Ogura H - Search Results

1

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

Arashiki N, Takakuwa Y, Mohandas N, Hale J, Yoshida K, Ogura H, Utsugisawa T, Ohga S, Miyano S, Ogawa S, Kojima S, Kanno H. Arashiki N, et al. Among authors: ogura h. Haematologica. 2016 May;101(5):559-65. doi: 10.3324/haematol.2016.142273. Epub 2016 Mar 4. Haematologica. 2016. PMID: 26944472 Free PMC article.

2

Genetic analysis of adenosine deaminase expression in adult T-cell leukemia.

Morisaki T, Horiuchi N, Tsutsumi H, Ogura H, Kanno H, Tani K, Fujii H, Miwa S. Morisaki T, et al. Among authors: ogura h. Am J Hematol. 1988 Jun;28(2):119-21. doi: 10.1002/ajh.2830280212. Am J Hematol. 1988. PMID: 2456011

3

A new glucose-6-phosphate dehydrogenase variant (G6PD Iwate) associated with congenital non-spherocytic hemolytic anemia.

Kanno H, Takano T, Fujii H, Tani K, Morisaki T, Hirono A, Kumakawa T, Ogura H, Takahashi K, Tsutsumi H, et al. Kanno H, et al. Among authors: ogura h. Nihon Ketsueki Gakkai Zasshi. 1988 Jul;51(4):715-9. Nihon Ketsueki Gakkai Zasshi. 1988. PMID: 3201886 No abstract available.

4

A new glucose-6-phosphate dehydrogenase variant (G6PD Tsukui) associated with congenital hemolytic anemia.

Ogura H, Morisaki T, Tani K, Kanno H, Tsutsumi H, Takahashi K, Miyamori T, Fujii H, Miwa S. Ogura H, et al. Hum Genet. 1988 Apr;78(4):369-71. doi: 10.1007/BF00291738. Hum Genet. 1988. PMID: 3360447

5

Two homozygous cases of erythrocyte pyruvate kinase (PK) deficiency in Japan: PK Sendai and PK Shinshu.

Tani K, Tsutsumi H, Takahashi K, Ogura H, Kanno H, Hayasaka K, Narisawa K, Nakahata T, Akabane T, Morisaki T, et al. Tani K, et al. Among authors: ogura h. Am J Hematol. 1988 Jul;28(3):186-90. doi: 10.1002/ajh.2830280312. Am J Hematol. 1988. PMID: 3407638

6

Transgenic rescue of hemolytic anemia due to red blood cell pyruvate kinase deficiency.

Kanno H, Utsugisawa T, Aizawa S, Koizumi T, Aisaki K, Hamada T, Ogura H, Fujii H. Kanno H, et al. Among authors: ogura h. Haematologica. 2007 Jun;92(6):731-7. doi: 10.3324/haematol.10945. Haematologica. 2007. PMID: 17550844 Free article.

7

[Glucose-6-phosphate dehydrogenase deficiency in Japan].

Kanno H, Ogura H. Kanno H, et al. Among authors: ogura h. Rinsho Ketsueki. 2015 Jul;56(7):771-7. doi: 10.11406/rinketsu.56.771. Rinsho Ketsueki. 2015. PMID: 26251139 Japanese.

8

Erythrocyte glutathione is a novel biomarker of Diamond-Blackfan anemia.

Utsugisawa T, Uchiyama T, Toki T, Ogura H, Aoki T, Hamaguchi I, Ishiguro A, Ohara A, Kojima S, Ohga S, Ito E, Kanno H. Utsugisawa T, et al. Among authors: ogura h. Blood Cells Mol Dis. 2016 Jul;59:31-6. doi: 10.1016/j.bcmd.2016.03.007. Epub 2016 Apr 11. Blood Cells Mol Dis. 2016. PMID: 27282564

9

Splenectomy resolves hemolytic anemia caused by adenylate kinase deficiency.

Niizuma H, Kanno H, Sato A, Ogura H, Imaizumi M. Niizuma H, et al. Among authors: ogura h. Pediatr Int. 2017 Feb;59(2):228-230. doi: 10.1111/ped.13166. Pediatr Int. 2017. PMID: 28211224 No abstract available.

10

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

Matsumaru S, Oguni H, Ogura H, Shimojima K, Nagata S, Kanno H, Yamamoto T. Matsumaru S, et al. Among authors: ogura h. Intractable Rare Dis Res. 2017 May;6(2):132-136. doi: 10.5582/irdr.2017.01020. Intractable Rare Dis Res. 2017. PMID: 28580215 Free PMC article.

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