These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
234 related articles for article (PubMed ID: 1904694)
1. [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]
2. 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]
3. Therapeutic modulation of cerebral L-lysine metabolism in a mouse model for glutaric aciduria type I. Sauer SW; Opp S; Hoffmann GF; Koeller DM; Okun JG; Kölker S Brain; 2011 Jan; 134(Pt 1):157-70. PubMed ID: 20923787 [TBL] [Abstract][Full Text] [Related]
4. [Saccharopinuria (a variant form of familial hyperlysinemia)]. Higashino K Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):191-4. PubMed ID: 9590025 [No Abstract] [Full Text] [Related]
5. Excretion of hypusine by children and by patients with familial hyperlysinemia. Woody NC; Pupene MB Pediatr Res; 1973 Dec; 7(12):994-5. PubMed ID: 4753051 [No Abstract] [Full Text] [Related]
6. 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]
7. Enzyme studies in a patient with saccharopinuria: a defect of lysine metabolism. Fellows FC; Carson NA Pediatr Res; 1974 Jan; 8(1):42-9. PubMed ID: 4809305 [No Abstract] [Full Text] [Related]
8. 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]
12. A Korean girl with alpha-aminoadipic and alpha-ketoadipic aciduria accompanied with elevation of 2-hydroxyglutarate and glutarate. Lee JS; Yoon HR; Coe CJ J Inherit Metab Dis; 2001 Aug; 24(4):509-10. PubMed ID: 11596655 [No Abstract] [Full Text] [Related]