Bettina Bessieres

Paris, France

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 78 publications

Identification of a Novel De Novo HECW2 Gene Pathogenic Variant in a Fetus With Cardiac Abnormalities.

Identification of a Novel De Novo HECW2 Gene Pathogenic Variant in a Fetus With Cardiac Abnormalities.

Journal: Prenatal diagnosis

Published: May 12, 2026

Neonatal lupus and congenital heart block

Neonatal lupus and congenital heart block

Journal: La Revue de medecine interne

Published: April 08, 2026

Maternal-Fetal Letermovir Exposure In Vivo and Physiologically Based Pharmacokinetic Modeling: A Rationale for Congenital Cytomegalovirus Therapy.

Maternal-Fetal Letermovir Exposure In Vivo and Physiologically Based Pharmacokinetic Modeling: A Rationale for Congenital Cytomegalovirus Therapy.

Journal: The Journal of infectious diseases

Published: August 15, 2025

Maternal-Fetal Letermovir Exposure in Vivo and PBPK-based: A Rationale for Congenital CMV Therapy.

Maternal-Fetal Letermovir Exposure in Vivo and PBPK-based: A Rationale for Congenital CMV Therapy.

Journal: The Journal of infectious diseases

Published: August 15, 2025

Early prediction of congenital cytomegalovirus infection and symptoms after maternal primary infection: an in vivo study using cytomegalovirus polymerase chain reaction in chorionic villi and in amniotic fluid.

Early prediction of congenital cytomegalovirus infection and symptoms after maternal primary infection: an in vivo study using cytomegalovirus polymerase chain reaction in chorionic villi and in amniotic fluid.

Journal: American journal of obstetrics and gynecology

Published: July 29, 2025

Dissecting the epigenetic regulation of the fetal hemoglobin genes to unravel a novel therapeutic approach for β-hemoglobinopathies.

Dissecting the epigenetic regulation of the fetal hemoglobin genes to unravel a novel therapeutic approach for β-hemoglobinopathies.

Journal: Nucleic acids research

Published: January 10, 2025

An exceptional anomaly of the coronary venous drainage: anatomic description.

An exceptional anomaly of the coronary venous drainage: anatomic description.

Journal: Cardiology in the young

Published: November 18, 2024

Histologic and molecular features shared between antibody-mediated rejection of kidney allografts and chronic histiocytic intervillositis support common pathogenesis.

Histologic and molecular features shared between antibody-mediated rejection of kidney allografts and chronic histiocytic intervillositis support common pathogenesis.

Journal: The Journal of pathology

Published: August 19, 2024

Foetal achondroplasia: Prenatal diagnosis, outcome and perspectives.

Foetal achondroplasia: Prenatal diagnosis, outcome and perspectives.

Journal: Journal of gynecology obstetrics and human reproduction

Published: July 16, 2024

COG6-related prenatal phenotype (CDG2L): Clinico-pathological report and review of the literature.

COG6-related prenatal phenotype (CDG2L): Clinico-pathological report and review of the literature.

Journal: Molecular genetics & genomic medicine

Published: January 03, 2024

Morphological and genetic causes of fetal cardiomyopathies.

Morphological and genetic causes of fetal cardiomyopathies.

Journal: Clinical genetics

Published: February 14, 2023

Two novel variations p.(Ser1275Thr) and p.(Ser1275Arg) in FLT4 causing prenatal hereditary lymphedema type 1.

Two novel variations p.(Ser1275Thr) and p.(Ser1275Arg) in FLT4 causing prenatal hereditary lymphedema type 1.

Journal: Birth defects research

Published: November 22, 2022

Showing 1-12 of 78

Last Updated: 09/26/2026