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Auteur Chen M

Documents disponibles écrits par cet auteur (18)

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Article

Journal of thoracic disease, 15, 6. Outcomes after thymectomy in non-thymomatous myasthenia gravis

Deboever N ; Xu Y ; Feldman HA ; Woodman KH ; Chen M ; Shih YT ; Rajaram R | 30/06/2023

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Article

Frontiers in pediatrics, 10. Circulating FGF21 and GDF15 as Biomarkers for Screening, Diagnosis, and Severity Assessment of Primary Mitochondrial Disorders in Children

Li Y ; Li S ; Qiu Y ; Zhou M ; Chen M ; Hu Y ; Hong S ; Jiang L ; Guo Y | 14/04/2022

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Article

Journal of pediatric rehabilitation medicine Respiratory outcomes in children with congenital myotonic dystrophy

Omura JC ; Chen M ; Haviland M ; Apkon S | Netherlands | 14/11/2021

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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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Article

Prenatal diagnosis, 40, 8. Noninvasive prenatal diagnosis for Duchenne muscular dystrophy based on the direct haplotype phasing

Chen M ; Chen C ; Huang X ; Sun J ; Jiang L ; Li Y ; Zhu Y ; Tian C ; Li Y ; Lu Z ; Wang Y ; Zeng F ; Yang Y ; Song X ; Peng Z ; Yin C ; Chen D | England | 2020

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Article

European journal of obstetrics, gynecology, and reproductive biology, 240. Haplotype-Based noninvasive prenatal diagnosis for duchenne muscular dystrophy: A pilot study in South China.

Chen M, Auteur ; Chen C ; Li Y ; Yuan Y ; Lai Z ; Guo F ; Wang Y ; Huang X ; Li S ; Wu R ; Peng Z ; Sun J ; Chen D | Ireland | 05/2019

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Article

Frontiers in neurology, 8. Serum Creatinine Distinguishes Duchenne Muscular Dystrophy from Becker Muscular Dystrophy in Patients Aged =3 Years: A Retrospective Study

Wang L, Auteur ; Chen M ; He R ; Sun Y ; Yang J ; Xiao L ; Cao J ; Zhang H ; Zhang C | 2017

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Article

The Cochrane database of systematic reviews, 11. Enzyme replacement therapy for infantile-onset Pompe disease

Chen M, Auteur ; Zhang L ; Quan S | 2017

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Article

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology, 49, 6. Targeted sequencing of maternal plasma for haplotype-based noninvasive prenatal testing of spinal muscular atrophy

Chen M, Auteur ; Lu S ; Lai Z ; Chen C ; Luo K ; Yuan Y ; Wang Y ; Li S ; Gao Y ; Chen F ; Asan ; Chen D | 2017

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Article

Human molecular genetics, 24, 21. Long-term engraftment of myogenic progenitors from adipose-derived stem cells and muscle regeneration in dystrophic mice

Zhang Y, Auteur ; Zhu Y ; Li Y ; Cao J ; Zhang H ; Chen M ; Wang L ; Zhang C | 2015

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Article

International journal of neuroscience, 120, 11. Vocal cord paresis and probable X-linked Charcot-Marie-Tooth disease with novel GJB1 mutation

Li Q ; Chen M ; Liu K ; Lin X ; Chui D | 2010

Accès au résumé PubMed / to PubMed abstract

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Article

Journal of clinical neuroscience, 15, 2. The clinical significance of anti-heat shock cognate protein 71 antibody in myasthenia gravis

Munakata S ; Chen M ; Aosai F ; Kawaguchi N ; Nemoto Y ; Norose K ; Hattori T ; Yano A | 2008

Accès au résumé PubMed / to PubMed abstract

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Article

Nature genetics, 29. The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy

Eisenberg I ; Avidan N ; Potikha T ; Hochner H ; Chen M ; Olender T ; Barash M ; Shemesh M ; Sadeh M ; Grabov-Nardini G ; Shmilevich I ; Friedmann A ; Karpati G ; Bradley WG ; Baumbach L ; Lancet D ; Ben Asher E ; Beckmann JS ; Argov Z ; Mitrani-Rosenbaum S | 09/2001

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Article

Cell transplantation, 2. Cell transplantation as an experimental treatment for Duchenne muscular dystrophy

Law PK ; Goodwin TG ; Fang Q ; Deering MB ; Duggirala V ; Larkin C ; Florendo JA ; Kirby DS ; Li HJ ; Chen M ; Cornett J ; Li LM ; Shirzad A ; Quinley T ; Yoo TJ ; Holcomb R | 1993

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Article

Acta paediatrica Japonica, 33,2. Myoblast transfer therapy for Duchenne muscular dystrophy.

Law PK ; Goodwin TG ; Fang QW ; Chen M ; Li HJ ; Florendo JA ; Kirby DS | 1991

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Article

Advances in experimental medicine and biology, 280. Myoblast transfer improves muscle genetics/structure/function and normalizes the behavior and life-span of dystrophic mice

Law PK ; Goodwin TG ; Li HJ ; Ajamoughli G ; Chen M | 1990

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Article

Advances in experimental medicine and biology, 280. Plausible structural/functional/behavioral/biochemical transformations following myoblast transfer therapy

Law PK ; Goodwin TG ; Li HJ ; Chen M | 1990

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Article

Lancet (Ed. ang.), 336. Dystrophin production induced by myoblast transfer therapy in Duchenne muscular dystrophy

Law PK ; Bertorini TE ; Goodwin TG ; Chen M ; Fang Q ; Li HJ | 1990

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Détail de l'auteur

Auteur Chen M

Documents disponibles écrits par cet auteur (18)

Journal of thoracic disease, 15, 6. Outcomes after thymectomy in non-thymomatous myasthenia gravis

Frontiers in pediatrics, 10. Circulating FGF21 and GDF15 as Biomarkers for Screening, Diagnosis, and Severity Assessment of Primary Mitochondrial Disorders in Children

Journal of pediatric rehabilitation medicine Respiratory outcomes in children with congenital myotonic dystrophy

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

Prenatal diagnosis, 40, 8. Noninvasive prenatal diagnosis for Duchenne muscular dystrophy based on the direct haplotype phasing

European journal of obstetrics, gynecology, and reproductive biology, 240. Haplotype-Based noninvasive prenatal diagnosis for duchenne muscular dystrophy: A pilot study in South China.

Frontiers in neurology, 8. Serum Creatinine Distinguishes Duchenne Muscular Dystrophy from Becker Muscular Dystrophy in Patients Aged =3 Years: A Retrospective Study

The Cochrane database of systematic reviews, 11. Enzyme replacement therapy for infantile-onset Pompe disease

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology, 49, 6. Targeted sequencing of maternal plasma for haplotype-based noninvasive prenatal testing of spinal muscular atrophy

Human molecular genetics, 24, 21. Long-term engraftment of myogenic progenitors from adipose-derived stem cells and muscle regeneration in dystrophic mice

International journal of neuroscience, 120, 11. Vocal cord paresis and probable X-linked Charcot-Marie-Tooth disease with novel GJB1 mutation

Journal of clinical neuroscience, 15, 2. The clinical significance of anti-heat shock cognate protein 71 antibody in myasthenia gravis

Nature genetics, 29. The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy

Cell transplantation, 2. Cell transplantation as an experimental treatment for Duchenne muscular dystrophy

Acta paediatrica Japonica, 33,2. Myoblast transfer therapy for Duchenne muscular dystrophy.

Advances in experimental medicine and biology, 280. Myoblast transfer improves muscle genetics/structure/function and normalizes the behavior and life-span of dystrophic mice

Advances in experimental medicine and biology, 280. Plausible structural/functional/behavioral/biochemical transformations following myoblast transfer therapy

Lancet (Ed. ang.), 336. Dystrophin production induced by myoblast transfer therapy in Duchenne muscular dystrophy