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H Ida

Showing results (31-40 of 152) with videos related to

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Pediatric Neurology|March 29, 2000
Communicating hydrocephalus in a patient with Gaucher's disease type 3T Shiihara, A Oka, I Suzaki, et al.
Biochemical and Biophysical Research Communications|January 30, 1990
Galactosylceramide and galactosylsphingosine loading studies in cultured skin fibroblasts in human and murine globoid cell leukodystrophyH Ida, K Kusano, H Suzuki, et al.
Blood Cells, Molecules & Diseases|June 6, 1998
Type 1 Gaucher disease: phenotypic expression and natural history in Japanese patientsH Ida, O M Rennert, T Ito, et al.
Acta Paediatrica Japonica : Overseas Edition|June 1, 1996
Clinical and genetic studies of five fatal cases of Japanese Gaucher disease type 1H Ida, O M Rennert, T Ito, et al.
Human Genetics|September 10, 1999
Clinical and genetic studies of Japanese homozygotes for the Gaucher disease L444P mutationH Ida, O M Rennert, K Iwasawa, et al.
Retina (Philadelphia, Pa.)|October 20, 2000
Histopathologic retinal changes with intravitreous fluorosilicone oil in rabbit eyesM Doi, M Ning, H Ida, et al.
Journal of Tropical Pediatrics|May 5, 2001
Type II Gaucher disease: compound heterozygote with RecNciI and L444P mutationsY S Lee, L K Poh, H Ida, et al.
Journal of Inherited Metabolic Disease|March 1, 1997
Mutation prevalence among 47 unrelated Japanese patients with Gaucher disease: identification of four novel mutationsH Ida, O M Rennert, H Kawame, et al.
Journal of Immunology (Baltimore, Md. : 1950)|September 1, 1997
CD94 ligation induces apoptosis in a subset of IL-2-stimulated NK cellsH Ida, M J Robertson, S Voss, et al.
Brain & Development|November 1, 1994
Pathological and biochemical studies of fetal Krabbe diseaseH Ida, O M Rennert, K Watabe, et al.
Pageof 16

Showing results (31-40 of 152) with videos related to

Sort By:
Pageof 16
Pediatric Neurology|March 29, 2000
Communicating hydrocephalus in a patient with Gaucher's disease type 3T Shiihara, A Oka, I Suzaki, et al.
Biochemical and Biophysical Research Communications|January 30, 1990
Galactosylceramide and galactosylsphingosine loading studies in cultured skin fibroblasts in human and murine globoid cell leukodystrophyH Ida, K Kusano, H Suzuki, et al.
Blood Cells, Molecules & Diseases|June 6, 1998
Type 1 Gaucher disease: phenotypic expression and natural history in Japanese patientsH Ida, O M Rennert, T Ito, et al.
Acta Paediatrica Japonica : Overseas Edition|June 1, 1996
Clinical and genetic studies of five fatal cases of Japanese Gaucher disease type 1H Ida, O M Rennert, T Ito, et al.
Human Genetics|September 10, 1999
Clinical and genetic studies of Japanese homozygotes for the Gaucher disease L444P mutationH Ida, O M Rennert, K Iwasawa, et al.
Retina (Philadelphia, Pa.)|October 20, 2000
Histopathologic retinal changes with intravitreous fluorosilicone oil in rabbit eyesM Doi, M Ning, H Ida, et al.
Journal of Tropical Pediatrics|May 5, 2001
Type II Gaucher disease: compound heterozygote with RecNciI and L444P mutationsY S Lee, L K Poh, H Ida, et al.
Journal of Inherited Metabolic Disease|March 1, 1997
Mutation prevalence among 47 unrelated Japanese patients with Gaucher disease: identification of four novel mutationsH Ida, O M Rennert, H Kawame, et al.
Journal of Immunology (Baltimore, Md. : 1950)|September 1, 1997
CD94 ligation induces apoptosis in a subset of IL-2-stimulated NK cellsH Ida, M J Robertson, S Voss, et al.
Brain & Development|November 1, 1994
Pathological and biochemical studies of fetal Krabbe diseaseH Ida, O M Rennert, K Watabe, et al.
Pageof 16