Morgane Stichelbout

Lille, France

Last Updated: 09/26/2026

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Found 22 publications

Genome sequencing identifies RMND1 as a strong candidate gene for severe prenatal kidney failure mimicking renal tubular dysgenesis associated with hyporeninism.

Genome sequencing identifies RMND1 as a strong candidate gene for severe prenatal kidney failure mimicking renal tubular dysgenesis associated with hyporeninism.

Journal: Pediatric nephrology (Berlin, Germany)

Published: February 20, 2025

Caracteristics of women presenting with chronic histiocytic intervillositis during pregnancy: A case-control study.

Caracteristics of women presenting with chronic histiocytic intervillositis during pregnancy: A case-control study.

Journal: Journal of gynecology obstetrics and human reproduction

Published: August 05, 2024

Gnathodiaphyseal dysplasia: Diagnostic clues from two fetal cases and literature review.

Gnathodiaphyseal dysplasia: Diagnostic clues from two fetal cases and literature review.

Journal: Prenatal diagnosis

Published: February 05, 2024

Pseudoxanthoma elasticum, a difficult diagnostic in patient with dark skin.

Pseudoxanthoma elasticum, a difficult diagnostic in patient with dark skin.

Journal: Skin health and disease

Published: December 05, 2023

Pregnancy as a susceptible state for thrombotic microangiopathies.

Pregnancy as a susceptible state for thrombotic microangiopathies.

Journal: Frontiers in medicine

Published: November 22, 2023

The challenging follow-up of pregnancy in women with known thrombotic thrombocytopenic purpura: a single-center experience of a preemptive management protocol.

The challenging follow-up of pregnancy in women with known thrombotic thrombocytopenic purpura: a single-center experience of a preemptive management protocol.

Journal: Journal of nephrology

Published: March 13, 2023

Total alkaline phosphatase levels by gestational age in a large sample of pregnant women.

Total alkaline phosphatase levels by gestational age in a large sample of pregnant women.

Journal: Placenta

Published: May 24, 2022

Associations between fetal heart rate variability and umbilical cord occlusions-induced neural injury: An experimental study in a fetal sheep model.

Associations between fetal heart rate variability and umbilical cord occlusions-induced neural injury: An experimental study in a fetal sheep model.

Journal: Acta obstetricia et gynecologica Scandinavica

Published: December 02, 2021

COL4A1/COL4A2 and inherited platelet disorder gene variants in fetuses showing intracranial hemorrhage.

COL4A1/COL4A2 and inherited platelet disorder gene variants in fetuses showing intracranial hemorrhage.

Journal: Prenatal diagnosis

Published: November 22, 2021

The first two non-Finnish HYLS1 variants: Expanding the phenotypic spectrum of hydrolethalus syndrome.

The first two non-Finnish HYLS1 variants: Expanding the phenotypic spectrum of hydrolethalus syndrome.

Journal: Clinical genetics

Published: April 12, 2021

Confirmation of risk of cancer in blepharocheilodontic syndrome.

Confirmation of risk of cancer in blepharocheilodontic syndrome.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: May 11, 2020

Risk factors for spontaneous hematoma of the umbilical cord: A case-control study.

Risk factors for spontaneous hematoma of the umbilical cord: A case-control study.

Journal: Placenta

Published: April 17, 2020

Showing 1-12 of 22

Last Updated: 09/26/2026