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Auteur Li H

Documents disponibles écrits par cet auteur (57)

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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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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 : the journal of the American Society for Experimental 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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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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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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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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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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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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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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Article

Aging Melatonin exerts immunoregulatory effects by balancing peripheral effector and regulatory T helper cells in myasthenia gravis

Chang T ; Niu C ; Sun C ; Ma Y ; Guo R ; Ruan Z ; Gao Y ; Lu X ; Li H ; Lin Y ; Lin J ; Li Z | United States | 02/11/2020

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BMC neurology, 20, 1. Prediction of generalization of ocular myasthenia gravis under immunosuppressive therapy in Northwest China.

Ding J ; Zhao S ; Ren K ; Dang D ; Li H ; Wu F ; Zhang M ; Li Z ; Guo J | 06/2020

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Health and quality of life outcomes, 18, 1. Gender differences in quality of life among patients with myasthenia gravis in China

Dong D, Auteur ; Chong MK ; Wu Y ; Kaminski H ; Cutter G ; Xu X ; Li H ; Zhao C ; Yin J ; Yu S ; Zhu J | 2020

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Article

Molecular therapy : the journal of the American Society of Gene Therapy, 28, 9. Correction of Three Prominent Mutations in Mouse and Human Models of Duchenne Muscular Dystrophy by Single-Cut Genome Editing

Min YL ; Chemello F ; Li H ; Rodriguez-Caycedo C ; Sanchez-Ortiz E ; Mireault AA ; McAnally JR ; Shelton JM ; Zhang Y ; Bassel Duby R ; Olson EN | 2020

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Article

International immunopharmacology, 75. Metformin attenuates autoimmune disease of the neuromotor system in animal models of myasthenia gravis

Cui Y, Auteur ; Chang L ; Wang C ; Han X ; Mu L ; Hao Y ; Liu C ; Zhao J ; Zhang T ; Zhang H ; Zhang Y ; Liu Y ; Zhao W ; Wang J ; Liu X ; Sun B ; Wang G ; Kong Q ; Han J ; Li H | Netherlands | 10/2019

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Nature communications, 10, 1. In vivo non-invasive monitoring of dystrophin correction in a new Duchenne muscular dystrophy reporter mouse

Amoasii L, Auteur ; Li H ; Zhang Y ; Min YL ; Sanchez-Ortiz E ; Shelton JM ; Long C ; Mireault AA ; Bhattacharyya S ; McAnally JR ; Bassel Duby R ; Olson EN | England | 10/2019

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Article

National science review, 7, 1. Disruption of splicing-regulatory elements using CRISPR/Cas9 to rescue spinal muscular atrophy in human iPSCs and mice

Li JJ ; Lin X ; Tang C ; Lu YQ ; Hu X ; Zuo E ; Li H ; Ying W ; Sun Y ; Lai LL ; Chen HZ ; Guo XX ; Zhang QJ ; Wu S ; Zhou C ; Shen X ; Wang Q ; Lin MT ; Ma LX ; Wang N ; Krainer AR ; Shi L ; Yang H ; Chen WJ | 03/09/2019

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Annals of clinical and translational neurology, 6, 9. Novel mutations in DNA2 associated with myopathy and mtDNA instability

Ronchi D, Auteur ; Liu C ; Caporali L ; Piga D ; Li H ; Tagliavini F ; Valentino ML ; Ferro MT ; Bini P ; Zheng L ; Carelli V ; Shen B ; Comi GP | United States | 09/2019

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Article

Developmental neurorehabilitation Cross-cultural Adaptation and Multi-centric Validation of the Motor Function Measure Chinese Version (MFM-32-CN) for Patients with Neuromuscular Diseases

Huang M, Auteur ; Cao J ; Sun J ; Li W ; Qin L ; Li H ; Zhai C ; Huang W ; Gui T ; Zhang K ; Wang J ; Vuillerot C ; Wang Y ; Dai M | 07/2019

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Science advances, 5, 3. CRISPR-Cas9 corrects Duchenne muscular dystrophy exon 44 deletion mutations in mice and human cells

Min YL, Auteur ; Li H ; Rodriguez-Caycedo C ; Mireault AA ; Huang J ; Shelton JM ; McAnally JR ; Amoasii L ; Mammen PPA ; Bassel Duby R ; Olson EN | 06/03/2019

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Molecular genetics & genomic medicine, 7, 3. Clinical application of single-molecule optical mapping to a multigeneration FSHD1 pedigree

Zhang Q, Auteur ; Xu X ; Ding L ; Li H ; Xu C ; Gong Y ; Liu Y ; Mu T ; Leigh D ; Cram DS ; Tang S | 03/2019

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Article

Science (New York, N.Y.), 362, 6410. Gene editing restores dystrophin expression in a canine model of Duchenne muscular dystrophy.

Amoasii L, Auteur ; Hildyard JCW ; Li H ; Sanchez-Ortiz E ; Mireault A ; Caballero D ; Harron R ; Stathopoulou TR ; Massey C ; Shelton JM ; Bassel Duby R ; Piercy RJ ; Olson EN | 10/2018

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Article

Orphanet journal of rare diseases, 13, 1. The clinical spectrum and genetic variability of limb-girdle muscular dystrophy in a cohort of Chinese patients

Wang L, Auteur ; Zhang VW ; Li S ; Li H ; Sun Y ; Li J ; Zhu Y ; He R ; Lin J ; Zhang C | 14/08/2018

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Article

Journal of cellular and molecular medicine Chemical, biochemical, preclinical and clinical studies of Ganoderma lucidum polysaccharide as an approved drug for treating myopathy and other diseases in China

Zeng P, Auteur ; Guo Z ; Zeng X ; Hao C ; Zhang Y ; Zhang M ; Liu Y ; Li H ; Li J ; Zhang L | 24/04/2018

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Détail de l'auteur

Auteur Li H

Documents disponibles écrits par cet auteur (57)

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 : the journal of the American Society for Experimental 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

Aging Melatonin exerts immunoregulatory effects by balancing peripheral effector and regulatory T helper cells in myasthenia gravis

BMC neurology, 20, 1. Prediction of generalization of ocular myasthenia gravis under immunosuppressive therapy in Northwest China.

Health and quality of life outcomes, 18, 1. Gender differences in quality of life among patients with myasthenia gravis in China

Molecular therapy : the journal of the American Society of Gene Therapy, 28, 9. Correction of Three Prominent Mutations in Mouse and Human Models of Duchenne Muscular Dystrophy by Single-Cut Genome Editing

International immunopharmacology, 75. Metformin attenuates autoimmune disease of the neuromotor system in animal models of myasthenia gravis

Nature communications, 10, 1. In vivo non-invasive monitoring of dystrophin correction in a new Duchenne muscular dystrophy reporter mouse

National science review, 7, 1. Disruption of splicing-regulatory elements using CRISPR/Cas9 to rescue spinal muscular atrophy in human iPSCs and mice

Annals of clinical and translational neurology, 6, 9. Novel mutations in DNA2 associated with myopathy and mtDNA instability

Developmental neurorehabilitation Cross-cultural Adaptation and Multi-centric Validation of the Motor Function Measure Chinese Version (MFM-32-CN) for Patients with Neuromuscular Diseases

Science advances, 5, 3. CRISPR-Cas9 corrects Duchenne muscular dystrophy exon 44 deletion mutations in mice and human cells

Molecular genetics & genomic medicine, 7, 3. Clinical application of single-molecule optical mapping to a multigeneration FSHD1 pedigree

Science (New York, N.Y.), 362, 6410. Gene editing restores dystrophin expression in a canine model of Duchenne muscular dystrophy.

Orphanet journal of rare diseases, 13, 1. The clinical spectrum and genetic variability of limb-girdle muscular dystrophy in a cohort of Chinese patients

Journal of cellular and molecular medicine Chemical, biochemical, preclinical and clinical studies of Ganoderma lucidum polysaccharide as an approved drug for treating myopathy and other diseases in China