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Documents disponibles écrits par cet auteur (23)

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Frontiers in neurology, 15. Efficacy and safety of different doses of vamorolone in boys with Duchenne muscular dystrophy: a systematic review and network meta-analysis

Wang Q ; Zeng Y ; Jiao L ; He J ; Li B ; Guo Y ; Song Z | 2024

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Rheumatology (Oxford, England), Epub. Single-cell landscape of peripheral immune response in patients with anti-melanoma differentiation-associated gene 5 dermatomyositis

He J ; Liu Z ; Cao Y ; Zhang X ; Yi C ; Zhou Y ; Yang C ; Guo Z ; Zheng Q ; Huang J | 06/11/2023

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Annals of neurology, Epub. Reply to SARS1 (SerRS) causing de novo dominant Charcot-Marie-Tooth disease with slow conduction

He J ; Liu XX ; Fan DS ; Chen WJ | 13/09/2023

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Clinical immunology (Orlando, Fla.), 255, Epub. Metagenome-wide association study of gut microbiome features for myositis

Li Y ; Xu J ; Hong Y ; Li Z ; Xing X ; Zhufeng Y ; Lu D ; Liu X ; He J ; Li Y ; Sun X | 16/08/2023

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Article

Neurology, 101, 3. Association of 4qA-Specific Distal D4Z4 Hypomethylation With Disease Severity and Progression in Facioscapulohumeral Muscular Dystrophy

Zheng F ; Qiu L ; Chen L ; Zheng Y ; Lin X ; He J ; Lin X ; He Q ; Lin Y ; Lin L ; Wang L ; Lin F ; Yang K ; Lin M ; Lin Y ; Fu Y ; Wang N ; Wang Z | 18/07/2023

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Article

Annals of neurology, 92, 2. Heterozygous Seryl-tRNA Synthetase 1 Variants Cause Charcot-Marie-Tooth Disease

He J ; Liu XX ; Ma MM ; Lin JJ ; Fu J ; Chen YK ; Xu GR ; Xu LQ ; Fu ZF ; Xu D ; Chen WF ; Cao CY ; Shi Y ; Zeng YH ; Zhang J ; Chen XC ; Zhang RX ; Wang N ; Kennerson M ; Fan DS ; Chen WJ | United States | 11/09/2022

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Article

Annals of neurology GGC repeat expansion of RILPL1 is associated with oculopharyngodistal myopathy

Zeng YH ; Yang K ; Du GQ ; Chen YK ; Cao CY ; Qiu YS ; He J ; Lv HD ; Qu QQ ; Chen JN ; Xu GR ; Chen L ; Zheng FZ ; Zhao M ; Lin MT ; Chen WJ ; Hu J ; Wang ZQ ; Wang N | United States | 14/06/2022

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Article

Neuroepidemiology Global prevalence of myotonic dystrophy: an updated systematic review and meta-analysis

Liao Q ; Zhang Y ; He J ; Huang K | Switzerland | 28/04/2022

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Article

Frontiers in cellular and infection microbiology, 12. Modification of Intestinal Microbiota Dysbiosis by Low-Dose Interleukin-2 in Dermatomyositis: A Post Hoc Analysis From a Clinical Trial Study

Zhufeng Y ; Xu J ; Miao M ; Wang Y ; Li Y ; Huang B ; Guo Y ; Tian J ; Sun X ; Li J ; Lu D ; Li Z ; Li Y ; He J | 14/03/2022

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Article

The Lancet regional health. Western Pacific, 18. Prevalence and disease progression of genetically-confirmed facioscapulohumeral muscular dystrophy type 1 (FSHD1) in China between 2001 and 2020: a nationwide population-based study

Wang Z ; Qiu L ; Lin M ; Chen L ; Zheng F ; Lin L ; Lin F ; Ye Z ; Lin X ; He J ; Wang L ; Lin X ; He Q ; Chen W ; Lin Y ; Fu Y ; Wang N | 22/11/2021

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Article

Frontiers in neurology, 12. Clinical and Genetic Features of Biallelic Mutations in SORD in a Series of Chinese Patients With Charcot-Marie-Tooth and Distal Hereditary Motor Neuropathy

Liu X ; He J ; Yilihamu M ; Duan X ; Fan D | 08/11/2021

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Article

Rheumatology and therapy Treatment of Active Idiopathic Inflammatory Myopathies by Low-Dose Interleukin-2: A Prospective Cohort Pilot Study

Miao M ; Li Y ; Huang B ; Chen J ; Jin Y ; Shao M ; Zhang X ; Sun X ; He J ; Li Z | England | 14/04/2021

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Article

Annals of clinical and translational neurology, 8, 1. Evaluation of SORD mutations as a novel cause of Charcot-Marie-Tooth disease

Yuan RY ; Ye ZL ; Zhang XR ; Xu LQ ; He J | United States | 01/2021

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Article

Journal of medical genetics Clinical and genetic features of somatic mosaicism in facioscapulohumeral dystrophy

Qiu L ; Ye Z ; Lin L ; Wang L ; Lin X ; He J ; Lin F ; Xu G ; Cai N ; Jin M ; Chen H ; Lin M ; Wang N ; Wang Z | England | 03/2020

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Article

Respiratory medicine, 165. Clinical characteristics of patients with anti-EJ antisynthetase syndrome associated interstitial lung disease and literature review

Liu Y, Auteur ; Liu X ; Xie M ; Chen Z ; He J ; Wang Z ; Dai J ; Cai H | England | 03/2020

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Article

Medicine, 99, 3. 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 ; Li L ; Tang X ; Wang L ; Guo J ; Jin C ; Tighe S ; Zhang Y ; Zhu Y ; Zhu B | United States | 01/2020

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Article

Neurogenetics Whole exome sequencing reveals a broader variant spectrum of Charcot-Marie-Tooth disease type 2

Lin S ; Xu LQ ; Xu GR ; Guo LL ; Lin BJ ; Chen WJ ; Wang N ; Lin Y ; He J | United States | 12/2019

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Article

Journal of cachexia, sarcopenia and muscle, 10, 3. Hemojuvelin is a novel suppressor for Duchenne muscular dystrophy and age-related muscle wasting

Zhang P, Auteur ; He J ; Wang F ; Gong J ; Wang L ; Wu Q ; Li W ; Liu H ; Wang J ; Zhang K ; Li M ; Huang X ; Pu C ; Li Y ; Jiang F ; Wang F ; Min J ; Chen X | 06/2019

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Article

Neurology, 87, 1. A randomized controlled trial of methotrexate for patients with generalized myasthenia gravis

Pasnoor M, Auteur ; He J ; Herbelin L ; Burns TM ; Nations S ; Bril V ; Wang AK ; Elsheikh BH ; Kissel JT ; Saperstein D ; Shaibani JA ; Jackson C ; Swenson A ; Howard Jr JF ; Goyal N ; David W ; Wicklund M ; Pulley M ; Becker M ; Mozaffar T ; Benatar M ; Pazcuzzi R ; Simpson E ; Rosenfeld J ; Dimachkie MM ; Statland JM ; Barohn RJ | 2016

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Article

Pediatric cardiology, 37, 7. Cardiac Disease Burden and Risk of Mortality in Hospitalized Muscular Dystrophy Patients

Punnoose AR, Auteur ; Kaltman JR ; Pastor W ; McCarter R ; He J ; Spurney CF | 2016

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Article

Science translational medicine, 8, 331. Targeting protein homeostasis in sporadic inclusion body myositis

Ahmed M ; Machado PM ; Miller A ; Spicer C ; Herbelin L ; He J ; Noel J ; Wang Y ; McVey AL ; Pasnoor M ; Gallagher P ; Statland J ; Lu CH ; Kalmar B ; Brady S ; Sethi H ; Samandouras G ; Parton M ; Holton JL ; Weston A ; Collinson L ; Taylor JP ; Schiavo G ; Hanna MG ; Barohn RJ ; Dimachkie MM ; Greensmith L | 2016

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Article

Journal of neurology, neurosurgery and psychiatry, 85, 9. Whole-genome sequencing and the clinician: a tale of two cities

Foley AR ; Pitceathly RD ; He J ; Kim J ; Pearson NM ; Muntoni F ; Hanna MG | 2014

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Article

Annals of the New York Academy of Sciences, 1275. Phase II trial of methotrexate in myasthenia gravis

Pasnoor M ; He J ; Herbelin L ; Dimachkie M ; Barohn RJ | 2012

Accès au résumé PubMed / to PubMed abstract

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Détail de l'auteur

Auteur He J

Documents disponibles écrits par cet auteur (23)

Frontiers in neurology, 15. Efficacy and safety of different doses of vamorolone in boys with Duchenne muscular dystrophy: a systematic review and network meta-analysis

Rheumatology (Oxford, England), Epub. Single-cell landscape of peripheral immune response in patients with anti-melanoma differentiation-associated gene 5 dermatomyositis

Annals of neurology, Epub. Reply to SARS1 (SerRS) causing de novo dominant Charcot-Marie-Tooth disease with slow conduction

Clinical immunology (Orlando, Fla.), 255, Epub. Metagenome-wide association study of gut microbiome features for myositis

Neurology, 101, 3. Association of 4qA-Specific Distal D4Z4 Hypomethylation With Disease Severity and Progression in Facioscapulohumeral Muscular Dystrophy

Annals of neurology, 92, 2. Heterozygous Seryl-tRNA Synthetase 1 Variants Cause Charcot-Marie-Tooth Disease

Annals of neurology GGC repeat expansion of RILPL1 is associated with oculopharyngodistal myopathy

Neuroepidemiology Global prevalence of myotonic dystrophy: an updated systematic review and meta-analysis

Frontiers in cellular and infection microbiology, 12. Modification of Intestinal Microbiota Dysbiosis by Low-Dose Interleukin-2 in Dermatomyositis: A Post Hoc Analysis From a Clinical Trial Study

The Lancet regional health. Western Pacific, 18. Prevalence and disease progression of genetically-confirmed facioscapulohumeral muscular dystrophy type 1 (FSHD1) in China between 2001 and 2020: a nationwide population-based study

Frontiers in neurology, 12. Clinical and Genetic Features of Biallelic Mutations in SORD in a Series of Chinese Patients With Charcot-Marie-Tooth and Distal Hereditary Motor Neuropathy

Rheumatology and therapy Treatment of Active Idiopathic Inflammatory Myopathies by Low-Dose Interleukin-2: A Prospective Cohort Pilot Study

Annals of clinical and translational neurology, 8, 1. Evaluation of SORD mutations as a novel cause of Charcot-Marie-Tooth disease

Journal of medical genetics Clinical and genetic features of somatic mosaicism in facioscapulohumeral dystrophy

Respiratory medicine, 165. Clinical characteristics of patients with anti-EJ antisynthetase syndrome associated interstitial lung disease and literature review

Medicine, 99, 3. 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

Neurogenetics Whole exome sequencing reveals a broader variant spectrum of Charcot-Marie-Tooth disease type 2

Journal of cachexia, sarcopenia and muscle, 10, 3. Hemojuvelin is a novel suppressor for Duchenne muscular dystrophy and age-related muscle wasting

Neurology, 87, 1. A randomized controlled trial of methotrexate for patients with generalized myasthenia gravis

Pediatric cardiology, 37, 7. Cardiac Disease Burden and Risk of Mortality in Hospitalized Muscular Dystrophy Patients

Science translational medicine, 8, 331. Targeting protein homeostasis in sporadic inclusion body myositis

Journal of neurology, neurosurgery and psychiatry, 85, 9. Whole-genome sequencing and the clinician: a tale of two cities

Annals of the New York Academy of Sciences, 1275. Phase II trial of methotrexate in myasthenia gravis