Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Rika Okano"'
Autor:
Takanori Utsumi, Satoshi Okada, Kazushi Izawa, Yoshitaka Honda, Gen Nishimura, Ryuta Nishikomori, Rika Okano, Masao Kobayashi
Publikováno v:
Frontiers in Endocrinology, Vol 8 (2017)
Spondyloenchondrodysplasia (SPENCD) is an autosomal recessive skeletal dysplasia caused by loss of function mutations in acid phosphatase 5, tartrate resistant (ACP5). Hypomorphic ACP5 mutations impair endochondral bone growth and create an interfero
Externí odkaz:
https://doaj.org/article/32bb9640f9444f6b8509c8e83154b1aa
Publikováno v:
Pediatrics International.
Autor:
Masao Kobayashi, Gen Nishimura, Kazushi Izawa, Ryuta Nishikomori, Yoshitaka Honda, Rika Okano, Satoshi Okada, Takanori Utsumi
Publikováno v:
Frontiers in Endocrinology, Vol 8 (2017)
Frontiers in Endocrinology
Frontiers in Endocrinology
Spondyloenchondrodysplasia (SPENCD) is an autosomal recessive skeletal dysplasia caused by loss of function mutations in acid phosphatase 5, tartrate resistant (ACP5). Hypomorphic ACP5 mutations impair endochondral bone growth and create an interfero
Publikováno v:
The FASEB Journal. 29
Autor:
Norihisa Iida, Kazuteru Kouno, Satoshi Ueno, Rika Okano, Hajime Fujii, Sumio Hyoudou, Michiko Fujitaka, Tooru Komazawa, Hiroshi Nakahara, Masatoshi Doumen
Publikováno v:
Nihon Shoni Arerugi Gakkaishi. The Japanese Journal of Pediatric Allergy and Clinical Immunology. 17:190-194
Two Cases of Hemorrhagic Shock and Encephalopathy Syndrome Associated with Influenza Virus Infection
Autor:
Hideo Mawatari, Minako Ohtani, Rika Okano, Yasumasa Iwasaki, Takao Yamanoue, Seishi Wada, Kiyoshi Okabayashi
Publikováno v:
Nihon Kyukyu Igakukai Zasshi. 12:54-58
Two girls--Case 1 aged 4 and Case 2 aged 5--were admitted due to sudden onset of fever, disturbed consciousness, and convulsions. On admission, laboratory and hematological data in both cases was normal, although AST, ALT, LDH and CPK were markedly i