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Journal of Cachexia, Sarcopenia and Muscle
|
April 4, 2022
Three-year quantitative magnetic resonance imaging and phosphorus magnetic resonance spectroscopy study in lower limb muscle in dysferlinopathy
Harmen Reyngoudt, Fiona E Smith, Ericky Caldas de Almeida Araújo, et al.
Neuromuscular Disorders : NMD
|
February 21, 2021
Miyoshi myopathy and limb girdle muscular dystrophy R2 are the same disease
Ursula Moore, Heather Gordish, Jordi Diaz-Manera, et al.
European Journal of Neurology
|
February 13, 2025
Disease Progression in Charcot-Marie-Tooth Disease Type 4B (CMT4B) Associated With Mutations in Myotubularin-Related Proteins 2 and 13
Alessandro Bertini, Mary M Reilly, Chiara Pisciotta, et al.
Orphanet Journal of Rare Diseases
|
December 19, 2014
An exploratory randomised double-blind and placebo-controlled phase 2 study of a combination of baclofen, naltrexone and sorbitol (PXT3003) in patients with Charcot-Marie-Tooth disease type 1A
Shahram Attarian, Jean-Michel Vallat, Laurent Magy, et al.
Journal of Neurology
|
September 24, 2021
Diagnostic interest of whole-body MRI in early- and late-onset LAMA2 muscular dystrophies: a large international cohort
Susana Quijano-Roy, Jana Haberlova, Claudia Castiglioni, et al.
Journal of Cachexia, Sarcopenia and Muscle
|
September 4, 2022
Water T2 could predict functional decline in patients with dysferlinopathy
Ursula Moore, Ericky Caldas de Almeida Araújo, Harmen Reyngoudt, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer
|
April 24, 2025
International survey on training of dermatology residents in supportive oncodermatology: the RESCUE study
Ariadna Ortiz-Brugués, Davide Fattore, Marie Boileau, 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.
Orphanet Journal of Rare Diseases
|
September 2, 2025
Prevalence and predictors of uncommon features in FSHD1 patients: insights from the French FSHD registry
Benoît Sanson, Abderhmane Slioui, Jérémy Garcia, et al.
Journal of Neuromuscular Diseases
|
March 22, 2021
Clinical and Molecular Spectrum Associated with COL6A3 c.7447A>G p.(Lys2483Glu) Variant: Elucidating its Role in Collagen VI-related Myopathies
Rocío N Villar-Quiles, Sandra Donkervoort, Alix de Becdelièvre, et al.
Page
of 107
Search research articles
Search
Showing results (1001-1010 of 1,067) with videos related to
Sort By:
Page
of 107
Journal of Cachexia, Sarcopenia and Muscle
|
April 4, 2022
Three-year quantitative magnetic resonance imaging and phosphorus magnetic resonance spectroscopy study in lower limb muscle in dysferlinopathy
Harmen Reyngoudt, Fiona E Smith, Ericky Caldas de Almeida Araújo, et al.
Neuromuscular Disorders : NMD
|
February 21, 2021
Miyoshi myopathy and limb girdle muscular dystrophy R2 are the same disease
Ursula Moore, Heather Gordish, Jordi Diaz-Manera, et al.
European Journal of Neurology
|
February 13, 2025
Disease Progression in Charcot-Marie-Tooth Disease Type 4B (CMT4B) Associated With Mutations in Myotubularin-Related Proteins 2 and 13
Alessandro Bertini, Mary M Reilly, Chiara Pisciotta, et al.
Orphanet Journal of Rare Diseases
|
December 19, 2014
An exploratory randomised double-blind and placebo-controlled phase 2 study of a combination of baclofen, naltrexone and sorbitol (PXT3003) in patients with Charcot-Marie-Tooth disease type 1A
Shahram Attarian, Jean-Michel Vallat, Laurent Magy, et al.
Journal of Neurology
|
September 24, 2021
Diagnostic interest of whole-body MRI in early- and late-onset LAMA2 muscular dystrophies: a large international cohort
Susana Quijano-Roy, Jana Haberlova, Claudia Castiglioni, et al.
Journal of Cachexia, Sarcopenia and Muscle
|
September 4, 2022
Water T2 could predict functional decline in patients with dysferlinopathy
Ursula Moore, Ericky Caldas de Almeida Araújo, Harmen Reyngoudt, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer
|
April 24, 2025
International survey on training of dermatology residents in supportive oncodermatology: the RESCUE study
Ariadna Ortiz-Brugués, Davide Fattore, Marie Boileau, 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.
Orphanet Journal of Rare Diseases
|
September 2, 2025
Prevalence and predictors of uncommon features in FSHD1 patients: insights from the French FSHD registry
Benoît Sanson, Abderhmane Slioui, Jérémy Garcia, et al.
Journal of Neuromuscular Diseases
|
March 22, 2021
Clinical and Molecular Spectrum Associated with COL6A3 c.7447A>G p.(Lys2483Glu) Variant: Elucidating its Role in Collagen VI-related Myopathies
Rocío N Villar-Quiles, Sandra Donkervoort, Alix de Becdelièvre, et al.
Page
of 107