Výsledky vyhledávání - "Akira, Hirono"

Development and validation of optimal cut-off value in inter-arm systolic blood pressure difference for prediction of cardiovascular events

Autor: Masataka Sata, Kenya Kusunose, Norihito Kageyama, Akira Hirono, Hiroyuki Fujinaga, Masahiro Abe, Masayuki Sumitomo

Publikováno v: Journal of Cardiology. 71:24-30

An inter-arm systolic blood pressure difference (IAD) is associated with cardiovascular disease. The aim of this study was to develop and validate the optimal cut-off value of IAD as a predictor of major adverse cardiac events in patients with arteri

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a601dce3e389fa34024be27754acaa3
https://doi.org/10.1016/j.jjcc.2017.06.010

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Left ventricular obstruction caused by a large hiatal hernia

Autor: Chiyo Ichimiya, Kenji Harada, Akira Hirono, Hirofumi Yamamoto, Norihito Kageyama, Takeshi Omura, Yuya Hiroshima, Ushio Tamura, Yasuhiro Yokoyama, Naho Terada, Hiroyuki Fujinaga

Publikováno v: Echocardiography. 34:1254-1256

A 76-year-old man was admitted to our emergency department owing to chest pain, which started immediately after lunch. Although electrocardiogram revealed ST-segment elevation with hyperacute T-wave changes in the anterior lead tracings, emergency co

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea6a20ee3ab4051c0898f0a8f917f3b7
https://doi.org/10.1111/echo.13563

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Chronic nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency: report of two families with novel mutations causing G6PD Bangkok and G6PD Bangkok Noi

Autor: Akira Hirono, Parichat Pung-Amritt, Wanchai Wanachiwanawin, Ajjima Treesucon, Voravarn S. Tanphaichitr

Publikováno v: Annals of Hematology. 90:769-775

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is one of the most common hereditary enzymopathies worldwide. Mostly G6PD deficient cases are asymptomatic though they may have the risk of neonatal jaundice (NNJ) and acute intravascular hemolysis

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5742edcf655d0c70621d194d791948d
https://doi.org/10.1007/s00277-010-1153-4

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An Improved Single-step Screening Method for Glucose-6-Phosphate Dehydrogenase Deficiency

Autor: Hisaichi Fujii, Akira Hirono, Shiro Miwa

Publikováno v: Japanese Journal of Tropical Medicine and Hygiene. 26:1-4

We have established a new simple and rapid screening method for glucose-6-phosphate dehydrogenase (G6PD) deficiency. The principle of this method is the formation of blue formazan with the reduced form of nicotinamide adenine dinucleotide phosphate (

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::32d43bbeebabf3676d5d72a4e034e95a
https://doi.org/10.2149/tmh1973.26.1

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Frame Shift Mutation, Exon Skipping, and a Two-Codon Deletion Caused by Splice Site Mutations Account for Pyruvate Kinase Deficiency

Autor: Hisaichi Fujii, Shiro Miwa, L.C. Chan, Akira Hirono, Ichiro Tsukimoto, Hitoshi Kanno, David C. Wei

Publikováno v: Blood. 89:4213-4218

Three novel splice site mutations and two novel missense mutations were identified by molecular analysis of pyruvate kinase (PK) deficiency associated with hereditary nonspherocytic hemolytic anemia. A Nepalese PK variant, PK Kowloon, was found to ha

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a0a90ef0bc4dcbfe8ad098667a9290f
https://doi.org/10.1182/blood.v89.11.4213

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Three cases of hereditary nonspherocytic hemolytic anemia associated with red blood cell glutathione deficiency

Autor: H Iyori, J Ueyama, Hiroshi Fujii, Shiro Miwa, Akira Hirono, Hitoshi Kanno, H Chiba, I Sekine

Publikováno v: Blood. 87:2071-2074

Three unrelated Japanese patients with chronic nonspherocytic hemolytic anemia wer found to have marked deficiency of red blood cell (RBC) reduced glutathoine (GSH) (4.4%, 13.1%, and 6.9% of normal, respectively). A panel of RBC enzyme assays showed

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54ad724eff9636cf9183cb42208b2b98
https://doi.org/10.1182/blood.v87.5.2071.bloodjournal8752071

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Hereditary spherocytic anemia with deletion of the short arm of chromosome 8

Autor: Yoshinao Wada, Shiro Miwa, Kikuno Murayama, Yoich Nakamura, Masahiro Nakayama, Hide-aki Chiyo, Akira Hirono, Yoshihito Yawata, Nobuhiko Okamoto, Akio Kanzaki, Takahumi Inoue

Publikováno v: American Journal of Medical Genetics. 58:225-229

We describe a 30-month-old boy with multiple anomalies and mental retardation with hereditary spherocytic anemia. His karyotype was 46,XY,del(8)(p11.23p21.1). Genes for ankyrin and glutathione reductase (GSR) were localized to chromosome areas 8p11.2

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::793de20f9806b38036b81d5ff9cff387
https://doi.org/10.1002/ajmg.1320580306

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Identification of two novel deletion mutations in glucose-6-phosphate dehydrogenase gene causing hemolytic anemia

Autor: Akira Hirono, Hisaichi Fujii, Shiro Miwa

Publikováno v: Blood. 85:1118-1121

Among over 50 distinct mutations causing glucose-6-phosphate dehydrogenase (G6PD) deficiency, only two deletion mutations have so far been reported. Using nonradioisotopic single-strand conformation polymorphism analysis, we found two additional dele

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::357cff3e3b77e7847a11cfbe675c7d10
https://doi.org/10.1182/blood.v85.4.1118.bloodjournal8541118

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