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749 results
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Novel 7-DHCR mutation in a child with Smith-Lemli-Opitz syndrome.
Patrono C, Rizzo C, Tessa A, Giannotti A, Borrelli P, Carrozzo R, Piemonte F, Bertini E, Dionisi-Vici C, Santorelli FM. Patrono C, et al. Among authors: bertini e. Am J Med Genet. 2000 Mar 13;91(2):138-40. doi: 10.1002/(sici)1096-8628(20000313)91:2<138::aid-ajmg12>;2-q. Am J Med Genet. 2000. PMID: 10748414
Respiratory chain defects in hereditary spastic paraplegias.
Piemonte F, Casali C, Carrozzo R, Schägger H, Patrono C, Tessa A, Tozzi G, Cricchi F, Di Capua M, Siciliano G, Amabile GA, Morocutti C, Bertini E, Santorelli FM. Piemonte F, et al. Among authors: bertini e. Neuromuscul Disord. 2001 Sep;11(6-7):565-9. doi: 10.1016/s0960-8966(01)00214-0. Neuromuscul Disord. 2001. PMID: 11525886
Glutathione in blood of patients with Friedreich's ataxia.
Piemonte F, Pastore A, Tozzi G, Tagliacozzi D, Santorelli FM, Carrozzo R, Casali C, Damiano M, Federici G, Bertini E. Piemonte F, et al. Among authors: bertini e. Eur J Clin Invest. 2001 Nov;31(11):1007-11. doi: 10.1046/j.1365-2362.2001.00922.x. Eur J Clin Invest. 2001. PMID: 11737244
Antioxidant enzymes in blood of patients with Friedreich's ataxia.
Tozzi G, Nuccetelli M, Lo Bello M, Bernardini S, Bellincampi L, Ballerini S, Gaeta LM, Casali C, Pastore A, Federici G, Bertini E, Piemonte F. Tozzi G, et al. Among authors: bertini e. Arch Dis Child. 2002 May;86(5):376-9. doi: 10.1136/adc.86.5.376. Arch Dis Child. 2002. PMID: 11970939 Free PMC article.
Mutation analysis in 16 patients with mtDNA depletion.
Carrozzo R, Bornstein B, Lucioli S, Campos Y, de la Pena P, Petit N, Dionisi-Vici C, Vilarinho L, Rizza T, Bertini E, Garesse R, Santorelli FM, Arenas J. Carrozzo R, et al. Among authors: bertini e. Hum Mutat. 2003 Apr;21(4):453-4. doi: 10.1002/humu.9135. Hum Mutat. 2003. PMID: 12655576
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