Maria Veiga-da-Cunha

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 6

Top Topics

Highly Efficient

Top Venues

Journal of inherited metabolic disease

Cellular and molecular life sciences : CMLS

Proceedings of the National Academy of Sciences of the United States of America

Diagnostics (Basel, Switzerland)

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

Publications

Jennifer Diederich, Pierre Mounkoro, Hernan A Tirado, Nathalie Chevalier, Emile Van Schaftingen, Maria Veiga-da-Cunha
SGLT5 is the renal transporter for 1,5-anhydroglucitol, a major player in two rare forms of neutropenia. Cellular and molecular life sciences : CMLS 80 (9) (2023)
Maria Veiga-da-Cunha, Saskia B Wortmann, Sarah Catharina Grünert, Emile Van Schaftingen
Treatment of the Neutropenia Associated with GSD1b and G6PC3 Deficiency with SGLT2 Inhibitors. Diagnostics (Basel, Switzerland) 13 (10) (2023)
Cecile Boulanger, Xavier Stephenne, Jennifer Diederich, Pierre Mounkoro, Nathalie Chevalier, Alina Ferster, Emile Van Schaftingen, Maria Veiga-da-Cunha
Successful use of empagliflozin to treat neutropenia in two G6PC3-deficient children: Impact of a mutation in SGLT5. Journal of inherited metabolic disease 45 (4) (2022)
Maria Veiga-da-Cunha, Emile Van Schaftingen, Guido T Bommer
Inborn errors of metabolite repair. Journal of inherited metabolic disease 43 (1) (2019)
Maria Veiga-da-Cunha, Nathalie Chevalier, Xavier Stephenne, Jean-Philippe Defour, Nicole Paczia, Alina Ferster, Younes Achouri, Joseph P Dewulf, Carole L Linster, Guido T Bommer, Emile Van Schaftingen
Failure to eliminate a phosphorylated glucose analog leads to neutropenia in patients with G6PT and G6PC3 deficiency. Proceedings of the National Academy of Sciences of the United States of America 116 (4) (2019)
Sebastian Kwiatkowski, Agnieszka K Seliga, Didier Vertommen, Marianna Terreri, Takao Ishikawa, Iwona Grabowska, Marcel Tiebe, Aurelio A Teleman, Adam K Jagielski, Maria Veiga-da-Cunha, Jakub Drozak
SETD3 protein is the actin-specific histidine N-methyltransferase. eLife 7 (2018)