Wenhua Zhu

Department of Neurology, Fudan University

Affiliated withFudan University National Center for Neurological Disorders (NCND)

Research Area

Biography

Wenhua Zhu has not added Biography.
If you are Wenhua Zhu and would like to personalize this page please email our Author Liaison for assistance.

JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 2	2025

Other Publications

Article	Year
The limitation of IL-10-exposed dendritic cells in the treatment of experimental autoimmune myasthenia gravis and myasthenia gravis. Cellular immunology\| PubMed ID: 17005165	2006
The presence of GM-CSF and IL-4 interferes with effect of TGF-beta1 on antigen presenting cells in patients with multiple sclerosis and in rats with experimental autoimmune encephalomyelitis... Cellular immunology\| PubMed ID: 18061154	2007
Clinical and pathological features in 15 Chinese patients with calpainopathy. Muscle & nerve\| PubMed ID: 21321956	2011
HLA-DQA103:02/DQB103:03:02 is strongly associated with susceptibility to childhood-onset ocular myasthenia gravis in Southern Han Chinese. Journal of neuroimmunology\| PubMed ID: 22503410	2012
Genetic variability and clinical spectrum of Chinese patients with limb-girdle muscular dystrophy type 2A. Muscle & nerve\| PubMed ID: 22926650	2012
Clinical features and ETFDH mutation spectrum in a cohort of 90 Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency. Journal of inherited metabolic disease\| PubMed ID: 24357026	2014
Giant cell polymyositis associated with myasthenia gravis and thymoma. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia\| PubMed ID: 25096712	2014
New disease allele and de novo mutation indicate mutational vulnerability of titin exon 343 in hereditary myopathy with early respiratory failure. Neuromuscular disorders : NMD\| PubMed ID: 25500009	2015
Muscle pathology and whole-body MRI in a polyglucosan myopathy associated with a novel glycogenin-1 mutation. Neuromuscular disorders : NMD\| PubMed ID: 26255073	2015
Congenital muscular dystrophy with fatty liver and infantile-onset cataract caused by TRAPPC11 mutations: broadening of the phenotype. Skeletal muscle\| PubMed ID: 26322222	2015
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition). Autophagy\| PubMed ID: 26799652	2016
Clinical features and long exercise test in Chinese patients with Andersen-Tawil syndrome. Muscle & nerve\| PubMed ID: 27145478	2016
Pediatric necrotizing myopathy associated with anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase antibodies. Rheumatology (Oxford, England)\| PubMed ID: 27818386	2017
Missing genetic variations in GNE myopathy: rearrangement hotspots encompassing 5'UTR and founder allele. Journal of human genetics\| PubMed ID: 27829678	2017
Neurolymphomatosis Caused by Nasal-type Extranodal Natural Killer/T-cell Lymphoma. Chinese medical journal\| PubMed ID: 28230000	2017
Multiple Spinal Lesions in an Immunocompetent Young Man. JAMA neurology\| PubMed ID: 28384798	2017
Novel mutations in the C-terminal region of GMPPB causing limb-girdle muscular dystrophy overlapping with congenital myasthenic syndrome. Neuromuscular disorders : NMD\| PubMed ID: 28433477	2017
Exertional myalgia, contractures and annular erythema in a patient with muscle lactate dehydrogenase (LDH) deficiency. Neuromuscular disorders : NMD\| PubMed ID: 29198466	2018
GNE myopathy caused by a synonymous mutation leading to aberrant mRNA splicing. Neuromuscular disorders : NMD\| PubMed ID: 29307446	2018
Fatty infiltration evaluation and selective pattern characterization of lower limbs in limb-girdle muscular dystrophy type 2A by muscle magnetic resonance imaging. Muscle & nerve\| PubMed ID: 29797799	2018
Statin-naïve anti-HMGCR antibody-mediated necrotizing myopathy in China. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia\| PubMed ID: 30205933	2018
GNE myopathy in Chinese population: hotspot and novel mutations. Journal of human genetics\| PubMed ID: 30390020	2019
Correction: GNE myopathy in Chinese population: hotspot and novel mutations. Journal of human genetics\| PubMed ID: 30585253	2019
Congenital muscular dystrophies in China. Clinical genetics\| PubMed ID: 31066047	2019
Identification of gene mutations in patients with primary periodic paralysis using targeted next-generation sequencing. BMC neurology\| PubMed ID: 31068157	2019
Clinical characteristics and long term follow-up of Lambert-Eaton myasthenia syndrome in patients with and without small cell lung cancer. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia\| PubMed ID: 31072737	2019
Inhibition of ROCK activity regulates the balance of Th1, Th17 and Treg cells in myasthenia gravis. Clinical immunology (Orlando, Fla.)\| PubMed ID: 31078707	2019
Myasthenia gravis and specific immunotherapy: monoclonal antibodies. Annals of the New York Academy of Sciences\| PubMed ID: 31393614	2019
Electromyographic Features in a Chinese Cohort With Hereditary Skeletal Muscle Channelopathies. Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society\| PubMed ID: 31567646	2020
Predictive Score for In-Hospital Mortality of Myasthenic Crisis: A Retrospective Chinese Cohort Study. European neurology\| PubMed ID: 31661691	2019
Molecular landscape of CAPN3 mutations in limb-girdle muscular dystrophy type R1: from a Chinese multicentre analysis to a worldwide perspective. Journal of medical genetics\| PubMed ID: 32994280	2021
Genetic variations and clinical spectrum of dystroglycanopathy in a large cohort of Chinese patients. Clinical genetics\| PubMed ID: 33200426	2021
The correlation of clinical evaluation with life quality and mental status in a Chinese cohort with dysferlinopathy. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia\| PubMed ID: 33222926	2020
5' UTR CGG repeat expansion in GIPC1 is associated with oculopharyngodistal myopathy. Brain : a journal of neurology\| PubMed ID: 33374016	2021
Short-term effect of low-dose rituximab on myasthenia gravis with muscle-specific tyrosine kinase antibody. Muscle & nerve\| PubMed ID: 33745138	2021
Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort. Orphanet journal of rare diseases\| PubMed ID: 34281576	2021
Molecular landscape of DYSF mutations in dysferlinopathy: From a Chinese multicenter analysis to a worldwide perspective. Human mutation\| PubMed ID: 34559919	2021
The CGG repeat expansion in RILPL1 is associated with oculopharyngodistal myopathy type 4. American journal of human genetics\| PubMed ID: 35148830	2022
Pneumonia and systemic inflammatory response syndrome as predictors for difficult-/prolonged-weaning after invasive ventilation in myasthenic crisis: A retrospective analysis of a Chinese co... Neuromuscular disorders : NMD\| PubMed ID: 35148922	2022
Melkerson-Rosenthal syndrome complicated by inflammatory myopathy. Muscle & nerve\| PubMed ID: 35485324	2022
Plasma exchange versus intravenous immunoglobulin in AChR subtype myasthenic crisis: A prospective cohort study. Clinical immunology (Orlando, Fla.)\| PubMed ID: 35690385	2022
Early respiratory muscle involvement in LGMDR25: a case report. Neuromuscular disorders : NMD\| PubMed ID: 35718670	2022
Human-induced pluripotent stem cell line (FDHSi001-A) derived from a patient with a CGG repeat expansion in the 5'UTR of GIPC1. Stem cell research\| PubMed ID: 36055118	2022
High-risk screening of late-onset Pompe disease: A different early portrait in China. Frontiers in neurology\| PubMed ID: 36237614	2022
Response to Eura et al. American journal of human genetics\| PubMed ID: 36332613	2022
Juvenile dermatomyositis in a Duchenne muscular dystrophy carrier. Clinical and experimental rheumatology\| PubMed ID: 36622134	2023
NOTCH2NLC-related oculopharyngodistal myopathy type 3 with cardiomyopathy and nephropathy. Muscle & nerve\| PubMed ID: 36840947	2023
Subclinical cardiac involvement present as electrocardiographic abnormalities in various neuromuscular diseases. Heliyon\| PubMed ID: 36895400	2023
Intrafamilial phenotypic heterogeneity in GIPC1-related oculopharyngodistal myopathy type 2: a case report. Neuromuscular disorders : NMD\| PubMed ID: 37550168	2023
Non-coding CGG repeat expansion in is associated with a phenotype of oculopharyngodistal myopathy. Journal of medical genetics\| PubMed ID: 37923380	2024
A 1-year analysis from a natural history study in Chinese individuals with Duchenne muscular dystrophy. The Lancet regional health. Western Pacific\| PubMed ID: 38089167	2024
Diagnostic delay in late-onset Pompe disease among Chinese patients: A retrospective study. JIMD reports\| PubMed ID: 38186848	2024
Clinical features and genetic spectrum of a multicenter Chinese cohort with myotonic dystrophy type 1. Orphanet journal of rare diseases\| PubMed ID: 38454488	2024
Diagnosis of Challenging Spinal Muscular Atrophy Cases with Long-Read Sequencing. The Journal of molecular diagnostics : JMD\| PubMed ID: 38490302	2024
Pseudoexon activation by deep intronic variation in GNE myopathy with thrombocytopenia. Muscle & nerve\| PubMed ID: 38558464	2024
(Bunge) Kitag. ex H.Hara inhibits pancreatic cancer progression by inducing caspase-dependent apoptosis and suppressing TGF-β-mediated epithelial-mesenchymal transition. Frontiers in pharmacology\| PubMed ID: 38881872	2024
Discovery of Novel 1-Phenylpiperidine Urea-Containing Derivatives Inhibiting β-Catenin/BCL9 Interaction and Exerting Antitumor Efficacy through the Activation of Antigen Presentation of cDC1... Journal of medicinal chemistry\| PubMed ID: 38912577	2024
Long-term impact of nusinersen on motor and electrophysiological outcomes in adolescent and adult spinal muscular atrophy: insights from a multicenter retrospective study. Journal of neurology\| PubMed ID: 39030456	2024
High-risk screening for late-onset Pompe disease in China: An expanded multicenter study. Journal of inherited metabolic disease\| PubMed ID: 39227307	2025
Human induced pluripotent stem cell line (FDHSi005-A) derived from a patient with a deep intronic variant in the GNE gene. Stem cell research\| PubMed ID: 39303320	2024
Novel variants and genotype-phenotype correlation in a multicentre cohort of GNE myopathy in China. Journal of medical genetics\| PubMed ID: 39332896	2024
4qA D4Z4 Methylation Test as a Valuable Complement for Differential Diagnosis in Patients with a Facioscapulohumeral Muscular Dystrophy-Like Phenotype. The Journal of molecular diagnostics : JMD\| PubMed ID: 40113166	2025
Efgartigimod for induction and maintenance therapy in muscle-specific kinase myasthenia gravis. Therapeutic advances in neurological disorders\| PubMed ID: 40144041	2025
Persistent exanthema mainly on the trunk with pathologically dermal interstitial mucin as anti-HMGCR myopathy-associated skin rash: Case series. The Journal of dermatology\| PubMed ID: 40152349	2025
Research trends on spinal muscular atrophy from 1995 to 2023: A bibliometric analysis. Medicine\| PubMed ID: 40153758	2025
Clinical, Pathologic, and Genetic Spectrum of Collagen VI-Related Disorder in China-A Retrospective Observational Multicenter Study. Human mutation\| PubMed ID: 40225934	2024
Diverse electrophysiological demyelinating features in a late-onset glycogen storage disease type IIIa case. Open medicine (Warsaw, Poland)\| PubMed ID: 40322467	2025
A cohort of GFPT1 related congenital myasthenic syndrome in China: high frequency of c.331 c > t variant. Orphanet journal of rare diseases\| PubMed ID: 40442802	2025
Pseudoexon activating by a deep intronic variant and phenotype variation in a Chinese family with dystrophinopathy. Journal of human genetics\| PubMed ID: 40583054	2025
Muscle Biopsy Findings in Valosin-Containing Protein Multisystem Proteinopathy. Neurology. Genetics\| PubMed ID: 40678441	2025