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Diabetologia
|
August 22, 2002
Haptoglobin genotype and diabetic microangiopathies in Japanese diabetic patients
Y Koda, M Soejima, S Yamagishi, et al.
Genetics
|
June 19, 2001
Contrasting patterns of polymorphisms at the ABO-secretor gene (FUT2) and plasma alpha(1,3)fucosyltransferase gene (FUT6) in human populations
Y Koda, H Tachida, H Pang, et al.
Clinical Nephrology
|
December 21, 2006
Idiopathic retroperitoneal fibrosis associated with Hashimoto's thyroiditis: a long-term follow-up
T Sanai, M Hirakawa, M Yokoyama, et al.
Human Genetics
|
August 14, 1998
Five novel missense mutations of the Lewis gene (FUT3) in African (Xhosa) and Caucasian populations in South Africa
H Pang, Y Liu, Y Koda, et al.
Clinical Rheumatology
|
March 27, 2009
Selective expression of MHC class I in the affected muscle of a patient with idiopathic inflammatory myopathy
T Gono, Y Katsumata, Y Kawaguchi, et al.
Medical Hypotheses
|
March 5, 2003
Polymorphisms of sorbitol dehydrogenase (SDH) gene and susceptibility to diabetic retinopathy
S Amano, S Yamagishi, Y Koda, et al.
Nephron
|
January 1, 1989
Waldenström's macroglobulinemia associated with amyloidosis and crescentic glomerulonephritis
Y Ogami, M Takasugi, M Soejima, et al.
Nihon Jinzo Gakkai Shi
|
November 1, 1984
[Gentamicin pharmacokinetics during hemodialysis]
M Takasugi, O Hasegawa, M Soejima, et al.
Blood
|
February 9, 2000
Simple PCR detection of haptoglobin gene deletion in anhaptoglobinemic patients with antihaptoglobin antibody that causes anaphylactic transfusion reactions
Y Koda, Y Watanabe, M Soejima, et al.
Journal of Human Genetics
|
May 13, 1999
The fusion gene at the ABO-secretor locus (FUT2): absence in Chinese populations
Y H Liu, Y Koda, M Soejima, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 64) with videos related to
Sort By:
Page
of 7
Diabetologia
|
August 22, 2002
Haptoglobin genotype and diabetic microangiopathies in Japanese diabetic patients
Y Koda, M Soejima, S Yamagishi, et al.
Genetics
|
June 19, 2001
Contrasting patterns of polymorphisms at the ABO-secretor gene (FUT2) and plasma alpha(1,3)fucosyltransferase gene (FUT6) in human populations
Y Koda, H Tachida, H Pang, et al.
Clinical Nephrology
|
December 21, 2006
Idiopathic retroperitoneal fibrosis associated with Hashimoto's thyroiditis: a long-term follow-up
T Sanai, M Hirakawa, M Yokoyama, et al.
Human Genetics
|
August 14, 1998
Five novel missense mutations of the Lewis gene (FUT3) in African (Xhosa) and Caucasian populations in South Africa
H Pang, Y Liu, Y Koda, et al.
Clinical Rheumatology
|
March 27, 2009
Selective expression of MHC class I in the affected muscle of a patient with idiopathic inflammatory myopathy
T Gono, Y Katsumata, Y Kawaguchi, et al.
Medical Hypotheses
|
March 5, 2003
Polymorphisms of sorbitol dehydrogenase (SDH) gene and susceptibility to diabetic retinopathy
S Amano, S Yamagishi, Y Koda, et al.
Nephron
|
January 1, 1989
Waldenström's macroglobulinemia associated with amyloidosis and crescentic glomerulonephritis
Y Ogami, M Takasugi, M Soejima, et al.
Nihon Jinzo Gakkai Shi
|
November 1, 1984
[Gentamicin pharmacokinetics during hemodialysis]
M Takasugi, O Hasegawa, M Soejima, et al.
Blood
|
February 9, 2000
Simple PCR detection of haptoglobin gene deletion in anhaptoglobinemic patients with antihaptoglobin antibody that causes anaphylactic transfusion reactions
Y Koda, Y Watanabe, M Soejima, et al.
Journal of Human Genetics
|
May 13, 1999
The fusion gene at the ABO-secretor locus (FUT2): absence in Chinese populations
Y H Liu, Y Koda, M Soejima, et al.
Page
of 7