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Barth syndrome.
Clarke SL, Bowron A, Gonzalez IL, Groves SJ, Newbury-Ecob R, Clayton N, Martin RP, Tsai-Goodman B, Garratt V, Ashworth M, Bowen VM, McCurdy KR, Damin MK, Spencer CT, Toth MJ, Kelley RI, Steward CG. Clarke SL, et al. Among authors: gonzalez il. Orphanet J Rare Dis. 2013 Feb 12;8:23. doi: 10.1186/1750-1172-8-23. Orphanet J Rare Dis. 2013. PMID: 23398819 Free PMC article. Review.
Barth syndrome: an X-linked cause of fetal cardiomyopathy and stillbirth.
Steward CG, Newbury-Ecob RA, Hastings R, Smithson SF, Tsai-Goodman B, Quarrell OW, Kulik W, Wanders R, Pennock M, Williams M, Cresswell JL, Gonzalez IL, Brennan P. Steward CG, et al. Among authors: gonzalez il. Prenat Diagn. 2010 Oct;30(10):970-6. doi: 10.1002/pd.2599. Prenat Diagn. 2010. PMID: 20812380 Free PMC article.
Cardiac and clinical phenotype in Barth syndrome.
Spencer CT, Bryant RM, Day J, Gonzalez IL, Colan SD, Thompson WR, Berthy J, Redfearn SP, Byrne BJ. Spencer CT, et al. Among authors: gonzalez il. Pediatrics. 2006 Aug;118(2):e337-46. doi: 10.1542/peds.2005-2667. Epub 2006 Jul 17. Pediatrics. 2006. PMID: 16847078
Tafazzin splice variants and mutations in Barth syndrome.
Kirwin SM, Manolakos A, Barnett SS, Gonzalez IL. Kirwin SM, et al. Among authors: gonzalez il. Mol Genet Metab. 2014 Jan;111(1):26-32. doi: 10.1016/j.ymgme.2013.11.006. Epub 2013 Nov 19. Mol Genet Metab. 2014. PMID: 24342716
Barth's syndrome-like disorder: a new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation).
De Kremer RD, Paschini-Capra A, Bacman S, Argaraña C, Civallero G, Kelley RI, Guelbert N, Latini A, Noher de Halac I, Giner-Ayala A, Johnston J, Proujansky R, Gonzalez I, Depetris-Boldini C, Oller-Ramírez A, Angaroni C, Theaux RA, Hliba E, Juaneda E. De Kremer RD, et al. Am J Med Genet. 2001 Mar 1;99(2):83-93. doi: 10.1002/1096-8628(2001)9999:9999<::aid-ajmg1136>3.0.co;2-x. Am J Med Genet. 2001. PMID: 11241464
Barth syndrome without 3-methylglutaconic aciduria.
Schmidt MR, Birkebaek N, Gonzalez I, Sunde L. Schmidt MR, et al. Acta Paediatr. 2004 Mar;93(3):419-21. doi: 10.1080/08035250410022837. Acta Paediatr. 2004. PMID: 15124852
Compositional Evolution of Individual CoNPs on Co/TiO2 during CO and Syngas Treatment Resolved through Soft XAS/X-PEEM.
Qiu C, Odarchenko Y, Meng Q, Dong H, Gonzalez IL, Panchal M, Olalde-Velasco P, Maccherozzi F, Zanetti-Domingues L, Martin-Fernandez ML, Beale AM. Qiu C, et al. Among authors: gonzalez il. ACS Catal. 2023 Nov 28;13(24):15956-15966. doi: 10.1021/acscatal.3c03214. eCollection 2023 Dec 15. ACS Catal. 2023. PMID: 38125980 Free PMC article.
47 results