Gaelle Hardy
Grenoble, France
Last Updated: 09/26/2026
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Found 13 publications
Confirmation of biallelic VPS11 variants as a cause of complex dystonic syndrome.
Journal: Clinical parkinsonism & related disorders
Published: September 29, 2025
French protocol for the diagnosis and management of hereditary angioedema.
Journal: La Revue de medecine interne
Published: September 01, 2025
Novel Dominant Splicing Variant in MPZ Associated With Unusual Charcot-Marie-Tooth Disease.
Journal: Journal of the peripheral nervous system : JPNS
Published: August 29, 2025
Early diagnosis of hereditary angioedema in children: genetic testing should be prioritized.
Journal: Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology
Published: August 02, 2024
Management of hereditary angioedema with normal C1Inh: a series of 163 French patients.
Journal: Orphanet journal of rare diseases
Published: May 13, 2024
Primary mitochondrial disorders and mimics: Insights from a large French cohort.
Journal: Annals of clinical and translational neurology
Published: February 26, 2024
Stroke-like manifestations of angioedema: A case report and the identification of a novel mutation.
Journal: Revue neurologique
Published: January 11, 2023
Acquired angioedema due to C1-inhibitor deficiency: CREAK recommendations for diagnosis and treatment
Journal: La Revue de medecine interne
Published: March 03, 2020
MyoNeuroGastroIntestinal Encephalopathy: Natural History and Means for Early Diagnosis.
Journal: Gastroenterology
Published: October 17, 2018
New mitochondrial DNA mutation in Leber's hereditary optic neuropathy: A case report
Journal: Journal francais d'ophtalmologie
Published: October 13, 2017
Last Updated: 09/26/2026