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European Journal of Human Genetics : EJHG
|
March 5, 2009
Identification and in silico analysis of 14 novel GJB1, MPZ and PMP22 gene mutations
Gabriel Miltenberger-Miltenyi, Thomas Schwarzbraun, Wolfgang N Löscher, et al.
Movement Disorders Clinical Practice
|
December 14, 2023
Pain in Multiple System Atrophy a Systematic Review and Meta-Analysis
Nicole Campese, Bianca Caliò, Fabian Leys, et al.
Plos One
|
March 6, 2014
Th1 response and systemic treg deficiency in inclusion body myositis
Yves Allenbach, Wahiba Chaara, Michelle Rosenzwajg, et al.
Journal of Neurology
|
January 17, 2019
High efficacy of rituximab for myasthenia gravis: a comprehensive nationwide study in Austria
Raffi Topakian, Fritz Zimprich, Stephan Iglseder, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 5, 2024
Pain in Multiple System Atrophy: A Community-Based Survey
Nicole Campese, Georg Göbel, Julia Wanschitz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 24, 2026
Types of Pain in Multiple System Atrophy
Nicole Campese, Mubasher A Qamar, Maria Alexandra Chiriac, et al.
Muscle & Nerve
|
February 9, 2024
Multifocal motor neuropathy as a mimic of amyotrophic lateral sclerosis: Serum neurofilament light chain as a reliable diagnostic biomarker
Vera E A Kleinveld, Omar Keritam, Corinne G C Horlings, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
May 17, 2007
Hypoxia up-regulates the angiogenic cytokine secretoneurin via an HIF-1alpha- and basic FGF-dependent pathway in muscle cells
Margot Egger, Wilfried Schgoer, Arno G E Beer, et al.
Neurology(R) Neuroimmunology & Neuroinflammation
|
June 4, 2020
Antibodies to nodal/paranodal proteins in paediatric immune-mediated neuropathy
Desiree De Simoni, Gerda Ricken, Michael Winklehner, et al.
European Journal of Neurology
|
March 3, 2022
Clinico-genetic spectrum of limb-girdle muscular weakness in Austria: A multicentre cohort study
Martin Krenn, Matthias Tomschik, Matias Wagner, et al.
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of 6
Search research articles
Search
Showing results (41-50 of 58) with videos related to
Sort By:
Page
of 6
European Journal of Human Genetics : EJHG
|
March 5, 2009
Identification and in silico analysis of 14 novel GJB1, MPZ and PMP22 gene mutations
Gabriel Miltenberger-Miltenyi, Thomas Schwarzbraun, Wolfgang N Löscher, et al.
Movement Disorders Clinical Practice
|
December 14, 2023
Pain in Multiple System Atrophy a Systematic Review and Meta-Analysis
Nicole Campese, Bianca Caliò, Fabian Leys, et al.
Plos One
|
March 6, 2014
Th1 response and systemic treg deficiency in inclusion body myositis
Yves Allenbach, Wahiba Chaara, Michelle Rosenzwajg, et al.
Journal of Neurology
|
January 17, 2019
High efficacy of rituximab for myasthenia gravis: a comprehensive nationwide study in Austria
Raffi Topakian, Fritz Zimprich, Stephan Iglseder, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 5, 2024
Pain in Multiple System Atrophy: A Community-Based Survey
Nicole Campese, Georg Göbel, Julia Wanschitz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 24, 2026
Types of Pain in Multiple System Atrophy
Nicole Campese, Mubasher A Qamar, Maria Alexandra Chiriac, et al.
Muscle & Nerve
|
February 9, 2024
Multifocal motor neuropathy as a mimic of amyotrophic lateral sclerosis: Serum neurofilament light chain as a reliable diagnostic biomarker
Vera E A Kleinveld, Omar Keritam, Corinne G C Horlings, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
May 17, 2007
Hypoxia up-regulates the angiogenic cytokine secretoneurin via an HIF-1alpha- and basic FGF-dependent pathway in muscle cells
Margot Egger, Wilfried Schgoer, Arno G E Beer, et al.
Neurology(R) Neuroimmunology & Neuroinflammation
|
June 4, 2020
Antibodies to nodal/paranodal proteins in paediatric immune-mediated neuropathy
Desiree De Simoni, Gerda Ricken, Michael Winklehner, et al.
European Journal of Neurology
|
March 3, 2022
Clinico-genetic spectrum of limb-girdle muscular weakness in Austria: A multicentre cohort study
Martin Krenn, Matthias Tomschik, Matias Wagner, et al.
Page
of 6