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.
365 related articles for article (PubMed ID: 15234333)
21. Creatine uptake in brain and skeletal muscle of mice lacking guanidinoacetate methyltransferase assessed by magnetic resonance spectroscopy. Kan HE; Meeuwissen E; van Asten JJ; Veltien A; Isbrandt D; Heerschap A J Appl Physiol (1985); 2007 Jun; 102(6):2121-7. PubMed ID: 17347380 [TBL] [Abstract][Full Text] [Related]
22. Creatine and creatine deficiency syndromes: biochemical and clinical aspects. Nasrallah F; Feki M; Kaabachi N Pediatr Neurol; 2010 Mar; 42(3):163-71. PubMed ID: 20159424 [TBL] [Abstract][Full Text] [Related]
23. Enzymes of creatine biosynthesis, arginine and methionine metabolism in normal and malignant cells. Bera S; Wallimann T; Ray S; Ray M FEBS J; 2008 Dec; 275(23):5899-909. PubMed ID: 19021765 [TBL] [Abstract][Full Text] [Related]
25. Guanidinoacetate and creatine plus creatinine assessment in physiologic fluids: an effective diagnostic tool for the biochemical diagnosis of arginine:glycine amidinotransferase and guanidinoacetate methyltransferase deficiencies. Carducci C; Birarelli M; Leuzzi V; Carducci C; Battini R; Cioni G; Antonozzi I Clin Chem; 2002 Oct; 48(10):1772-8. PubMed ID: 12324495 [TBL] [Abstract][Full Text] [Related]
26. Biochemical and behavioural phenotyping of a mouse model for GAMT deficiency. Torremans A; Marescau B; Possemiers I; Van Dam D; D'Hooge R; Isbrandt D; De Deyn PP J Neurol Sci; 2005 Apr; 231(1-2):49-55. PubMed ID: 15792821 [TBL] [Abstract][Full Text] [Related]
27. Creatine deficiency in the brain: a new, treatable inborn error of metabolism. Stöckler S; Holzbach U; Hanefeld F; Marquardt I; Helms G; Requart M; Hänicke W; Frahm J Pediatr Res; 1994 Sep; 36(3):409-13. PubMed ID: 7808840 [TBL] [Abstract][Full Text] [Related]
28. Two new severe mutations causing guanidinoacetate methyltransferase deficiency. Carducci C; Leuzzi V; Carducci C; Prudente S; Mercuri L; Antonozzi I Mol Genet Metab; 2000 Dec; 71(4):633-8. PubMed ID: 11136556 [TBL] [Abstract][Full Text] [Related]
29. High cerebral guanidinoacetate and variable creatine concentrations in argininosuccinate synthetase and lyase deficiency: implications for treatment? van Spronsen FJ; Reijngoud DJ; Verhoeven NM; Soorani-Lunsing RJ; Jakobs C; Sijens PE Mol Genet Metab; 2006 Nov; 89(3):274-6. PubMed ID: 16580861 [TBL] [Abstract][Full Text] [Related]
30. Diagnosis of creatine metabolism disorders by determining creatine and guanidinoacetate in plasma and urine. Sun Q; O'Brien WE Methods Mol Biol; 2010; 603():175-85. PubMed ID: 20077070 [TBL] [Abstract][Full Text] [Related]
31. Evidence-based treatment of guanidinoacetate methyltransferase (GAMT) deficiency. Viau KS; Ernst SL; Pasquali M; Botto LD; Hedlund G; Longo N Mol Genet Metab; 2013 Nov; 110(3):255-62. PubMed ID: 24071436 [TBL] [Abstract][Full Text] [Related]
37. Guanidinoacetate methyltransferase deficiency: new clinical features. Ganesan V; Johnson A; Connelly A; Eckhardt S; Surtees RA Pediatr Neurol; 1997 Sep; 17(2):155-7. PubMed ID: 9367297 [TBL] [Abstract][Full Text] [Related]
38. Case study for the evaluation of current treatment recommendations of guanidinoacetate methyltransferase deficiency: ineffectiveness of sodium benzoate. Mercimek-Mahmutoglu S; Salomons GS; Chan A Pediatr Neurol; 2014 Jul; 51(1):133-7. PubMed ID: 24766785 [TBL] [Abstract][Full Text] [Related]
40. A mutation on exon 6 of guanidinoacetate methyltransferase (GAMT) gene supports a different function for isoform a and b of GAMT enzyme. Leuzzi V; Carducci C; Carducci C; Matricardi M; Bianchi MC; Di Sabato ML; Artiola C; Antonozzi I Mol Genet Metab; 2006 Jan; 87(1):88-90. PubMed ID: 16293431 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]