Zobrazeno 1 - 10
of 47
pro vyhledávání: '"S, Shike"'
Conference
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
S, Kojima, T, Matsuyama, T, Miyazaki, K, Sakurada, S, Shike, E, Okino, T, Akabane, T, Nakahata, M, Okuni, H, Mugishima
Publikováno v:
[Rinsho ketsueki] The Japanese journal of clinical hematology. 31(7)
Thirty-nine patients with severe or moderate aplastic anemia received treatment with recombinant human granulocyte colony-stimulating factor (rhG-CSF). The first group of eight patients received rhG-CSF in doses of 100 to 400 micrograms/m2/d by a dai
Autor:
T. Nagao, K. Yoshioka, J. Akatsuka, S. Shike, Kaneo Yamada, Shunichi Miyazaki, Y. Kobayashi, Hidekazu Kamitsuji, M. Nakashima, Akira Shirahata, S. Tanaka, Hiroshi Fukui, S. Maki, Minoru Inagaki
Publikováno v:
Thrombosis Research. 56:667-675
Arthral, abdominal and renal symptoms in Henoch-Schonlein purpura (HSP) were scored. Coagulation factor XIII (F XIII) activity was determined in fifty-six children with HSP and the correlation with the severity score of the clinical symptoms was inve
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
[Rinsho ketsueki] The Japanese journal of clinical hematology. 15(11)
Autor:
I, Sekine, J, Utsmi, N, Kuriya, O, Auma, J, Mimaya, S, Shike, S, Koizumi, S, Imajuku, S, Yamamoto, T, Ninomiya
Publikováno v:
[Rinsho ketsueki] The Japanese journal of clinical hematology. 24(9)
Publikováno v:
Jinrui idengaku zasshi. The Japanese journal of human genetics. 19(1)
Publikováno v:
[Rinsho ketsueki] The Japanese journal of clinical hematology. 16(10)
Publikováno v:
Human genetics. 78(1)
A case of hereditary spherocytosis (HS) is reported. Cytogenetic study revealed a de novo minute deletion of chromosome 8. The critical portion which affected the expression of the HS phenotype appeared to be localized to 8p11.22----8p21.1.
Autor:
E, Okino, C, Mori, S, Yamazaki, K, Toyota, T, Yamada, K, Tachi, S, Shike, A, Kanzaki, A, Ikeda, Y, Yawata
Publikováno v:
[Rinsho ketsueki] The Japanese journal of clinical hematology. 30(7)
We have experienced a case of cytohemolytic hereditary elliptocytosis (HE) in a six-year-old boy. Metabolisms of the erythrocytic membrane were investigated on the members from his pedigree. The results were as follows; 1) The presence or absence of