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Marie-Cécile Nassogne

Researcher at Cliniques Universitaires Saint-Luc

Publications -  114
Citations -  3702

Marie-Cécile Nassogne is an academic researcher from Cliniques Universitaires Saint-Luc. The author has contributed to research in topics: Microcephaly & Epilepsy. The author has an hindex of 29, co-authored 106 publications receiving 3230 citations. Previous affiliations of Marie-Cécile Nassogne include Université catholique de Louvain.

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Pediatric diffusion tensor imaging: normal database and observation of the white matter maturation in early childhood.

TL;DR: The establishment of a database of DTI images in children can be used as a normal standard of reference for diagnosis of pediatric neurological abnormalities, and visual observations that maturation of the white matter and the normality of its architecture can be assessed with DTI in young children are confirmed.
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Sustained Engraftment and Tissue Enzyme Activity After Liver Cell Transplantation for Argininosuccinate Lyase Deficiency

TL;DR: Liver cell transplantation can achieve donor cell engraftment in humans in a significant proportion, leading to sustained metabolic and clinical control with psychomotor catch-up, changing the clinical phenotype from a severe neonatal one to a moderate late-onset type.
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Neural correlates of symbolic number comparison in developmental dyscalculia

TL;DR: The findings suggest that dyscalculia is associated with impairment in areas involved in number magnitude processing and, to a lesser extent, in areas dedicated to domain-general magnitude processing.
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A gene encoding a putative FAD-dependent l-2-hydroxyglutarate dehydrogenase is mutated in l-2-hydroxyglutaric aciduria

TL;DR: It is concluded that L-2-hydroxyglutaric aciduria is normally metabolized to alpha-ketoglutarate in mammalian tissues and that the pathological findings observed in this metabolic disorder must be due to a toxic effect of L- 2-hydroxglutarate on the central nervous system.
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Inherited CARD9 deficiency in otherwise healthy children and adults with Candida species-induced meningoencephalitis, colitis, or both

TL;DR: Invasive infections of the central nervous system (CNS) or digestive tract caused by commensal fungi of the genus Candida are rare and life-threatening as discussed by the authors, with patients often displaying a history of multiple infections.