Connection
Scott Cramer to Hyperoxaluria, Primary
This is a "connection" page, showing publications Scott Cramer has written about Hyperoxaluria, Primary.
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Takayama T, Nagata M, Ozono S, Nonomura K, Cramer SD. A novel mutation in the GRHPR gene in a Japanese patient with primary hyperoxaluria type 2. Nephrol Dial Transplant. 2007 Aug; 22(8):2371-4.
Score: 0.289
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Knight J, Holmes RP, Milliner DS, Monico CG, Cramer SD. Glyoxylate reductase activity in blood mononuclear cells and the diagnosis of primary hyperoxaluria type 2. Nephrol Dial Transplant. 2006 Aug; 21(8):2292-5.
Score: 0.267
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Webster KE, Ferree PM, Holmes RP, Cramer SD. Identification of missense, nonsense, and deletion mutations in the GRHPR gene in patients with primary hyperoxaluria type II (PH2). Hum Genet. 2000 Aug; 107(2):176-85.
Score: 0.180
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Webster KE, Cramer SD. Genetic basis of primary hyperoxaluria type II. Mol Urol. 2000; 4(4):355-64.
Score: 0.173
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Levin-Iaina N, Dinour D, Romero L, Ron R, Brady RL, Cramer SD, Holtzman EJ. Late diagnosis of primary hyperoxaluria type 2 in the adult: effect of a novel mutation in GRHPR gene on enzymatic activity and molecular modeling. J Urol. 2009 May; 181(5):2146-51.
Score: 0.082