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Acta Paediatrica Japonica : Overseas Edition
|
June 1, 1987
A case of congenital myopathy without specific features
N Tachi, S Hosoya, M Watanabe, et al.
The Journal of Pediatrics
|
February 1, 1979
The mechanism of hyperammonemia in congenital lysinuria
K Oyanagi, H Sogawa, R Minami, et al.
Brain & Development
|
January 1, 1982
A case of type 2 Gm1-gangliosidosis with long survival
K Kikuchi, R Minami, T Kudoh, et al.
Brain & Development
|
November 1, 1995
Preservation of central motor conduction in patients with spinal muscular atrophy type II
T Imai, M Matsuya, H Matsumoto, et al.
The Tohoku Journal of Experimental Medicine
|
October 1, 1976
Atypical Hurler syndrome without alpha-L-iduronidase deficiency
T Orii, K Sukegawa, R Minami, et al.
The Tohoku Journal of Experimental Medicine
|
March 1, 1983
Characterization of keratan sulfate isolated from liver affected by Morquio syndrome
R Minami, T Ikeno, C Igarashi, et al.
The Tohoku Journal of Experimental Medicine
|
December 1, 1974
Influence of fresh plasma infusions on patients with genetic mucopolysaccharidosis
T Orii, M Yamaguchi, R Minami, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
May 1, 1991
[Occipital horn syndrome (Ehlers-Danlos syndrome type IX) with severe psychomotor retardation and muscle atrophy--a first Japanese case]
S Wakai, Y Ishikawa, M Nagaoka, et al.
The Tohoku Journal of Experimental Medicine
|
August 1, 1977
alpha-L-Iduronidase activity in established lymphoblastoid cells from patients with Hurler and Scheie syndromes transformed by Epstein-Barr virus
R Minami, M Suzuki, T Kudoh, et al.
Journal of Pediatric Orthopedics
|
February 15, 2001
Correlation between progression of spinal deformity and pulmonary function in Duchenne muscular dystrophy
T Yamashita, K Kanaya, K Yokogushi, et al.
Page
of 19
Search research articles
Search
Showing results (61-70 of 184) with videos related to
Sort By:
Page
of 19
Acta Paediatrica Japonica : Overseas Edition
|
June 1, 1987
A case of congenital myopathy without specific features
N Tachi, S Hosoya, M Watanabe, et al.
The Journal of Pediatrics
|
February 1, 1979
The mechanism of hyperammonemia in congenital lysinuria
K Oyanagi, H Sogawa, R Minami, et al.
Brain & Development
|
January 1, 1982
A case of type 2 Gm1-gangliosidosis with long survival
K Kikuchi, R Minami, T Kudoh, et al.
Brain & Development
|
November 1, 1995
Preservation of central motor conduction in patients with spinal muscular atrophy type II
T Imai, M Matsuya, H Matsumoto, et al.
The Tohoku Journal of Experimental Medicine
|
October 1, 1976
Atypical Hurler syndrome without alpha-L-iduronidase deficiency
T Orii, K Sukegawa, R Minami, et al.
The Tohoku Journal of Experimental Medicine
|
March 1, 1983
Characterization of keratan sulfate isolated from liver affected by Morquio syndrome
R Minami, T Ikeno, C Igarashi, et al.
The Tohoku Journal of Experimental Medicine
|
December 1, 1974
Influence of fresh plasma infusions on patients with genetic mucopolysaccharidosis
T Orii, M Yamaguchi, R Minami, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
May 1, 1991
[Occipital horn syndrome (Ehlers-Danlos syndrome type IX) with severe psychomotor retardation and muscle atrophy--a first Japanese case]
S Wakai, Y Ishikawa, M Nagaoka, et al.
The Tohoku Journal of Experimental Medicine
|
August 1, 1977
alpha-L-Iduronidase activity in established lymphoblastoid cells from patients with Hurler and Scheie syndromes transformed by Epstein-Barr virus
R Minami, M Suzuki, T Kudoh, et al.
Journal of Pediatric Orthopedics
|
February 15, 2001
Correlation between progression of spinal deformity and pulmonary function in Duchenne muscular dystrophy
T Yamashita, K Kanaya, K Yokogushi, et al.
Page
of 19