Maria Veiga-da-Cunha

8PUBLICATIONS
13CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Medical biochemistry - inorganic elements and compoundsNephrology and urologyEpigenetics (incl. genome methylation and epigenomics)Infant and child health
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Publications (8)

|Mar 02, 2026
Clinical Outcomes and Management in Late Diagnosed Siblings Affected With Attenuated GSD Ib.

Gregory Lynch, Alison Woodall, Charlotte Dawson

|Sep 17, 2025
Pathophysiology of the Neutropenia of GSDIb and G6PC3 Deficiency: Origin, Metabolism and Elimination of 1,5-Anhydroglucitol.

Maria Veiga-da-Cunha, Lila Gannoun, Joseph Dewulf

|Aug 18, 2023
SGLT5 is the renal transporter for 1,5-anhydroglucitol, a major player in two rare forms of neutropenia.

Jennifer Diederich, Pierre Mounkoro, Hernan A Tirado

|May 27, 2023
Treatment of the Neutropenia Associated with GSD1b and G6PC3 Deficiency with SGLT2 Inhibitors.

Maria Veiga-da-Cunha, Saskia B Wortmann, Sarah C Grünert

|May 04, 2022
Successful use of empagliflozin to treat neutropenia in two G6PC3-deficient children: Impact of a mutation in SGLT5.

Cécile Boulanger, Xavier Stephenne, Jennifer Diederich

|Nov 07, 2019
Inborn errors of metabolite repair.

Maria Veiga-da-Cunha, Emile Van Schaftingen, Guido T Bommer

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