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Auteur Mori-Yoshimura M |
Documents disponibles écrits par cet auteur



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New MRI Findings in Fukuyama Congenital Muscular Dystrophy: Brain Stem and Venous System Anomalies.
Hirasawa-Inoue A, Sato N, Shigemoto Y, et al.
AJNR. American journal of neuroradiology, 2020, 41, 6, p 1094
Revue : AJNR. American journal of neuroradiology, 41, 6 Titre : New MRI Findings in Fukuyama Congenital Muscular Dystrophy: Brain Stem and Venous System Anomalies. Type de document : Article Auteurs : Hirasawa-Inoue A ; Sato N ; Shigemoto Y ; Kimura Y ; Ishiyama A ; Takeshita E ; Mori-Yoshimura M ; Oya Y ; Takahashi Y ; Komaki H ; Matsuda H ; Sasaki M Editeur : United States Année de publication : 06/2020 Pages : p 1094 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 32439644 / DOI : 10.3174/ajnr.A6577
N° Profil MNM : 2020052 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32439644 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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Obstruction-related dysphagia in inclusion body myositis: Cricopharyngeal bar on videofluoroscopy indicates risk of aspiration
Taira K, Yamamoto T, Mori-Yoshimura M, et al.
Journal of the neurological sciences, 2020, 413
Revue : Journal of the neurological sciences, 413 Titre : Obstruction-related dysphagia in inclusion body myositis: Cricopharyngeal bar on videofluoroscopy indicates risk of aspiration Type de document : Article Auteurs : Taira K, Auteur ; Yamamoto T ; Mori-Yoshimura M ; Fujita S ; Oya Y ; Nishino I ; Takahashi Y Editeur : Netherlands Année de publication : 02/2020 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 32172012 / DOI : 10.1016/j.jns.2020.116764
N° Profil MNM : 2020032 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32172012 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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ADSSL1 myopathy is the most common nemaline myopathy in Japan with variable clinical features
Saito Y, Nishikawa A, Iida A, et al.
Neurology, 2020
Revue : Neurology Titre : ADSSL1 myopathy is the most common nemaline myopathy in Japan with variable clinical features Type de document : Article Auteurs : Saito Y ; Nishikawa A ; Iida A ; Mori-Yoshimura M ; Oya Y ; Ishiyama A ; Komaki H ; Nakamura S ; Fujikawa S ; Kanda T ; Yamadera M ; Sakiyama H ; Hayashi S ; Nonaka I ; Noguchi S ; Nishino I Editeur : United States Année de publication : 2020 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 32646962 / DOI : 10.1212/WNL.0000000000010237
N° Profil MNM : 2020071 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32646962 Voir aussiAvis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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Pregnancy in GNE myopathy patients: a nationwide repository survey in Japan
Yoshioka W, Miyasaka N, Okubo R, et al.
Orphanet journal of rare diseases, 2020, 15, 1, p 245
Revue : Orphanet journal of rare diseases, 15, 1 Titre : Pregnancy in GNE myopathy patients: a nationwide repository survey in Japan Type de document : Article Auteurs : Yoshioka W ; Miyasaka N ; Okubo R ; Shimizu R ; Takahashi Y ; Oda Y ; Nishino I ; Nakamura H ; Mori-Yoshimura M Année de publication : 2020 Pages : p 245 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 32917266 / DOI : 10.1186/s13023-020-01487-5
N° Profil MNM : 2020091 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32917266 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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Psychiatric and neurodevelopmental aspects of Becker muscular dystrophy
Mori-Yoshimura M, Mizuno Y, Yoshida S, et al.
Neuromuscular disorders : NMD, 2019
Revue : Neuromuscular disorders : NMD Titre : Psychiatric and neurodevelopmental aspects of Becker muscular dystrophy Type de document : Article Auteurs : Mori-Yoshimura M, Auteur ; Mizuno Y ; Yoshida S ; Ishihara N ; Minami N ; Morimoto E ; Maruo K ; Nonaka I ; Komaki H ; Nishino I ; Sekiguchi M ; Sato N ; Takeda S ; Takahashi Y Editeur : England Année de publication : 09/2019 Langues : Anglais (eng) Mots-clés : dystrophie musculaire de Becker ; dystrophinopathie ; épidémiologie ; étude de cohorte ; maladie neuromusculaire ; psychopathologie ; trouble neuropsychologique Pubmed / DOI : Pubmed : 31708335 / DOI : 10.1016/j.nmd.2019.09.006
N° Profil MNM : 2019112 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/31708335 Voir aussiAvis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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Safety and efficacy of intravenous bimagrumab in inclusion body myositis (RESILIENT): a randomised, double-blind, placebo-controlled phase 2b trial
Hanna MG, Badrising UA, Benveniste O, et al.
The Lancet. Neurology, 2019, 18, 9, p 834
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Emery-Dreifuss muscular dystrophy-related myopathy with TMEM43 mutations
Mukai T, Mukai T, Mori-Yoshimura M, et al.
Muscle & Nerve, 2018
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National registry of patients with Fukuyama congenital muscular dystrophy in Japan
Ishigaki K, Ihara C, Nakamura H, et al.
Neuromuscular disorders : NMD, 2018, 28, 10, p. 885
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Muscle MRI in patients with dysferlinopathy: pattern recognition and implications for clinical trials
Diaz-Manera J, Fernández-Torrón R, Llauger J, et al.
Journal of neurology, neurosurgery, and psychiatry, 2018
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Characteristics of Japanese Patients with Becker Muscular Dystrophy and Intermediate Muscular Dystrophy in a Japanese National Registry of Muscular Dystrophy (Remudy): Heterogeneity and Clinical Variation
Mori-Yoshimura M, Mitsuhashi S, Nakamura H, et al.
Journal of Neuromuscular Diseases, 2018
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Social involvement issues in patients with Becker muscular dystrophy: A questionnaire survey of subjects from a patient registry
Mori-Yoshimura M, Mizuno Y, Yoshida S, et al.
Brain & development, 2018, 40, 4, p 268
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Two novel VCP missense variants identified in Japanese patients with multisystem proteinopathy
Inoue M, Inoue M, Iida A, et al.
Human genome variation, 2018, 5
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Teenage exercise is associated with earlier symptom onset in dysferlinopathy: a retrospective cohort study
Moore UR, Jacobs M, Fernández-Torrón R, et al.
Journal of neurology, neurosurgery, and psychiatry, 2018, 89, 11, p 1224
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Detection and management of cardiomyopathy in female dystrophinopathy carriers
Adachi K, Hashiguchi S, Saito M, et al.
Journal of the neurological sciences, 2018, 386, p 74
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Missing genetic variations in GNE myopathy: rearrangement hotspots encompassing 5'UTR and founder allele
Zhu W, Mitsuhashi S, Yonekawa T, et al.
Journal of human genetics, 2017, 62, 2, p 159
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Cardiopulmonary dysfunction in patients with limb-girdle muscular dystrophy 2A
Mori-Yoshimura M, Segawa K, Minami N, et al.
Muscle & Nerve, 2017, 55, 4, p 465
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Brain gray matter structural network in myotonic dystrophy type 1
Sugiyama A, Sone D, Sato N, et al.
PLoS ONE, 2017, 12, 11
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Pediatric necrotizing myopathy associated with anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase antibodies
Liang WC, Uruha A, Suzuki S, et al.
Rheumatology (Oxford, England), 2017, 56, 2, p 287
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The Clinical Outcome Study for dysferlinopathy: An international multicenter study
Harris E, Bladen CL, Mayhew A, et al.
Neurology. Genetics, 2016, 2, 4
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Necklace cytoplasmic bodies in hereditary myopathy with early respiratory failure
Uruha A, Hayashi YK, Oya Y, et al.
Journal of neurology, neurosurgery, and psychiatry, 2015, 86, 5, p 483
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GNE myopathy: A prospective natural history study of disease progression
Mori-Yoshimura M, Oya Y, Yajima H, et al.
Neuromuscular disorders : NMD, 2014, 24, 5, p 380
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Nationwide patient registry for GNE myopathy in Japan
Mori-Yoshimura M, Hayashi YK, Yonemoto N, et al.
Orphanet journal of rare diseases, 2014, 9
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Surgical treatment of severe blepharoptosis and facial palsy caused by oculopharyngodistal myopathy
Shimizu Y, Suzuki S, Mori-Yoshimura M, et al.
Journal of Plastic, Reconstructive and Aesthetic Surgery, 2013, 66, 10, p. e277-e280
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Respiratory dysfunction in patients severely affected by GNE myopathy (distal myopathy with rimmed vacuoles)
Mori-Yoshimura M, Oya Y, Hayashi YK, et al.
Neuromuscular disorders : NMD, 2013, 23, 1, p. 84-88
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Characteristics of Japanese Duchenne and Becker muscular dystrophy patients in a novel Japanese national registry of muscular dystrophy (Remudy)
Nakamura H, Kimura E, Mori-Yoshimura M, et al.
Orphanet journal of rare diseases, 2013, 8, 1, 60, 17 p.
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