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Pediatric Neurology
|
March 29, 2000
Communicating hydrocephalus in a patient with Gaucher's disease type 3
T 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 leukodystrophy
H 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 patients
H 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 1
H 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 mutation
H Ida, O M Rennert, K Iwasawa, et al.
Retina (Philadelphia, Pa.)
|
October 20, 2000
Histopathologic retinal changes with intravitreous fluorosilicone oil in rabbit eyes
M Doi, M Ning, H Ida, et al.
Journal of Tropical Pediatrics
|
May 5, 2001
Type II Gaucher disease: compound heterozygote with RecNciI and L444P mutations
Y 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 mutations
H 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 cells
H Ida, M J Robertson, S Voss, et al.
Brain & Development
|
November 1, 1994
Pathological and biochemical studies of fetal Krabbe disease
H Ida, O M Rennert, K Watabe, et al.
Page
of 16
Search research articles
Search
Showing results (31-40 of 152) with videos related to
Sort By:
Page
of 16
Pediatric Neurology
|
March 29, 2000
Communicating hydrocephalus in a patient with Gaucher's disease type 3
T 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 leukodystrophy
H 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 patients
H 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 1
H 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 mutation
H Ida, O M Rennert, K Iwasawa, et al.
Retina (Philadelphia, Pa.)
|
October 20, 2000
Histopathologic retinal changes with intravitreous fluorosilicone oil in rabbit eyes
M Doi, M Ning, H Ida, et al.
Journal of Tropical Pediatrics
|
May 5, 2001
Type II Gaucher disease: compound heterozygote with RecNciI and L444P mutations
Y 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 mutations
H 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 cells
H Ida, M J Robertson, S Voss, et al.
Brain & Development
|
November 1, 1994
Pathological and biochemical studies of fetal Krabbe disease
H Ida, O M Rennert, K Watabe, et al.
Page
of 16