1. Greco E, Minasi MG and Fiorentino F. |
Healthy Babies after Intrauterine Transfer of Mosaic Aneuploid Blastocysts |
2. S. Bono, A. Biricik, L. Spizzichino, A. Nuccitelli, M.G. Minasi, E. Greco, F. Spinella, and F. Fiorentino |
Validation of a semiconductor next-generation sequencing (NGS)-based protocol for preimplantation genetic diagnosis of reciprocal translocations |
3. Fiorentino F., Bono S., Biricik A., Nuccitelli A., Cotroneo E., Cottone G., Kokocinski F., Michel C., Minasi M.G., Greco E. |
Application of next-generation sequencing technology for comprehensive aneuploidy screening of blastocysts in clinical preimplantation genetic screening cycles. |
4. Greco E, Bono S, Ruberti A, Lobascio AM, Greco P, Biricik A, Spizzichino L, Greco A, Tesarik J, Minasi MG, Fiorentino F |
Comparative genomic hybridization selection of blastocysts for repeated implantation failure treatment: a pilot study |
5. Fiorentino F., Biricik A., Bono S., Spizzichino L., Cotroneo E., Cottone G., Kokocinski F., Michel C |
Development and validation of a next-generation sequencing (NGS)-based protocol for 24-chromosome aneuploidy screening of embryos |
6. Fiorentino F., Spizzichino L., Bono S., Biricik A., Kokkali G., Rienzi L., Ubaldi F.M., Iammarrone E., Gordon A., Pantos K.. |
PGD for reciprocal and Robertsonian translocations using array comparative genomic hybridization |
7. Fiorentino F, Kokkali G, Biricik A, Stavrou D, Ismailoglu B, De Palma R, Arizzi L, Harton G, Sessa M, Pantos K. |
Polymerase chain reaction-based detection of chromosomal imbalances on embryos: the evolution of preimplantation genetic diagnosis for chromosomal translocations. |
8. 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. |
What next for preimplantation genetic screening (PGS)? A position statement from the ESHRE PGD Consortium steering committee. |
9. Fusco C, Frattini D, Farnetti E, Nicoli D, Casali B, Fiorentino F, Nuccitelli A, Giustina ED. |
Hereditary spastic paraplegia and axonal motor neuropathy caused by a novel SPG3A de novo mutation. |
10. Van de Velde H, De Rycke M, De Man C, De Hauwere K, Fiorentino F, Kahraman S, Pennings G, Verpoest W, Devroey P, Liebaers I. |
The experience of two European preimplantation genetic diagnosis centres on human leukocyte antigen typing. |
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