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COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement.
Diomedi-Camassei F, Di Giandomenico S, Santorelli FM, Caridi G, Piemonte F, Montini G, Ghiggeri GM, Murer L, Barisoni L, Pastore A, Muda AO, Valente ML, Bertini E, Emma F. Diomedi-Camassei F, et al. Among authors: pastore a. J Am Soc Nephrol. 2007 Oct;18(10):2773-80. doi: 10.1681/ASN.2006080833. Epub 2007 Sep 12. J Am Soc Nephrol. 2007. PMID: 17855635
Modulation of CTNS gene expression by intracellular thiols.
Bellomo F, Corallini S, Pastore A, Palma A, Laurenzi C, Emma F, Taranta A. Bellomo F, et al. Among authors: pastore a. Free Radic Biol Med. 2010 Apr 1;48(7):865-72. doi: 10.1016/j.freeradbiomed.2010.01.011. Epub 2010 Jan 14. Free Radic Biol Med. 2010. PMID: 20079424
Pediatric reference intervals for muscle coenzyme Q(10).
Pastore A, Di Giovamberardino G, Petrillo S, Boenzi S, Bertini E, Dionisi-Vici C, Piemonte F. Pastore A, et al. Biomarkers. 2012 Dec;17(8):764-6. doi: 10.3109/1354750X.2012.727029. Epub 2012 Oct 1. Biomarkers. 2012. PMID: 23020092
Glutathione metabolism in cobalamin deficiency type C (cblC).
Pastore A, Martinelli D, Piemonte F, Tozzi G, Boenzi S, Di Giovamberardino G, Petrillo S, Bertini E, Dionisi-Vici C. Pastore A, et al. J Inherit Metab Dis. 2014 Jan;37(1):125-9. doi: 10.1007/s10545-013-9605-3. Epub 2013 Apr 9. J Inherit Metab Dis. 2014. PMID: 23568438
1,081 results