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Profil bibliographique

Rosa-Maria Guéant Rodriguez

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

3Publications signalées
12Citations signalées
2Affiliations récentes

Les institutions déclarées

Les domaines associés

Folate and B Vitamins ResearchPorphyrin Metabolism and DisordersMetabolism and Genetic DisordersVitamin K Research Studies

Les publications récentes

Accès ouvert 2026 article OpenAlex

Expert Perspectives on Diagnosis and Management of Vitamin B12 Deficiency in Adults

Jean‐Louis Guéant, David Alpers, Lindsay H. Allen, Emmanuel Andres et autres

There is no universally-accepted definition of vitamin B 12 deficiency despite the severity of its medical consequences if not properly diagnosed and treated. B 12 deficiency can arise either from inadequate dietary intake, in particular in vegans/vegetarians, or various causes of impaired …

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2 citations Advances in Nutrition
Accès ouvert 2024 erratum OpenAlex

Corrigendum to Multiomic analysis in fibroblasts of patients with inborn errors of cobalamin metabolism reveals concordance with clinical and metabolic variability [eBioMedicine 99 (2024), 104911]

Arnaud Wiedemann, Abderrahim Oussalah, Rosa-Maria Guéant Rodriguez, Élise Jeannesson et autres

Following a request from Sebastien Hergalant, bioinformatics engineer at Inserm unit NGERE 1256, the authors accepted to include him in the list of authors rather than in the acknowledgements, given his significant contribution in the analysis of the online data of reference …

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0 citations EBioMedicine
Accès ouvert 2024 article OpenAlex

Multiomic analysis in fibroblasts of patients with inborn errors of cobalamin metabolism reveals concordance with clinical and metabolic variability

Arnaud Wiedemann, Abderrahim Oussalah, Rosa-Maria Guéant Rodriguez, Élise Jeannesson et autres

BACKGROUND: The high variability in clinical and metabolic presentations of inborn errors of cobalamin (cbl) metabolism (IECM), such as the cblC/epicblC types with combined deficits in methylmalonyl-coA mutase (MUT) and methionine synthase (MS), are not well understood. They could be explained by …

fr (code pays fourni par la source)

10 citations EBioMedicine

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