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3. [Cystine-lysine-ornithine-argininuria. Current genetic and clinico-therapeutic problems]. Berio A Minerva Pediatr; 1979 Oct; 31(20):1443-52. PubMed ID: 537610 [No Abstract] [Full Text] [Related]
4. Hyperdibasicaminoaciduria and hyperammonemia in familial protein intolerance. Kato T; Tanaka E; Horisawa S Am J Dis Child; 1976 Dec; 130(12):1340-4. PubMed ID: 998577 [TBL] [Abstract][Full Text] [Related]
5. Cystinuria phenotyping by oral lysine and arginine loading. de Sanctis L; Bonetti G; Bruno M; De Luca F; Bisceglia L; Palacin M; Dianzani I; Ponzone A Clin Nephrol; 2001 Dec; 56(6):467-74. PubMed ID: 11770798 [TBL] [Abstract][Full Text] [Related]
6. Lysinuric protein intolerance. Simell O; Perheentupa J; Rapola J; Visakorpi JK; Eskelin LE Am J Med; 1975 Aug; 59(2):229-40. PubMed ID: 1155480 [TBL] [Abstract][Full Text] [Related]
7. Congenital lysinuria: a new inherited transport disorder of dibasic amino acids. Oyanagi K; Miura R; Yamanouchi T J Pediatr; 1970 Aug; 77(2):259-66. PubMed ID: 5431208 [No Abstract] [Full Text] [Related]
8. Prolonged coma and isoelectric electroencephalogram in a child with lysinuric protein intolerance. Chan H; Billmeier GJ; Molinary SV; Tucker HN; Shin BC; Schaffer A; Cavallo K J Pediatr; 1977 Jul; 91(1):79-81. PubMed ID: 874670 [No Abstract] [Full Text] [Related]
10. Lysine transport in human kidney. Atanasova E Acta Med Iugosl; 1990; 44(2):163-75. PubMed ID: 2112825 [TBL] [Abstract][Full Text] [Related]
11. Hyperdibasicaminoaciduria in a mentally retarded homozygote with a peculiar response to phenothiazines. Kihara H; Valente M; Porter MT; Fluharty AL Pediatrics; 1973 Feb; 51(2):223-9. PubMed ID: 4144453 [No Abstract] [Full Text] [Related]
12. Defective metabolic clearance of plasma arginine and ornithine in lysinuric protein intolerance. Simell O; Perheentupa J Metabolism; 1974 Aug; 23(8):691-701. PubMed ID: 4851276 [No Abstract] [Full Text] [Related]
13. Tissue transport defects of dibasic amino acids. Segal S Bibl Paediatr; 1968; 87():56-71. PubMed ID: 4888869 [No Abstract] [Full Text] [Related]
14. Hyperammonemia in lysinuric protein intolerance. Kato T; Mizutani N; Ban M Pediatrics; 1984 Apr; 73(4):489-92. PubMed ID: 6424086 [TBL] [Abstract][Full Text] [Related]
15. Protein intolerance with deficient transport of basic aminoacids. Another inborn error of metabolism. Perheentupa J; Visakorpi JK Lancet; 1965 Oct; 2(7417):813-6. PubMed ID: 4158034 [No Abstract] [Full Text] [Related]
16. Lysine malabsorption syndrome: a new type of transport defect. Omura K; Yamanaka N; Higami S; Matsuoka O; Fujimoto A Pediatrics; 1976 Jan; 57(1):102-5. PubMed ID: 1246485 [TBL] [Abstract][Full Text] [Related]
17. Haemophagocytosis by myeloid precursors in lysinuric protein intolerance. Gordon WC; Gibson B; Leach MT; Robinson P Br J Haematol; 2007 Jul; 138(1):1. PubMed ID: 17474972 [No Abstract] [Full Text] [Related]
18. A defect in intestinal amino acid transport in Lowe's syndrome. Bartsocas CS; Levy HL; Crawford JD; Thier SO Am J Dis Child; 1969 Jan; 117(1):93-5. PubMed ID: 5782535 [No Abstract] [Full Text] [Related]
19. Clinical and biochemical studies on periodic hyperammonemia with hyperlysinemia and homocitrullinuria. Oyanagi K; Sogawa H; Sato S; Orii T; Nakao T Tohoku J Exp Med; 1976 Oct; 120(2):105-12. PubMed ID: 982431 [TBL] [Abstract][Full Text] [Related]
20. A new transport interaction of dibasic amino acids and citrulline in human kidney. Oyanagi K; Sogawa H; Minami R; Nakao T; Karube K; Tsugawa S Tohoku J Exp Med; 1981 May; 134(1):55-8. PubMed ID: 6797099 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]