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Auteur Liu M

Documents disponibles écrits par cet auteur (26)

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Article

Frontiers in pharmacology, 15. Comprehensive analysis of adverse events associated with onasemnogene abeparvovec (Zolgensma) in spinal muscular atrophy patients: insights from FAERS database

Zhang W ; Yin Y ; Yang D ; Liu M ; Ye C ; Yan R ; Li R | 07/01/2025

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Article

Cell Allogeneic CD19-targeted CAR-T therapy in patients with severe myositis and systemic sclerosis

Wang X ; Wu X ; Tan B ; Zhu L ; Zhang Y ; Lin L ; Xiao Y ; Sun A ; Wan X ; Liu S ; Liu Y ; Ta N ; Zhang H ; Song J ; Li T ; Zhou L ; Yin J ; Ye L ; Lu H ; Hong J ; Cheng H ; Wang P ; Li W ; Chen J ; Zhang J ; Luo J ; Huang M ; Guo L ; Pan X ; Jin Y ; Ye W ; Dai L ; Zhu J ; Sun L ; Zheng B ; Li D ; He Y ; Liu M ; Wu H ; Du B ; Xu H | 09/07/2024

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Article

Frontiers in immunology, 15. Therapeutic efficacy and safety of JAK inhibitors in treating polymyositis/dermatomyositis: a single-arm systemic meta-analysis

Ma C ; Liu M ; Cheng Y ; Wang X ; Zhao Y ; Wang K ; Wang W | 21/03/2024

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Article

Alternative therapies in health and medicine Effects of Qishen Dihuang Granules on Intestinal Microbiota in Experimental Autoimmune Myasthenia Gravis Model Rats

Wu T ; Wang B ; Xu P ; Lv Z ; Zhang Y ; Zhang D ; Chang T ; Lu J ; Wu L ; Liu M ; Chen Z ; Lan T ; Wang J | 12/05/2023

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Article

Frontiers in immunology, 14. Characteristics of cardiac involvement in immune-mediated necrotizing myopathy

Liu M ; Lin Y ; Qiao L ; Chen J ; Shi Q | Switzerland | 28/02/2023

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Article

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology Becker muscular dystrophy: case report, review of the literature, and analysis of differentially expressed hub genes

Li M ; Han Y ; Wang S ; Yu Y ; Liu M ; Xia Y ; Weng Z ; Zhou L ; He X ; Wang J ; He Z ; Yu L ; Zha Y | Italy | 03/11/2021

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Article

Journal of neuropathology and experimental neurology, 79, 5. Gasdermine E-Dependent Mitochondrial Pyroptotic Pathway in Dermatomyositis: A Possible Mechanism of Perifascicular Atrophy

Liu M, Auteur ; Li L ; Dai T ; Hou Y ; Li W ; Zhao Y ; Fang Q ; Yan C | England | 05/2020

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Article

BMC neurology, 20, 1. Myotonic dystrophy type 1 accompanied with normal pressure hydrocephalus: a case report and literature review

Wang J ; Liu M ; Shang W ; Chen Z ; Peng G | England | 02/2020

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Article

Frontiers in neurology, 10. GJB1 Mutation-A Disease Spectrum: Report of Case Series

Niu J ; Dai Y ; Liu M ; Li Y ; Ding Q ; Guan Y ; Cui L ; Jin L | 01/2020

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Article

Annals of clinical and translational neurology, 6, 9. Variants in MME are associated with autosomal-recessive distal hereditary motor neuropathy

Hong D, Auteur ; Fang P ; Yao S ; Chen J ; Zhang X ; Chen S ; Zhang J ; Tan D ; Wang L ; Han X ; Xin L ; Wang Y ; Liu M ; Cong L ; Zhong S ; Ouyang H ; Gao X ; Zhang J | United States | 2019

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Article

Disability and rehabilitation, 40, 12. A comparison of swallowing dysfunction in Becker muscular dystrophy and Duchenne muscular dystrophy

Yamada Y, Auteur ; Kawakami M ; Wada A ; Otsuka T ; Muraoka K ; Liu M | 2018

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Article

Frontiers in neurology, 8. Multiple Sites Ultrasonography of Peripheral Nerves in Differentiating Charcot-Marie-Tooth Type 1A from Chronic Inflammatory Demyelinating Polyradiculoneuropathy

Niu J, Auteur ; Cui L ; Liu M | 2017

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Article

Respiratory care, 62, 4. Feasibility of a Respiratory Movement Evaluation Tool to Quantify Thoracoabdominal Movement for Neuromuscular Diseases

Liu F, Auteur ; Kawakami M ; Tamura K ; Taki Y ; Shimizu K ; Otsuka T ; Tsuji T ; Miyata C ; Tashiro S ; Wada A ; Mizuno K ; Aoki Y ; Liu M | 2017

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Article

PLoS ONE, 11, 11. Activin Receptor Type IIB Inhibition Improves Muscle Phenotype and Function in a Mouse Model of Spinal Muscular Atrophy

Liu M, Auteur ; Hammers DW ; Barton ER ; Sweeney HL | 2016

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Article

Human molecular genetics, 24, 20. Muscle hypertrophy induced by myostatin inhibition accelerates degeneration in dysferlinopathy

Lee YS, Auteur ; Lehar A ; Sebald S ; Liu M ; Swaggart KA ; Talbot CC ; Pytel P ; Barton ER ; McNally EM ; Lee SJ | 2015

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Article

BioMed Central neuroscience, 11, 117. Change in brain activity through virtual reality-based brain-machine communication in a chronic tetraplegic subject with muscular dystrophy

Hashimoto Y ; Ushiba J ; Kimura A ; Liu M ; Tomita Y | 2010

Accès au résumé PubMed / to PubMed abstract

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Article

Disability and rehabilitation, 30, 7. Dysphagia in patients with Duchenne muscular dystrophy evaluated with a questionnaire and videofluorography

Hanayama K ; Liu M ; Higuchi Y ; Fujiwara T ; Tsuji T ; Hase K ; Ishihara T | 2008

Accès au résumé PubMed / to PubMed abstract

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Article

EMBO journal (The), 27, 20. An isogenetic myoblast expression screen identifies DUX4-mediated FSHD-associated molecular pathologies

Bosnakovski D ; Xu Z ; Gang EJ ; Galindo CL ; Liu M ; Simsek T ; Garner HR ; Agha Mohammadi S ; Tassin A ; Coppée F ; Belayew A ; Perlingeiro RR ; Kyba M | 2008

Accès au résumé PubMed / to PubMed abstract

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Article

Neuromuscular disorders : NMD, 18, 9-10. Transient overexpression of the Rho family exchange factor GEFT stimulates myogenic differentiation of inclusion-body myositis (IBM) mesoangioblasts (Poster)

Collectif ; Morosetti R ; Gliubizzi C ; Broccolini A ; Gidaro T ; Tonali PA ; Liu M ; Ricci E ; Mirabella M | 2008

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Article

Molecular therapy, 14, 1. C-terminal-truncated microdystrophin recruits dystrobrevin and syntrophin to the dystrophin-associated glycoprotein complex and reduces muscular dystrophy in symptomatic utrophin/dystrophin double-knockout mice

Yue Y ; Liu M ; Duan D | 07/2006

Accès au résumé PubMed / to PubMed abstract

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Article

Molecular therapy, 11, 2. Adeno-associated virus-mediated microdystrophin expression protects young mdx muscle from contraction-induced injury

Liu M ; Yue Y ; Harper SQ ; Grange RW ; Chamberlain JS ; Duan D | 02/2005

Accès au résumé PubMed / to PubMed abstract

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Article

Journal of molecular medicine, 83. Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family

Wang Q ; Liu M ; Xu C ; Tang Z ; Liao Y ; Du R ; Li W ; Wu X ; Wang X ; Liu P ; Zhang X ; Zhu J ; Ren X ; Ke T ; Yang J | 2005

Accès au résumé PubMed / to PubMed abstract

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Article

Journal of rehabilitation medicine, 36, 3. Functional status and muscle strength in people with Duchenne muscular dystrophy living in the community

Uchikawa K ; Liu M ; Hanayama K ; Tsuji T ; Fujiwara T ; Chino N | 2004

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Article

Archives of physical medicine and rehabilitation, 84, 6. Practical problems and management of seating through the clinical stages of Duchenne's Muscular Dystrophy

Liu M ; Mineo K ; Hanayama K ; Fujiwara T ; Chino N | 06/2003

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Article

American journal of physical medicine & rehabilitation, 77, 1. Functional independence measure for children (WeeFIM). A preliminary study in nondisabled japanese children.

Liu M ; Toikawa H ; Seki M ; Domen K ; Chino N | 01/1998

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Détail de l'auteur

Auteur Liu M

Documents disponibles écrits par cet auteur (26)

Frontiers in pharmacology, 15. Comprehensive analysis of adverse events associated with onasemnogene abeparvovec (Zolgensma) in spinal muscular atrophy patients: insights from FAERS database

Cell Allogeneic CD19-targeted CAR-T therapy in patients with severe myositis and systemic sclerosis

Frontiers in immunology, 15. Therapeutic efficacy and safety of JAK inhibitors in treating polymyositis/dermatomyositis: a single-arm systemic meta-analysis

Alternative therapies in health and medicine Effects of Qishen Dihuang Granules on Intestinal Microbiota in Experimental Autoimmune Myasthenia Gravis Model Rats

Frontiers in immunology, 14. Characteristics of cardiac involvement in immune-mediated necrotizing myopathy

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology Becker muscular dystrophy: case report, review of the literature, and analysis of differentially expressed hub genes

Journal of neuropathology and experimental neurology, 79, 5. Gasdermine E-Dependent Mitochondrial Pyroptotic Pathway in Dermatomyositis: A Possible Mechanism of Perifascicular Atrophy

BMC neurology, 20, 1. Myotonic dystrophy type 1 accompanied with normal pressure hydrocephalus: a case report and literature review

Frontiers in neurology, 10. GJB1 Mutation-A Disease Spectrum: Report of Case Series

Annals of clinical and translational neurology, 6, 9. Variants in MME are associated with autosomal-recessive distal hereditary motor neuropathy

Disability and rehabilitation, 40, 12. A comparison of swallowing dysfunction in Becker muscular dystrophy and Duchenne muscular dystrophy

Frontiers in neurology, 8. Multiple Sites Ultrasonography of Peripheral Nerves in Differentiating Charcot-Marie-Tooth Type 1A from Chronic Inflammatory Demyelinating Polyradiculoneuropathy

Respiratory care, 62, 4. Feasibility of a Respiratory Movement Evaluation Tool to Quantify Thoracoabdominal Movement for Neuromuscular Diseases

PLoS ONE, 11, 11. Activin Receptor Type IIB Inhibition Improves Muscle Phenotype and Function in a Mouse Model of Spinal Muscular Atrophy

Human molecular genetics, 24, 20. Muscle hypertrophy induced by myostatin inhibition accelerates degeneration in dysferlinopathy

BioMed Central neuroscience, 11, 117. Change in brain activity through virtual reality-based brain-machine communication in a chronic tetraplegic subject with muscular dystrophy

Disability and rehabilitation, 30, 7. Dysphagia in patients with Duchenne muscular dystrophy evaluated with a questionnaire and videofluorography

EMBO journal (The), 27, 20. An isogenetic myoblast expression screen identifies DUX4-mediated FSHD-associated molecular pathologies

Neuromuscular disorders : NMD, 18, 9-10. Transient overexpression of the Rho family exchange factor GEFT stimulates myogenic differentiation of inclusion-body myositis (IBM) mesoangioblasts (Poster)

Molecular therapy, 14, 1. C-terminal-truncated microdystrophin recruits dystrobrevin and syntrophin to the dystrophin-associated glycoprotein complex and reduces muscular dystrophy in symptomatic utrophin/dystrophin double-knockout mice

Molecular therapy, 11, 2. Adeno-associated virus-mediated microdystrophin expression protects young mdx muscle from contraction-induced injury

Journal of molecular medicine, 83. Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family

Journal of rehabilitation medicine, 36, 3. Functional status and muscle strength in people with Duchenne muscular dystrophy living in the community

Archives of physical medicine and rehabilitation, 84, 6. Practical problems and management of seating through the clinical stages of Duchenne's Muscular Dystrophy

American journal of physical medicine & rehabilitation, 77, 1. Functional independence measure for children (WeeFIM). A preliminary study in nondisabled japanese children.