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Therapeutic Monitoring of Patients With Hereditary Tyrosinemia Type 1-A Belgian Monocentric Experience.

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Title: Therapeutic Monitoring of Patients With Hereditary Tyrosinemia Type 1-A Belgian Monocentric Experience.
Authors: Adam AS; Department of Clinical Chemistry, Laboratoire Hospitalier Universitaire de Bruxelles Université Libre de Bruxelles Brussels Belgium., Marcélis L; Laboratory of Paediatric Research Université Libre de Bruxelles Brussels Belgium., Fage D; Department of Clinical Chemistry, Laboratoire Hospitalier Universitaire de Bruxelles Université Libre de Bruxelles Brussels Belgium., Mathieu E; Department of Clinical Chemistry, Laboratoire Hospitalier Universitaire de Bruxelles Université Libre de Bruxelles Brussels Belgium., Empain A; Nutrition and Metabolic Clinic Brussels University Hospital, Academic Children Hospital Queen Fabiola, Université libre de Bruxelles Brussels Belgium.; European Reference Network for Hereditary Metabolic Disorders (MetabERN) Member Padova Italy., Dufour C; Nutrition and Metabolic Clinic Brussels University Hospital, Academic Children Hospital Queen Fabiola, Université libre de Bruxelles Brussels Belgium.; European Reference Network for Hereditary Metabolic Disorders (MetabERN) Member Padova Italy., Cotton F; Department of Clinical Chemistry, Laboratoire Hospitalier Universitaire de Bruxelles Université Libre de Bruxelles Brussels Belgium., de Laet C; Nutrition and Metabolic Clinic Brussels University Hospital, Academic Children Hospital Queen Fabiola, Université libre de Bruxelles Brussels Belgium.; European Reference Network for Hereditary Metabolic Disorders (MetabERN) Member Padova Italy.
Source: JIMD reports [JIMD Rep] 2026 Jan 07; Vol. 67 (1), pp. e70062. Date of Electronic Publication: 2026 Jan 07 (Print Publication: 2026).
Publication Type: Journal Article
Journal Info: Publisher: Wiley Country of Publication: United States NLM ID: 101568557 Publication Model: eCollection Cited Medium: Print ISSN: 2192-8304 (Print) Linking ISSN: 21928304 NLM ISO Abbreviation: JIMD Rep Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
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  Data: <searchLink fieldCode="AU" term="%22Adam+AS%22">Adam AS</searchLink>; Department of Clinical Chemistry, Laboratoire Hospitalier Universitaire de Bruxelles Université Libre de Bruxelles Brussels Belgium.<br /><searchLink fieldCode="AU" term="%22Marcélis+L%22">Marcélis L</searchLink>; Laboratory of Paediatric Research Université Libre de Bruxelles Brussels Belgium.<br /><searchLink fieldCode="AU" term="%22Fage+D%22">Fage D</searchLink>; Department of Clinical Chemistry, Laboratoire Hospitalier Universitaire de Bruxelles Université Libre de Bruxelles Brussels Belgium.<br /><searchLink fieldCode="AU" term="%22Mathieu+E%22">Mathieu E</searchLink>; Department of Clinical Chemistry, Laboratoire Hospitalier Universitaire de Bruxelles Université Libre de Bruxelles Brussels Belgium.<br /><searchLink fieldCode="AU" term="%22Empain+A%22">Empain A</searchLink>; Nutrition and Metabolic Clinic Brussels University Hospital, Academic Children Hospital Queen Fabiola, Université libre de Bruxelles Brussels Belgium.; European Reference Network for Hereditary Metabolic Disorders (MetabERN) Member Padova Italy.<br /><searchLink fieldCode="AU" term="%22Dufour+C%22">Dufour C</searchLink>; Nutrition and Metabolic Clinic Brussels University Hospital, Academic Children Hospital Queen Fabiola, Université libre de Bruxelles Brussels Belgium.; European Reference Network for Hereditary Metabolic Disorders (MetabERN) Member Padova Italy.<br /><searchLink fieldCode="AU" term="%22Cotton+F%22">Cotton F</searchLink>; Department of Clinical Chemistry, Laboratoire Hospitalier Universitaire de Bruxelles Université Libre de Bruxelles Brussels Belgium.<br /><searchLink fieldCode="AU" term="%22de+Laet+C%22">de Laet C</searchLink>; Nutrition and Metabolic Clinic Brussels University Hospital, Academic Children Hospital Queen Fabiola, Université libre de Bruxelles Brussels Belgium.; European Reference Network for Hereditary Metabolic Disorders (MetabERN) Member Padova Italy.
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