Wang H Catalogue en ligne

Détail de l'auteur

Auteur Wang H

Documents disponibles écrits par cet auteur (49)

trié(s) par (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

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

Plus d'information...

Ajouter au panier

En ligne

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

Plus d'information...

Ajouter au panier

En ligne

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

Plus d'information...

Ajouter au panier

En ligne

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

Plus d'information...

Ajouter au panier

En ligne

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

Plus d'information...

Ajouter au panier

En ligne

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

Plus d'information...

Ajouter au panier

En ligne

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

Plus d'information...

Ajouter au panier

En ligne

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

Plus d'information...

Ajouter au panier

En ligne

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

Plus d'information...

Ajouter au panier

En ligne

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

Plus d'information...

Ajouter au panier

En ligne

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

Plus d'information...

Ajouter au panier

En ligne

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

Plus d'information...

Ajouter au panier

En ligne

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

Plus d'information...

Ajouter au panier

En ligne

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

Plus d'information...

Ajouter au panier

En ligne

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

Plus d'information...

Ajouter au panier

En ligne

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

Plus d'information...

Ajouter au panier

En ligne

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

Plus d'information...

Ajouter au panier

En ligne

Article

Journal of human genetics Transmission characteristics of SMN from 227 spinal muscular atrophy core families in China

Cao Y ; Qu Y ; Bai J ; Cheng M ; Jin Y ; Wang H ; Song F | England | 02/2020

Plus d'information...

Ajouter au panier

En ligne

Article

Annals of clinical and translational neurology, 7, 1. Transmembrane protease serine 5: a novel Schwann cell plasma marker for CMT1A

Wang H ; Davison M ; Wang K ; Xia TH ; Kramer M ; Call K ; Luo J ; Wu X ; Zuccarino R ; Bacon C ; Bai Y ; Moran JJ ; Gutmann L ; Feely SME ; Grider T ; Rossor AM ; Reilly MM ; Svaren J ; Shy ME | United States | 01/2020

Plus d'information...

Ajouter au panier

En ligne

Article

Cell Research Dosage effect of multiple genes accounts for multisystem disorder of myotonic dystrophy type 1

Yin Q ; Wang H ; Li N ; Ding Y ; Xie Z ; Jin L ; Li Y ; Wang Q ; Liu X ; Xu L ; Li Q ; Ma Y ; Cheng Y ; Wang K ; Zhong C ; Yu Q ; Tang W ; Chen W ; Yang W ; Zhang F ; Ding C ; Bao L ; Zhou B ; Hu P ; Li J | England | 12/2019

Plus d'information...

Ajouter au panier

En ligne

Article

Genetics in medicine : official journal of the American College of Medical Genetics The genomic and clinical landscape of fetal akinesia

Pergande M, Auteur ; Motameny S ; Ozdemir O ; Kreutzer M ; Wang H ; Daimaguler HS ; Becker K ; Karakaya M ; Ehrhardt H ; Elcioglu N ; Ostojic S ; Chao CM ; Kawalia A ; Duman O ; Koy A ; Hahn A ; Reimann J ; Schoner K ; Schänzer A ; Westhoff JH ; Schwaibold EMC ; Cossee M ; Imbert-Bouteille M ; von Pein H ; Haliloglu G ; Topaloglu H ; Altmuller J ; Nurnberg P ; Thiele H ; Heller R ; Cirak S | United States | 11/2019

Plus d'information...

Ajouter au panier

En ligne

Article

Frontiers in neuroscience Genotype-Phenotype Correlations in Charcot-Marie-Tooth Disease Due to MTMR2 Mutations and Implications in Membrane Trafficking

Wang H, Auteur ; Kacar Bayram A ; Sprute R ; Ozdemir O ; Cooper E ; Pergande M ; Efthymiou S ; Nedic I ; Mazaheri N ; Stumpfe K ; Azizi Malamiri R ; Shariati G ; Zeighami J ; Bayram N ; Naghibzadeh SK ; Tajik M ; Yasar M ; Sami Guven A ; Bibi F ; Sultan T ; Salpietro V ; Houlden H ; Per H ; Galehdari H ; Shalbafan B ; Jamshidi Y ; Cirak S | Switzerland | 10/2019

Plus d'information...

Ajouter au panier

En ligne

Article

eLife, 8. A mechanism in agrin signaling revealed by a prevalent Rapsyn mutation in congenital myasthenic syndrome

Xing G, Auteur ; Jing H ; Zhang L ; Cao Y ; Li L ; Zhao K ; Dong Z ; Chen W ; Wang H ; Cao R ; Xiong WC ; Mei L | England | 09/2019

Plus d'information...

Ajouter au panier

En ligne

Article

The Turkish journal of pediatrics, 61, 6. Bi-allelic mutations in PRUNE lead to neurodegeneration with spinal motor neuron involvement and hyperCKaemia

Okur D ; Daimaguler HS ; Danyeli AE ; Tekgul H ; Wang H ; Wunderlich G ; Cirak S ; Yis U | Turkey | 2019

Plus d'information...

Ajouter au panier

En ligne

Article

Nucleic acids research Efficient CRISPR/Cas9-mediated editing of trinucleotide repeat expansion in myotonic dystrophy patient-derived iPS and myogenic cells

Dastidar S, Auteur ; Ardui S ; Singh K ; Majumdar D ; Nair N ; Fu Y ; Reyon D ; Samara E ; Gerli MFM ; Klein AF ; De Schrijver W ; Tipanee J ; Seneca S ; Tulalamba W ; Wang H ; Chai YC ; In't Veld P ; Furling D ; Tedesco FS ; Vermeesch JR ; Joung JK ; Chuah MK ; Vandendriessche T | 27/06/2018

Plus d'information...

Ajouter au panier

En ligne

MYOBASE

Newsletters

Bibliographies

Portail documentaire sur les maladies neuromusculaires

Se connecter

Accueil

Sélection de la langue

Adresse

Détail de l'auteur

Auteur Wang H

Documents disponibles écrits par cet auteur (49)

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

Journal of human genetics Transmission characteristics of SMN from 227 spinal muscular atrophy core families in China

Annals of clinical and translational neurology, 7, 1. Transmembrane protease serine 5: a novel Schwann cell plasma marker for CMT1A

Cell Research Dosage effect of multiple genes accounts for multisystem disorder of myotonic dystrophy type 1

Genetics in medicine : official journal of the American College of Medical Genetics The genomic and clinical landscape of fetal akinesia

Frontiers in neuroscience Genotype-Phenotype Correlations in Charcot-Marie-Tooth Disease Due to MTMR2 Mutations and Implications in Membrane Trafficking

eLife, 8. A mechanism in agrin signaling revealed by a prevalent Rapsyn mutation in congenital myasthenic syndrome

The Turkish journal of pediatrics, 61, 6. Bi-allelic mutations in PRUNE lead to neurodegeneration with spinal motor neuron involvement and hyperCKaemia

Nucleic acids research Efficient CRISPR/Cas9-mediated editing of trinucleotide repeat expansion in myotonic dystrophy patient-derived iPS and myogenic cells