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Journal of Inherited Metabolic Disease
|
January 1, 1983
Biochemical studies in mouse Krabbe's disease (Twitcher)
Y Eto, F Umezawa, E Kasai, 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.
Archives of Neurology
|
February 1, 1974
Multiple sulfatase deficiencies in cultured skin fibroblasts. Occurrence in patients with a variant form of metachromatic leukodystrophy
Y Eto, U N Wiesmann, J H Carson, et al.
European Journal of Haematology
|
November 20, 1998
Efficient and persistent expression of beta-glucuronidase gene in CD34+ cells from human umbilical cord blood by retroviral vector
T Ohashi, S Iizuka, W S Sly, 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.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 24, 1999
Psychiatric inpatients and chromosome deletions within 22q11.2
S Sugama, T Namihira, R Matsuoka, et al.
Molecular and Cellular Biochemistry
|
February 17, 1993
Molecular characteristics in Japanese patients with lipidosis: novel mutations in metachromatic leukodystrophy and Gaucher disease
Y Eto, H Kawame, Y Hasegawa, et al.
Clinical Nephrology
|
April 5, 2000
Focal segmental glomerulosclerosis in a patient with Prader-Willi syndrome
H Mochizuki, K Joh, N Matsuyama, et al.
Human Reproduction (Oxford, England)
|
September 1, 1993
Presence and possible function of activin-like substance in human follicular fluid
M Sadatsuki, O Tsutsumi, R Sakai, et al.
Page
of 31
Search research articles
Search
Showing results (151-160 of 307) with videos related to
Sort By:
Page
of 31
Journal of Inherited Metabolic Disease
|
January 1, 1983
Biochemical studies in mouse Krabbe's disease (Twitcher)
Y Eto, F Umezawa, E Kasai, 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.
Archives of Neurology
|
February 1, 1974
Multiple sulfatase deficiencies in cultured skin fibroblasts. Occurrence in patients with a variant form of metachromatic leukodystrophy
Y Eto, U N Wiesmann, J H Carson, et al.
European Journal of Haematology
|
November 20, 1998
Efficient and persistent expression of beta-glucuronidase gene in CD34+ cells from human umbilical cord blood by retroviral vector
T Ohashi, S Iizuka, W S Sly, 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.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 24, 1999
Psychiatric inpatients and chromosome deletions within 22q11.2
S Sugama, T Namihira, R Matsuoka, et al.
Molecular and Cellular Biochemistry
|
February 17, 1993
Molecular characteristics in Japanese patients with lipidosis: novel mutations in metachromatic leukodystrophy and Gaucher disease
Y Eto, H Kawame, Y Hasegawa, et al.
Clinical Nephrology
|
April 5, 2000
Focal segmental glomerulosclerosis in a patient with Prader-Willi syndrome
H Mochizuki, K Joh, N Matsuyama, et al.
Human Reproduction (Oxford, England)
|
September 1, 1993
Presence and possible function of activin-like substance in human follicular fluid
M Sadatsuki, O Tsutsumi, R Sakai, et al.
Page
of 31