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European Journal of Pediatrics
|
November 1, 1979
Urinary acid mucopolysaccharides in multiple sulfatase deficiency (mucosulfatidosis)
Y Eto, S Numaguchi, T Handa
Journal of Craniofacial Genetics and Developmental Biology
|
March 24, 2000
Pfeiffer syndrome caused by haploinsufficient mutation of FGFR2
M Tsukuno, H Suzuki, Y Eto
Bone
|
August 24, 1999
Local administration of activin promotes fracture healing in the rat fibula fracture model
R Sakai, K Miwa, Y Eto
Endocrine Journal
|
February 1, 1995
Expression of immunoreactive activin A in fetal rat pancreas
M Furukawa, Y Eto, I Kojima
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 17, 1978
Effects of macromolecular compounds on human leukocyte beta-galactosidase activity
K Kiguchi, Y Eto, K Aoki
Human Mutation
|
January 1, 1993
Molecular screening of Japanese patients with Gaucher disease: phenotypic variability in the same genotypes
H Kawame, K Maekawa, Y Eto
DNA and Cell Biology
|
July 1, 1993
Mutations in the arylsulfatase A gene of Japanese patients with metachromatic leukodystrophy
Y Hasegawa, H Kawame, Y Eto
Nihon Rinsho. Japanese Journal of Clinical Medicine
|
September 1, 1993
[Molecular analysis of Japanese patients with metachromatic leukodystrophy]
Y Hasegawa, H Kawame, Y Eto
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 1, 1977
Bile lysosomal enzymes: characteristics and pathological significance for various hepatobiliary disorders
S Toyoda, Y Eto, K Aoki
Acta Paediatrica Japonica : Overseas Edition
|
February 1, 1990
Biochemical pathogenesis of demyelination in globoid cell leukodystrophy (Krabbe's disease): the effects of psychosine upon oligodendroglial cell culture
H Ida, Y Eto, K Maekawa
Page
of 31
Search research articles
Search
Showing results (51-60 of 307) with videos related to
Sort By:
Page
of 31
European Journal of Pediatrics
|
November 1, 1979
Urinary acid mucopolysaccharides in multiple sulfatase deficiency (mucosulfatidosis)
Y Eto, S Numaguchi, T Handa
Journal of Craniofacial Genetics and Developmental Biology
|
March 24, 2000
Pfeiffer syndrome caused by haploinsufficient mutation of FGFR2
M Tsukuno, H Suzuki, Y Eto
Bone
|
August 24, 1999
Local administration of activin promotes fracture healing in the rat fibula fracture model
R Sakai, K Miwa, Y Eto
Endocrine Journal
|
February 1, 1995
Expression of immunoreactive activin A in fetal rat pancreas
M Furukawa, Y Eto, I Kojima
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 17, 1978
Effects of macromolecular compounds on human leukocyte beta-galactosidase activity
K Kiguchi, Y Eto, K Aoki
Human Mutation
|
January 1, 1993
Molecular screening of Japanese patients with Gaucher disease: phenotypic variability in the same genotypes
H Kawame, K Maekawa, Y Eto
DNA and Cell Biology
|
July 1, 1993
Mutations in the arylsulfatase A gene of Japanese patients with metachromatic leukodystrophy
Y Hasegawa, H Kawame, Y Eto
Nihon Rinsho. Japanese Journal of Clinical Medicine
|
September 1, 1993
[Molecular analysis of Japanese patients with metachromatic leukodystrophy]
Y Hasegawa, H Kawame, Y Eto
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 1, 1977
Bile lysosomal enzymes: characteristics and pathological significance for various hepatobiliary disorders
S Toyoda, Y Eto, K Aoki
Acta Paediatrica Japonica : Overseas Edition
|
February 1, 1990
Biochemical pathogenesis of demyelination in globoid cell leukodystrophy (Krabbe's disease): the effects of psychosine upon oligodendroglial cell culture
H Ida, Y Eto, K Maekawa
Page
of 31