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6. alpha-Aminoadipic and alpha-ketoadipic aciduria: detection of a new case by a screening program using two-dimensional thin layer chromatography of amino acids. Vianey-Liaud C; Divry P; Cotte J; Teyssier G J Inherit Metab Dis; 1985; 8 Suppl 2():133-4. PubMed ID: 3930865 [No Abstract] [Full Text] [Related]
7. Biochemical and clinical studies of a new case of alpha-aminoadipic aciduria. Casey RE; Zaleski WA; Philp M; Mendelson IS; MacKenzie SL J Inherit Metab Dis; 1978; 1(4):129-35. PubMed ID: 117247 [TBL] [Abstract][Full Text] [Related]
8. Dicarboxylic aciduria: the response to fasting. Truscott RJ; Hick L; Pullin C; Halpern B; Wilcken B; Griffiths H; Silink M; Kilham H; Grunseit F Clin Chim Acta; 1979 May; 94(1):31-9. PubMed ID: 455718 [TBL] [Abstract][Full Text] [Related]
9. Genetic basis of alpha-aminoadipic and alpha-ketoadipic aciduria. Hagen J; te Brinke H; Wanders RJ; Knegt AC; Oussoren E; Hoogeboom AJ; Ruijter GJ; Becker D; Schwab KO; Franke I; Duran M; Waterham HR; Sass JO; Houten SM J Inherit Metab Dis; 2015 Sep; 38(5):873-9. PubMed ID: 25860818 [TBL] [Abstract][Full Text] [Related]
10. A patient with alpha-ketoadipic and alpha-aminoadipic aciduria. Duran M; Beemer FA; Wadman SK; Wendel U; Janssen B J Inherit Metab Dis; 1984; 7(2):61. PubMed ID: 6434826 [No Abstract] [Full Text] [Related]
11. Asymptomatic alpha-ketoadipic aciduria detected during a pilot study of neonatal urine screening. Peng H; Shinka T; Inoue Y; Mitsubuchi H; Ishimatsu J; Yoshino M; Kuhara T Acta Paediatr; 1999 Aug; 88(8):911-4. PubMed ID: 10503694 [No Abstract] [Full Text] [Related]
12. Ethylmalonic adipic aciduria--a treatable hepatomuscular disorder in two adult brothers. Elias E; Gray RG; Poulton K; Green A J Hepatol; 1997 Feb; 26(2):433-6. PubMed ID: 9059968 [TBL] [Abstract][Full Text] [Related]
14. Carnitine palmitoyltransferase 2 deficiency: the time-course of blood and urinary acylcarnitine levels during initial L-carnitine supplementation. Hori T; Fukao T; Kobayashi H; Teramoto T; Takayanagi M; Hasegawa Y; Yasuno T; Yamaguchi S; Kondo N Tohoku J Exp Med; 2010 Jul; 221(3):191-5. PubMed ID: 20543534 [TBL] [Abstract][Full Text] [Related]
15. C6-C10-dicarboxylic aciduria: investigations of a patient with riboflavin responsive multiple acyl-CoA dehydrogenation defects. Gregersen N; Wintzensen H; Christensen SK; Christensen MF; Brandt NJ; Rasmussen K Pediatr Res; 1982 Oct; 16(10):861-8. PubMed ID: 7145508 [TBL] [Abstract][Full Text] [Related]
16. Dihydrolipoamide dehydrogenase deficiency: a still overlooked cause of recurrent acute liver failure and Reye-like syndrome. Brassier A; Ottolenghi C; Boutron A; Bertrand AM; Valmary-Degano S; Cervoni JP; Chrétien D; Arnoux JB; Hubert L; Rabier D; Lacaille F; de Keyzer Y; Di Martino V; de Lonlay P Mol Genet Metab; 2013 May; 109(1):28-32. PubMed ID: 23478190 [TBL] [Abstract][Full Text] [Related]
17. Alpha-ketoadipic aciduria: a description of a new metabolic error in lysine-tryptophan degradation. Wilson RW; Wilson CM; Gates SC; Higgins JV Pediatr Res; 1975 Jun; 9(6):522-6. PubMed ID: 1161338 [TBL] [Abstract][Full Text] [Related]
18. [Inborn errors of lysine metabolism]. Divry P; Vianey-Liaud C; Mathieu M Ann Biol Clin (Paris); 1991; 49(1):27-35. PubMed ID: 1904694 [TBL] [Abstract][Full Text] [Related]
19. Reye syndrome: rate of oxidation of fatty acids in leukocytes and serum levels of lipid peroxides. Yoshida Y; Singh I; Singh AK; Tecklenberg FW; Brown FR; Darby CP J Exp Pathol; 1989; 4(3):133-9. PubMed ID: 2769452 [TBL] [Abstract][Full Text] [Related]