Lucie Pierron
Paris, France
Last Updated: 09/26/2026
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Found 9 publications
A Patient-Reported Outcome Measure of Communication Difficulties in Friedreich Ataxia: COMATAX.
Journal: Cerebellum (London, England)
Published: February 08, 2026
BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.
Journal: Journal of medical genetics
Published: December 26, 2025
Patient-reported, psychosocial and health economic outcomes in mild to moderate Friedreich's ataxia: baseline results of the PROFA study.
Journal: The Lancet regional health. Europe
Published: August 06, 2025
Lessons learned from 30 years of presymptomatic testing in Huntington Disease.
Journal: Revue neurologique
Published: May 25, 2025
Basic helix-loop-helix transcription factor BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, tone and movement abnormalities.
Journal: medRxiv : the preprint server for health sciences
Published: November 06, 2024
End-of-Life Discussions With Patients and Caregivers Affected By Neurogenetic Diseases.
Journal: Neurology. Clinical practice
Published: March 23, 2023
Reproductive choices and intrafamilial communication in neurogenetic diseases with different self-estimated severities.
Journal: Journal of medical genetics
Published: January 26, 2022
Informing about genetic risk in families with Huntington disease: comparison of attitudes across two decades.
Journal: European journal of human genetics : EJHG
Published: July 09, 2020
Double chromosomal translocation in an infertile man: one-step FISH meiotic segregation analysis and reproductive prognosis.
Journal: Journal of assisted reproduction and genetics
Published: November 15, 2018
Showing 1-9 of 9
Last Updated: 09/26/2026