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Case report: Motor neuron disease phenotype associated with symptomatic copper deficiency: Challenging diagnosis and treatment by Adam Benkirane, Thibault Warlop, Thibault Warlop, Adrian Ivanoiu, Pierre Baret, Elsa Wiame, Vincent Haufroid, Vincent Haufroid, Thierry Duprez, Philippe Hantson, Philippe Hantson
Published 2023-01-01
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A mouse model of L-2-hydroxyglutaric aciduria, a disorder of metabolite repair. by Rim Rzem, Younes Achouri, Etienne Marbaix, Olivier Schakman, Elsa Wiame, Sandrine Marie, Philippe Gailly, Marie-Françoise Vincent, Maria Veiga-da-Cunha, Emile Van Schaftingen
Published 2015-01-01
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