Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Madoka Yoshimura"'
Publikováno v:
Nosotchu. 29:44-48
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86052cf33d87fcb185920bd6065b9547
https://doi.org/10.3995/jstroke.29.44
https://doi.org/10.3995/jstroke.29.44
Low dose pergolide induced systemic edema and pleural effusion in a patient with parkinson's disease
Publikováno v:
Rinsho Shinkeigaku. 48:143-145
A 77-year-old woman was admitted to our department due to leg edema of 2-year duration. The patient has been suffered from Parkinson's disease for 12 years and prescribed levodopa, selegiline, and small dosage of pergolide (200 microg/day). Leg edema
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cac86f1ec316f2a201ba9f4730d55f8a
https://doi.org/10.5692/clinicalneurol.48.143
https://doi.org/10.5692/clinicalneurol.48.143
Autor:
Madoka Yoshimura, Kazuhiro Masuoka, Masahiro Kami, Yuji Miura, Naoko Murashige, Shuichi Taniguchi, Eiji Kusumi, Shintaro Tachibana
Publikováno v:
American Journal of Hematology. 81:222-224
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78813a691466d5f1f0ab92e8d9f17db7
https://doi.org/10.1002/ajh.20527
https://doi.org/10.1002/ajh.20527
Autor:
Takao Hijikata, Katsutoshi Yuasa, S. Ohshima, Madoka Yoshimura, John McC Howell, Shin'ichi Takeda, Yuko Miyagoe-Suzuki, Nobuyuki Urasawa, Akinori Nakamura
Publikováno v:
Gene therapy. 14(17)
Using murine models, we have previously demonstrated that recombinant adeno-associated virus (rAAV)-mediated microdystrophin gene transfer is a promising approach to treatment of Duchenne muscular dystrophy (DMD). To examine further therapeutic effec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9ec88699c7490c495dd9f46d67564cd
https://pubmed.ncbi.nlm.nih.gov/17581597
https://pubmed.ncbi.nlm.nih.gov/17581597
Autor:
Madoka, Yoshimura
Publikováno v:
Brain and nerve = Shinkei kenkyu no shinpo. 59(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e8d656eee4079d2cefc1e739d7840677
https://pubmed.ncbi.nlm.nih.gov/17354383
https://pubmed.ncbi.nlm.nih.gov/17354383
Autor:
Akio Takahashi, Naoko Yugeta, Masao Nakura, Nobuyuki Urasawa, Yoshiki Shimatsu, Yoshito Wakao, Akinori Nakamura, Madoka Yoshimura, Masayuki Tomohiro, Noboru Machida, Shin'ichi Takeda, Katsutoshi Yuasa, Yoko Fujii, Michiko R Wada
Publikováno v:
BMC Cardiovascular Disorders
BMC Cardiovascular Disorders, Vol 6, Iss 1, p 47 (2006)
BMC Cardiovascular Disorders, Vol 6, Iss 1, p 47 (2006)
Background Cardiac mortality in Duchenne muscular dystrophy (DMD) has recently become important, because risk of respiratory failure has been reduced due to widespread use of the respirator. The cardiac involvement is characterized by distinctive ele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c142ce64f44b980d3fe7416ff9ca9234
https://doi.org/10.1186/1471-2261-6-47
https://doi.org/10.1186/1471-2261-6-47
Autor:
Yoshiki, Shimatsu, Madoka, Yoshimura, Katsutoshi, Yuasa, Nobuyuki, Urasawa, Masayuki, Tomohiro, Masao, Nakura, Manabu, Tanigawa, Akinori, Nakamura, Shin'ichi, Takeda
Publikováno v:
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology. 24(2)
Canine X-linked muscular dystrophy (CXMD), which was found in a colony of golden retriever, is caused by a mutation in the dystrophin gene and it is a useful model of Duchenne muscular dystrophy (DMD). To investigate the pathogenesis and to develop t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e13a18282d9a70b4117c86ad6fc2531e
https://pubmed.ncbi.nlm.nih.gov/16550932
https://pubmed.ncbi.nlm.nih.gov/16550932
Micro-dystrophin cDNA ameliorates dystrophic phenotypes when introduced into mdx mice as a transgene
Autor:
Misao Suzuki, George Dickson, Yuko Miyagoe-Suzuki, Shin'ichi Takeda, Takaaki Ikemoto, Katsutoshi Yuasa, Toshifumi Yokota, Madoka Yoshimura, Miki Sakamoto
Publikováno v:
Biochemical and biophysical research communications. 293(4)
The adeno-associated virus vector is a good tool for gene transfer into skeletal muscle, but the length of a gene that can be incorporated is limited. To develop a gene therapy for Duchenne muscular dystrophy, we generated a series of rod-truncated m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::088b94e54029150d5a6b0817d2c6a81f
https://pubmed.ncbi.nlm.nih.gov/12054513
https://pubmed.ncbi.nlm.nih.gov/12054513
Autor:
Katsutoshi Yuasa, Akiyo Nishiyama, Madoka Ikemoto, Shin'ichi Takeda, Madoka Yoshimura, John McC Howell, Yuko Miyagoe-Suzuki
Publikováno v:
Molecular Therapy. 11:S99-S100
Duchenne muscular dystrophy (DMD) is an X-linked, lethal muscle disorder caused by mutations in the dystrophin gene (14 kb cDNA). An adeno-associated virus (AAV) vector-mediated gene transfer is one of attractive approaches to the treatment of DMD, b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94346ba9c8b84c1a1e433483774a67f5
https://doi.org/10.1016/j.ymthe.2005.06.256
https://doi.org/10.1016/j.ymthe.2005.06.256
Autor:
Yasushi Mochizuki, Madoka Yoshimura, Katsutoshi Yuasa, Shin'ichi Takeda, Toshifumi Yokota, Madoka Ikemoto, Miki Sakamoto, Yuko Miyagoe-Suzuki
Publikováno v:
Molecular Therapy. 9:S144-S145
Top of pageAbstract [Background] Duchenne muscular dystrophy (DMD) is an X-linked, lethal muscle disorder caused by mutations in the dystrophin gene. An adeno-associated virus (AAV) vector-mediated gene transfer is one of attractive approaches to the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c352186db81e3de471eef3baef0ba43d
https://doi.org/10.1016/j.ymthe.2004.06.312
https://doi.org/10.1016/j.ymthe.2004.06.312