Rennert OM - Search Results

1

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: rennert om. 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.

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: rennert om. Hum Genet. 1995 Jun;95(6):717-20. doi: 10.1007/BF00209497. Hum Genet. 1995. PMID: 7789963

3

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

4

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: rennert om. Acta Paediatr Jpn. 1996 Jun;38(3):233-6. doi: 10.1111/j.1442-200x.1996.tb03476.x. Acta Paediatr Jpn. 1996. PMID: 8741312

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

6

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. Among authors: rennert om. J Inherit Metab Dis. 1999 Feb;22(1):63-73. doi: 10.1023/a:1005451300167. J Inherit Metab Dis. 1999. PMID: 10070619

7

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

8

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. Among authors: rennert om. Eur J Pediatr. 2001 Jan;160(1):21-5. doi: 10.1007/pl00008411. Eur J Pediatr. 2001. PMID: 11195013

9

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: rennert om. 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.

10

Pathological and biochemical studies of fetal Krabbe disease.

Ida H, Rennert OM, Watabe K, Eto Y, Maekawa K. Ida H, et al. Among authors: rennert om. Brain Dev. 1994 Nov-Dec;16(6):480-4. doi: 10.1016/0387-7604(94)90013-2. Brain Dev. 1994. PMID: 7695000 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

254 results

Search Page

Filters