IRG / Selected Publications: 
Scientific Consultant Dr. Domenico Valerio 

​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 result 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 - fetal https://pubmed.ncbi.nlm.nih.gov/8999384

Minerva Ginecologica 1996; 48,9;365-369​

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​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

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​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

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​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 2008

1. First trimester combined screening in a low risk population

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

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Dissezione cito - molecolare di anomalie cromosomiche sbilanciate alla diagnosi prenatale: Valutazione prognostica dell'outcome fenotipico postnatale

 

1. 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​

2. 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

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