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Maria Veiga-da-Cunha

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Assistant Professor (Chargé de cours)

Université catholique de Louvain

Belgium

Research Interests

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Professors in Belgium

Recent Grants

Grant: Open

Understanding the dysregulation of glucose phosphorylation as a cause of neurological problems

Open Date: 2025-01-01

Close Date: 2026-12-01

Grant: Close

Biochemical investigation on the pathophysiology of G6PC3 deficiency, an inborn error of metabolite repair

Open Date: 2021-01-01

Close Date: 2025-12-01

Grant: Close

Studies on the pathophysiology of G6PC3 and G6PT deficiencies. Can we understand even be?er these defects?

Open Date: 2020-01-01

Close Date: 2022-12-01

Grant: Close

The neutropenias in G6PC3 and G6PT deficiency: a default in metabolite repair?

Open Date: 2018-01-01

Close Date: 2020-12-01

Articles (11)

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2026

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2026

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2025

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2024

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2023

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2023

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2023

Collaborators (8)

Melodie Aubart

Imagine Institute for Genetic Diseases

FRANCE

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Terry Derks

NETHERLANDS

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Ellen Crushell

Consultant Paediatrician SI Inherited Metabolic Disorders, Clinical Prof

University College Dublin

IRELAND

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Maite Iriarte

Full Professor

Public University of Navarre

SPAIN

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Joseph Dewulf

Head of Laboratory of Bochemical Genetics and newborn screening

Cliniques Universitaires Saint-Luc

BELGIUM

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Ignacio Moriyon

Emeritus Professor

Universidad de Navarra

SPAIN

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Nathalie Boddaert

professor

Assistance Publique - Hôpitaux de Paris

FRANCE

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Amaia Zúñiga-Ripa

Public University of Navarre

SPAIN

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Maria Veiga-da-Cunha

Research Interests

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Recent Grants

Articles (11)

Clinical Outcomes and Management in Late Diagnosed Siblings Affected With Attenuated GSD Ib

Identification of the function of the metabolite repair enzyme Nit1: the story of a collaboration with Arthur Cooper

Pathophysiology of the Neutropenia of GSDIb and G6PC3 Deficiency: Origin, Metabolism and Elimination of 1,5‐Anhydroglucitol

Empagliflozin for treating neutropenia and neutrophil dysfunction in 21 infants with glycogen storage disease 1b

Treatment recommendations for glycogen storage disease type IB- associated neutropenia and neutrophil dysfunction with empagliflozin

A novel gluconeogenic route enables efficient use of erythritol in zoonotic <i>Brucella</i>.

Clinical, Neuroimaging, and Metabolic Footprint of the Neurodevelopmental Disorder Caused by Monoallelic HK1 Variants

Successful repurposing of empagliflozin to treat neutropenia in a severe congenital neutropenia patient with G6PC3 mutations.

DBS are suitable for 1,5-anhydroglucitol monitoring in GSD1b and G6PC3-deficient patients taking SGLT2 inhibitors to treat neutropenia

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

Treatment of the Neutropenia Associated with GSD1b and G6PC3 Deficiency with SGLT2 Inhibitors

Collaborators (8)

Melodie Aubart

Terry Derks

Ellen Crushell

Maite Iriarte

Joseph Dewulf

Ignacio Moriyon

Nathalie Boddaert

Amaia Zúñiga-Ripa

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