Eto Y - Search Results

1

Clinical and genetic studies of Japanese homozygotes for the Gaucher disease L444P mutation.

Ida H, Rennert OM, Iwasawa K, Kobayashi M, Eto Y. Ida H, et al. Among authors: eto y. Hum Genet. 1999 Jul-Aug;105(1-2):120-6. doi: 10.1007/s004399900076. Hum Genet. 1999. PMID: 10480365

2

Characteristics of gene mutations among 32 unrelated Japanese Gaucher disease patients: absence of the common Jewish 84GG and 1226G mutations.

Ida H, Iwasawa K, Kawame H, Rennert OM, Maekawa K, Eto Y. Ida H, et al. Among authors: eto y. Hum Genet. 1995 Jun;95(6):717-20. doi: 10.1007/BF00209497. Hum Genet. 1995. PMID: 7789963

3

Molecular characteristics in Japanese patients with lipidosis: novel mutations in metachromatic leukodystrophy and Gaucher disease.

Eto Y, Kawame H, Hasegawa Y, Ohashi T, Ida H, Tokoro T. Eto Y, et al. Mol Cell Biochem. 1993 Feb 17;119(1-2):179-84. doi: 10.1007/BF00926869. Mol Cell Biochem. 1993. PMID: 8455580

4

Identification of three novel mutations in the acid sphinogomyelinase gene of Japanese patients with Niemann-Pick disease type A and B.

Ida H, Rennert OM, Maekawa K, Eto Y. Ida H, et al. Among authors: eto y. Hum Mutat. 1996;7(1):65-7. doi: 10.1002/(SICI)1098-1004(1996)7:1<65::AID-HUMU10>3.0.CO;2-Q. Hum Mutat. 1996. PMID: 8664904 No abstract available.

5

Mutation screening of 17 Japanese patients with neuropathic Gaucher disease.

Ida H, Rennert OM, Kawame H, Ito T, Maekawa K, Eto Y. Ida H, et al. Among authors: eto y. Hum Genet. 1996 Aug;98(2):167-71. doi: 10.1007/s004390050182. Hum Genet. 1996. PMID: 8698334

6

Clinical and genetic studies of five fatal cases of Japanese Gaucher disease type 1.

Ida H, Rennert OM, Ito T, Maekawa K, Eto Y. Ida H, et al. Among authors: eto y. Acta Paediatr Jpn. 1996 Jun;38(3):233-6. doi: 10.1111/j.1442-200x.1996.tb03476.x. Acta Paediatr Jpn. 1996. PMID: 8741312

7

[Molecular studies of Gaucher disease].

Eto Y, Ida H. Eto Y, et al. Rinsho Byori. 1996 Apr;44(4):327-34. Rinsho Byori. 1996. PMID: 8847814 Review. Japanese.

8

Mutation prevalence among 47 unrelated Japanese patients with Gaucher disease: identification of four novel mutations.

Ida H, Rennert OM, Kawame H, Maekawa K, Eto Y. Ida H, et al. Among authors: eto y. J Inherit Metab Dis. 1997 Mar;20(1):67-73. doi: 10.1023/a:1005313724361. J Inherit Metab Dis. 1997. PMID: 9061570

9

Differences in origin of the 1448C mutation in patients with Gaucher disease.

Iwasawa K, Ida H, Eto Y. Iwasawa K, et al. Among authors: eto y. Acta Paediatr Jpn. 1997 Aug;39(4):451-3. doi: 10.1111/j.1442-200x.1997.tb03616.x. Acta Paediatr Jpn. 1997. PMID: 9316290

10

Type 1 Gaucher disease: phenotypic expression and natural history in Japanese patients.

Ida H, Rennert OM, Ito T, Maekawa K, Eto Y. Ida H, et al. Among authors: eto y. Blood Cells Mol Dis. 1998 Mar;24(1):73-81. doi: 10.1006/bcmd.1998.0172. Blood Cells Mol Dis. 1998. PMID: 9541479 Free article.

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