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Auteur Li H

Documents disponibles écrits par cet auteur (71)

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Article

Orphanet journal of rare diseases, 19, 1. Comprehensive analysis of 2097 patients with dystrophinopathy based on a database from 2011 to 2021

Zhao L ; Shi Y ; Hu C ; Zhou S ; Li H ; Zhang L ; Qian C ; Zhou Y ; Wang Y ; Li X | 24/08/2024

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Article

Molecular neurobiology Advances on the Mechanisms and Therapeutic Strategies in Non-coding CGG Repeat Expansion Diseases

Zhang Y ; Liu X ; Li Z ; Li H ; Miao Z ; Wan B ; Xu X | 23/05/2024

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$Bispecific BCMA/CD19 targeted CAR-T cell therapy forces sustained disappearance of symptoms and anti-acetylcholine receptor antibodies in refractory myasthenia gravis: a case report$

Article

Journal of neurology, Epub. Bispecific BCMA/CD19 targeted CAR-T cell therapy forces sustained disappearance of symptoms and anti-acetylcholine receptor antibodies in refractory myasthenia gravis: a case report

Zhang Y ; Liu D ; Zhang Z ; Huang X ; Cao J ; Wang G ; Du X ; Wang Z ; Yang M ; Luo T ; Liu S ; Zhang W ; Sheng Y ; Li H ; Zhang W ; Chen H ; Zhang S ; Wang X ; Meng W ; Zong S ; Shi M ; Zheng J ; Cui G | 11/04/2024

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Article

JAMA Neurology Batoclimab vs Placebo for Generalized Myasthenia Gravis: A Randomized Clinical Trial

Yan C ; Yue Y ; Guan Y ; Bu B ; Ke Q ; Duan R ; Deng H ; Xue Q ; Jiang H ; Xiao F ; Yang H ; Chang T ; Zou Z ; Li H ; Tan S ; Xiao H ; Zhou H ; Zhang H ; Meng Q ; Li W ; Li W ; Guo J ; Zhang Y ; Li Z ; Tu J ; Shi J ; Li W ; Lee M ; Chen Y ; Tao X ; Zhao S ; Li P ; Zhao C | 04/03/2024

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Article

Aging and disease, Epub. Responsiveness to Tocilizumab in Anti-Acetylcholine Receptor-Positive Generalized Myasthenia Gravis

Jia D ; Zhang F ; Li H ; Shen Y ; Jin Z ; Shi FD ; Zhang C | 06/07/2023

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Article

Molecular therapy. Nucleic acids, 32. Single-swap editing for the correction of common Duchenne muscular dystrophy mutations

Chai AC ; Chemello F ; Li H ; Nishiyama T ; Chen K ; Zhang Y ; Sanchez-Ortiz E ; Alomar A ; Xu L ; Liu N ; Bassel-Duby R ; Olson EN | 19/04/2023

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Nature communications, 14, 1. Defective BVES-mediated feedback control of cAMP in muscular dystrophy

Li H ; Wang P ; Zhang C ; Zuo Y ; Zhou Y ; Han R | England | 30/03/2023

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Article

Frontiers in neurology, 14. Outcome and clinical features in juvenile myasthenia gravis: A systematic review and meta-analysis

Lin Y ; Kuang Q ; Li H ; Liang B ; Lu J ; Jiang Q ; Yang X | Switzerland | 08/03/2023

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Article

Journal of proteome research Proteomics Analysis of Plasma-Derived Exosomes Unveils the Aberrant Complement and Coagulation Cascades in Dermatomyositis/Polymyositis

Meng S ; Wang T ; Zhao Q ; Hu Q ; Chen Y ; Li H ; Liu C ; Liu D ; Hong X | United States | 12/12/2022

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Article

Molecular therapy : the journal of the American Society of Gene Therapy Systemic AAV9.BVES delivery ameliorates muscular dystrophy in a mouse model of LGMDR25

Li H ; Wang P ; Hsu E ; Pinckard KM ; Stanford KI ; Han R | United States | 25/11/2022

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Article

Frontiers in cardiovascular medicine, 9. Autophagy in striated muscle diseases

Li H ; Zhang L ; Zhang L ; Han R | Switzerland | 13/10/2022

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Article

Cells, 11, 19. CRISPR-Based Therapeutic Gene Editing for Duchenne Muscular Dystrophy: Advances, Challenges and Perspectives

Chen G ; Wei T ; Yang H ; Li G ; Li H | 22/09/2022

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Article

Frontiers in neurology, 13. Efficacy and Safety of the Ketogenic Diet for Mitochondrial Disease With Epilepsy: A Prospective, Open-labeled, Controlled Study

Huang L ; Li H ; Zhong J ; Yang L ; Chen G ; Wang D ; Zheng G ; Han H ; Han X ; Long Y ; Wang X ; Liang J ; Yu M ; Shen X ; Fan M ; Fang F ; Liao J ; Sun D | 08/2022

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Article

Molecular therapy. Nucleic acids, 29. A humanized knockin mouse model of Duchenne muscular dystrophy and its correction by CRISPR-Cas9 therapeutic gene editing

Zhang Y ; Li H ; Nishiyama T ; McAnally JR ; Sanchez-Ortiz E ; Huang J ; Mammen PPA ; Bassel-Duby R ; Olson EN | 01/08/2022

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Article

European journal of neurology Association of immunosuppression treatment with generalization among patients with ocular myasthenia gravis: A propensity score analysis

Ruan Z ; Guo R ; Zhou H ; Gao F ; Lin Y ; Xu Q ; Yu L ; Wu S ; Lei T ; Zhang M ; Gao Y ; Lu X ; Li H ; Sun C ; Tang B ; Li Z ; Chang T | England | 21/02/2022

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Article

Journal of neuroimmunology, 362. Eculizumab treatment for myasthenia gravis subgroups: 2021 update

Jiao L ; Li H ; Guo S | Netherlands | 18/11/2021

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Article

Neurotherapeutics Thymectomy and Risk of Generalization in Patients with Ocular Myasthenia Gravis: A Multicenter Retrospective Cohort Study

Li H ; Ruan Z ; Gao F ; Zhou H ; Guo R ; Sun C ; Xu Q ; Lu Q ; Zhou Y ; Zhao Z ; Yu L ; Wu S ; Lei T ; Gao T ; Tang Y ; Li C ; Huo F ; Zhu Y ; Sun J ; Tang B ; Zhang M ; Gao Y ; Lu X ; Li Z ; Chang T | United States | 08/10/2021

Correction to: Thymectomy and Risk of Generalization in Patients with Ocular Myasthenia Gravis: a Multicenter Retrospective Cohort Study Li H et al Neurotherapeutics. 2021 Nov 8. doi: 10.1007/s13311-021-01144-0. Correction for the affiliati[...]

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Article

Clinical rheumatology Myocardial involvement in idiopathic inflammatory myopathies: a multi-center cross-sectional study in the CRDC-MYO Registry

Zhang L ; Zhu H ; Yang P ; Duan X ; Wei W ; Wu Z ; Fang Y ; Li Q ; Liu S ; Shi X ; Li H ; Wu C ; Zhou S ; Leng X ; Zhao J ; Xu D ; Wu Q ; Tian X ; Li M ; Zhao Y ; Wang Q ; Zeng X | Germany | 29/06/2021

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Article

Nature communications, 12, 1. Efficient precise in vivo base editing in adult dystrophic mice

Xu L ; Zhang C ; Li H ; Wang P ; Gao Y ; Mokadam NA ; Ma J ; Arnold WD ; Han R | 17/06/2021

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Article

Molecular therapy. Methods & clinical development, 22. A consolidated AAV system for single-cut CRISPR correction of a common Duchenne muscular dystrophy mutation

Zhang Y ; Nishiyama T ; Li H ; Huang J ; Atmanli A ; Sanchez-Ortiz E ; Wang Z ; Mireault AA ; Mammen PPA ; Bassel Duby R ; Olson EN | 04/06/2021

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Article

Science advances, 7, 18. Precise correction of Duchenne muscular dystrophy exon deletion mutations by base and prime editing

Chemello F ; Chai AC ; Li H ; Rodriguez-Caycedo C ; Sanchez-Ortiz E ; Atmanli A ; Mireault AA ; Liu N ; Bassel Duby R ; Olson EN | 30/04/2021

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Article

13, 1. In vivo genome editing in mouse restores dystrophin expression in Duchenne muscular dystrophy patient muscle fibers

Chen M ; Shi H ; Gou S ; Wang X ; Li L ; Jin Q ; Wu H ; Zhang H ; Li Y ; Wang L ; Li H ; Lin J ; Guo W ; Jiang Z ; Yang X ; Xu A ; Zhu Y ; Zhang C ; Lai L ; Li X | 12/04/2021

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Science translational medicine, 13, 588. Urolithin A improves muscle function by inducing mitophagy in muscular dystrophy

Luan P ; D'Amico D ; Andreux PA ; Laurila PP ; Wohlwend M ; Li H ; Imamura de Lima T ; Place N ; Rinsch C ; Zanou N ; Auwerx J | United States | 07/04/2021

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Article

Journal of neuroimmunology, 354. Low-dose rituximab treatment for new-onset generalized myasthenia gravis

Li H ; Huang Z ; Jia D ; Xue H ; Pan J ; Zhang M ; Shi K ; Shi FD ; Zhang C | Netherlands | 24/02/2021

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Article

Proceedings of the national Academy of sciences of the United States of America, 118, 2. Ataluren and aminoglycosides stimulate read-through of nonsense codons by orthogonal mechanisms

Ng MY ; Li H ; Ghelfi MD ; Goldman YE ; Cooperman BS | 12/01/2021

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Détail de l'auteur

Auteur Li H

Documents disponibles écrits par cet auteur (71)

Orphanet journal of rare diseases, 19, 1. Comprehensive analysis of 2097 patients with dystrophinopathy based on a database from 2011 to 2021

Molecular neurobiology Advances on the Mechanisms and Therapeutic Strategies in Non-coding CGG Repeat Expansion Diseases

Journal of neurology, Epub. Bispecific BCMA/CD19 targeted CAR-T cell therapy forces sustained disappearance of symptoms and anti-acetylcholine receptor antibodies in refractory myasthenia gravis: a case report

JAMA Neurology Batoclimab vs Placebo for Generalized Myasthenia Gravis: A Randomized Clinical Trial

Aging and disease, Epub. Responsiveness to Tocilizumab in Anti-Acetylcholine Receptor-Positive Generalized Myasthenia Gravis

Molecular therapy. Nucleic acids, 32. Single-swap editing for the correction of common Duchenne muscular dystrophy mutations

Nature communications, 14, 1. Defective BVES-mediated feedback control of cAMP in muscular dystrophy

Frontiers in neurology, 14. Outcome and clinical features in juvenile myasthenia gravis: A systematic review and meta-analysis

Journal of proteome research Proteomics Analysis of Plasma-Derived Exosomes Unveils the Aberrant Complement and Coagulation Cascades in Dermatomyositis/Polymyositis

Molecular therapy : the journal of the American Society of Gene Therapy Systemic AAV9.BVES delivery ameliorates muscular dystrophy in a mouse model of LGMDR25

Frontiers in cardiovascular medicine, 9. Autophagy in striated muscle diseases

Cells, 11, 19. CRISPR-Based Therapeutic Gene Editing for Duchenne Muscular Dystrophy: Advances, Challenges and Perspectives

Frontiers in neurology, 13. Efficacy and Safety of the Ketogenic Diet for Mitochondrial Disease With Epilepsy: A Prospective, Open-labeled, Controlled Study

Molecular therapy. Nucleic acids, 29. A humanized knockin mouse model of Duchenne muscular dystrophy and its correction by CRISPR-Cas9 therapeutic gene editing

European journal of neurology Association of immunosuppression treatment with generalization among patients with ocular myasthenia gravis: A propensity score analysis

Journal of neuroimmunology, 362. Eculizumab treatment for myasthenia gravis subgroups: 2021 update

Neurotherapeutics Thymectomy and Risk of Generalization in Patients with Ocular Myasthenia Gravis: A Multicenter Retrospective Cohort Study

Clinical rheumatology Myocardial involvement in idiopathic inflammatory myopathies: a multi-center cross-sectional study in the CRDC-MYO Registry

Nature communications, 12, 1. Efficient precise in vivo base editing in adult dystrophic mice

Molecular therapy. Methods & clinical development, 22. A consolidated AAV system for single-cut CRISPR correction of a common Duchenne muscular dystrophy mutation

Science advances, 7, 18. Precise correction of Duchenne muscular dystrophy exon deletion mutations by base and prime editing

13, 1. In vivo genome editing in mouse restores dystrophin expression in Duchenne muscular dystrophy patient muscle fibers

Science translational medicine, 13, 588. Urolithin A improves muscle function by inducing mitophagy in muscular dystrophy

Journal of neuroimmunology, 354. Low-dose rituximab treatment for new-onset generalized myasthenia gravis

Proceedings of the national Academy of sciences of the United States of America, 118, 2. Ataluren and aminoglycosides stimulate read-through of nonsense codons by orthogonal mechanisms