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Catheterization and Cardiovascular Interventions : Official Journal of the Society for Cardiac Angiography & Interventions
|
August 26, 2025
The Influence of Radiographic Equipment, Setup, and Operator Experience on Radiation Exposure in Chronic Total Occlusion Interventions
Gerald S Werner, Alexandre Avran, Nicolas Boudou, et al.
European Journal of Neurology
|
September 4, 2025
Diagnostic Impasse and Wandering in Patients With Rare Neuromuscular Diseases: Insights Into Patient Characteristics From the French National Network for Rare Neuromuscular Diseases (FILNEMUS) and the French National Rare Disease Database (BNDMR)
Rémy Dumas, Anne-Sophie Jannot, Nabila Elarouci, et al.
Human Mutation
|
September 11, 2014
Mosaicism for dominant collagen 6 mutations as a cause for intrafamilial phenotypic variability
Sandra Donkervoort, Ying Hu, Tanya Stojkovic, et al.
Journal of Neurology
|
May 26, 2026
Identification of prognostic biomarkers in a large cohort of patients with LGMD R2
Carla F Bolano-Diaz, Jose Verdu-Diaz, Dan Hao, et al.
Neurology. Genetics
|
July 20, 2023
Phenotype Presentation and Molecular Diagnostic Yield in Non-5q Spinal Muscular Atrophy
Gorka Fernández-Eulate, Julian Theuriet, Christopher J Record, et al.
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.
Journal of Neurology
|
July 17, 2017
Mutations in GFPT1-related congenital myasthenic syndromes are associated with synaptic morphological defects and underlie a tubular aggregate myopathy with synaptopathy
Stéphanie Bauché, Geoffroy Vellieux, Damien Sternberg, et al.
The Lancet. Rheumatology
|
January 26, 2024
Sirolimus for treatment of patients with inclusion body myositis: a randomised, double-blind, placebo-controlled, proof-of-concept, phase 2b trial
Olivier Benveniste, Jean-Yves Hogrel, Lisa Belin, et al.
European Journal of Neurology
|
June 1, 2021
Genotype-phenotype correlation in French patients with myelin protein zero gene-related inherited neuropathy
Marie Subréville, Nathalie Bonello-Palot, Douniazed Yahiaoui, et al.
Neuromuscular Disorders : NMD
|
March 27, 2023
Expanding the muscle imaging spectrum in dysferlinopathy: description of an outlier population from the classical MRI pattern
Laura Llansó, Ursula Moore, Carla Bolano-Diaz, et al.
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of 107
Search research articles
Search
Showing results (981-990 of 1,067) with videos related to
Sort By:
Page
of 107
Catheterization and Cardiovascular Interventions : Official Journal of the Society for Cardiac Angiography & Interventions
|
August 26, 2025
The Influence of Radiographic Equipment, Setup, and Operator Experience on Radiation Exposure in Chronic Total Occlusion Interventions
Gerald S Werner, Alexandre Avran, Nicolas Boudou, et al.
European Journal of Neurology
|
September 4, 2025
Diagnostic Impasse and Wandering in Patients With Rare Neuromuscular Diseases: Insights Into Patient Characteristics From the French National Network for Rare Neuromuscular Diseases (FILNEMUS) and the French National Rare Disease Database (BNDMR)
Rémy Dumas, Anne-Sophie Jannot, Nabila Elarouci, et al.
Human Mutation
|
September 11, 2014
Mosaicism for dominant collagen 6 mutations as a cause for intrafamilial phenotypic variability
Sandra Donkervoort, Ying Hu, Tanya Stojkovic, et al.
Journal of Neurology
|
May 26, 2026
Identification of prognostic biomarkers in a large cohort of patients with LGMD R2
Carla F Bolano-Diaz, Jose Verdu-Diaz, Dan Hao, et al.
Neurology. Genetics
|
July 20, 2023
Phenotype Presentation and Molecular Diagnostic Yield in Non-5q Spinal Muscular Atrophy
Gorka Fernández-Eulate, Julian Theuriet, Christopher J Record, et al.
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.
Journal of Neurology
|
July 17, 2017
Mutations in GFPT1-related congenital myasthenic syndromes are associated with synaptic morphological defects and underlie a tubular aggregate myopathy with synaptopathy
Stéphanie Bauché, Geoffroy Vellieux, Damien Sternberg, et al.
The Lancet. Rheumatology
|
January 26, 2024
Sirolimus for treatment of patients with inclusion body myositis: a randomised, double-blind, placebo-controlled, proof-of-concept, phase 2b trial
Olivier Benveniste, Jean-Yves Hogrel, Lisa Belin, et al.
European Journal of Neurology
|
June 1, 2021
Genotype-phenotype correlation in French patients with myelin protein zero gene-related inherited neuropathy
Marie Subréville, Nathalie Bonello-Palot, Douniazed Yahiaoui, et al.
Neuromuscular Disorders : NMD
|
March 27, 2023
Expanding the muscle imaging spectrum in dysferlinopathy: description of an outlier population from the classical MRI pattern
Laura Llansó, Ursula Moore, Carla Bolano-Diaz, et al.
Page
of 107