Re-evaluation of the penicillamine challenge test in the diagnosis of Wilson's disease in children
- Author
- MÜLLER, Thomas1 2 ; KOPPIKAR, Smita3 ; STAUDINGER, Roland10 ; MIELI-VERGANI, Giorgina3 ; DHAWAN, Anil3 ; TAYLOR, Rachel M3 ; CARRAGHER, Fiona4 ; SCHLENCK, Barbara5 ; HEINZ-ERIAN, Peter1 ; KRONENBERG, Florian6 ; FERENCI, Peter7 ; TANNER, Stuart8 ; SIEBERT, Uwe2 9
[1] Department of Pediatrics II, Medical University of Innsbruck, Innsbruck, Austria
[2] Institute of Public Health, Medical Decision Making and HTA. UMIT -University for Health Sciences, Medical Informatics and Technology, Hall, Austria
[3] Paediatric Liver Centre, King's College Hospital London, London, United Kingdom
[4] Clinical Biochemistry, King's College School of Medicine and Dentistry, King's College Hospital London, London, United Kingdom
[5] Division of Pediatric Urology, Department of Urology, Medical University of Innsbruck, Austria
[6] Division of Genetic Epidemiology, Department of Medical Genetics, Molecular and Clinical Pharmacology, Innsbruck Medical University, Austria
[7] Department of Internal Medicine IV, Gastroenterology and Hepatology, Medical University of Vienna, Austria
[8] Department of Child Health, University of Sheffield, Sheffield, United Kingdom
[9] Institute of Technology Assessment, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States
[10] Institute for Medical Law, Human Resources and Health politic, UMIT-University for Health Sciences, Medical Informatics and Technology, Hall, Austria - Source
Journal of hepatology. 2007, Vol 47, Num 2, pp 270-276, 7 p ; ref : 19 ref
- CODEN
- JOHEEC
- ISSN
- 0168-8278
- Scientific domain
- Gastroenterology
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Author keyword
- Copper Liver Penicillamine Wilson's disease
- Keyword (fr)
- Antirhumatismal Cuivre Diagnostic Enfant Evaluation performance Foie pathologie Foie Pénicillamine Sensibilité Spécificité Urine Wilson maladie Cupriurie Test thérapeutique Aminoacide soufré Appareil digestif pathologie Chélateur Enzymopathie Homme Maladie héréditaire Métabolisme pathologie Système nerveux pathologie
- Keyword (en)
- Antirheumatic agent Copper Diagnosis Child Performance evaluation Hepatic disease Liver Penicillamine Sensitivity Specificity Urine Wilson disease Sulfur containing aminoacid Digestive diseases Chelating agent Enzymopathy Human Genetic disease Metabolic diseases Nervous system diseases
- Keyword (es)
- Antireumático Cobre Diagnóstico Niño Evaluación prestación Hígado patología Hígado Penicilamina Sensibilidad Especificidad Orina Wilson enfermedad Aminoácido azufrado Aparato digestivo patología Quelante Enzimopatía Hombre Enfermedad hereditaria Metabolismo patología Sistema nervioso patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B02 Pharmacology. Drug treatments / 002B02L Bones, joints and connective tissue. Antiinflammatory agents
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B22 Metabolic diseases / 002B22E Other metabolic disorders / 002B22E03 Metals (hemochromatosis...)
- Discipline
- Metabolic diseases Pharmacological treatments
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 18943898
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
10.1016/j.jhep.2007.03.011 
https://dx.doi.org/10.1016/j.jhep.2007.03.011
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