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Nephron
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June 27, 2000
L-Carnitine supplementation in a hemodialysis patient with a mutation in the mitochondrial tRNA(Leu(UUR)) gene
M Matsumura, A Nakashima, T Araki, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
March 13, 1999
Fatal cardiac beta2-microglobulin amyloidosis in patients on long-term hemodialysis
M Kawano, H Muramoto, M Yamada, et al.
Clinical Nephrology
|
December 6, 2000
Nephrotic syndrome due to focal glomerulosclerosis and undifferentiated carcinoma
T Konoshita, M Itoh, S Hatakeyama, et al.
Molecular & General Genetics : MGG
|
June 25, 1995
Mutations causing high basal level transcription that is independent of transcriptional activators but dependent on chromosomal position in Saccharomyces cerevisiae
S Harashima, T Mizuno, H Mabuchi, et al.
Japanese Journal of Medicine
|
January 1, 1991
A study of the clinical significance of lipoprotein (a) in nephrotic syndrome
T Takegoshi, C Kitoh, T Haba, et al.
Metabolism: Clinical and Experimental
|
February 1, 1989
A young type III hyperlipoproteinemic patient associated with apolipoprotein E deficiency
H Mabuchi, H Itoh, M Takeda, et al.
Human Genetics
|
March 1, 1993
Rapid detection and prevalence of cholesteryl ester transfer protein deficiency caused by an intron 14 splicing defect in hyperalphalipoproteinemia
A Inazu, J Koizumi, T Haraki, et al.
Atherosclerosis
|
November 1, 1987
A new low density lipoprotein apheresis system using two dextran sulfate cellulose columns in an automated column regenerating unit (LDL continuous apheresis)
H Mabuchi, I Michishita, M Takeda, et al.
Japanese Circulation Journal
|
September 18, 1997
Quantitative evaluation of the rate of myocardial interstitial fibrosis using a personal computer
M Kitamura, M Shimizu, Y Kita, et al.
Hepato-Gastroenterology
|
May 6, 1999
Effectiveness of paraaortic lymph node dissection for advanced gastric cancer
H Isozaki, K Okajima, K Fujii, et al.
Page
of 30
Search research articles
Search
Showing results (191-200 of 293) with videos related to
Sort By:
Page
of 30
Nephron
|
June 27, 2000
L-Carnitine supplementation in a hemodialysis patient with a mutation in the mitochondrial tRNA(Leu(UUR)) gene
M Matsumura, A Nakashima, T Araki, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
March 13, 1999
Fatal cardiac beta2-microglobulin amyloidosis in patients on long-term hemodialysis
M Kawano, H Muramoto, M Yamada, et al.
Clinical Nephrology
|
December 6, 2000
Nephrotic syndrome due to focal glomerulosclerosis and undifferentiated carcinoma
T Konoshita, M Itoh, S Hatakeyama, et al.
Molecular & General Genetics : MGG
|
June 25, 1995
Mutations causing high basal level transcription that is independent of transcriptional activators but dependent on chromosomal position in Saccharomyces cerevisiae
S Harashima, T Mizuno, H Mabuchi, et al.
Japanese Journal of Medicine
|
January 1, 1991
A study of the clinical significance of lipoprotein (a) in nephrotic syndrome
T Takegoshi, C Kitoh, T Haba, et al.
Metabolism: Clinical and Experimental
|
February 1, 1989
A young type III hyperlipoproteinemic patient associated with apolipoprotein E deficiency
H Mabuchi, H Itoh, M Takeda, et al.
Human Genetics
|
March 1, 1993
Rapid detection and prevalence of cholesteryl ester transfer protein deficiency caused by an intron 14 splicing defect in hyperalphalipoproteinemia
A Inazu, J Koizumi, T Haraki, et al.
Atherosclerosis
|
November 1, 1987
A new low density lipoprotein apheresis system using two dextran sulfate cellulose columns in an automated column regenerating unit (LDL continuous apheresis)
H Mabuchi, I Michishita, M Takeda, et al.
Japanese Circulation Journal
|
September 18, 1997
Quantitative evaluation of the rate of myocardial interstitial fibrosis using a personal computer
M Kitamura, M Shimizu, Y Kita, et al.
Hepato-Gastroenterology
|
May 6, 1999
Effectiveness of paraaortic lymph node dissection for advanced gastric cancer
H Isozaki, K Okajima, K Fujii, et al.
Page
of 30