Ida H - Search Results

1

Imprint cytology of Gaucher's disease presenting as a splenic mass. A case report with molecular approaches.

Kobayashi TK, Tamagaki T, Yoneyama C, Watanabe S, Sugihara H, Ida H. Kobayashi TK, et al. Among authors: ida h. Acta Cytol. 1998 Mar-Apr;42(2):419-24. doi: 10.1159/000331630. Acta Cytol. 1998. PMID: 9568149

2

Communicating hydrocephalus in a patient with Gaucher's disease type 3.

Shiihara T, Oka A, Suzaki I, Ida H, Takeshita K. Shiihara T, et al. Among authors: ida h. Pediatr Neurol. 2000 Mar;22(3):234-6. doi: 10.1016/s0887-8994(99)00140-x. Pediatr Neurol. 2000. PMID: 10734257

3

An autopsy case of fetal Gaucher disease.

Adachi Y, Kobayashi Y, Ida H, Yasumizu R, Okamura A, Kayatani H, Teranishi N, Inaba M, Sugihara A, Genba H, Eto Y, Ikehara S. Adachi Y, et al. Among authors: ida h. Acta Paediatr Jpn. 1998 Aug;40(4):374-7. doi: 10.1111/j.1442-200x.1998.tb01952.x. Acta Paediatr Jpn. 1998. PMID: 9745785

4

Enzyme enhancement activity of N-octyl-beta-valienamine on beta-glucosidase mutants associated with Gaucher disease.

Lei K, Ninomiya H, Suzuki M, Inoue T, Sawa M, Iida M, Ida H, Eto Y, Ogawa S, Ohno K, Suzuki Y. Lei K, et al. Among authors: ida h. Biochim Biophys Acta. 2007 May;1772(5):587-96. doi: 10.1016/j.bbadis.2007.02.003. Epub 2007 Feb 14. Biochim Biophys Acta. 2007. PMID: 17363227 Free article.

5

Enzyme therapy in Gaucher disease type 2: an autopsy case.

Takahashi T, Yoshida Y, Sato W, Yano T, Shoji Y, Sawaishi Y, Sakuma I, Sashi T, Enomoto K, Ida H, Takada G. Takahashi T, et al. Among authors: ida h. Tohoku J Exp Med. 1998 Oct;186(2):143-9. doi: 10.1620/tjem.186.143. Tohoku J Exp Med. 1998. PMID: 10223617 Free article.

6

N-octyl-beta-valienamine up-regulates activity of F213I mutant beta-glucosidase in cultured cells: a potential chemical chaperone therapy for Gaucher disease.

Lin H, Sugimoto Y, Ohsaki Y, Ninomiya H, Oka A, Taniguchi M, Ida H, Eto Y, Ogawa S, Matsuzaki Y, Sawa M, Inoue T, Higaki K, Nanba E, Ohno K, Suzuki Y. Lin H, et al. Among authors: ida h. Biochim Biophys Acta. 2004 Aug 4;1689(3):219-28. doi: 10.1016/j.bbadis.2004.03.007. Biochim Biophys Acta. 2004. PMID: 15276648 Free article.

7

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. Among authors: ida h. Mol Cell Biochem. 1993 Feb 17;119(1-2):179-84. doi: 10.1007/BF00926869. Mol Cell Biochem. 1993. PMID: 8455580

8

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

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

9

Severe skeletal complications in Japanese patients with type 1 Gaucher disease.

Ida H, Rennert OM, Kato S, Ueda T, Oishi K, Maekawa K, Eto Y. Ida H, et al. J Inherit Metab Dis. 1999 Feb;22(1):63-73. doi: 10.1023/a:1005451300167. J Inherit Metab Dis. 1999. PMID: 10070619

10

Gaucher disease type 1: revised recommendations on evaluations and monitoring for adult patients.

Weinreb NJ, Aggio MC, Andersson HC, Andria G, Charrow J, Clarke JT, Erikson A, Giraldo P, Goldblatt J, Hollak C, Ida H, Kaplan P, Kolodny EH, Mistry P, Pastores GM, Pires R, Prakash-Cheng A, Rosenbloom BE, Scott CR, Sobreira E, Tylki-Szymańska A, Vellodi A, vom Dahl S, Wappner RS, Zimran A; International Collaborative Gaucher Group (ICGG). Weinreb NJ, et al. Among authors: ida h. Semin Hematol. 2004 Oct;41(4 Suppl 5):15-22. doi: 10.1053/j.seminhematol.2004.07.010. Semin Hematol. 2004. PMID: 15468046

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