List of works - Patrick Vermersch

Acute fulminant demyelinating disease: a descriptive study of 60 patients

scientific article published on 01 October 2007

Adult-onset genetic leukoencephalopathies: a MRI pattern-based approach in a comprehensive study of 154 patients.

scientific article published on 19 December 2014

Altered B lymphocyte homeostasis and functions in systemic sclerosis.

scientific article published on 14 January 2018

Anti-JCV antibody prevalence in a French cohort of MS patients under natalizumab therapy

scientific article published on 12 April 2012

Asymptomatic optic nerve lesions: An underestimated cause of silent retinal atrophy in MS

scientific article published on 20 May 2020

Bent spine syndrome as the initial symptom of late-onset Pompe disease.

scientific article published on 15 November 2016

Central nervous system abnormalities in patients with PMP22 gene mutations: a prospective study.

scientific article published on 15 December 2012

Cognitive Impairment in Secondary Progressive Multiple Sclerosis: Effect of Disease Duration, Age, and Progressive Phenotype

scientific article published on 30 January 2022

Cognitive functions in neuromyelitis optica.

scientific article published in January 2008

Effective immune restoration after immunosuppressant discontinuation in a lupus patient presenting progressive multifocal leukoencephalopathy

scientific article published on 7 October 2009

Extensive myelitis associated with anti-NMDA receptor antibodies.

scientific article

JC-virus seroconversion in multiple sclerosis patients receiving natalizumab.

scientific article published on 26 September 2013

Kjellin Syndrome: Long-term Neuro-ophthalmologic Follow-up and Novel Mutations in the SPG11 Gene

article

Methionine synthase deficiency: a rare cause of adult-onset leukoencephalopathy

scientific article

NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe

Optical coherence tomography in clinically isolated syndrome: no evidence of subclinical retinal axonal loss.

scientific article published in November 2009

Punctate pattern: A promising imaging marker for the diagnosis of natalizumab-associated PML.

scientific article

Rituximab in refractory and non‐refractory myasthenia: A retrospective multicenter study ⬇️

scientific article published on August 31, 2012

Siponimod and cognition in secondary progressive multiple sclerosis: EXPAND secondary analyses

scientific article published on 16 December 2020

Sustained-released fampridine in multiple sclerosis: effects on gait parameters, arm function, fatigue, and quality of life

scientific article published on 5 June 2015

Tear analysis in clinically isolated syndrome as new multiple sclerosis criterion

scientific article published on 22 December 2009

List of works by Patrick Vermersch

Acute fulminant demyelinating disease: a descriptive study of 60 patients

Adult-onset genetic leukoencephalopathies: a MRI pattern-based approach in a comprehensive study of 154 patients.

Altered B lymphocyte homeostasis and functions in systemic sclerosis.

Anti-JCV antibody prevalence in a French cohort of MS patients under natalizumab therapy

Asymptomatic optic nerve lesions: An underestimated cause of silent retinal atrophy in MS

Bent spine syndrome as the initial symptom of late-onset Pompe disease.

Central nervous system abnormalities in patients with PMP22 gene mutations: a prospective study.

Cognitive Impairment in Secondary Progressive Multiple Sclerosis: Effect of Disease Duration, Age, and Progressive Phenotype

Cognitive functions in neuromyelitis optica.

Effective immune restoration after immunosuppressant discontinuation in a lupus patient presenting progressive multifocal leukoencephalopathy

Extensive myelitis associated with anti-NMDA receptor antibodies.

JC-virus seroconversion in multiple sclerosis patients receiving natalizumab.

Kjellin Syndrome: Long-term Neuro-ophthalmologic Follow-up and Novel Mutations in the SPG11 Gene

Methionine synthase deficiency: a rare cause of adult-onset leukoencephalopathy

NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe

Optical coherence tomography in clinically isolated syndrome: no evidence of subclinical retinal axonal loss.

Punctate pattern: A promising imaging marker for the diagnosis of natalizumab-associated PML.

Rituximab in refractory and non‐refractory myasthenia: A retrospective multicenter study ⬇️

Siponimod and cognition in secondary progressive multiple sclerosis: EXPAND secondary analyses

Sustained-released fampridine in multiple sclerosis: effects on gait parameters, arm function, fatigue, and quality of life

Tear analysis in clinically isolated syndrome as new multiple sclerosis criterion