Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Azuma Hiramoto"'
Publikováno v:
Brain and Development. 37:344-346
Pelger-Huët anomalies, which are characterized by an abnormal nuclear shape and chromatin organization in blood granulocytes, and are frequently confused with myelodysplastic syndrome. We herein report a case of Lenox syndrome in a patient treated w
Two unrelated patients with MRE11A mutations and Nijmegen breakage syndrome-like severe microcephaly
Autor:
Shinya Matsuura, Yoshiyuki Matsumoto, Hirofumi Ohashi, Azuma Hiramoto, Yoshihiro Sakemi, Hiromi Sakamoto, Tomoo Ogi, Toshihide Shiiki, Hidetoshi Tahara, Hideki Izumi, Tatsuo Miyamoto, Yoshiki Fujisawa, Shozo Oku, Yuka Nakazawa
Publikováno v:
DNA repair. 10(3)
MRE11 and NBS1 function together as components of a MRE11/RAD50/NBS1 protein complex, however deficiency of either protein does not result in the same clinical features. Mutations in the NBN gene underlie Nijmegen breakage syndrome (NBS), a chromosom
Autor:
Tomoyuki Hanaoka, Reiko Kishi, Kitoku Okada, Toshio Nakadate, Katsumi Mita, Shizuo Maruyama, Yasuyuki Suzuki, Azuma Hiramoto, Yasuhiko Egusa
Publikováno v:
Journal of Epidemiology
Background: Although the prognosis for survival in people with severe functional disabilities is a serious concern for their families and health care practitioners, there have been few reports on survival rates for this population. Every year, the Ja
Autor:
Kayomi Matsumoto, Azuma Hiramoto, Masanori Yosida, Hajime Kurosawa, Rika Imanishi, Yuko Sano, Noboru Chiba, Naoki Mori, Tamio keitoku
Publikováno v:
Chest. 148:781A
Autor:
Hajime Kurosawa, Yuko Sano, Kayomi Matumoto, Naoki Mori, Hiromi Fujii, Emiko Fukuda, Masahiro Kohzuki, Azuma Hiramoto
Publikováno v:
Chest. 128:355S