Veronica Barbieri

Reggio Nell'emilia, Italy

Last Updated: 09/26/2026

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Found 12 publications

Hydranencephaly Secondary to Placental Fetal Vascular Malperfusion in a Pregnancy with Extensive Uterine Fibromatosis.

Hydranencephaly Secondary to Placental Fetal Vascular Malperfusion in a Pregnancy with Extensive Uterine Fibromatosis.

Journal: Fetal and pediatric pathology

Published: July 28, 2026

Bladder Exstrophy in a Female Fetus: Ultrasound and Autopsy Findings.

Bladder Exstrophy in a Female Fetus: Ultrasound and Autopsy Findings.

Journal: Fetal and pediatric pathology

Published: March 04, 2026

Renal Hypoplasia and Oligomeganephronia in a Fetus with Wolf-Hirschhorn Syndrome.

Renal Hypoplasia and Oligomeganephronia in a Fetus with Wolf-Hirschhorn Syndrome.

Journal: Diagnostics (Basel, Switzerland)

Published: September 12, 2025

Prenatal Array-CGH Detection of 3q26.32q26.33 Interstitial Deletion Encompassing the SOX2 Gene: Ultrasound, Pathological, and Cytogenetic Findings.

Prenatal Array-CGH Detection of 3q26.32q26.33 Interstitial Deletion Encompassing the SOX2 Gene: Ultrasound, Pathological, and Cytogenetic Findings.

Journal: Fetal and pediatric pathology

Published: September 25, 2023

Prenatal Detection of Vesico-Allantoic Cyst: Ultrasound and Autopsy Findings.

Prenatal Detection of Vesico-Allantoic Cyst: Ultrasound and Autopsy Findings.

Journal: Fetal and pediatric pathology

Published: November 12, 2022

Fetal Presentation of Mediastinal Immature Teratoma: Ultrasound, Autopsy and Cytogenetic Findings.

Fetal Presentation of Mediastinal Immature Teratoma: Ultrasound, Autopsy and Cytogenetic Findings.

Journal: Diagnostics (Basel, Switzerland)

Published: August 02, 2021

Whole Exome Sequencing Is the Minimal Technological Approach in Probands Born to Consanguineous Couples.

Whole Exome Sequencing Is the Minimal Technological Approach in Probands Born to Consanguineous Couples.

Journal: Genes

Published: May 24, 2021

Prenatal Diagnosis of Fetal Trisomy 5 Mosaicism with Congenital Pulmonary Airway Malformation Type 3: A Case Report.

Prenatal Diagnosis of Fetal Trisomy 5 Mosaicism with Congenital Pulmonary Airway Malformation Type 3: A Case Report.

Journal: Fetal and pediatric pathology

Published: January 07, 2021

Mosaic Trisomy 12: Prenatal Diagnosis at Amniocentesis and Molecular Genetic Analysis on Fetal Tissues.

Mosaic Trisomy 12: Prenatal Diagnosis at Amniocentesis and Molecular Genetic Analysis on Fetal Tissues.

Journal: Fetal and pediatric pathology

Published: July 02, 2020

Amniotic fluid stem cell exosomes: Therapeutic perspective.

Amniotic fluid stem cell exosomes: Therapeutic perspective.

Journal: BioFactors (Oxford, England)

Published: October 23, 2017

Development of a novel method for amniotic fluid stem cell storage.

Development of a novel method for amniotic fluid stem cell storage.

Journal: Cytotherapy

Published: March 07, 2017

Endocrinological Abnormalities Are a Main Feature of 17p13.1 Microduplication Syndrome: A New Case and Literature Review.

Endocrinological Abnormalities Are a Main Feature of 17p13.1 Microduplication Syndrome: A New Case and Literature Review.

Journal: Molecular syndromology

Published: August 23, 2016

Showing 1-12 of 12

Last Updated: 09/26/2026