Hong-Phuc Cudre-Cung
Overview
Explore the profile of Hong-Phuc Cudre-Cung including associated specialties, affiliations and a list of published articles.
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Articles
5
Citations
31
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Recent Articles
1.
Gonzalez Melo M, Remacle N, Cudre-Cung H, Roux C, Poms M, Cudalbu C, et al.
Mol Genet Metab
. 2021 May;
133(2):157-181.
PMID: 33965309
Glutaric aciduria type I (GA-I, OMIM # 231670) is an inborn error of metabolism caused by a deficiency of glutaryl-CoA dehydrogenase (GCDH). Patients develop acute encephalopathic crises (AEC) with striatal...
2.
Cudre-Cung H, Remacle N, do Vale-Pereira S, Gonzalez M, Henry H, Ivanisevic J, et al.
Mol Genet Metab
. 2019 Jan;
126(4):416-428.
PMID: 30686684
Glutaric Aciduria type I (GA-I) is caused by mutations in the GCDH gene. Its deficiency results in accumulation of the key metabolites glutaric acid (GA) and 3-hydroxyglutaric acid (3-OHGA) in...
3.
Remacle N, Forny P, Cudre-Cung H, Gonzalez-Melo M, do Vale-Pereira S, Henry H, et al.
Mol Genet Metab
. 2018 Jun;
124(4):266-277.
PMID: 29934063
Background: Methylmalonic aciduria (MMAuria) is an inborn error of metabolism leading to neurological deterioration. In this study, we used 3D organotypic brain cell cultures derived from embryos of a brain-specific...
4.
Braissant O, Jafari P, Remacle N, Cudre-Cung H, Do Vale Pereira S, Ballhausen D
Neuroscience
. 2016 Dec;
343:355-363.
PMID: 27984186
Glutaryl-CoA dehydrogenase (GCDH) is a mitochondrial enzyme that is involved in the degradation of tryptophan, lysine and hydroxylysine. Deficient enzyme activity leads to glutaric aciduria type-I (GA-I). This neurometabolic disease...
5.
Cudre-Cung H, Zavadakova P, do Vale-Pereira S, Remacle N, Henry H, Ivanisevic J, et al.
Mol Genet Metab
. 2016 Sep;
119(1-2):57-67.
PMID: 27599447
Using 3D organotypic rat brain cell cultures in aggregates we recently identified 2-methylcitrate (2-MCA) as the main toxic metabolite for developing brain cells in methylmalonic aciduria. Exposure to 2-MCA triggered...