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I Koni

Showing results (11-20 of 52) with videos related to

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Clinical Nephrology|September 2, 1998
Clinical characteristics of polycystic kidney disease with end-stage renal disease. The Kanazawa Renal Disease Study GroupT Konoshita, K Okamoto, I Koni, et al.
Nihon Jinzo Gakkai Shi|September 1, 1991
Urine anion gap in patients with chronic renal insufficiencyY Tofuku, I Koni, R Takeda, et al.
Clinical and Experimental Immunology|June 11, 1999
Elevated serum levels of soluble membrane cofactor protein (CD46, MCP) in patients with systemic lupus erythematosus (SLE)M Kawano, T Seya, I Koni, et al.
American Journal of Nephrology|September 8, 1998
Effect of L-carnitine and palmitoyl-L-carnitine on erythroid colony formation in fetal mouse liver cell cultureM Matsumura, S Hatakeyama, I Koni, et al.
Diabetes Care|January 1, 1995
Increased plasma levels of immunoreactive endothelin and von Willebrand factor in NIDDM patientsT Morise, Y Takeuchi, M Kawano, et al.
Nephron|January 1, 1996
Correlation between serum carnitine levels and erythrocyte osmotic fragility in hemodialysis patientsM Matsumura, S Hatakeyama, I Koni, et al.
The Journal of Rheumatology|October 24, 2001
Clinical and laboratory features of anticentromere antibody positive primary Sjögren's syndromeK Katano, M Kawano, I Koni, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 27, 1999
Significance of serum pepsinogens and their relationship to Helicobacter pylori infection and histological gastritis in dialysis patientsH Araki, R Miyazaki, T Matsuda, et al.
Lancet (London, England)|February 19, 1994
Angiotensin-converting enzyme gene polymorphism in haemodialysis patientsH Nomura, I Koni, Y Michishita, et al.
Clinical Nephrology|April 24, 2001
A missense mutation, A156T, in the alpha-galactosidase A gene causes typical Fabry diseaseT Konoshita, H Mutoh, T Yokoi, et al.
Pageof 6

Showing results (11-20 of 52) with videos related to

Sort By:
Pageof 6
Clinical Nephrology|September 2, 1998
Clinical characteristics of polycystic kidney disease with end-stage renal disease. The Kanazawa Renal Disease Study GroupT Konoshita, K Okamoto, I Koni, et al.
Nihon Jinzo Gakkai Shi|September 1, 1991
Urine anion gap in patients with chronic renal insufficiencyY Tofuku, I Koni, R Takeda, et al.
Clinical and Experimental Immunology|June 11, 1999
Elevated serum levels of soluble membrane cofactor protein (CD46, MCP) in patients with systemic lupus erythematosus (SLE)M Kawano, T Seya, I Koni, et al.
American Journal of Nephrology|September 8, 1998
Effect of L-carnitine and palmitoyl-L-carnitine on erythroid colony formation in fetal mouse liver cell cultureM Matsumura, S Hatakeyama, I Koni, et al.
Diabetes Care|January 1, 1995
Increased plasma levels of immunoreactive endothelin and von Willebrand factor in NIDDM patientsT Morise, Y Takeuchi, M Kawano, et al.
Nephron|January 1, 1996
Correlation between serum carnitine levels and erythrocyte osmotic fragility in hemodialysis patientsM Matsumura, S Hatakeyama, I Koni, et al.
The Journal of Rheumatology|October 24, 2001
Clinical and laboratory features of anticentromere antibody positive primary Sjögren's syndromeK Katano, M Kawano, I Koni, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 27, 1999
Significance of serum pepsinogens and their relationship to Helicobacter pylori infection and histological gastritis in dialysis patientsH Araki, R Miyazaki, T Matsuda, et al.
Lancet (London, England)|February 19, 1994
Angiotensin-converting enzyme gene polymorphism in haemodialysis patientsH Nomura, I Koni, Y Michishita, et al.
Clinical Nephrology|April 24, 2001
A missense mutation, A156T, in the alpha-galactosidase A gene causes typical Fabry diseaseT Konoshita, H Mutoh, T Yokoi, et al.
Pageof 6