Congenital macrothrombocytopenias

Blood Reviews

Volumn 20, Issue 2, 2006, Pages 111-121

  Kunishima, Shinji ^a   Saito, Hidehiko ^a  

^a NATIONAL HOSPITAL ORGANIZATION NAGOYA MEDICAL CENTER   (Japan)

Author keywords

Bernard Soulier syndrome; Giant platelets; Idiopathic thrombocytopenic purpura; Macrothrombocytopenia with leukocyte inclusions; May Hegglin anomaly

Indexed keywords

AMINOCAPROIC ACID; ANTIFIBRINOLYTIC AGENT; BLOOD CLOTTING FACTOR 7; CORTICOSTEROID; GLYCOPROTEIN IB; IMMUNOGLOBULIN; PROTEIN; PROTEIN MYH9; RECOMBINANT PROTEIN; TRANEXAMIC ACID; UNCLASSIFIED DRUG;

BERNARD SOULIER DISEASE; BLEEDING; CELL INCLUSION; CLINICAL FEATURE; DIAGNOSTIC ERROR; DIAGNOSTIC PROCEDURE; DIGEORGE SYNDROME; DISEASE CLASSIFICATION; DYSERYTHROPOIESIS; FECHTNER SYNDROME; GENE MUTATION; GENOTYPE PHENOTYPE CORRELATION; GRAY THROMBOCYTE SYNDROME; HEMATOPOIETIC STEM CELL TRANSPLANTATION; HETEROZYGOSITY; HUMAN; LABORATORY TEST; LEUKOCYTE; MACROTHROMBOCYTOPENIA WITH LEUKOCYTE INCLUSION; MAY HEGGLIN ANOMALY; MEDITERRANEAN MACROTHROMBOCYTOPENIA; MUTATIONAL ANALYSIS; NEPHROTIC SYNDROME; NONHUMAN; PARIS TROUSSEAU SYNDROME; PATHOGENESIS; PATHOPHYSIOLOGY; POSTOPERATIVE COMPLICATION; PRIORITY JOURNAL; REVIEW; SEBASTIAN SYNDROME; SPLENECTOMY; THROMBOCYTE TRANSFUSION; THROMBOCYTOPENIA; VON WILLEBRAND DISEASE TYPE 2B; X CHROMOSOME LINKED DISORDER; X CHROMOSOME LINKED MACROTHROMBOCYTOPENIA WITH DYSERYTHROPOIESIS;

EID: 33644522742     PISSN: 0268960X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.blre.2005.08.001     Document Type: Article

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