Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Marie-Odile Greneche"'
Autor:
Marie-Odile Greneche, Catherine Delanoë, Samia Pichard, Laurent François, Silvana de Lucia, Manuel Schiff, Stéphane Auvin, Adina Ilea
Publikováno v:
European Journal of Paediatric Neurology. 20:674-677
The ketogenic diet is an evidence-based treatment for resistant epilepsy including Lennox-Gastaut syndrome. This diet is based on low carbohydrate-high fat intakes. Dietary treatment is also therapeutic for inborn errors of metabolism such as aminoac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75e43182e895d86d4ac23f370a3c15ab
https://doi.org/10.1016/j.ejpn.2016.02.015
https://doi.org/10.1016/j.ejpn.2016.02.015
Autor:
Catherine Delanoë, Stéphane Auvin, Vanina Bellavoine, Marie-Odile Greneche, Domitille Gras, Sofiane Amalou, Adina Ilea, Laurent François
Publikováno v:
Developmental medicine and child neurology. 58(11)
Aim Glucose transporter type 1 deficiency syndrome (GLUT1-DS) results from impaired glucose transport into the brain, and is treated with a ketogenic diet. A few reports have suggested effectiveness of treatment using the modified Atkins diet (MAD).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f7df4064986b31382fba3c4c3834a5f
https://pubmed.ncbi.nlm.nih.gov/27445040
https://pubmed.ncbi.nlm.nih.gov/27445040
Autor:
A. Davit-Spraul, Marie-Odile Greneche, S. Roche, J.-F. Benoist, A. Imbard, H. Ogier de Baulny, N. Garcia Segarra
Publikováno v:
Journal of Inherited Metabolic Disease. 33:507-510
A 22 year-old woman with tyrosinemia type I (HT1) married her first cousin who is heterozygous for the same FAH mutation for which the patient is homozygous. During her pregnancy she was treated with diet (prescribed tyrosine intake 300 mg/day), and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33b4990fddb8bb094ccf8a04544f6cf2
https://doi.org/10.1007/s10545-012-9569-8
https://doi.org/10.1007/s10545-012-9569-8