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.
284 related articles for article (PubMed ID: 23843353)
1. Barth syndrome. Jefferies JL Am J Med Genet C Semin Med Genet; 2013 Aug; 163C(3):198-205. PubMed ID: 23843353 [TBL] [Abstract][Full Text] [Related]
2. Intrafamilial variability for novel TAZ gene mutation: Barth syndrome with dilated cardiomyopathy and heart failure in an infant and left ventricular noncompaction in his great-uncle. Ronvelia D; Greenwood J; Platt J; Hakim S; Zaragoza MV Mol Genet Metab; 2012 Nov; 107(3):428-32. PubMed ID: 23031367 [TBL] [Abstract][Full Text] [Related]
6. A Barth Syndrome Patient-Derived Snider PL; Sierra Potchanant EA; Sun Z; Edwards DM; Chan KK; Matias C; Awata J; Sheth A; Pride PM; Payne RM; Rubart M; Brault JJ; Chin MT; Nalepa G; Conway SJ Int J Mol Sci; 2024 Jul; 25(15):. PubMed ID: 39125771 [TBL] [Abstract][Full Text] [Related]
7. Barth syndrome-related cardiomyopathy is associated with a reduction in myocardial glucose oxidation. Greenwell AA; Gopal K; Altamimi TR; Saed CT; Wang F; Tabatabaei Dakhili SA; Ho KL; Zhang L; Eaton F; Kruger J; Al Batran R; Lopaschuk GD; Oudit GY; Ussher JR Am J Physiol Heart Circ Physiol; 2021 Jun; 320(6):H2255-H2269. PubMed ID: 33929899 [TBL] [Abstract][Full Text] [Related]
8. Identification of TAZ mutations in pediatric patients with cardiomyopathy by targeted next-generation sequencing in a Chinese cohort. Wang J; Guo Y; Huang M; Zhang Z; Zhu J; Liu T; Shi L; Li F; Huang H; Fu L Orphanet J Rare Dis; 2017 Feb; 12(1):26. PubMed ID: 28183324 [TBL] [Abstract][Full Text] [Related]
9. Cardiolipin Remodeling Defects Impair Mitochondrial Architecture and Function in a Murine Model of Barth Syndrome Cardiomyopathy. Zhu S; Chen Z; Zhu M; Shen Y; Leon LJ; Chi L; Spinozzi S; Tan C; Gu Y; Nguyen A; Zhou Y; Feng W; Vaz FM; Wang X; Gustafsson AB; Evans SM; Kunfu O; Fang X Circ Heart Fail; 2021 Jun; 14(6):e008289. PubMed ID: 34129362 [TBL] [Abstract][Full Text] [Related]
10. Advances in the understanding of Barth syndrome. Aprikyan AA; Khuchua Z Br J Haematol; 2013 May; 161(3):330-8. PubMed ID: 23432031 [TBL] [Abstract][Full Text] [Related]
12. Targeted overexpression of catalase to mitochondria does not prevent cardioskeletal myopathy in Barth syndrome. Johnson JM; Ferrara PJ; Verkerke ARP; Coleman CB; Wentzler EJ; Neufer PD; Kew KA; de Castro BrĂ¡s LE; Funai K J Mol Cell Cardiol; 2018 Aug; 121():94-102. PubMed ID: 30008435 [TBL] [Abstract][Full Text] [Related]
13. Increased mtDNA Abundance and Improved Function in Human Barth Syndrome Patient Fibroblasts Following AAV- Suzuki-Hatano S; Sriramvenugopal M; Ramanathan M; Soustek M; Byrne BJ; Cade WT; Kang PB; Pacak CA Int J Mol Sci; 2019 Jul; 20(14):. PubMed ID: 31336787 [TBL] [Abstract][Full Text] [Related]
14. Phospholipid abnormalities in children with Barth syndrome. Schlame M; Kelley RI; Feigenbaum A; Towbin JA; Heerdt PM; Schieble T; Wanders RJ; DiMauro S; Blanck TJ J Am Coll Cardiol; 2003 Dec; 42(11):1994-9. PubMed ID: 14662265 [TBL] [Abstract][Full Text] [Related]
15. A case of infantile Barth syndrome with severe heart failure: Importance of splicing variants in the TAZ gene. Takeda A; Ueki M; Abe J; Maeta K; Horiguchi T; Yamazawa H; Izumi G; Chida-Nagai A; Sasaki D; Tsujioka T; Sato I; Shiraishi M; Matsuo M Mol Genet Genomic Med; 2023 Jul; 11(7):e2190. PubMed ID: 37186429 [TBL] [Abstract][Full Text] [Related]