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K Sukegawa

Showing results (11-20 of 101) with videos related to

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Pediatrics|November 1, 1977
Hurler's syndromes without alpha-L-iduronidase deficiencyT Orii, K Sukegawa, R Minami, et al.
Ryoikibetsu Shokogun Shirizu|June 30, 1998
[Mucopolysaccharidosis type II (Hunter syndrome)]K Sukegawa, S Tomatsu, N Kondo, et al.
Human Genetics|January 1, 1990
Non-existence of a tight association between a 444leucine to proline mutation and phenotypes of Gaucher disease: high frequency of a NciI polymorphism in the non-neuronopathic formM Masuno, S Tomatsu, K Sukegawa, et al.
Kaibogaku Zasshi. Journal of Anatomy|April 1, 1978
[A quantitative study on the left-right asymmetry in the area consisting of the posterior part of the superior temporal gyrus, the angular gyrus and the supramarginal gyrus (author's transl)]T Yamadori, M Ohnishi, K Sukegawa, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications|September 24, 1999
Application of delayed extraction matrix-assisted laser desorption ionization time-of-flight mass spectrometry for analysis of sphingolipids in tissues from sphingolipidosis patientsT Fujiwaki, S Yamaguchi, K Sukegawa, et al.
Nihon Rinsho. Japanese Journal of Clinical Medicine|December 1, 1995
[Mucopolysaccharidoses]S Fukuda, K Sukegawa, S Tomatsu, et al.
Acta Paediatrica Japonica : Overseas Edition|April 1, 1989
Restriction fragment length polymorphism analysis in healthy Japanese individuals and Japanese families with Gaucher diseaseM Masuno, T Orii, K Sukegawa, et al.
Journal of Biochemistry|December 1, 1991
N-acetylgalactosamine-6-sulfate sulfatase in human placenta: purification and characteristicsM Masue, K Sukegawa, T Orii, et al.
Ryoikibetsu Shokogun Shirizu|June 30, 1998
[Mucopolysaccharidosis type I (Hurler syndrome, Scheie syndrome)]K Sukegawa, S Tomatsu, N Kondo, et al.
Ryoikibetsu Shokogun Shirizu|June 30, 1998
[Mucopolysaccharidosis type III (Sanfilippo syndrome)]K Sukegawa, S Tomatsu, N Kondo, et al.
Pageof 11

Showing results (11-20 of 101) with videos related to

Sort By:
Pageof 11
Pediatrics|November 1, 1977
Hurler's syndromes without alpha-L-iduronidase deficiencyT Orii, K Sukegawa, R Minami, et al.
Ryoikibetsu Shokogun Shirizu|June 30, 1998
[Mucopolysaccharidosis type II (Hunter syndrome)]K Sukegawa, S Tomatsu, N Kondo, et al.
Human Genetics|January 1, 1990
Non-existence of a tight association between a 444leucine to proline mutation and phenotypes of Gaucher disease: high frequency of a NciI polymorphism in the non-neuronopathic formM Masuno, S Tomatsu, K Sukegawa, et al.
Kaibogaku Zasshi. Journal of Anatomy|April 1, 1978
[A quantitative study on the left-right asymmetry in the area consisting of the posterior part of the superior temporal gyrus, the angular gyrus and the supramarginal gyrus (author's transl)]T Yamadori, M Ohnishi, K Sukegawa, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications|September 24, 1999
Application of delayed extraction matrix-assisted laser desorption ionization time-of-flight mass spectrometry for analysis of sphingolipids in tissues from sphingolipidosis patientsT Fujiwaki, S Yamaguchi, K Sukegawa, et al.
Nihon Rinsho. Japanese Journal of Clinical Medicine|December 1, 1995
[Mucopolysaccharidoses]S Fukuda, K Sukegawa, S Tomatsu, et al.
Acta Paediatrica Japonica : Overseas Edition|April 1, 1989
Restriction fragment length polymorphism analysis in healthy Japanese individuals and Japanese families with Gaucher diseaseM Masuno, T Orii, K Sukegawa, et al.
Journal of Biochemistry|December 1, 1991
N-acetylgalactosamine-6-sulfate sulfatase in human placenta: purification and characteristicsM Masue, K Sukegawa, T Orii, et al.
Ryoikibetsu Shokogun Shirizu|June 30, 1998
[Mucopolysaccharidosis type I (Hurler syndrome, Scheie syndrome)]K Sukegawa, S Tomatsu, N Kondo, et al.
Ryoikibetsu Shokogun Shirizu|June 30, 1998
[Mucopolysaccharidosis type III (Sanfilippo syndrome)]K Sukegawa, S Tomatsu, N Kondo, et al.
Pageof 11