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Auteur Ito M

Documents disponibles écrits par cet auteur (23)

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Article

Brain & development Epidemiological investigation of spinal muscular atrophy in Japan

Ito M ; Yamauchi A ; Urano M ; Kato T ; Matsuo M ; Nakashima K ; Saito K | Netherlands | 24/08/2021

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International Journal of molecular sciences, 22, 5. Secreted Signaling Molecules at the Neuromuscular Junction in Physiology and Pathology

Ohkawara B ; Ito M ; Ohno K | 28/02/2021

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Scientific Reports, 10, 1. Inhibition of cyclooxygenase-1 by nonsteroidal anti-inflammatory drugs demethylates MeR2 enhancer and promotes Mbnl1 transcription in myogenic cells

Huang K ; Masuda A ; Chen G ; Bushra S ; Kamon M ; Araki T ; Kinoshita M ; Ohkawara B ; Ito M ; Ohno K | England | 02/2020

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Journal of rehabilitation medicine, 52, 9. Strategies for learning glossopharyngeal breathing in boys with Duchenne muscular dystrophy: A feasibility case series

Haruyama K ; Yamaha Y ; Ito M ; Otsuka T ; Kawakami M | Sweden | 2020

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Matrix biology : journal of the International Society for Matrix Biology Protein-anchoring therapy to target extracellular matrix proteins to their physiological destinations

Ito M, Auteur ; Ohno K | 20/02/2018

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BMC Pediatrics, 17, 1. Carnitine-related hypoglycemia caused by 3 days of pivalate antibiotic therapy in a patient with severe muscular dystrophy: a case report

Ito M, Auteur ; Fukuda M ; Suzuki Y ; Wakamoto H ; Ishii E | 2017

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Expert opinion on therapeutic targets, 21, 10. Agrin-LRP4-MuSK signaling as a therapeutic target for myasthenia gravis and other neuromuscular disorders

Ohno K, Auteur ; Ohkawara B ; Ito M | 2017

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Article

Chemico-biological interactions, 259, Pt B. Roles of collagen Q in MuSK antibody-positive myasthenia gravis

Ohno K, Auteur ; Otsuka K ; Ito M | 2016

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Article

International Heart Journal, 57, 1. Generation of Induced Pluripotent Stem Cells From Patients With Duchenne Muscular Dystrophy and Their Induction to Cardiomyocytes

Hashimoto A, Auteur ; Naito AT ; Lee JK ; Kitazume-Taneike R ; Ito M ; Yamaguchi T ; Nakata R ; Sumida T ; Okada K ; Nakagawa A ; Higo T ; Kuramoto Y ; Sakai T ; Tominaga K ; Okinaga T ; Kogaki S ; Ozono K ; Miyagawa S ; Sawa Y ; Sakata Y ; Morita H ; Umezawa A ; Komuro I | 2015

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Neuromuscular disorders : NMD, 25, 8. A missense mutation in domain III in HSPG2 in Schwartz-Jampel syndrome compromises secretion of perlecan into the extracellular space

Iwata S, Auteur ; Ito M ; Nakata T ; Noguchi Y ; Okuno T ; Ohkawara B ; Masuda A ; Goto T ; Adachi M ; Osaka H ; Nonaka R ; Arikawa-Hirasawa E ; Ohno K | 2015

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Chemico-biological interactions, 203, 1. Specific binding of collagen Q to the neuromuscular junction is exploited to cure congenital myasthenia and to explore bases of myasthenia gravis

Ohno K ; Ito M ; Kawakami Y ; Krejci E ; Engel AG | 2013

Accès au résumé PubMed / to PubMed abstract

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Journal of bone and mineral metabolism, 31, 1. Clinically applicable antianginal agents suppress osteoblastic transformation of myogenic cells and heterotopic ossifications in mice

Yamamoto R ; Matsushita M ; Kitoh H ; Masuda A ; Ito M ; Katagiri T ; Kawai T ; Ishiguro N ; Ohno K | 2013

Accès au résumé PubMed / to PubMed abstract

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Medical gas research, 1, 1. Open-label trial and randomized, double-blind, placebo-controlled, crossover trial of hydrogen-enriched water for mitochondrial and inflammatory myopathies

Ibi T ; Sahashi K ; Ichihara M ; Ito M ; Ohno K | 2011

Accès au résumé PubMed / to PubMed abstract

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Annals of neurology, 65, 2. Phase 2 trial of leuprorelin in patients with spinal and bulbar muscular atrophy

Banno H ; Katsuno M ; Suzuki K ; Takeuchi Y ; Kawashima M ; Suga N ; Takamori M ; Ito M ; Nakamura T ; Matsuo K ; Yamada S ; Oki Y ; Adachi H ; Minamiyama M ; Waza M ; Atsuta N ; Watanabe H ; Fujimoto Y ; Nakashima T ; Tanaka F ; Doyu M ; Sobue G | 02/2009

Accès au résumé PubMed / to PubMed abstract 11/05/2009 - Amélioration clinique du syndrome de Kennedy par la leuproréline : un essai de phase 2 japonais concluant Le syndrome de Kennedy, ou amyotrophie spino-bulbaire (SBMA), est u[...]

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Brain, 131, 1. CAG repeat size correlates to electrophysiological motor and sensory phenotypes in SBMA

Suzuki K ; Katsuno M ; Banno H ; Takeuchi Y ; Atsuta N ; Ito M ; Watanabe H ; Yamashita F ; Hori N ; Nakamura T ; Hirayama M ; Tanaka F ; Sobue G | 2008

Accès au résumé PubMed / to PubMed abstract

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Muscle & Nerve, 38, 2. Walking capacity evaluated by the 6-minute walk test in spinal and bulbar muscular atrophy

Takeuchi Y ; Katsuno M ; Banno H ; Suzuki K ; Kawashima M ; Atsuta N ; Ito M ; Watanabe H ; Tanaka F ; Sobue G | 2008

Accès au résumé PubMed / to PubMed abstract

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Article

International journal of cardiology, 98, 1. Electron microscopic findings of cardiomyopathy with limb girdle muscular dystrophy

Funabiki K ; Onishi K ; Tanabe M ; Kuru S ; Konagaya M ; Sato F ; Ito M ; Nakano T | 2005

Accès au résumé PubMed / to PubMed abstract

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Metabolism clinical and experimental, 50, 10. Paradoxical weight loss with extra energy expenditure at brown adipose tissue in adolescent patients with Duchenne muscular dystrophy

Satomura S ; Yokota I ; Tatara K ; Naito E ; Ito M ; Kuroda Y | 10/2001

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Article

Journal of applied physiology, 82, 1. Determination of fascicle length and pennation in a contracting human muscle in vivo

Ichinose Y ; Ito M ; Kawakami Y ; Fukashiro S | 1997

Accès au résumé PubMed / to PubMed abstract

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Article

Human gene therapy Humoral and cellular immunity to an encoded protein induced by direct DNA injection

Katsumi A ; Emi N ; Abe A ; Hasegawa Y ; Ito M ; Saito H | 1994

Pour voir le résumé sur PubMed, cliquez ici

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Article

Spine, 18/15. Tree-dimensional spinal deformity in scoliosis associated with cerebral palsy and with progressive muscular dystroph*

Ito M ; Tadano S ; Kaneda K | 1993

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Article

Journal of pediatrics (The), 116, 1. Complex I (reduced nicotinamide-adenine dinucleotide-coenzyme Q reductase) deficiency in two patients with probable Leigh syndrome

Fujii T ; Ito M ; Okuno T ; Mutoh K ; Nishikomari R ; Mikawa H | 1990

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Archives of pathology and laboratory medicine, 112, 5. Brown adipose tissue in Duchenne's progressive muscular dystrophy

Ito M ; Sekine I ; Fujii H ; Ogawa M | 1988

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Détail de l'auteur

Auteur Ito M

Documents disponibles écrits par cet auteur (23)

Brain & development Epidemiological investigation of spinal muscular atrophy in Japan

International Journal of molecular sciences, 22, 5. Secreted Signaling Molecules at the Neuromuscular Junction in Physiology and Pathology

Scientific Reports, 10, 1. Inhibition of cyclooxygenase-1 by nonsteroidal anti-inflammatory drugs demethylates MeR2 enhancer and promotes Mbnl1 transcription in myogenic cells

Journal of rehabilitation medicine, 52, 9. Strategies for learning glossopharyngeal breathing in boys with Duchenne muscular dystrophy: A feasibility case series

Matrix biology : journal of the International Society for Matrix Biology Protein-anchoring therapy to target extracellular matrix proteins to their physiological destinations

BMC Pediatrics, 17, 1. Carnitine-related hypoglycemia caused by 3 days of pivalate antibiotic therapy in a patient with severe muscular dystrophy: a case report

Expert opinion on therapeutic targets, 21, 10. Agrin-LRP4-MuSK signaling as a therapeutic target for myasthenia gravis and other neuromuscular disorders

Chemico-biological interactions, 259, Pt B. Roles of collagen Q in MuSK antibody-positive myasthenia gravis

International Heart Journal, 57, 1. Generation of Induced Pluripotent Stem Cells From Patients With Duchenne Muscular Dystrophy and Their Induction to Cardiomyocytes

Neuromuscular disorders : NMD, 25, 8. A missense mutation in domain III in HSPG2 in Schwartz-Jampel syndrome compromises secretion of perlecan into the extracellular space

Chemico-biological interactions, 203, 1. Specific binding of collagen Q to the neuromuscular junction is exploited to cure congenital myasthenia and to explore bases of myasthenia gravis

Journal of bone and mineral metabolism, 31, 1. Clinically applicable antianginal agents suppress osteoblastic transformation of myogenic cells and heterotopic ossifications in mice

Medical gas research, 1, 1. Open-label trial and randomized, double-blind, placebo-controlled, crossover trial of hydrogen-enriched water for mitochondrial and inflammatory myopathies

Annals of neurology, 65, 2. Phase 2 trial of leuprorelin in patients with spinal and bulbar muscular atrophy

Brain, 131, 1. CAG repeat size correlates to electrophysiological motor and sensory phenotypes in SBMA

Muscle & Nerve, 38, 2. Walking capacity evaluated by the 6-minute walk test in spinal and bulbar muscular atrophy

International journal of cardiology, 98, 1. Electron microscopic findings of cardiomyopathy with limb girdle muscular dystrophy

Metabolism clinical and experimental, 50, 10. Paradoxical weight loss with extra energy expenditure at brown adipose tissue in adolescent patients with Duchenne muscular dystrophy

Journal of applied physiology, 82, 1. Determination of fascicle length and pennation in a contracting human muscle in vivo

Human gene therapy Humoral and cellular immunity to an encoded protein induced by direct DNA injection

Spine, 18/15. Tree-dimensional spinal deformity in scoliosis associated with cerebral palsy and with progressive muscular dystroph*

Journal of pediatrics (The), 116, 1. Complex I (reduced nicotinamide-adenine dinucleotide-coenzyme Q reductase) deficiency in two patients with probable Leigh syndrome

Archives of pathology and laboratory medicine, 112, 5. Brown adipose tissue in Duchenne's progressive muscular dystrophy