Elevated plasma total homocysteine in severe methionine adenosyltransferase I/III deficiency
- Auteur
- STABLER, Sally P; STEEGBORN, Clemens; WAHL, Markus C; OLIVERIUSOVA, Jana; KRAUS, Jan P; ALLEN, Robert H; WAGNER, Conrad; MUDD, S. Harvey
Abteilung Strukturjorschung, Max Planck Institut für Biochemie, Planegg-Martinsried, Germany
Department of Biochemistry and the Clinical Nutrition Research Unit, Vanderbilt University, Nashville, United States
Department of Veterans Affair, Medical Center, Nashville, TN, United States
Departments of Medicine, Pediatrics, and Cellular and Structural Biology, University of Colorado Health Sciences Center, Denver, CO, United States
Laboratory of Molecular Biology, National Institute of Mental Health, Bethesda, MD, United States - Source
Metabolism, clinical and experimental. 2002, Vol 51, Num 8, pp 981-988 ; ref : 52 ref
- ISSN
- 0026-0495
- Domaine scientifique
- Endocrinology; Nutrition, obesity, metabolic disorders
- Editeur
- Elsevier, New York, NY
- Pays de publication
- United States
- Type de document
- Article
- Langue
- English
- Mot clé (fr)
- Aminoacide soufré Aminoacide Augmentation Diagnostic différentiel Diagnostic Déficit Etude cas Grave Homme Homocystéine Methionine adenosyltransferase Métabolite Méthionine Plasma sanguin Thiol Aminoacidopathie Enzyme Maladie héréditaire Métabolisme pathologie Transferases
- Mot clé (en)
- Sulfur containing aminoacid Aminoacid Increase Differential diagnostic Diagnosis Deficiency Case study Severe Human Homocystein Methionine adenosyltransferase Metabolite Methionine Blood plasma Thiol Aminoacid disorder Enzyme Genetic disease Metabolic diseases Transferases
- Mot clé (es)
- Aminoácido azufrado Aminoácido Aumentación Diagnóstico diferencial Diagnóstico Déficiencia Estudio caso Grave Hombre Homocisteína Methionine adenosyltransferase Metabolito Metionina Plasma sanguíneo Tiol Aminoacido alteración Enzima Enfermedad hereditaria Metabolismo patología Transferases
- Classification
- Pascal
- 002 Sciences biologiques et medicales / 002B Sciences medicales / 002B22 Maladies metaboliques / 002B22D Maladies métaboliques héréditaires et congénitales / 002B22D01 Aminoacidopathies
- Discipline
- Metabolic diseases
- Provenance
- Inist-CNRS
- Base de données
- PASCAL
- Identifiant INIST
- 13808106
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1053/meta.2002.34017 
https://dx.doi.org/10.1053/meta.2002.34017
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