Détail de l'auteur
Documents disponibles écrits par cet auteur
trié(s) par (Pertinence décroissant(e), Date de parution décroissant(e), Date de parution décroissant(e), Système de projection du document croissant(e)) Mettre toutes les notices dans le panier Faire une suggestion Ajouter un critère de recherche
The diagnostic value of GDF-15 for myocardial involvement in idiopathic inflammatory myopathy
Qiu M, Sun X, Qi X, et al.
Rheumatology (Oxford, England), 2020
A symptomatic female patient with duchenne muscular dystrophy gene mutation showing rimmed vacuoles in muscle biopsy
Ban R, Lu X, Pu C, et al.
Neurology India, 2020, 68, 2, p 518
Analysis of myositis autoantibodies in Chinese patients with cancer-associated myositis
Li L, Liu C, Wang Q, et al.
Journal of clinical laboratory analysis, 2020
Applying genome-wide CRISPR-Cas9 screens for therapeutic discovery in facioscapulohumeral muscular dystrophy
Lek A, Zhang Y, Woodman KG, et al.
Science translational medicine, 2020, 12, 536
Mutations of MACF1, Encoding Microtubule-Actin Crosslinking-Factor 1, Cause Spectraplakinopathy
Kang L, Liu Y, Jin Y, et al.
Frontiers in neurology, 2020, 10
Clinical and Genetic Diversity of PMP22 Mutations in a Large Cohort of Chinese Patients With Charcot-Marie-Tooth Disease
Liu X, Duan X, Zhang Y, et al.
Frontiers in neurology, 2020, 11, p 630
Cross-Sectional Study in a Large Cohort of Chinese Patients With GJB1 Gene Mutations
Liu X, Duan X, Zhang Y, et al.
Frontiers in neurology, 2020, 11, p 690
The analysis of the association between the copy numbers of survival motor neuron gene 2 and neuronal apoptosis inhibitory protein genes and the clinical phenotypes in 40 patients with spinal muscular atrophy: Observational study
Zhang Y, He J, Zhang Y, et al.
Medicine, 2020, 99, 3
A novel application of tau PET in the diagnosis of sporadic inclusion body myositis: A case report
Zhang Y, Li K, Pu C, et al.
Medicine, 2020, 99, 31
Correction of Three Prominent Mutations in Mouse and Human Models of Duchenne Muscular Dystrophy by Single-Cut Genome Editing
Min YL, Chemello F, Li H, et al.
Molecular therapy : the journal of the American Society of Gene Therapy, 2020, 28, 9, p 2044
Late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (MADD): case reports and epidemiology of ETFDH gene mutations
Chen W, Zhang Y, Ni Y, et al.
BMC neurology, 2019, 19, 1, p 330
Metformin attenuates autoimmune disease of the neuromotor system in animal models of myasthenia gravis
Cui Y, Chang L, Wang C, et al.
International immunopharmacology, 2019, 75
In vivo non-invasive monitoring of dystrophin correction in a new Duchenne muscular dystrophy reporter mouse
Amoasii L, Li H, Zhang Y, et al.
Nature communications, 2019, 10, 1
Clinical analysis of Chinese anti-low-density-lipoprotein-receptor-associated protein 4 antibodies in patients with myasthenia gravis
Li M, Han J, Zhang Y, et al.
European journal of neurology, 2019
Diffuse pruritic erythema as a clinical manifestation in anti-SAE antibody-associated dermatomyositis: a case report and literature review
Jia E, Wei J, Geng H, et al.
Clinical rheumatology, 2019
Overexpression of miR-29 Leads to Myopathy that Resemble Pathology of Ullrich Congenital Muscular Dystrophy
Liu C, Li L, Ge M, et al.
Cells, 2019, 8, 5, p 459
Management strategies in facioscapulohumeral muscular dystrophy
Lu J, Yao Z, Yang Y, et al.
Intractable & rare diseases research, 2019, 8, 1, p 9
Protein kinase A activation inhibits DUX4 gene expression in myotubes from patients with facioscapulohumeral muscular dystrophy
Cruz JM Jr, Hupper N, Wilson LS, et al.
The Journal of biological chemistry, 2018
Chemical, biochemical, preclinical and clinical studies of Ganoderma lucidum polysaccharide as an approved drug for treating myopathy and other diseases in China
Zeng P, Guo Z, Zeng X, et al.
Journal of cellular and molecular medicine, 2018
Clinical characteristics of AChRAb and MuSKAb double seropositive myasthenia gravis patients
Li M, Li M, Ren L, et al.
Clinical neurology and neurosurgery, 2018, 172, p 69
Dual AAV gene therapy for Duchenne muscular dystrophy with a 7-kb mini-dystrophin gene in the canine model
Kodippili K, Hakim C, Pan X, et al.
Human gene therapy, 2018, 29, 3, p 299
Myoediting: Toward Prevention of Muscular Dystrophy by Therapeutic Genome Editing
Zhang Y, Long C, Bassel-Duby R, et al.
Physiological reviews, 2018, 98, 3, p 1205
A novel SYNE1 gene mutation in a Chinese family of Emery-Dreifuss muscular dystrophy-like
Chen Z, Ren Z, Mei W, et al.
BMC Medical Genetics, 2017, 18, 1
Anti-LRP4 Autoantibodies in Chinese Patients with Myasthenia Gravis
Li Y, Zhang Y, Cai G, et al.
Muscle & Nerve, 2017, 56, 5, p 938
