Annunziata A. Epifania

Matera, 75100, Italy

Last Updated: 09/26/2026

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Found 13 publications

7q35q36.3 deletion and concomitant 20q13.2q13.33 duplication in a newborn: familiar case.

7q35q36.3 deletion and concomitant 20q13.2q13.33 duplication in a newborn: familiar case.

Journal: European review for medical and pharmacological sciences

Published: April 20, 2021

Mayer-Rokitansky-Küster-Hauser syndrome with 22q11.21 microduplication: a case report.

Mayer-Rokitansky-Küster-Hauser syndrome with 22q11.21 microduplication: a case report.

Journal: Journal of medical case reports

Published: October 14, 2020

Methylenetetrahydrofolate reductase gene C677T and A1298C polymorphisms and susceptibility to recurrent pregnancy loss.

Methylenetetrahydrofolate reductase gene C677T and A1298C polymorphisms and susceptibility to recurrent pregnancy loss.

Journal: Biomedical reports

Published: October 02, 2017

Prevention of neural tube defects and maternal gestational diabetes through the inositol supplementation: preliminary results.

Prevention of neural tube defects and maternal gestational diabetes through the inositol supplementation: preliminary results.

Journal: European review for medical and pharmacological sciences

Published: August 04, 2017

The influence of D-chiro-inositol and D-myo-inositol in pregnant women with glucose intolerance.

The influence of D-chiro-inositol and D-myo-inositol in pregnant women with glucose intolerance.

Journal: Biomedical reports

Published: April 24, 2017

Limitations of the biochemical research in the identification of the thalassemic trait carrier.

Limitations of the biochemical research in the identification of the thalassemic trait carrier.

Journal: Minerva ginecologica

Published: June 16, 2016

Analysis of cystic fibrosis gene mutations in children with cystic fibrosis and in 964 infertile couples within the region of Basilicata, Italy: a research study.

Analysis of cystic fibrosis gene mutations in children with cystic fibrosis and in 964 infertile couples within the region of Basilicata, Italy: a research study.

Journal: Journal of medical case reports

Published: April 02, 2014

Identification of patients with defects in the globin genes.

Identification of patients with defects in the globin genes.

Journal: Journal of prenatal medicine

Published: March 11, 2014

Effect of multivitamins on plasma homocysteine in patients with the 5,10 methylenetetrahydrofolate reductase C677T homozygous state.

Effect of multivitamins on plasma homocysteine in patients with the 5,10 methylenetetrahydrofolate reductase C677T homozygous state.

Journal: Molecular medicine reports

Published: February 24, 2013

Incidence of β-thalassemia carrier on 1495 couples in preconceptional period.

Incidence of β-thalassemia carrier on 1495 couples in preconceptional period.

Journal: The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians

Published: October 09, 2012

Clinical correlation between premature ovarian failure and a chromosomal anomaly in a 22-year-old Caucasian woman: a case report.

Clinical correlation between premature ovarian failure and a chromosomal anomaly in a 22-year-old Caucasian woman: a case report.

Journal: Journal of medical case reports

Published: June 05, 2012

Study of a family in the province of Matera presenting with glucose-6-phosphate dehydrogenase deficiency and Gilbert's syndrome.

Study of a family in the province of Matera presenting with glucose-6-phosphate dehydrogenase deficiency and Gilbert's syndrome.

Journal: Molecular medicine reports

Published: November 23, 2011

Showing 1-12 of 13

Last Updated: 09/26/2026