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Pubblicazioni scientifiche

27/08/2012
Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 1000 consecutive clinical cases - Reply letter
Fiorentino F, Caiazzo F, Napolitano S, Spizzichino L, Bono S, Sessa M, Nuccitelli A, Biricik A, Gordon A, Rizzo G, Baldi M.

01/08/2012
Array comparative genomic hybridization: its role in preimplantation genetic diagnosis
Francesco Fiorentino Curr Opin Obstet Gynecol. 2012 Aug;24(4):203-9.

01/08/2012
Molecular Genetic Analysis of Single Cells
Francesco Fiorentino Semin Reprod Med. 2012 Aug;30(4):267-82.

03/05/2012
Re: Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011.
Fiorentino F, Baldi M. Ultrasound Obstet Gynecol. 2012 May;39(5):601-2.

31/12/2011
Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 1000 consecutive clinical cases.
Fiorentino F, Caiazzo F, Napolitano S, Spizzichino L, Bono S, Sessa M, Nuccitelli A, Biricik A, Gordon A, Rizzo G, Baldi M. Prenat Diagn. 2011 Dec;31(13):1270-82.

26/07/2011
PGD for reciprocal and Robertsonian translocations using array comparative genomic hybridization
Fiorentino F, Spizzichino L, Bono S, Biricik A, Kokkali G, Rienzi L, Ubaldi FM, Iammarrone E, Gordon A, Pantos K. Hum Reprod. 2011 Jul;26(7):1925-35.

03/01/2011
ESHRE PGD consortium best practice guidelines for amplification-based PGD.
Harton GL, De Rycke M, Fiorentino F, Moutou C, SenGupta S, Traeger-Synodinos J, Harper JC; European Society for Human Reproduction and Embryology (ESHRE) PGD Consortium. Hum Reprod. 2011 Jan;26(1):33-40.

11/11/2010
Polymerase chain reaction-based detection of chromosomal imbalances on embryos: the evolution of preimplantation genetic diagnosis for chromosomal translocations.
Fiorentino F, Kokkali G, Biricik A, Stavrou D, Ismailoglu B, De Palma R, Arizzi L, Harton G, Sessa M, Pantos K. Fertil Steril. 2010 Nov;94(6):2001-11,

01/08/2010
Hereditary spastic paraplegia and axonal motor neuropathy caused by a novel SPG3A de novo mutation.
Fusco C, Frattini D, Farnetti E, Nicoli D, Casali B, Fiorentino F, Nuccitelli A, Giustina ED. Brain Dev. 2010 Aug;32(7):592-4.

16/04/2010
What next for preimplantation genetic screening (PGS)? A position statement from the ESHRE PGD Consortium steering committee.
Harper J, Coonen E, De Rycke M, Fiorentino F, Geraedts J, Goossens V, Harton G, Moutou C, Pehlivan Budak T, Renwick P, Sengupta S, Traeger-Synodinos J, Vesela K. Hum Reprod. 2010 Apr;25(4):821-3.