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  • 1-10 of  96 results for ""Muscular Dystrophy, Duchenne""
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Academic Journal

Social difficulties and care burden of adult Duchenne muscular dystrophy in Japan: a questionnaire survey based on the Japanese Registry of Muscular Dystrophy (Remudy).

  • Authors : Mori-Yoshimura M; Department of Neurology, National Center Hospital, National Center of Neurology and Psychiatry, 4-1-1 Ogawahigashi, Kodaira, Tokyo, 187-8551, Japan. .; Ishigaki K

Subjects: Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/economics ; Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/therapy ; Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/psychology

  • Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2024 Apr 30; Vol. 19 (1), pp. 182. Date of Electronic Publication: 2024 Apr 30.Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172

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Academic Journal

Caregiver Burden with Duchenne and Becker Muscular Dystrophy in Japan: A Clinical Observation Study.

  • Authors : Ishizaki M; Department of Neurology, National Hospital Organization Kumamoto Saishun Medical Center, Japan.; Kobayashi M

Subjects: Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/genetics; Humans ; Female

  • Source: Internal medicine (Tokyo, Japan) [Intern Med] 2024 Feb 01; Vol. 63 (3), pp. 365-372. Date of Electronic Publication: 2023 Jun 21.Publisher: Japanese Society of Internal Medicine Country of Publication: Japan NLM ID: 9204241 Publication Model:

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Academic Journal

[Muscular Dystrophy].

  • Authors : Matsumura T; Department of Neurology, National Hospital Organization Osaka Toneyama Medical Center.; Saito T

Subjects: Muscular Dystrophies*/Muscular Dystrophies*/Muscular Dystrophies*/therapy ; Muscular Dystrophy, Duchenne* ; Neurology*

  • Source: Brain and nerve = Shinkei kenkyu no shinpo [Brain Nerve] 2022 Jun; Vol. 74 (6), pp. 795-799.Publisher: igaku Shoin Country of Publication: Japan NLM ID: 101299709 Publication Model: Print Cited Medium: Print

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Academic Journal

Development of outcome measures according to dystrophic phenotypes in canine X-linked muscular dystrophy in Japan.

  • Authors : Kuraoka M; Laboratory of Experimental Animal Science, Nippon Veterinary and Life Science University, 1-7-1 Kyonancho, Musashino, Tokyo 180-8602, Japan.; Department of Molecular Therapy, National Institute of Neuroscience, National Center of Neurology and Psychiatry, 4-1-1 Ogawa-Higashi, Kodaira, Tokyo 187-8502, Japan.

Subjects: Motor Activity*; Biomarkers/Biomarkers/Biomarkers/*blood ; Muscular Dystrophy, Duchenne/Muscular Dystrophy, Duchenne/Muscular Dystrophy, Duchenne/*physiopathology

  • Source: Experimental animals [Exp Anim] 2021 Nov 10; Vol. 70 (4), pp. 419-430. Date of Electronic Publication: 2021 Jun 16.Publisher: Japanese Association for Laboratory Animal Science Country of Publication: Japan NLM ID: 9604830 Publication Model:

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Academic Journal

Viltolarsen in Japanese Duchenne muscular dystrophy patients: A phase 1/2 study.

  • Authors : Komaki H; Translational Medical Center, National Center of Neurology and Psychiatry, Kodaira, Tokyo, Japan.; Takeshima Y

Subjects: Dystrophin/Dystrophin/Dystrophin/*drug effects ; Muscular Dystrophy, Duchenne/Muscular Dystrophy, Duchenne/Muscular Dystrophy, Duchenne/*drug therapy ; Oligonucleotides/Oligonucleotides/Oligonucleotides/*pharmacology

  • Source: Annals of clinical and translational neurology [Ann Clin Transl Neurol] 2020 Dec; Vol. 7 (12), pp. 2393-2408. Date of Electronic Publication: 2020 Dec 07.Publisher: Wiley Periodicals, Inc on behalf of American Neurological Association Country of Publication: United States NLM ID: 101623278 Publication Model:

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Academic Journal

[Study of medical management for patients with Duchenne muscular dystrophy in Japan: what was changed by a practical guideline].

  • Authors : Matsumura T; Department of Neurology, National Hospital Organization Osaka Toneyama Medical Center.; Komaki H

Subjects: Practice Guidelines as Topic*; Muscular Dystrophy, Duchenne/Muscular Dystrophy, Duchenne/Muscular Dystrophy, Duchenne/*rehabilitation ; Muscular Dystrophy, Duchenne/Muscular Dystrophy, Duchenne/Muscular Dystrophy, Duchenne/*therapy

  • Source: Rinsho shinkeigaku = Clinical neurology [Rinsho Shinkeigaku] 2019 Nov 08; Vol. 59 (11), pp. 723-729. Date of Electronic Publication: 2019 Oct 26.Publisher: Nihon Shinkei Gakkai Country of Publication: Japan NLM ID: 0417466 Publication Model: Print-Electronic Cited

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Academic Journal

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.

  • Authors : Mori-Yoshimura M; Department of Neurology, National Center Hospital, National Center of Neurology and Psychiatry, Kodaira, Tokyo, Japan.; Mitsuhashi S

Subjects: Mobility Limitation* ; Registries*; Muscular Dystrophy, Duchenne/Muscular Dystrophy, Duchenne/Muscular Dystrophy, Duchenne/*physiopathology

  • Source: Journal of neuromuscular diseases [J Neuromuscul Dis] 2018; Vol. 5 (2), pp. 193-203.Publisher: IOS Press Country of Publication: Netherlands NLM ID: 101649948 Publication Model: Print Cited Medium: Print ISSN: 2214-3599 (Print)

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Academic Journal

Amelioration of intracellular Ca 2+ regulation by exon-45 skipping in Duchenne muscular dystrophy-induced pluripotent stem cell-derived cardiomyocytes.

  • Authors : Sato M; Third Department of Medicine, Shinshu University School of Medicine, Matsumoto, Nagano, 390-8621, Japan.; Shiba N

Subjects: Calcium/Calcium/Calcium/*metabolism ; Induced Pluripotent Stem Cells/Induced Pluripotent Stem Cells/Induced Pluripotent Stem Cells/*cytology ; Muscular Dystrophy, Duchenne/Muscular Dystrophy, Duchenne/Muscular Dystrophy, Duchenne/*genetics

  • Source: Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2019 Nov 26; Vol. 520 (1), pp. 179-185. Date of Electronic Publication: 2019 Oct 01.Publisher: Elsevier Country of Publication: United States NLM ID: 0372516 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Clinical practice with steroid therapy for Duchenne muscular dystrophy: An expert survey in Asia and Oceania.

  • Authors : Takeuchi F; Department of Clinical Research Support, Translational Medical Center, National Center of Neurology and Psychiatry, 4-1-1 Ogawa-higashi, Kodaira, Tokyo 187-8551, Japan.; Nakamura H

Subjects: Muscular Dystrophy, Duchenne/Muscular Dystrophy, Duchenne/Muscular Dystrophy, Duchenne/*drug therapy ; Practice Patterns, Physicians'/Practice Patterns, Physicians'/Practice Patterns, Physicians'/*statistics & numerical data ; Prednisolone/Prednisolone/Prednisolone/*therapeutic use

  • Source: Brain & development [Brain Dev] 2020 Mar; Vol. 42 (3), pp. 277-288. Date of Electronic Publication: 2020 Jan 21.Publisher: Elsevier Country of Publication: Netherlands NLM ID: 7909235 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

[Changes in clinical condition and causes of death of inpatients with Duchenne muscular dystrophy in Japan from 1999 to 2012].

  • Authors : Saito T; Division of Child Neurology, Department of Neurology, National Hospital Organization Toneyama National Hospital.; Tatara K

Subjects: Muscular Dystrophy, Duchenne/Muscular Dystrophy, Duchenne/Muscular Dystrophy, Duchenne/*mortality; Adolescent ; Adult

  • Source: Rinsho shinkeigaku = Clinical neurology [Rinsho Shinkeigaku] 2014; Vol. 54 (10), pp. 783-90.Publisher: Nihon Shinkei Gakkai Country of Publication: Japan NLM ID: 0417466 Publication Model: Print Cited Medium:

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  • 1-10 of  96 results for ""Muscular Dystrophy, Duchenne""