Search research articles
Contact Us
Filters
Showing results (241-250 of 276) with videos related to
Page
of 28
Sort By:
Scandinavian Journal of Immunology
|
July 1, 1992
Common variable immunodeficiency with increased surface IgM-positive double-bearing B cells
F Motoyoshi, S Mori, N Kondo, et al.
International Archives of Allergy and Immunology
|
January 1, 1994
Suppression of proliferative responses of lymphocytes to food antigens by an anti-allergic drug, ketotifen fumarate, in patients with food-sensitive atopic dermatitis
N Kondo, O Fukutomi, T Kameyama, et al.
Pediatric Research
|
September 27, 2000
Temperature-sensitive mutation of PEX6 in peroxisome biogenesis disorders in complementation group C (CG-C): comparative study of PEX6 and PEX1
A Imamura, N Shimozawa, Y Suzuki, et al.
Clinical Genetics
|
May 1, 1997
Two novel missense mutations in the ATP-binding domain of the adrenoleukodystrophy gene: immunoblotting and immunocytological study of two patients
A Imamura, Y Suzuki, X Q Song, et al.
Human Molecular Genetics
|
May 18, 2000
Biochemical and structural analysis of missense mutations in N-acetylgalactosamine-6-sulfate sulfatase causing mucopolysaccharidosis IVA phenotypes
K Sukegawa, H Nakamura, Z Kato, et al.
Biochemical and Biophysical Research Communications
|
February 15, 1993
Congenitally defective aldosterone biosynthesis in humans: inactivation of the P-450C18 gene (CYP11B2) due to nucleotide deletion in CMO I deficient patients
Y Mitsuuchi, T Kawamoto, K Miyahara, et al.
Epilepsia
|
February 1, 1997
Epilepsy in peroxisomal diseases
Y Takahashi, Y Suzuki, K Kumazaki, et al.
American Journal of Human Genetics
|
November 5, 1997
D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder
Y Suzuki, L L Jiang, M Souri, et al.
Bone Marrow Transplantation
|
May 30, 1998
Treatment of MPS VII (Sly disease) by allogeneic BMT in a female with homozygous A619V mutation
Y Yamada, K Kato, K Sukegawa, et al.
Current Pharmaceutical Biotechnology
|
April 22, 2011
Mucopolysaccharidosis type IVA (Morquio A disease): clinical review and current treatment
S Tomatsu, A M Montaño, H Oikawa, et al.
Page
of 28
Search research articles
Search
Showing results (241-250 of 276) with videos related to
Sort By:
Page
of 28
Scandinavian Journal of Immunology
|
July 1, 1992
Common variable immunodeficiency with increased surface IgM-positive double-bearing B cells
F Motoyoshi, S Mori, N Kondo, et al.
International Archives of Allergy and Immunology
|
January 1, 1994
Suppression of proliferative responses of lymphocytes to food antigens by an anti-allergic drug, ketotifen fumarate, in patients with food-sensitive atopic dermatitis
N Kondo, O Fukutomi, T Kameyama, et al.
Pediatric Research
|
September 27, 2000
Temperature-sensitive mutation of PEX6 in peroxisome biogenesis disorders in complementation group C (CG-C): comparative study of PEX6 and PEX1
A Imamura, N Shimozawa, Y Suzuki, et al.
Clinical Genetics
|
May 1, 1997
Two novel missense mutations in the ATP-binding domain of the adrenoleukodystrophy gene: immunoblotting and immunocytological study of two patients
A Imamura, Y Suzuki, X Q Song, et al.
Human Molecular Genetics
|
May 18, 2000
Biochemical and structural analysis of missense mutations in N-acetylgalactosamine-6-sulfate sulfatase causing mucopolysaccharidosis IVA phenotypes
K Sukegawa, H Nakamura, Z Kato, et al.
Biochemical and Biophysical Research Communications
|
February 15, 1993
Congenitally defective aldosterone biosynthesis in humans: inactivation of the P-450C18 gene (CYP11B2) due to nucleotide deletion in CMO I deficient patients
Y Mitsuuchi, T Kawamoto, K Miyahara, et al.
Epilepsia
|
February 1, 1997
Epilepsy in peroxisomal diseases
Y Takahashi, Y Suzuki, K Kumazaki, et al.
American Journal of Human Genetics
|
November 5, 1997
D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder
Y Suzuki, L L Jiang, M Souri, et al.
Bone Marrow Transplantation
|
May 30, 1998
Treatment of MPS VII (Sly disease) by allogeneic BMT in a female with homozygous A619V mutation
Y Yamada, K Kato, K Sukegawa, et al.
Current Pharmaceutical Biotechnology
|
April 22, 2011
Mucopolysaccharidosis type IVA (Morquio A disease): clinical review and current treatment
S Tomatsu, A M Montaño, H Oikawa, et al.
Page
of 28