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Page 1
Visual function in infants with West syndrome: correlation with EEG patterns.
Randò T, Bancale A, Baranello G, Bini M, De Belvis AG, Epifanio R, Frisone MF, Guzzetta A, La Torre G, Ricci D, Signorini S, Tinelli F, Biagioni E, Veggiotti P, Mercuri E, Fazzi E, Cioni G, Guzzetta F. Randò T, et al. Among authors: fazzi e. Epilepsia. 2004 Jul;45(7):781-6. doi: 10.1111/j.0013-9580.2004.41403.x. Epilepsia. 2004. PMID: 15230702 Free article.
Ring chromosome 9: an atypical case.
Lanzi G, Fazzi E, Veggiotti P, Pagliano E, Gariglio M, Bonaglia C, Landolfo S. Lanzi G, et al. Among authors: fazzi e. Brain Dev. 1996 May-Jun;18(3):216-9. doi: 10.1016/0387-7604(95)00144-1. Brain Dev. 1996. PMID: 8836504
Leber's congenital amaurosis: an update.
Fazzi E, Signorini SG, Scelsa B, Bova SM, Lanzi G. Fazzi E, et al. Eur J Paediatr Neurol. 2003;7(1):13-22. doi: 10.1016/s1090-3798(02)00135-6. Eur J Paediatr Neurol. 2003. PMID: 12615170 Review.
Auditory attention at the onset of West syndrome: correlation with EEG patterns and visual function.
Baranello G, Randò T, Bancale A, D'Acunto MG, Epifanio R, Frisone MF, Guzzetta A, La Torre G, Mannocci A, Ricci D, Signorini S, Tinelli F, Biagioni E, Veggiotti P, Fazzi E, Mercuri E, Cioni G, Guzzetta F. Baranello G, et al. Among authors: fazzi e. Brain Dev. 2006 Jun;28(5):293-9. doi: 10.1016/j.braindev.2005.10.004. Epub 2006 Feb 14. Brain Dev. 2006. PMID: 16481138
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders.
Brancati F, Barrano G, Silhavy JL, Marsh SE, Travaglini L, Bielas SL, Amorini M, Zablocka D, Kayserili H, Al-Gazali L, Bertini E, Boltshauser E, D'Hooghe M, Fazzi E, Fenerci EY, Hennekam RC, Kiss A, Lees MM, Marco E, Phadke SR, Rigoli L, Romano S, Salpietro CD, Sherr EH, Signorini S, Stromme P, Stuart B, Sztriha L, Viskochil DH, Yuksel A, Dallapiccola B; International JSRD Study Group; Valente EM, Gleeson JG. Brancati F, et al. Among authors: fazzi e. Am J Hum Genet. 2007 Jul;81(1):104-13. doi: 10.1086/519026. Epub 2007 May 18. Am J Hum Genet. 2007. PMID: 17564967 Free PMC article.
260 results