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.
133 related articles for article (PubMed ID: 15532707)
21. Severe epilepsy in X-linked creatine transporter defect (CRTR-D). Mancardi MM; Caruso U; Schiaffino MC; Baglietto MG; Rossi A; Battaglia FM; Salomons GS; Jakobs C; Zara F; Veneselli E; Gaggero R Epilepsia; 2007 Jun; 48(6):1211-3. PubMed ID: 17553121 [TBL] [Abstract][Full Text] [Related]
22. Incidence of brain creatine transporter deficiency in males with developmental delay referred for brain magnetic resonance imaging. Newmeyer A; Cecil KM; Schapiro M; Clark JF; Degrauw TJ J Dev Behav Pediatr; 2005 Aug; 26(4):276-82. PubMed ID: 16100500 [TBL] [Abstract][Full Text] [Related]
23. Variable White Matter Atrophy and Intellectual Development in a Family With X-linked Creatine Transporter Deficiency Despite Genotypic Homogeneity. Heussinger N; Saake M; Mennecke A; Dörr HG; Trollmann R Pediatr Neurol; 2017 Feb; 67():45-52. PubMed ID: 28065824 [TBL] [Abstract][Full Text] [Related]
24. Deletion of the creatine transporter gene in neonatal, but not adult, mice leads to cognitive deficits. Udobi KC; Delcimmuto N; Kokenge AN; Abdulla ZI; Perna MK; Skelton MR J Inherit Metab Dis; 2019 Sep; 42(5):966-974. PubMed ID: 31209903 [TBL] [Abstract][Full Text] [Related]
25. Creatine transporter deficiency leads to increased whole body and cellular metabolism. Perna MK; Kokenge AN; Miles KN; Udobi KC; Clark JF; Pyne-Geithman GJ; Khuchua Z; Skelton MR Amino Acids; 2016 Aug; 48(8):2057-65. PubMed ID: 27401086 [TBL] [Abstract][Full Text] [Related]
27. Intradialytic creatine supplementation: A scientific rationale for improving the health and quality of life of dialysis patients. Wallimann T; Riek U; Möddel M Med Hypotheses; 2017 Feb; 99():1-14. PubMed ID: 28110688 [TBL] [Abstract][Full Text] [Related]
28. Treatment of X-linked creatine transporter (SLC6A8) deficiency: systematic review of the literature and three new cases. Dunbar M; Jaggumantri S; Sargent M; Stockler-Ipsiroglu S; van Karnebeek CD Mol Genet Metab; 2014 Aug; 112(4):259-74. PubMed ID: 24953403 [TBL] [Abstract][Full Text] [Related]
29. 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]
30. Acute and moderate-term creatine monohydrate supplementation does not affect creatine transporter mRNA or protein content in either young or elderly humans. Tarnopolsky M; Parise G; Fu MH; Brose A; Parshad A; Speer O; Wallimann T Mol Cell Biochem; 2003 Feb; 244(1-2):159-66. PubMed ID: 12701826 [TBL] [Abstract][Full Text] [Related]
31. Oxidative phosphorylation in creatine transporter deficiency. Li S; Bianconi S; van der Veen JW; Dang Do A; Stolinski J; Cecil KM; Hannah-Shmouni F; Porter FD; Shen J NMR Biomed; 2021 Jan; 34(1):e4419. PubMed ID: 32990357 [TBL] [Abstract][Full Text] [Related]
32. [Cerebral creatine transporter deficiency: an infradiagnosed neurometabolic disease]. Campistol J; Arias-Dimas A; Poo P; Pineda M; Hoffman M; Vilaseca MA; Artuch R; Ribes A Rev Neurol; 2007 Mar 16-31; 44(6):343-7. PubMed ID: 17385170 [TBL] [Abstract][Full Text] [Related]
33. Myocellular creatine and creatine transporter serine phosphorylation after starvation. Zhao CR; Shang L; Wang W; Jacobs DO J Surg Res; 2002 Jun; 105(1):10-6. PubMed ID: 12069495 [TBL] [Abstract][Full Text] [Related]
34. Response to creatine analogs in fibroblasts and patients with creatine transporter deficiency. Fons C; Arias A; Sempere A; Póo P; Pineda M; Mas A; López-Sala A; Garcia-Villoria J; Vilaseca MA; Ozaez L; Lluch M; Artuch R; Campistol J; Ribes A Mol Genet Metab; 2010 Mar; 99(3):296-9. PubMed ID: 19955008 [TBL] [Abstract][Full Text] [Related]
35. A mouse model for creatine transporter deficiency reveals early onset cognitive impairment and neuropathology associated with brain aging. Baroncelli L; Molinaro A; Cacciante F; Alessandrì MG; Napoli D; Putignano E; Tola J; Leuzzi V; Cioni G; Pizzorusso T Hum Mol Genet; 2016 Oct; 25(19):4186-4200. PubMed ID: 27466184 [TBL] [Abstract][Full Text] [Related]
36. Inborn errors of creatine metabolism and epilepsy: clinical features, diagnosis, and treatment. Leuzzi V J Child Neurol; 2002 Dec; 17 Suppl 3():3S89-97; discussion 3S97. PubMed ID: 12597058 [TBL] [Abstract][Full Text] [Related]
37. Cardiac manifestations in a child with a novel mutation in creatine transporter gene SLC6A8. Anselm IA; Coulter DL; Darras BT Neurology; 2008 Apr; 70(18):1642-4. PubMed ID: 18443316 [No Abstract] [Full Text] [Related]