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Gaelle Hardy

Showing results (1-10 of 5) with videos related to

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Allergy|June 29, 2018
Plasminogen gene mutation with normal C1 inhibitor hereditary angioedema: Three additional French familiesAude Belbézier, Gaelle Hardy, Raphael Marlu, et al.
Clinical Parkinsonism & Related Disorders|January 19, 2026
Confirmation of biallelic <i>VPS11</i> variants as a cause of complex dystonic syndromeArnaud Storck, Marie Thérèse Abiwarde, Gaelle Hardy, et al.
Orphanet Journal of Rare Diseases|December 2, 2025
Management of hereditary angioedema with normal C1Inh: a series of 163 French patientsAlexis Bocquet, Laurence Bouillet, Gaelle Hardy, et al.
La Revue De Medecine Interne|October 30, 2025
French protocol for the diagnosis and management of hereditary angioedemaIsabelle Boccon-Gibod, Olivier Fain, Delphine Gobert, et al.
Presse Medicale (Paris, France : 1983)|November 13, 2018
Laurence Bouillet, Frederica Defendi, Gaelle Hardy, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Allergy|June 29, 2018
Plasminogen gene mutation with normal C1 inhibitor hereditary angioedema: Three additional French familiesAude Belbézier, Gaelle Hardy, Raphael Marlu, et al.
Clinical Parkinsonism & Related Disorders|January 19, 2026
Confirmation of biallelic <i>VPS11</i> variants as a cause of complex dystonic syndromeArnaud Storck, Marie Thérèse Abiwarde, Gaelle Hardy, et al.
Orphanet Journal of Rare Diseases|December 2, 2025
Management of hereditary angioedema with normal C1Inh: a series of 163 French patientsAlexis Bocquet, Laurence Bouillet, Gaelle Hardy, et al.
La Revue De Medecine Interne|October 30, 2025
French protocol for the diagnosis and management of hereditary angioedemaIsabelle Boccon-Gibod, Olivier Fain, Delphine Gobert, et al.
Presse Medicale (Paris, France : 1983)|November 13, 2018
Laurence Bouillet, Frederica Defendi, Gaelle Hardy, et al.
Pageof 1