A novel PGK1 mutation associated with neurological dysfunction and the absence of episodes of hemolytic anemia or myoglobinuria

gan Matsumaru, Shigeto, Oguni, Hirokazu, Ogura, Hiromi, Shimojima, Keiko, Nagata, Satoru, Kanno, Hitoshi, Yamamoto, Toshiyuki
Cyhoeddwyd yn Intractable Rare Dis Res (2017)

Effect of Interferon‐α in Patients with Chronic Myelogenous Leukemia in the Accelerated Phase: Cytogenetic and Molecular Studies

gan Ogura, Hiromi, Tani, Kenzaburo, Kozai, Yasuji, Watari, Kiyoshi, Kodo, Hideki, Ozawa, Keiya, Asano, Shigetaka, Takaku, Fumimaro
Cyhoeddwyd yn Jpn J Cancer Res (1990)

ATP11C is a major flippase in human erythrocytes and its defect causes congenital hemolytic anemia

gan Arashiki, Nobuto, Takakuwa, Yuichi, Mohandas, Narla, Hale, John, Yoshida, Kenichi, Ogura, Hiromi, Utsugisawa, Taiju, Ohga, Shouichi, Miyano, Satoru, Ogawa, Seishi, Kojima, Seiji, Kanno, Hitoshi
Cyhoeddwyd yn Haematologica (2016)

Novel COL4A1 mutations identified in infants with congenital hemolytic anemia in association with brain malformations

gan Ogura, Hiromi, Ohga, Shouichi, Aoki, Takako, Utsugisawa, Taiju, Takahashi, Hidehiro, Iwai, Asayuki, Watanabe, Kenichiro, Okuno, Yusuke, Yoshida, Kenichi, Ogawa, Seishi, Miyano, Satoru, Kojima, Seiji, Yamamoto, Toshiyuki, Yamamoto-Shimojima, Keiko, Kanno, Hitoshi
Cyhoeddwyd yn Hum Genome Var (2020)