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Journal of Investigational Allergology & Clinical Immunology
|
March 1, 1995
IgE production by B-cells stimulated with interleukin-4 and Epstein-Barr virus in patients with elevated serum IgE levels
Lorenzo PR 1st, N Kuwabara, N Kondo, et al.
The Tohoku Journal of Experimental Medicine
|
April 1, 1974
Hyperglycopeptiduria in genetic mucolipidoses
T Orii, Chiba, R Minami, et al.
Cell Structure and Function
|
April 1, 1992
Optimization of electroporation for transfection of human fibroblast cell lines with origin-defective SV40 DNA: development of human transformed fibroblast cell lines with mucopolysaccharidoses (I-VII)
H Okamoto, K Sukegawa, S Tomatsu, et al.
No to Hattatsu = Brain and Development
|
November 1, 1988
[Peroxisomal disorders--clinical and biochemical studies]
N Shimozawa, Y Suzuki, S Yamaguchi, et al.
Acta Paediatrica Scandinavica
|
September 1, 1987
An unusually mild variant of Hunter's syndrome in a 14-year-old boy. Normal growth and development
S Tsuzaki, N Matsuo, T Nagai, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
May 1, 1982
[A case of mucopolysaccharidosis III A (Sanfilippo) with retinal changes]
T Tabira, I Goto, T Kurokawa, et al.
European Journal of Pediatrics
|
March 1, 1997
Use of buccal smears for rapid detection of peroxisomes
Y Suzuki, Z Zhang, N Shimozawa, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics
|
June 1, 1995
Methylation patterns of I epsilon region in B cells stimulated with interleukin 4 and Epstein-Barr virus in patients with a high level of serum IgE
N Kuwabara, N Kondo, O Fukutomi, et al.
The Tohoku Journal of Experimental Medicine
|
October 1, 1976
Clinical and biochemical studies on periodic hyperammonemia with hyperlysinemia and homocitrullinuria
K Oyanagi, H Sogawa, S Sato, et al.
Journal of Inherited Metabolic Disease
|
July 10, 2009
Retinitis pigmentosa and mucopolysaccharidosis type II: an extremely attenuated phenotype
Y Suzuki, A Aoyama, T Kato, et al.
Page
of 40
Search research articles
Search
Showing results (91-100 of 397) with videos related to
Sort By:
Page
of 40
Journal of Investigational Allergology & Clinical Immunology
|
March 1, 1995
IgE production by B-cells stimulated with interleukin-4 and Epstein-Barr virus in patients with elevated serum IgE levels
Lorenzo PR 1st, N Kuwabara, N Kondo, et al.
The Tohoku Journal of Experimental Medicine
|
April 1, 1974
Hyperglycopeptiduria in genetic mucolipidoses
T Orii, Chiba, R Minami, et al.
Cell Structure and Function
|
April 1, 1992
Optimization of electroporation for transfection of human fibroblast cell lines with origin-defective SV40 DNA: development of human transformed fibroblast cell lines with mucopolysaccharidoses (I-VII)
H Okamoto, K Sukegawa, S Tomatsu, et al.
No to Hattatsu = Brain and Development
|
November 1, 1988
[Peroxisomal disorders--clinical and biochemical studies]
N Shimozawa, Y Suzuki, S Yamaguchi, et al.
Acta Paediatrica Scandinavica
|
September 1, 1987
An unusually mild variant of Hunter's syndrome in a 14-year-old boy. Normal growth and development
S Tsuzaki, N Matsuo, T Nagai, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
May 1, 1982
[A case of mucopolysaccharidosis III A (Sanfilippo) with retinal changes]
T Tabira, I Goto, T Kurokawa, et al.
European Journal of Pediatrics
|
March 1, 1997
Use of buccal smears for rapid detection of peroxisomes
Y Suzuki, Z Zhang, N Shimozawa, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics
|
June 1, 1995
Methylation patterns of I epsilon region in B cells stimulated with interleukin 4 and Epstein-Barr virus in patients with a high level of serum IgE
N Kuwabara, N Kondo, O Fukutomi, et al.
The Tohoku Journal of Experimental Medicine
|
October 1, 1976
Clinical and biochemical studies on periodic hyperammonemia with hyperlysinemia and homocitrullinuria
K Oyanagi, H Sogawa, S Sato, et al.
Journal of Inherited Metabolic Disease
|
July 10, 2009
Retinitis pigmentosa and mucopolysaccharidosis type II: an extremely attenuated phenotype
Y Suzuki, A Aoyama, T Kato, et al.
Page
of 40