 19 patients

Journal of the neurological sciences, 2009-03, Vol.278 (1), p.77-81

2009

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Phenotypic variability in autosomal recessive axonal Charcot–Marie–Tooth disease due to the R298C mutation in lamin A/C

Brain (London, England : 1878), 2004-01, Vol.127 (1), p.154-163

2004

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Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations

Neurology, 2006-08, Vol.67 (4), p.602-606

2006

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Polyneuropathy associated with IgG/IgA monoclonal gammopathy: a clinical and electrophysiological study of 15 cases

European journal of neurology, 2003-11, Vol.10 (6), p.677-685

2003

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Interferon beta-1a as an investigational treatment for CIDP

Neurology, 2003-04, Vol.60 (8 Suppl 3), p.S23

2003

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Polyneuropathy with demyelinating features in mixed cryoglobulinemia with hepatitis C virus infection

European journal of neurology, 2006-09, Vol.13 (9), p.937-941

2006

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IVIg increases interleukin‐11 levels, which in turn contribute to increased platelets, VWF and FVIII in mice and humans

Clinical and experimental immunology, 2021-05, Vol.204 (2), p.258-266

2021

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Cell culture evidence for neuronal degeneration in amyotrophic lateral sclerosis being linked to glutamate AMPA/kainate receptors

The Lancet (British edition), 1993-01, Vol.341 (8840), p.265-268

1993

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Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutation

Neurology, 2000-03, Vol.54 (5), p.1075-1079

2000

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Non-Hodgkin malignant lymphomas and peripheral neuropathies—13 cases

Brain (London, England : 1878), 1995-10, Vol.118 (5), p.1233-1245

1995

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Demyelinating X-linked Charcot-Marie-Tooth disease: Unusual electrophysiological findings

Muscle & nerve, 1999-10, Vol.22 (10), p.1442-1447

1999

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Identification of seven novel mutations in the GAN gene

Human mutation, 2003-04, Vol.21 (4), p.446-446

2003

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Krox20 inactivation in the PNS leads to CNS/PNS boundary transgression by central glia

Revue neurologique, 2011, Vol.167 (1), p.51-56

2011

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Homozygous Defects in LMNA, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy in Human (Charcot-Marie-Tooth Disorder Type 2) and Mouse

American journal of human genetics, 2002-03, Vol.70 (3), p.726-736

2002

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Microglia-neuron interaction at nodes of Ranvier depends on neuronal activity through potassium release and contributes to remyelination

Antibody‐ and macrophage‐mediated segmental demyelination in chronic inflammatory demyelinating polyneuropathy: clinical, electrophysiological, immunological and pathological correlates

Intramuscular interferon beta-1a in chronic inflammatory demyelinating polyradiculoneuropathy

Motor neuronopathy in Chediak–Higashi syndrome

Severe early-onset axonal neuropathy with homozygous and compound heterozygous MFN2 mutations

The clinical and laboratory features of chronic sensory ataxic neuropathy with anti-disialosyl IgM antibodies

Nutritional status is a prognostic factor for survival in ALS patients

POEMS syndrome with prominent acute axonal lesions

Peripheral nervous system neuroimmunology seen by a neuro-pathologist

Pain as the presenting symptom of chronic inflammatory demyelinating polyradiculoneuropathy (CIDP)

Classifications of neurogenetic diseases: An increasingly complex problem

Ataxia with oculomotor apraxia type 2: A clinical and genetic study of 19 patients

Phenotypic variability in autosomal recessive axonal Charcot–Marie–Tooth disease due to the R298C mutation in lamin A/C

Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations

Polyneuropathy associated with IgG/IgA monoclonal gammopathy: a clinical and electrophysiological study of 15 cases

Interferon beta-1a as an investigational treatment for CIDP

Polyneuropathy with demyelinating features in mixed cryoglobulinemia with hepatitis C virus infection

IVIg increases interleukin‐11 levels, which in turn contribute to increased platelets, VWF and FVIII in mice and humans

Cell culture evidence for neuronal degeneration in amyotrophic lateral sclerosis being linked to glutamate AMPA/kainate receptors

Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutation

Non-Hodgkin malignant lymphomas and peripheral neuropathies—13 cases

Demyelinating X-linked Charcot-Marie-Tooth disease: Unusual electrophysiological findings

Identification of seven novel mutations in the GAN gene

Krox20 inactivation in the PNS leads to CNS/PNS boundary transgression by central glia

Homozygous Defects in LMNA, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy in Human (Charcot-Marie-Tooth Disorder Type 2) and Mouse

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