Search research articles
Contact Us
Filters
Showing results (111-120 of 130) with videos related to
Page
of 13
Sort By:
European Journal of Neurology
|
March 14, 2021
Deep phenotyping of an international series of patients with late-onset dysferlinopathy
Gorka Fernández-Eulate, Giorgia Querin, Ursula Moore, et al.
The New England Journal of Medicine
|
June 15, 2012
Hereditary systemic amyloidosis due to Asp76Asn variant β2-microglobulin
Sophie Valleix, Julian D Gillmore, Frank Bridoux, et al.
Brain : a Journal of Neurology
|
January 14, 2012
A phase I trial of adeno-associated virus serotype 1-γ-sarcoglycan gene therapy for limb girdle muscular dystrophy type 2C
Serge Herson, Faycal Hentati, Aude Rigolet, et al.
Journal of Neurology
|
May 20, 2024
Clinical, paraclinical and outcome features of 166 patients with acute anti-GQ1b antibody syndrome
Martin Coly, David Adams, Shahram Attarian, et al.
European Journal of Neurology
|
March 20, 2026
Multiple Mononeuropathy Secondary to Parvovirus B19 Infection: A Case Series
Julian Theuriet, Maud Michaud, Guillaume Fargeot, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology
|
February 5, 2013
HTLV-1-associated inflammatory myopathies: low proviral load and moderate inflammation in 13 patients from West Indies and West Africa
Marion Desdouits, Olivier Cassar, Thierry Maisonobe, et al.
The Lancet Regional Health. Europe
|
February 3, 2025
Features of myositis and myasthenia gravis in patients treated with immune checkpoint inhibitors: a multicentric, retrospective cohort study
Lotta Plomp, Hortense Chassepot, Dimitri Psimaras, et al.
Annals of Neurology
|
May 14, 2020
GGPS1 Mutations Cause Muscular Dystrophy/Hearing Loss/Ovarian Insufficiency Syndrome
A Reghan Foley, Yaqun Zou, James E Dunford, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
February 21, 2020
Electrophysiological features of chronic inflammatory demyelinating polyradiculoneuropathy associated with IgG4 antibodies targeting neurofascin 155 or contactin 1 glycoproteins
Ludivine Kouton, José Boucraut, Jérome Devaux, et al.
Journal of Neuromuscular Diseases
|
November 18, 2025
Unveiling MYH2-related myopathy: Histological-genetic insights from a case series and systematic review
Beatrice Labella, Guy Brochier, Maud Beuvin, et al.
Page
of 13
Search research articles
Search
Showing results (111-120 of 130) with videos related to
Sort By:
Page
of 13
European Journal of Neurology
|
March 14, 2021
Deep phenotyping of an international series of patients with late-onset dysferlinopathy
Gorka Fernández-Eulate, Giorgia Querin, Ursula Moore, et al.
The New England Journal of Medicine
|
June 15, 2012
Hereditary systemic amyloidosis due to Asp76Asn variant β2-microglobulin
Sophie Valleix, Julian D Gillmore, Frank Bridoux, et al.
Brain : a Journal of Neurology
|
January 14, 2012
A phase I trial of adeno-associated virus serotype 1-γ-sarcoglycan gene therapy for limb girdle muscular dystrophy type 2C
Serge Herson, Faycal Hentati, Aude Rigolet, et al.
Journal of Neurology
|
May 20, 2024
Clinical, paraclinical and outcome features of 166 patients with acute anti-GQ1b antibody syndrome
Martin Coly, David Adams, Shahram Attarian, et al.
European Journal of Neurology
|
March 20, 2026
Multiple Mononeuropathy Secondary to Parvovirus B19 Infection: A Case Series
Julian Theuriet, Maud Michaud, Guillaume Fargeot, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology
|
February 5, 2013
HTLV-1-associated inflammatory myopathies: low proviral load and moderate inflammation in 13 patients from West Indies and West Africa
Marion Desdouits, Olivier Cassar, Thierry Maisonobe, et al.
The Lancet Regional Health. Europe
|
February 3, 2025
Features of myositis and myasthenia gravis in patients treated with immune checkpoint inhibitors: a multicentric, retrospective cohort study
Lotta Plomp, Hortense Chassepot, Dimitri Psimaras, et al.
Annals of Neurology
|
May 14, 2020
GGPS1 Mutations Cause Muscular Dystrophy/Hearing Loss/Ovarian Insufficiency Syndrome
A Reghan Foley, Yaqun Zou, James E Dunford, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
February 21, 2020
Electrophysiological features of chronic inflammatory demyelinating polyradiculoneuropathy associated with IgG4 antibodies targeting neurofascin 155 or contactin 1 glycoproteins
Ludivine Kouton, José Boucraut, Jérome Devaux, et al.
Journal of Neuromuscular Diseases
|
November 18, 2025
Unveiling MYH2-related myopathy: Histological-genetic insights from a case series and systematic review
Beatrice Labella, Guy Brochier, Maud Beuvin, et al.
Page
of 13