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As seen in: Journal of Clinical Pathology
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Articles

Syndrome de Dravet

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By Maladies Rares
| medizinonline.com
Cette forme rare et grave d’épilepsie a été décrite pour la première fois par le docteur Charlotte Dravet, médecin français. L’ancienne dénomination était “épilepsie myoclonique infantile sévère”. La première manifestation du syndrome de Dravet a lieu au cours de la première année de vie et se caractérise par des convulsions motrices fébriles et focales, généralement unilatérales. Dieser Inhalt ist nur für registrierte Benutzer zugänglich () Einloggen Jetzt registrieren
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Lysis Timer: a new sensitive tool to diagnose hyperfibrinolysis in liver transplantation

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By Stéphanie Roullet, CHU Bordeaux, Université de Bordeaux, Maladies Rares
| Journal of Clinical Pathology Verified
Lysis Timer: a new sensitive tool to diagnose hyperfibrinolysis in liver transplantation Stéphanie Roullet1,2, Sylvie Labrouche3,4, Christine Mouton5, Alice Quinart6, Karine Nouette-Gaulain1,2, Christophe Laurent7, Geneviève Freyburger4 1 CHU Bordeaux, Service d’Anesthésie-Réanimation Pellegrin, Bordeaux, France 2 Université de Bordeaux, INSERM U 12-11, Maladies rares: Génétique et Métabolisme, Bordeaux, France 3 CHU Bordeaux, Laboratoire d’Hématologie – PTRR, Hôpital Pellegrin, Bordeaux,...
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Lysis Timer: a new sensitive tool to diagnose hyperfibrinolysis in liver transplantation

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By CHU Bordeaux, Université de Bordeaux, Maladies Rares, Stéphanie Roullet
| Journal of Clinical Pathology Verified
Aims Diagnosis of hyperfibrinolysis in orthotopic liver transplantation (OLT) remains challenging. Euglobulin clot lysis time (ECLT) is not adapted to clinical situations. ROTEM is specific but seldom sensitive to hyperfibrinolysis. The Lysis Timer assesses ‘Global Fibrinolytic Capacity’ in citrated plasma (GFC/LT).
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