Functional polymorphism in gamma-glutamylcarboxylase is a risk factor for severe neonatal hemorrhage

Journal of Pediatrics

Volumn 159, Issue 2, 2011, Pages 347-349

  Vanakker, Olivier M ^a   De Coen, Kris ^a   Costrop, Laura ^a   Coucke, Paul J ^a   Vanhaesebrouck, Piet ^a   De Paepe, Anne ^a  

^a GHENT UNIVERSITY HOSPITAL   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

UNCLASSIFIED DRUG; VITAMIN K DEPENDENT CARBOXYLASE; VITAMIN K EPOXIDE REDUCTASE C1; VITAMIN K GROUP;

ARTICLE; BLOOD CLOTTING DISORDER; BRAIN HEMORRHAGE; CASE REPORT; DISEASE COURSE; DISEASE SEVERITY; ECCHYMOSIS; ENZYME ACTIVITY; GASTROINTESTINAL HEMORRHAGE; GENE EXPRESSION; GENETIC ANALYSIS; HEMATEMESIS; HETEROZYGOSITY; HUMAN; MOLECULAR DIAGNOSIS; NEONATAL HEMORRHAGE; NEWBORN; NUCLEAR MAGNETIC RESONANCE IMAGING; ONSET AGE; PALATAL ECCHYMOSIS; PARTIAL THROMBOPLASTIN TIME; PRIORITY JOURNAL; PROTHROMBIN TIME; RISK FACTOR; SINGLE NUCLEOTIDE POLYMORPHISM; SOMNOLENCE; SUBDURAL HEMATOMA; THROMBOCYTE COUNT; VITAMIN SUPPLEMENTATION;

ANTIFIBRINOLYTIC AGENTS; BLOOD COAGULATION; CARBON-CARBON LIGASES; DNA; FEMALE; HUMANS; INFANT, NEWBORN; POLYMORPHISM, GENETIC; RISK FACTORS; SEVERITY OF ILLNESS INDEX; VITAMIN K; VITAMIN K DEFICIENCY BLEEDING;

EID: 79960454874     PISSN: 00223476     EISSN: 10976833     Source Type: Journal    
DOI: 10.1016/j.jpeds.2011.04.044     Document Type: Article

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