Fanny Pelluard-Nehme
Bordeaux, France
Last Updated: 09/26/2026
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Found 37 publications
Extensive Cystic lymphatic malformation with PIK3CA-Related Overgrowth Spectrum: Prenatal Diagnosis and Autopsy Findings in 3 Fetal Cases.
Journal: Fetal and pediatric pathology
Published: June 24, 2025
Celastrol has beneficial effects on pulmonary hypertension associated with bronchopulmonary dysplasia: Preclinical study outcomes.
Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
Published: August 07, 2024
Morphological and genetic causes of fetal cardiomyopathies.
Journal: Clinical genetics
Published: February 14, 2023
Extending the prenatal Noonan's phenotype by review of ultrasound and autopsy data.
Journal: Prenatal diagnosis
Published: December 23, 2021
COL4A1/COL4A2 and inherited platelet disorder gene variants in fetuses showing intracranial hemorrhage.
Journal: Prenatal diagnosis
Published: November 22, 2021
Occupational Exposure to Ultrafine Particles and Placental Histopathological Lesions: A Retrospective Study about 130 Cases.
Journal: International journal of environmental research and public health
Published: November 07, 2021
Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita.
Journal: Journal of medical genetics
Published: November 16, 2020
Chronic Intervillositis of Unknown Etiology: Development of a Grading and Scoring System That Is Strongly Associated With Poor Perinatal Outcomes.
Journal: The American journal of surgical pathology
Published: August 11, 2020
p57-discordant villi in hydropic products of conception: a clinicopathological study of 70 cases.
Journal: Human pathology
Published: March 30, 2020
Foetal onset of EIF2B related disorder in two siblings: cerebellar hypoplasia with absent Bergmann glia and severe hypomyelination.
Journal: Acta neuropathologica communications
Published: February 24, 2020
Last Updated: 09/26/2026