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22. Renal handling of lysozyme in experimental Fanconi syndrome. Fujita T, Itakura M. J Lab Clin Med; 1978 Jul; 92(1):135-40. PubMed ID: 149177 [Abstract] [Full Text] [Related]
23. HARTNUP DISEASE: A GENETIC MODIFICATION OF INTESTINAL AND RENAL TRANSPORT OF CERTAIN NEUTRAL ALPHA-AMINO ACIDS. SCRIVER CR. N Engl J Med; 1965 Sep 02; 273():530-2. PubMed ID: 14324515 [No Abstract] [Full Text] [Related]
24. [Aminoaciduria and ocular pathology]. Ardouin M, Urvoy M, Turquois JP, Chaneac M. Bull Soc Ophtalmol Fr; 1980 Sep 02; 80(4-5):409-12. PubMed ID: 7460175 [No Abstract] [Full Text] [Related]
25. Amino acid metabolism and its disorders. Scriver CR, Rosenberg LE. Major Probl Clin Pediatr; 1973 Sep 02; 10():1-478. PubMed ID: 4768607 [No Abstract] [Full Text] [Related]
26. Idiopathic de Toni-Debré-Fanconi syndrome with absence of proximal tubular brush border. Manz F, Waldherr R, Fritz HP, Lutz P, Nützenadel W, Reitter B, Schärer K, Schmidt H, Trefz F. Clin Nephrol; 1984 Sep 02; 22(3):149-57. PubMed ID: 6488596 [Abstract] [Full Text] [Related]
27. [Physiological and pathological aminoacidurias]. Brodehl J. Monatsschr Kinderheilkd (1902); 1973 May 02; 121(5):190-200. PubMed ID: 4713389 [No Abstract] [Full Text] [Related]
29. The prognosis and management of renal tubular disorders. Milne MD. Proc R Soc Med; 1967 Nov 01; 60(11 Part 1):1149-52. PubMed ID: 6060714 [No Abstract] [Full Text] [Related]
31. Disorders of intestinal transport of amino acids. Thier SO, Alpers DH. Am J Dis Child; 1969 Jan 01; 117(1):13-23. PubMed ID: 4883974 [No Abstract] [Full Text] [Related]
32. Genetics of renal transport disorders. Segal S. Prog Clin Biol Res; 1989 Jan 01; 305():101-9. PubMed ID: 2668967 [No Abstract] [Full Text] [Related]
33. [Genetic bases of metabolic tubular nephropathies]. Savi M. Minerva Med; 1979 Oct 13; 70(44):3001-13. PubMed ID: 386171 [No Abstract] [Full Text] [Related]
34. The genetics of heteromeric amino acid transporters. Palacín M, Nunes V, Font-Llitjós M, Jiménez-Vidal M, Fort J, Gasol E, Pineda M, Feliubadaló L, Chillarón J, Zorzano A. Physiology (Bethesda); 2005 Apr 13; 20():112-24. PubMed ID: 15772300 [Abstract] [Full Text] [Related]
35. Membrane permeability as a cause of transport defects in experimental Fanconi syndrome. A new hypothesis. Bergeron M, Dubord L, Hausser C, Schwab C. J Clin Invest; 1976 May 13; 57(5):1181-9. PubMed ID: 1262464 [Abstract] [Full Text] [Related]
36. Dibasic amino acid transport: lessons from human disease. Thier SO. Trans Am Clin Climatol Assoc; 1984 May 13; 95():132-6. PubMed ID: 6433526 [No Abstract] [Full Text] [Related]
37. [Amino acid transfer systems and their importance in pathology. II. Specific abnormalities in renal and intestinal amino acid transfer]. Boisse J, Moatti N. Ann Biol Clin (Paris); 1973 May 13; 31(4):249-55. PubMed ID: 4579284 [No Abstract] [Full Text] [Related]
38. Effects of succinylacetone on the uptake of sugars and amino acids by brush border vesicles. Spencer PD, Medow MS, Moses LC, Roth KS. Kidney Int; 1988 Nov 13; 34(5):671-7. PubMed ID: 3199678 [Abstract] [Full Text] [Related]
39. [The hyperaminoacidurias with special reference to cystinuria]. Perfumo F, Basile G, Ginevri F, Gusmano R. Minerva Med; 1979 Oct 13; 70(44):3065-74. PubMed ID: 386173 [Abstract] [Full Text] [Related]
40. Tissue transport defects of dibasic amino acids. Segal S. Bibl Paediatr; 1968 Oct 13; 87():56-71. PubMed ID: 4888869 [No Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]