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Auteur Wang H

Documents disponibles écrits par cet auteur (57)

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Article

Journal of neurology, Epub. Nusinersen effectiveness and safety in pediatric patients with 5q-spinal muscular atrophy: a multi-center disease registry in China

Yao X ; Peng J ; Luo R ; Wang X ; Lu X ; Wu L ; Jin R ; Zhong J ; Liang J ; Hong S ; Yang L ; Zhang X ; Mao S ; Hu J ; Tao Z ; Sun D ; Wang H ; Zhang L ; Xia Y ; Chen K ; Wang Y | 02/07/2024

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Article

Neurological research, 46, 7. microRNA-mRNA expression profiles in the skeletal muscle of myotonic dystrophy type 1

Li M ; Li Y ; Wang Z ; Cui F ; Yang F ; Wang H ; Shi Q ; Huang X | 07/2024

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Article

Canadian journal of ophthalmology. Journal canadien d'ophtalmologie, Epub. Omalizumab-induced ocular myasthenia gravis?

Wang H ; Supramaniam D ; Cugati S ; Chen C | 14/04/2024

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Article

Heliyon, 10, 4. Curcumin protects mice with myasthenia gravis by regulating the gut microbiota, short-chain fatty acids, and the Th17/Treg balance

Sun J ; Xie Q ; Sun M ; Zhang W ; Wang H ; Liu N ; Wang M | 29/02/2024

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Article

Frontiers in immunology, 15. Efgartigimod as a promising add-on therapy for myasthenic crisis: a prospective case series

Song J ; Wang H ; Huan X ; Jiang Q ; Wu Z ; Yan C ; Xi J ; Zhao C ; Feng H ; Luo S | 2024

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Article

Journal of inflammation (London, England), 20, 1. Sodium butyrate alleviates R97-116 peptide-induced myasthenia gravis in mice by improving the gut microbiota and modulating immune response

Sun J ; Chen J ; Xie Q ; Sun M ; Zhang W ; Wang H ; Liu N ; Wang Q ; Wang M | 03/11/2023

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Article

Human molecular genetics The clinical features and TCAP mutation Spectrum in a Chinese cohort of patients with limb-girdle muscular dystrophy R7

Lv X ; Lin F ; Wu W ; Wang H ; Luo Y ; Wang Z ; Yan C ; Lv H ; Luo S ; Lin P | 22/05/2023

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Article

Frontiers in neurology, 14. Altered gut microbiota and metabolites in untreated myasthenia gravis patients

Ding XJ ; Li HY ; Wang H ; Zhang XH ; Song M ; Jiang XH ; Zhang X ; Yue YX ; Li XH | 2023

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Article

Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology, 146. Distinguishing normal, neuropathic and myopathic EMG with an automated machine learning approach

Tannemaat MR ; Kefalas M ; Geraedts VJ ; Remijn-Nelissen L ; Verschuuren AJM ; Koch M ; Kononova AV ; Wang H ; Bäck THW | Netherlands | 09/12/2022

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Article

Zeitschrift fur Rheumatologie Associations between anti-mitochondrial antibodies and cardiac involvement in idiopathic inflammatory myopathy patients : A systematic review and meta-analysis

Wang H ; Zhu Y ; Hu J ; Jin J ; Lu J ; Shen C ; Cai Z | Germany | 16/05/2022

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Article

Frontiers in medicine, 8. Coronary Heart Disease and Cardiovascular Risk Factors in Patients With Idiopathic Inflammatory Myopathies: A Systemic Review and Meta-Analysis

Qin L ; Li F ; Luo Q ; Chen L ; Yang X ; Wang H | 14/01/2022

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Article

Frontiers in bioscience (Landmark edition), 27, 1. The protective role of mesencephalic astrocyte-derived neurotrophic factor in endoplasmic reticulum stress in RT4-D6P2T schwannoma sells with the S63del MPZ mutation

Sun B ; Wang H ; Li Y ; He Z ; Cui F ; Yang F ; Huang X | Singapore | 04/01/2022

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Article

Rheumatology (Oxford, England) Comment on: Cardiovascular events in adult polymyositis and dermatomyositis: a meta-analysis of observational studies

Qin L ; Wang H | England | 28/12/2021

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Article

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research Plasma Soluble Biomarkers for Fibrodysplasia Ossificans Progressiva (FOP) Reflect Acute and Chronic Inflammatory States

Pignolo RJ ; McCarrick-Walmsley R ; Wang H ; Qiu S ; Hunter J ; Barr S ; He K ; Zhang H ; Kaplan FS | United States | 26/12/2021

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Article

Human molecular genetics Antisense oligonucleotides targeting the SMN2 promoter region enhance SMN2 expression in spinal muscular atrophy cell lines and mouse model

Wang J ; Bai J ; Ouyang S ; Wang H ; Jin Y ; Peng X ; Ge X ; Jiao H ; Zou J ; He C ; Xiao P ; Song F ; Qu Y | England | 09/12/2021

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Article

Clinical rheumatology, 40, 10. The risk of ischemic stroke in patients with idiopathic inflammatory myopathies: a systematic review and meta-analysis

Zhen C ; Wang Y ; Wang H ; Wang X | Germany | 10/2021

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Article

Neurology, 97, 5. MicroRNAs as Biomarkers of Charcot-Marie-Tooth Disease Type 1A

Wang H ; Davison M ; Wang K ; Xia TH ; Call KM ; Luo J ; Wu X ; Zuccarino R ; Bacha A ; Bai Y ; Gutmann L ; Feely SME ; Grider T ; Rossor AM ; Reilly MM ; Shy ME ; Svaren J | 03/08/2021

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Article

Bone, 149. Spatial patterns of heterotopic ossification in fibrodysplasia ossificans progressiva correlate with anatomic temperature gradients

Wang H ; De Cunto CL ; Pignolo RJ ; Kaplan FS | United States | 08/2021

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Article

Frontiers in neuroscience, 15. The Pathological Features of Common Hereditary Mitochondrial Dynamics Neuropathy

Wu R ; Lv H ; Wang H ; Wang Z ; Yuan Y | 22/07/2021

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Article

Neuron, 109, 12. Membraneless condensates by Rapsn phase separation as a platform for neuromuscular junction formation

Xing G ; Jing H ; Yu Z ; Chen P ; Wang H ; Xiong WC ; Mei L | 16/06/2021

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Article

Human molecular genetics Proteomic analysis identifies key differences in the cardiac interactomes of dystrophin and micro-dystrophin

Wang H ; Marrosu E ; Brayson D ; Wasala NB ; Johnson EK ; Scott CS ; Yue Y ; Hau KL ; Trask AJ ; Froehner SC ; Adams ME ; Zhang L ; Duan D ; Montanaro F | England | 05/05/2021

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Article

Annals of translational medicine, 9, 9. Genetic identification of pathogenic variations of the DMD gene: a retrospective study from 10,481 neonatal patients based on next-generation sequencing data

Xiao T ; Wu B ; Cao Y ; Liu R ; Cheng G ; Wang L ; Zhuang D ; Zhao Z ; Wang H ; Zhou W | 05/2021

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Article

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 42, 3. AChRAb and MuSKAb double-seropositive myasthenia gravis: a distinct subtype?

Zhang J ; Chen Y ; Chen J ; Huang X ; Wang H ; Li Y ; Liu W ; Feng H | 01/2021

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Article

Neurology India, 68, 2. A symptomatic female patient with duchenne muscular dystrophy gene mutation showing rimmed vacuoles in muscle biopsy

Ban R ; Lu X ; Pu C ; Shi Q ; Wang H ; Liu H ; Zhang Y ; Fang F | India | 05/2020

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Article

Human gene therapy Different serotypes of AAV vectors and lentivirus meditated tropism in choroid plexus by intracerebroventricular delivery

Chen X, Auteur ; He Y ; Tian Y ; Wang Y ; Wu Z ; Lan T ; Wang H ; Cheng K ; Xie P | United States | 02/2020

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Détail de l'auteur

Auteur Wang H

Documents disponibles écrits par cet auteur (57)

Journal of neurology, Epub. Nusinersen effectiveness and safety in pediatric patients with 5q-spinal muscular atrophy: a multi-center disease registry in China

Neurological research, 46, 7. microRNA-mRNA expression profiles in the skeletal muscle of myotonic dystrophy type 1

Canadian journal of ophthalmology. Journal canadien d'ophtalmologie, Epub. Omalizumab-induced ocular myasthenia gravis?

Heliyon, 10, 4. Curcumin protects mice with myasthenia gravis by regulating the gut microbiota, short-chain fatty acids, and the Th17/Treg balance

Frontiers in immunology, 15. Efgartigimod as a promising add-on therapy for myasthenic crisis: a prospective case series

Journal of inflammation (London, England), 20, 1. Sodium butyrate alleviates R97-116 peptide-induced myasthenia gravis in mice by improving the gut microbiota and modulating immune response

Human molecular genetics The clinical features and TCAP mutation Spectrum in a Chinese cohort of patients with limb-girdle muscular dystrophy R7

Frontiers in neurology, 14. Altered gut microbiota and metabolites in untreated myasthenia gravis patients

Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology, 146. Distinguishing normal, neuropathic and myopathic EMG with an automated machine learning approach

Zeitschrift fur Rheumatologie Associations between anti-mitochondrial antibodies and cardiac involvement in idiopathic inflammatory myopathy patients : A systematic review and meta-analysis

Frontiers in medicine, 8. Coronary Heart Disease and Cardiovascular Risk Factors in Patients With Idiopathic Inflammatory Myopathies: A Systemic Review and Meta-Analysis

Frontiers in bioscience (Landmark edition), 27, 1. The protective role of mesencephalic astrocyte-derived neurotrophic factor in endoplasmic reticulum stress in RT4-D6P2T schwannoma sells with the S63del MPZ mutation

Rheumatology (Oxford, England) Comment on: Cardiovascular events in adult polymyositis and dermatomyositis: a meta-analysis of observational studies

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research Plasma Soluble Biomarkers for Fibrodysplasia Ossificans Progressiva (FOP) Reflect Acute and Chronic Inflammatory States

Human molecular genetics Antisense oligonucleotides targeting the SMN2 promoter region enhance SMN2 expression in spinal muscular atrophy cell lines and mouse model

Clinical rheumatology, 40, 10. The risk of ischemic stroke in patients with idiopathic inflammatory myopathies: a systematic review and meta-analysis

Neurology, 97, 5. MicroRNAs as Biomarkers of Charcot-Marie-Tooth Disease Type 1A

Bone, 149. Spatial patterns of heterotopic ossification in fibrodysplasia ossificans progressiva correlate with anatomic temperature gradients

Frontiers in neuroscience, 15. The Pathological Features of Common Hereditary Mitochondrial Dynamics Neuropathy

Neuron, 109, 12. Membraneless condensates by Rapsn phase separation as a platform for neuromuscular junction formation

Human molecular genetics Proteomic analysis identifies key differences in the cardiac interactomes of dystrophin and micro-dystrophin

Annals of translational medicine, 9, 9. Genetic identification of pathogenic variations of the DMD gene: a retrospective study from 10,481 neonatal patients based on next-generation sequencing data

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 42, 3. AChRAb and MuSKAb double-seropositive myasthenia gravis: a distinct subtype?

Neurology India, 68, 2. A symptomatic female patient with duchenne muscular dystrophy gene mutation showing rimmed vacuoles in muscle biopsy

Human gene therapy Different serotypes of AAV vectors and lentivirus meditated tropism in choroid plexus by intracerebroventricular delivery