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Clinical Genetics
|
November 18, 2003
Peroxisome proliferator-activated receptor gamma C161T polymorphisms and survival of Japanese patients with immunoglobulin A nephropathy
J Song, M Sakatsume, I Narita, et al.
Internal Medicine (Tokyo, Japan)
|
October 3, 2001
Association of gene polymorphism of polymeric immunoglobulin receptor and IgA nephropathy
I Narita, D Kondo, S Goto, et al.
Scandinavian Journal of Rheumatology
|
February 6, 2010
Cystatin C is a sensitive marker for detecting a reduced glomerular filtration rate when assessing chronic kidney disease in patients with rheumatoid arthritis and secondary amyloidosis
H Sato, T Kuroda, N Tanabe, et al.
Annals of Clinical Biochemistry
|
November 1, 1995
A new enzymatic method for the determination of inulin
O Sugita, Y Tomiyama, T Matsuto, et al.
Clinical Chemistry
|
January 1, 1990
Glycosaminoglycans of the hemodialysis-associated carpal synovial amyloid and of amyloid-rich tissues and fibrils of heart, liver, and spleen
H Ohishi, M Skinner, N Sato-Araki, et al.
The Journal of Biological Chemistry
|
February 5, 1986
The complete amino acid sequence of the A-chain of human plasma alpha 2HS-glycoprotein
Y Yoshioka, F Gejyo, T Marti, et al.
Clinical Nephrology
|
December 3, 2003
Development of hungry bone syndrome after rapid lowering of PTH with intravenous maxacalcitol therapy in a patient with non-uremic secondary hyperparathyroidism
J J Kazama, K Suzuki, A Yokoseki, et al.
Clinical Nephrology
|
July 29, 2005
Maxacalcitol therapy decreases circulating osteoprotegerin levels in dialysis patients with secondary hyperparathyroidism
J J Kazama, K Omori, N Takahashi, et al.
Artificial Organs
|
December 1, 1995
Long-term clinical evaluation of an adsorbent column (BM-01) of direct hemoperfusion type for beta 2-microglobulin on the treatment of dialysis-related amyloidosis
F Gejyo, T Teramura, I Ei, et al.
Gene
|
August 15, 2000
Characterization and chromosomal mapping of a novel human gene, ANKHZN
H Kuriyama, S Asakawa, S Minoshima, et al.
Page
of 25
Search research articles
Search
Showing results (181-190 of 243) with videos related to
Sort By:
Page
of 25
Clinical Genetics
|
November 18, 2003
Peroxisome proliferator-activated receptor gamma C161T polymorphisms and survival of Japanese patients with immunoglobulin A nephropathy
J Song, M Sakatsume, I Narita, et al.
Internal Medicine (Tokyo, Japan)
|
October 3, 2001
Association of gene polymorphism of polymeric immunoglobulin receptor and IgA nephropathy
I Narita, D Kondo, S Goto, et al.
Scandinavian Journal of Rheumatology
|
February 6, 2010
Cystatin C is a sensitive marker for detecting a reduced glomerular filtration rate when assessing chronic kidney disease in patients with rheumatoid arthritis and secondary amyloidosis
H Sato, T Kuroda, N Tanabe, et al.
Annals of Clinical Biochemistry
|
November 1, 1995
A new enzymatic method for the determination of inulin
O Sugita, Y Tomiyama, T Matsuto, et al.
Clinical Chemistry
|
January 1, 1990
Glycosaminoglycans of the hemodialysis-associated carpal synovial amyloid and of amyloid-rich tissues and fibrils of heart, liver, and spleen
H Ohishi, M Skinner, N Sato-Araki, et al.
The Journal of Biological Chemistry
|
February 5, 1986
The complete amino acid sequence of the A-chain of human plasma alpha 2HS-glycoprotein
Y Yoshioka, F Gejyo, T Marti, et al.
Clinical Nephrology
|
December 3, 2003
Development of hungry bone syndrome after rapid lowering of PTH with intravenous maxacalcitol therapy in a patient with non-uremic secondary hyperparathyroidism
J J Kazama, K Suzuki, A Yokoseki, et al.
Clinical Nephrology
|
July 29, 2005
Maxacalcitol therapy decreases circulating osteoprotegerin levels in dialysis patients with secondary hyperparathyroidism
J J Kazama, K Omori, N Takahashi, et al.
Artificial Organs
|
December 1, 1995
Long-term clinical evaluation of an adsorbent column (BM-01) of direct hemoperfusion type for beta 2-microglobulin on the treatment of dialysis-related amyloidosis
F Gejyo, T Teramura, I Ei, et al.
Gene
|
August 15, 2000
Characterization and chromosomal mapping of a novel human gene, ANKHZN
H Kuriyama, S Asakawa, S Minoshima, et al.
Page
of 25