Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sachie Nakazato"'
Autor:
Toshifumi Yoshida, Sachie Nakazato, Fumio Nagumo, Yoshinori Shimamoto, Kanako Tsuchiya, Kazutoshi Ono
Publikováno v:
European Journal of Haematology. 58:130-132
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63760d56d987c67e11ef7cbd857a1cad
https://doi.org/10.1111/j.1600-0609.1997.tb00938.x
https://doi.org/10.1111/j.1600-0609.1997.tb00938.x
Autor:
Yoshinori Shimamoto, Osamu Kohashi, Noriko Funai, Yoshinori Nagai, Shin-ichi Yoshida, Sachie Nakazato
Publikováno v:
Clinical Immunology and Immunopathology. 80:325-332
A variety of immunologic tests were compared between human T-lymphotropic virus type I (HTLV-I) carriers and patients with adult T-cell leukemia/lymphoma (ATL). The mitogenic responses of the lymphocytes to concanavalin A and phytohemagglutinin were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53c0c6424d5f7eaa8ff52c34cdb71225
https://doi.org/10.1006/clin.1996.0131
https://doi.org/10.1006/clin.1996.0131
Autor:
Yutaka Imamura, Sachie Nakazato, Masaaki Moroi, Masayuki Sano, Ritsuko Seki, Taisuke Kanaji, Takashi Okamura, Yuka Takata, Eisaburo Sueoka
Publikováno v:
International journal of hematology. 96(6)
Bernard–Soulier syndrome (BSS) is an inherited bleeding disorder caused by a defect in the platelet glycoprotein (GP) Ib/IX complex. The GPIX W127X mutation is the most common genetic defect in Japanese patients with BSS, which is often misdiagnose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6393b8dcdb641df4d052c3e277dfd8a4
https://pubmed.ncbi.nlm.nih.gov/23143686
https://pubmed.ncbi.nlm.nih.gov/23143686
Autor:
Fumio Nagumo, Miho Honda, Kenji Izuhara, Sachiko Kanaji, Taisuke Kanaji, Ikuko Nakamura, Shoichiro Shibata, Masaharu Miyahara, Takashi Okamura, Shoichiro Ohta, Yoshitomi Tabata, Koichi Node, Hisashi Gondo, Sachie Nakazato, Masanori Miura, Kazuo Wakayama
Publikováno v:
International journal of hematology. 89(1)
Coagulation factor V (FV) deficiency is a rare bleeding disorder characterized by low coagulant and antigen levels of FV with bleeding symptoms ranging from mild to severe. Only a limited number of mutations have been reported because of the large si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::474c459e42c926799d10c49477f913a4
https://pubmed.ncbi.nlm.nih.gov/19052695
https://pubmed.ncbi.nlm.nih.gov/19052695
Publikováno v:
Pediatric neurology. 35(2)
This study examined the possibility that children with and without a history of febrile seizures might mount different immune responses to double-stranded ribonucleic acid, which is a common viral factor that induces host cell immune responses, and i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3ac93efd5b7ff3800fd73e1ae47a465
https://pubmed.ncbi.nlm.nih.gov/16876005
https://pubmed.ncbi.nlm.nih.gov/16876005
Autor:
Yutaka Imamura, Masayuki Sano, Kenji Izuhara, Eijiro Oku, Takashi Okamura, Masaaki Moroi, Yuka Takata, Eizaburo Sueoka, Taisuke Kanaji, Ritsuko Seki, Sachie Nakazato
Publikováno v:
Blood. 112:1234-1234
A W127X mutation in platelet glycoprotein (GP)IX is the most common genetic defect in Japanese Bernard-Soulier Syndrome (BSS). Patients having this mutation are often misdiagnosed as having immune thrombocytopenia (ITP) because of residual expression
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03bef9741d67fd1cac1e0abc1de3e8a7
https://doi.org/10.1182/blood.v112.11.1234.1234
https://doi.org/10.1182/blood.v112.11.1234.1234