Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Midori Asada"'
Autor:
Tetsunori Saikawa, Midori Asada, Shuji Ishida, Susumu Shimada, Naohiko Takahashi, Mikiko Nakagawa, Tetsu Iwao, Hidetoshi Yonemochi, Morio Ito
Publikováno v:
Japanese Circulation Journal. 62:215-218
A case report of a 15-year-old girl who experienced syncope and torsades de pointes is presented. The girl had a normal QT interval (QTc=0.37 sec) on the resting electrocardiogram (ECG). Infusion of isoproterenol induced QT prolongation (QTc=0.62 sec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80c169be5c3562e69037e7068a8fe9ce
https://doi.org/10.1253/jcj.62.215
https://doi.org/10.1253/jcj.62.215
Publikováno v:
Pharmacogenetics. 7:341-344
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2d61a7b31f757d6810e33264d4b06f8
https://doi.org/10.1097/00008571-199708000-00011
https://doi.org/10.1097/00008571-199708000-00011
Autor:
Midori Asada, Masaji Okada, Fumiaki Tanaka, Shigehiko Haeno, Yasuyo Suzuki, Tomokazu Suzuki, Ryouji Hiramatsu, Toyoki Maeda
Publikováno v:
Internal Medicine. 35:200-202
Two sisters with Ehlers-Danlos syndrome, inherited as an autosomal recessive trait, and congenital heart disease are herein reported. One was a 20-year-old woman with Ehlers-Danlos syndrome and multiple aphthous stomatitis, bronchial asthma, an emphy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3e83db127106df47630dea4dcd3a795
https://doi.org/10.2169/internalmedicine.35.200
https://doi.org/10.2169/internalmedicine.35.200
Publikováno v:
Journal of human genetics. 47(7)
We previously reported a patient with hereditary hypotransferrinemia who suffered from severe anemia and growth retardation and was diagnosed on the basis of an extremely low level of serum transferrin (TF). By an isoelectric focusing analysis, we fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::238f60cc30983c636cfce6fd7b9a2559
https://pubmed.ncbi.nlm.nih.gov/12111369
https://pubmed.ncbi.nlm.nih.gov/12111369
Autor:
Takashi Omori, Fumiaki Tanaka, Yasuyo Suzuki, Shigehiko Haeno, Tomokazu Suzuki, Masaji Okada, Midori Asada, Shunichi Murakami, Hiroshi Watanabe, Toyoki Maeda, Ryoji Hiramatsu
Publikováno v:
Internal medicine (Tokyo, Japan). 34(11)
A case of hypoparathyroidism accompanied with Turner's syndrome is reported. On admission, a 44-year-old woman had facial dystonia, deafness, and primary amenorrhea. Laboratory examinations showed a decrease in serum PTH and mosaicism of 45,X and 46,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bbf2e5cbe91143fc8316128033aeaac4
https://pubmed.ncbi.nlm.nih.gov/8774966
https://pubmed.ncbi.nlm.nih.gov/8774966