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Mise au point et intérêt du diagnostic de la maladie de Gilbert par biologie moléculaire

Other title
Adaptation and interest of Gilbert syndrome molecular diagnosis (en)
Author
LE BIHAN-LEVAUFRE, B1 ; FRANCOUAL, J1 ; LABRUNE, P2 ; CHALAS, J1 ; CAPEL, L1 ; LINDENBAUM, A1
[1] Laboratoire de biochimie, Hôpital Antoine-Béclère (AP-HP), BP 405, 92141 Clamart, France
[2] Service de pédiatrie, Hôpital Antoine-Béclère (AP-HP), BP 405, 92141 Clamart, France
Conference title
Colloque de virologie de Versailles
Conference name
Colloque de virologie de Versailles (13 ; Versailles 2000-10-12)
Source

Annales de biologie clinique (Paris). 2001, Vol 59, Num 1, pp 61-66 ; ref : 15 ref

CODEN
ABCLAI
ISSN
0003-3898
Scientific domain
Biochemistry, molecular biology, biophysics; Medical laboratory techniques; General medicine general surgery
Publisher
Libbey-Eurotext, Montrouge
Publication country
France
Document type
Conference Paper
Language
French
Keyword (fr)
Adaptation Anticancéreux Biologie moléculaire Diagnostic Epidémiologie Exon Génotype HELLP syndrome Homme Ictère héréditaire Gilbert Irinotécan Mise au point Mutation Pharmacogénétique Phénotype Promoteur Toxicité UDP-glucuronosyltransferase Pyrano indolizino quinoléine dérivé Appareil digestif pathologie Biologie clinique Enzyme Foie pathologie Glycosyltransferases Génétique Hexosyltransferases Hyperbilirubinémie Maladie héréditaire Transferases Voie biliaire pathologie
Keyword (en)
Adaptation Antineoplastic agent Molecular biology Diagnosis Epidemiology Exon Genotype HELLP syndrome Human Gilbert disease Irinotecan Perfecting Mutation Pharmacogenetics Phenotype Promoter Toxicity UDP-glucuronosyltransferase Digestive diseases Clinical biology Enzyme Hepatic disease Glycosyltransferases Genetics Hexosyltransferases Hyperbilirubinemia Genetic disease Transferases Biliary tract disease
Keyword (es)
Adaptación Anticanceroso Biología molecular Diagnóstico Epidemiología Exón Genotipo HELLP síndrome Hombre Ictericia hereditaria Gilbert Irinotecán Puesta a punto Mutación Farmacogenética Fenotipo Promotor Toxicidad UDP-glucuronosyltransferase Aparato digestivo patología Biología clínica Enzima Hígado patología Glycosyltransferases Genética Hexosyltransferases Hiperbilirrubinemia Enfermedad hereditaria Transferases Vía biliar patología
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B13 Gastroenterology. Liver. Pancreas. Abdomen / 002B13C Liver. Biliary tract. Portal circulation. Exocrine pancreas / 002B13C03 Other diseases. Semiology

Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B22 Metabolic diseases / 002B22D Errors of metabolism / 002B22D05 Miscellaneous hereditary metabolic disorders

Discipline
Gastroenterology. Liver. Pancreas. Abdomen Metabolic diseases
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
949965

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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