Bilaketaren emaitzak

Renal clearances of amino acids in normal adults and in patients with aminoaciduria nork D. C. Cusworth, C. E. Dent

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The Fanconi syndrome and mechanisms of tubular transport dysfunction nork Karl S. Roth, John W. Foreman, Stanton Segal

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Effects of non-metabolizable analogs on the distribution of amino acids in the rat nork Halvor N. Christensen, Andrea M. Cullen

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Fanconi's Syndrome in HIV+ Adults: Report of Three Cases and Literature Review nork Karen Earle, Tara Seneviratne, Joseph Shaker, Dolores Shoback

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Hyperdibasicaminoaciduria: An Inherited Disorder of Amino Acid Transport[34] nork Donald T. Whelan, Charles R. Scriver

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Fanconi Syndrome Accompanied by Renal Function Decline with Tenofovir Disoproxil Fumarate: A Prospective, Case-Control Study of Predictors and Resolution in HIV-Infected Patients nork Samir K. Gupta, Albert M. Anderson, Ramin Ebrahimi, Todd Fralich, Hiba Graham, Valeska Scharen-Guivel, John F. Flaherty, Claude Fortin, Robert C. Kalayjian, Anita Rachlis, Christina Wyatt

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INVESTIGATION OF THE AMINOACIDURIA IN WILSON'S DISEASE (HEPATOLENTICULAR DEGENERATION): DEMONSTRATION OF A DEFECT IN RENAL FUNCTION 1 nork Arnold M. Cooper, Richard D. Eckhardt, William W. Faloon, Charles S. Davidson

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Dipeptide Absorption in Cystinuria nork M.D. Hellier, David I. Perrett, C D Holdsworth

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Nephrolithiasis related to inborn metabolic diseases nork Pierre Cochat, Valérie Pichault, Justine Bacchetta, Laurence Dubourg, Jean-François Sabot, Christine Saban, Michel Daudon, A. Liutkus

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A novel missense mutation in SLC5A2 encoding SGLT2 underlies autosomal-recessive renal glucosuria and aminoaciduria nork Daniella Magen, E Sprecher, Israel Zelikovic, Karl Skorecki

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The<i>HNF4A</i>R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype nork Alexander Hamilton, Coralie Bingham, Timothy J. McDonald, Paul Cook, Richard Caswell, Michael N. Weedon, Richard A. Oram, Beverley M. Shields, Maggie Shepherd, Carol Inward, Julian Hamilton‐Shield, Jürgen Kohlhase, Sian Ellard, Andrew T. Hattersley

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Biochemical and genetic studies in cystinuria: observations on double heterozygotes of genotype I/II nork Claude Morin, Margaret Thompson, Sanford H. Jackson, Andrew Sass-Kortsāk

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Transport of Neutral and Dibasic Amino Acids by Human Leukocytes: Absence of Defect in Cystinuria* nork León E. Rosenberg, Sylvia J. Downing

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Cystinuria subtype and the risk of nephrolithiasis nork Paul Goodyer, Irfan Saadi, Patricia Ong, Gay Elkas, Rima Rozen

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Mouse Model for Lowe Syndrome/Dent Disease 2 Renal Tubulopathy nork Susan P. Bothwell, Emily Chan, Isa Bernardini, Yien–Ming Kuo, William A. Gahl, Robert L. Nussbaum

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Hyperparathyroidism as the Cause of Hyperaminoaciduia and Phosphaturia in Human Vitamin D Deficiency nork David R. Fraser, Sang Whay Kooh, C. R. Scriver

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Aminoaciduria, but normal thyroid hormone levels and signalling, in mice lacking the amino acid and thyroid hormone transporter <i>Slc7a8</i> nork Doreen Braun, Eva K. Wirth, Franziska Wohlgemuth, Nathalie Reix, Marc Klein, Annette Grüters, Josef Köhrle, Ulrich Schweizer

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Abnormalities of Copper Metabolism in Wilson's Disease and Their Relationship to the Aminoaciduria nork Alexander G. Bearn, Henry G. Kunkel

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Plasma and muscle free carnitine deficiency due to renal Fanconi syndrome. nork Isa Bernardini, William B. Rizzo, Marinos C. Dalakas, Juan Bernar, William A. Gahl

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The Renal Clearance of Amino Acids in Cystinuria* nork J.C. Crawhall, E. F. Scowen, C. J. Thompson, R. W. E. Watts

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