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Frontiers in Immunology
|
October 14, 2024
Seroprevalence of binding and neutralizing antibodies against 18 adeno-associated virus types in patients with neuromuscular disorders
Xiaoyan Wang, Patrick Julian Klann, Ellen Wiedtke, et al.
Neuropathology and Applied Neurobiology
|
February 26, 2015
Th2-M2 immunity in lesions of muscular sarcoidosis and macrophagic myofasciitis
Corinna Preusse, Hans-H Goebel, Debora Pehl, et al.
JIMD Reports
|
August 27, 2014
Urge incontinence and gastrointestinal symptoms in adult patients with pompe disease: a cross-sectional survey
Nesrin Karabul, Anika Skudlarek, Janine Berndt, et al.
NMR in Biomedicine
|
May 25, 2024
Quantitative muscle magnetic resonance imaging in limb-girdle muscular dystrophy type R1 (LGMDR1): A prospective longitudinal cohort study
Johannes Forsting, Marian Wächter, Martijn Froeling, et al.
Journal of Cachexia, Sarcopenia and Muscle
|
June 1, 2026
Longitudinal Assessment of Muscle Involvement in Late-Onset Pompe Disease Using Quantitative MRI: A Prospective Cohort Study
Alice De Lorenzo, Johannes Forsting, Martijn Froeling, et al.
Neuropediatrics
|
August 12, 2014
Long survival in Leigh syndrome: new cases and review of literature
Wiebke Aulbert, Katharina Weigt-Usinger, Charlotte Thiels, et al.
Genes
|
October 27, 2022
Homozygous Inversion on Chromosome 13 Involving SGCG Detected by Short Read Whole Genome Sequencing in a Patient Suffering from Limb-Girdle Muscular Dystrophy
Natalie Pluta, Sabine Hoffjan, Frederic Zimmer, et al.
Animal Models and Experimental Medicine
|
April 7, 2026
Evaluation of quantitative muscle MRI and an intelligent phenotyping housing system as advanced phenotyping methods in a mouse model of calpain 3-deficient muscular dystrophy
Nicolina Südkamp, Marlena Rohm, Gabriele Russo, et al.
European Journal of Human Genetics : EJHG
|
June 22, 2017
Phenotypic extremes of BICD2-opathies: from lethal, congenital muscular atrophy with arthrogryposis to asymptomatic with subclinical features
Markus Storbeck, Beate Horsberg Eriksen, Andreas Unger, et al.
American Journal of Human Genetics
|
June 2, 2005
A mutation in the dimerization domain of filamin c causes a novel type of autosomal dominant myofibrillar myopathy
Matthias Vorgerd, Peter F M van der Ven, Vera Bruchertseifer, et al.
Page
of 14
Search research articles
Search
Showing results (81-90 of 140) with videos related to
Sort By:
Page
of 14
Frontiers in Immunology
|
October 14, 2024
Seroprevalence of binding and neutralizing antibodies against 18 adeno-associated virus types in patients with neuromuscular disorders
Xiaoyan Wang, Patrick Julian Klann, Ellen Wiedtke, et al.
Neuropathology and Applied Neurobiology
|
February 26, 2015
Th2-M2 immunity in lesions of muscular sarcoidosis and macrophagic myofasciitis
Corinna Preusse, Hans-H Goebel, Debora Pehl, et al.
JIMD Reports
|
August 27, 2014
Urge incontinence and gastrointestinal symptoms in adult patients with pompe disease: a cross-sectional survey
Nesrin Karabul, Anika Skudlarek, Janine Berndt, et al.
NMR in Biomedicine
|
May 25, 2024
Quantitative muscle magnetic resonance imaging in limb-girdle muscular dystrophy type R1 (LGMDR1): A prospective longitudinal cohort study
Johannes Forsting, Marian Wächter, Martijn Froeling, et al.
Journal of Cachexia, Sarcopenia and Muscle
|
June 1, 2026
Longitudinal Assessment of Muscle Involvement in Late-Onset Pompe Disease Using Quantitative MRI: A Prospective Cohort Study
Alice De Lorenzo, Johannes Forsting, Martijn Froeling, et al.
Neuropediatrics
|
August 12, 2014
Long survival in Leigh syndrome: new cases and review of literature
Wiebke Aulbert, Katharina Weigt-Usinger, Charlotte Thiels, et al.
Genes
|
October 27, 2022
Homozygous Inversion on Chromosome 13 Involving SGCG Detected by Short Read Whole Genome Sequencing in a Patient Suffering from Limb-Girdle Muscular Dystrophy
Natalie Pluta, Sabine Hoffjan, Frederic Zimmer, et al.
Animal Models and Experimental Medicine
|
April 7, 2026
Evaluation of quantitative muscle MRI and an intelligent phenotyping housing system as advanced phenotyping methods in a mouse model of calpain 3-deficient muscular dystrophy
Nicolina Südkamp, Marlena Rohm, Gabriele Russo, et al.
European Journal of Human Genetics : EJHG
|
June 22, 2017
Phenotypic extremes of BICD2-opathies: from lethal, congenital muscular atrophy with arthrogryposis to asymptomatic with subclinical features
Markus Storbeck, Beate Horsberg Eriksen, Andreas Unger, et al.
American Journal of Human Genetics
|
June 2, 2005
A mutation in the dimerization domain of filamin c causes a novel type of autosomal dominant myofibrillar myopathy
Matthias Vorgerd, Peter F M van der Ven, Vera Bruchertseifer, et al.
Page
of 14