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Nephron
|
January 1, 1990
Progressive renal failure despite discontinuation of mefenamic acid
N Itami, Y Akutsu, K Yasoshima, et al.
Nephron
|
January 1, 1989
Glomerular deposition of C4 cleavage fragment (C4d) and C4-binding protein in idiopathic membranous glomerulonephritis
Y Kusunoki, N Itami, H Tochimaru, et al.
Clinical Nephrology
|
August 1, 1990
IgA nephritis in Behçet's disease: case report and review of the literature
Y Akutsu, N Itami, M Tanaka, et al.
Nephron
|
July 1, 1998
Gabexate mesilate plus intravenous gammaglobulin treatment in children with diarrhoea-associated haemolytic uraemic syndrome
Y Kusunoki, K Nobumoto, M Ohkawa, et al.
Endocrine Journal
|
February 12, 2000
A Japanese case with Frasier syndrome caused by the splice junction mutation of WT1 gene
K Okuhara, S Tajima, J Nakae, et al.
American Journal of Medical Genetics
|
June 24, 1998
4q33-qter deletion and absorptive hypercalciuria: report of two unrelated girls
K Imamura, H Tonoki, K Wakui, et al.
Biochemistry and Molecular Biology International
|
December 1, 1996
Identification and immunohistochemical localization of macrophage migration inhibitory factor in human kidney
K Imamura, J Nishihira, M Suzuki, et al.
Nephron
|
January 1, 1991
Urinary excretion of terminal complement complexes in glomerular disease
Y Kusunoki, Y Akutsu, N Itami, et al.
Pediatric Research
|
March 1, 1992
Inherited copper toxicity in Long-Evans cinnamon rats exhibiting spontaneous hepatitis: a model of Wilson's disease
T Okayasu, H Tochimaru, T Hyuga, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
Nephron
|
January 1, 1990
Progressive renal failure despite discontinuation of mefenamic acid
N Itami, Y Akutsu, K Yasoshima, et al.
Nephron
|
January 1, 1989
Glomerular deposition of C4 cleavage fragment (C4d) and C4-binding protein in idiopathic membranous glomerulonephritis
Y Kusunoki, N Itami, H Tochimaru, et al.
Clinical Nephrology
|
August 1, 1990
IgA nephritis in Behçet's disease: case report and review of the literature
Y Akutsu, N Itami, M Tanaka, et al.
Nephron
|
July 1, 1998
Gabexate mesilate plus intravenous gammaglobulin treatment in children with diarrhoea-associated haemolytic uraemic syndrome
Y Kusunoki, K Nobumoto, M Ohkawa, et al.
Endocrine Journal
|
February 12, 2000
A Japanese case with Frasier syndrome caused by the splice junction mutation of WT1 gene
K Okuhara, S Tajima, J Nakae, et al.
American Journal of Medical Genetics
|
June 24, 1998
4q33-qter deletion and absorptive hypercalciuria: report of two unrelated girls
K Imamura, H Tonoki, K Wakui, et al.
Biochemistry and Molecular Biology International
|
December 1, 1996
Identification and immunohistochemical localization of macrophage migration inhibitory factor in human kidney
K Imamura, J Nishihira, M Suzuki, et al.
Nephron
|
January 1, 1991
Urinary excretion of terminal complement complexes in glomerular disease
Y Kusunoki, Y Akutsu, N Itami, et al.
Pediatric Research
|
March 1, 1992
Inherited copper toxicity in Long-Evans cinnamon rats exhibiting spontaneous hepatitis: a model of Wilson's disease
T Okayasu, H Tochimaru, T Hyuga, et al.
Page
of 2