المؤلفون: Christian Lavigne, Lena Damaj, Esther Noel, François Maillot, Sybill Charriere, Adrien Bigot, Vincent Rigalleau, Claire Douillard, Fanny Mochel, Elsa Kaphan, Ségolène Toquet, Amélie Servettaz, Samir Mesli, Gérard Besson, Roselyne Garnotel, Caroline Moreau, Agathe Roubertie, Sylvie Odent, Isabelle Redonnet-Vernhet, Jean Baptiste Arnoux, Marta Spodenkiewicz, Aude Servais

المساهمون: Laboratoire Maladies Rares: Génétique et Métabolisme (Bordeaux) (U1211 INSERM/MRGM), Université de Bordeaux (UB)-Groupe hospitalier Pellegrin-Institut National de la Santé et de la Recherche Médicale (INSERM), Bordeaux population health (BPH), Université de Bordeaux (UB)-Institut de Santé Publique, d'Épidémiologie et de Développement (ISPED)-Institut National de la Santé et de la Recherche Médicale (INSERM)

المصدر: Journal of Inherited Metabolic Disease
Journal of Inherited Metabolic Disease, Springer Verlag, 2021, ⟨10.1002/jimd.12403⟩

مصطلحات موضوعية: Adult, Male, Ornithine, Pediatrics, medicine.medical_specialty, Adolescent, Argininosuccinic Aciduria, Context (language use), Inherited metabolic diseases, Urea cycle disorders, 03 medical and health sciences, Young Adult, Sex Factors, Intensive care, Genetics, Medicine, Adults, Humans, Hyperammonemia, Decompensation, Family history, Age of Onset, Urea Cycle Disorders, Inborn, Genetics (clinical), 030304 developmental biology, Aged, Retrospective Studies, Coma, Aged, 80 and over, 0303 health sciences, biology, business.industry, 030305 genetics & heredity, Middle Aged, medicine.disease, 3. Good health, Ornithine Carbamoyltransferase Deficiency Disease, Citrin, Argininosuccinic aciduria, Late-onset diagnosis, Cohort, biology.protein, [SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie, Female, France, medicine.symptom, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88826c8496ec65eeeef85daf47f752f6Test
https://pubmed.ncbi.nlm.nih.gov/34014557Test

المؤلفون: Christelle Corne, Laetitia Van Noolen, François Maillot, Patrice Faure, Lysiane Boulet, Gérard Besson

المصدر: Journal of inherited metabolic diseaseREFERENCES. 43(5)

مصطلحات موضوعية: Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Population, Phenylalanine, 03 medical and health sciences, chemistry.chemical_compound, Kynurenic acid, Tandem Mass Spectrometry, Internal medicine, Phenylketonurias, Genetics, medicine, Humans, Prospective Studies, education, Genetics (clinical), 030304 developmental biology, 0303 health sciences, education.field_of_study, business.industry, 030305 genetics & heredity, Tryptophan, nutritional and metabolic diseases, Metabolism, medicine.disease, Endocrinology, chemistry, Inborn error of metabolism, Female, France, business, Kynurenine, Blood Chemical Analysis, Cohort study, Chromatography, Liquid

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9dd8b504534924f78c23dce3542ebd93Test
https://pubmed.ncbi.nlm.nih.gov/32392388Test