Elodie Lebredonchel (E Lebredonchel)

Years Active: 2021-2022
Publications (10 Years): 3

This page only lists publications with an associated author ORCID identifier.

Publications

Elodie Lebredonchel, A Riquet, D Neut, F Broly, G Matthijs, A Klein, F Foulquier
A PMM2-CDG caused by an A108V mutation associated with a heterozygous 70 kilobases deletion case report. Italian journal of pediatrics 48 (1) (2022)
Elodie Lebredonchel, Sandrine Duvet, Claire Douillard, François Foulquier, André Klein
Variation of the serum N-glycosylation during the pregnancy of a MPI-CDG patient. JIMD reports 62 (1) (2021)
Vasily Smirnov, Olivier Grunewald, Jean Muller, Christina Zeitz, Carolin D Obermaier, Aurore Devos, Valérie Pelletier, Béatrice Bocquet, Camille Andrieu, Jean-Louis Bacquet, Elodie Lebredonchel, Saddek Mohand-Saïd, Sabine Defoort-Dhellemmes, José-Alain Sahel, Hélène Dollfus, Xavier Zanlonghi, Isabelle Audo, Isabelle Meunier, Elise Boulanger-Scemama, Claire-Marie Dhaenens
Novel TTLL5 Variants Associated with Cone-Rod Dystrophy and Early-Onset Severe Retinal Dystrophy. International journal of molecular sciences 22 (12) (2021)

Elodie Lebredonchel.css-eqlu8i{font-size:small;padding-left:4px;} (E Lebredonchel)