Ida H - Search Results

1

Type II Gaucher disease: compound heterozygote with RecNciI and L444P mutations.

Lee YS, Poh LK, Ida H, Loke KY. Lee YS, et al. Among authors: ida h. J Trop Pediatr. 2001 Apr;47(2):115-7. doi: 10.1093/tropej/47.2.110-a. J Trop Pediatr. 2001. PMID: 11336129

2

Effects of enzyme replacement therapy in thirteen Japanese paediatric patients with Gaucher disease.

Ida H, Rennert OM, Kobayashi M, Eto Y. Ida H, et al. Eur J Pediatr. 2001 Jan;160(1):21-5. doi: 10.1007/pl00008411. Eur J Pediatr. 2001. PMID: 11195013

3

A new variant neuropathic type of Gaucher's disease characterized by hydrocephalus, corneal opacities, deformed toes, and fibrous thickening of spleen and liver capsules.

Inui K, Yanagihara K, Otani K, Suzuki Y, Akagi M, Nakayama M, Ida H, Okada S. Inui K, et al. Among authors: ida h. J Pediatr. 2001 Jan;138(1):137-9. doi: 10.1067/mpd.2001.109789. J Pediatr. 2001. PMID: 11148530

4

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. Hum Genet. 1999 Jul-Aug;105(1-2):120-6. doi: 10.1007/s004399900076. Hum Genet. 1999. PMID: 10480365

5

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. J Inherit Metab Dis. 1997 Mar;20(1):67-73. doi: 10.1023/a:1005313724361. J Inherit Metab Dis. 1997. PMID: 9061570

6

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. Hum Genet. 1996 Aug;98(2):167-71. doi: 10.1007/s004390050182. Hum Genet. 1996. PMID: 8698334

7

[Gaucher disease].

Ida H. Ida H. Ryoikibetsu Shokogun Shirizu. 1998;(19 Pt 2):356-9. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9645082 Review. Japanese. No abstract available.

8

Clinical and molecular characteristics of Japanese Gaucher disease.

Eto Y, Ida H. Eto Y, et al. Among authors: ida h. Neurochem Res. 1999 Feb;24(2):207-11. doi: 10.1023/a:1022553819241. Neurochem Res. 1999. PMID: 9972866

9

[Molecular studies of Gaucher disease].

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

10

Initiation of enzyme replacement therapy for an adult patient with asymptomatic type 1 Gaucher's disease.

Tanaka N, Saito H, Ito T, Momose K, Ishida F, Hora K, Kiyosawa K, Ida H. Tanaka N, et al. Among authors: ida h. Intern Med. 2001 Aug;40(8):716-21. doi: 10.2169/internalmedicine.40.716. Intern Med. 2001. PMID: 11518109 Free article.

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