Elenco Pubblicazioni Scientifiche I.R.G
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  • Maternal serum screening and triploidy

     https://pubmed.ncbi.nlm.nih.gov/7521965

Prenatal Diagnosis 1994,14

  • Culture of fetal erythroid progenitor cells from maternal blood for non invasive prenatal diagnosis

​https://pubmed.ncbi.nlm.nih.gov/8994241

Prenatal Diagnosis 1996;16;1073-1082

  • Maternal serum screening of fetal chromosomal abnormalities by AFP, UE3, HCG and free BHCG:

Prospective and retrospective results

https://pubmed.ncbi.nlm.nih.gov/8783867

Minerva Ginecologica 1996; 48,5;169-173

  • Caratterizzazione citogenetica di cromosomi markers individuati all'amniocentesi:

Implicazioni per correlazioni cario tipo - fetale

https://pubmed.ncbi.nlm.nih.gov/8999384

Minerva Ginecologica 1996; 48,9;365-369

  • Isolation of fetal erythroid cells from maternal blood based on expression of erythropoietin receptors

      https://pubmed.ncbi.nlm.nih.gov/9239731

Molecular Human Reproduction ;1997. 3,451-455

  • Characterization of fetal hematopoietic progenitors circulating in maternal blood of seven aneuploid pregnancies

https://pubmed.ncbi.nlm.nih.gov/9467814

Prenatal Diagnosis 1997;.17;1159-1169

                                                                              

  • Detection of fetal trisomy 18 by short term culture of maternal peripheral blood

https://pubmed.ncbi.nlm.nih.gov/10920335             

Am J. Obstet Gynecol 2000;183:222-225

  • Prenatal diagnosis of congenital diseases:

5 years experience of Prenatal Diagnosis Center at the "Second University of Naples" 

Gazzetta Medica Italiana Arch Sci Med 2004;163;249-256

  • Prenatal diagnosis of partial trisomy 6q: a case report

​https://pubmed.ncbi.nlm.nih.gov/16845680

Prenatal Diagnosis 2006; 26;917-919

Abstract 7 th International Congress of Fetal Medicine Foundation at Sorrento Conference 2008

  1. First trimester combined screening in a low risk population

  2. Prenatal detection of partial fetal chromosomal deletionsby first trimester combined screening

Dissezione cito - molecolare di anomalie cromosomiche sbilanciate alla diagnosi prenatale: 

Valutazione prognostica dell'outcome fenotipico postnatale

  • Cohesin SA1 and SA2 proteins and NAD + deacetylase protein modulate telomere homeostasis in cumulus cells and are eligible biomarkers of oocyte ontogeny and ovarian ageing​

  • Gene expression and apoptosis in cumulus cells of patients with polymorphisms of FSHR and LHB undergoing in vitro fertilization program

https://pubmed.ncbi.nlm.nih.gov/29481647

Paper in collaboration submitted for publication in a peer review journal, 2017