Glanzmann thrombasthenia: An update. Export

@article{citeulike:6049199, abstract = {Glanzmann thrombasthenia (GT) is a rare autosomal recessive disorder characterized by qualitative or quantitative abnormalities of the platelet membrane glycoprotein (GP) IIb/IIIa. Physiologically, this platelet receptor normally binds several adhesive plasma proteins, and this facilitates attachment and aggregation of platelets to ensure thrombus formation at sites of vascular injury. The lack of resultant platelet aggregation in GT leads to mucocutaneous bleeding whose manifestation may be clinically variable, ranging from easy bruising to severe and potentially life-threatening hemorrhages. In this review we discuss the main characteristics of GT, focusing on molecular defects, diagnostic evaluation and treatment strategies.}, author = {Franchini, Massimo and Favaloro, Emmanuel J. and Lippi, Giuseppe}, citeulike-article-id = {6049199}, citeulike-linkout-0 = {http://dx.doi.org/10.1016/j.cca.2009.10.016}, citeulike-linkout-1 = {http://linkinghub.elsevier.com/retrieve/pii/S0009898109005439}, citeulike-linkout-2 = {http://view.ncbi.nlm.nih.gov/pubmed/19854165}, citeulike-linkout-3 = {http://www.hubmed.org/display.cgi?uids=19854165}, day = {23}, doi = {10.1016/j.cca.2009.10.016}, issn = {1873-3492}, journal = {Clinica chimica acta; international journal of clinical chemistry}, keywords = {glanzmann, glycoprotein, glycoproteins, gpiibiiia, review}, month = {October}, posted-at = {2009-11-03 13:55:02}, priority = {3}, title = {Glanzmann thrombasthenia: An update.}, url = {http://dx.doi.org/10.1016/j.cca.2009.10.016}, year = {2009} }

TY - JOUR ID - citeulike:6049199 L3 - citeulike-article-id:6049199 N2 - Glanzmann thrombasthenia (GT) is a rare autosomal recessive disorder characterized by qualitative or quantitative abnormalities of the platelet membrane glycoprotein (GP) IIb/IIIa. Physiologically, this platelet receptor normally binds several adhesive plasma proteins, and this facilitates attachment and aggregation of platelets to ensure thrombus formation at sites of vascular injury. The lack of resultant platelet aggregation in GT leads to mucocutaneous bleeding whose manifestation may be clinically variable, ranging from easy bruising to severe and potentially life-threatening hemorrhages. In this review we discuss the main characteristics of GT, focusing on molecular defects, diagnostic evaluation and treatment strategies. JF - Clinica chimica acta; international journal of clinical chemistry SN - 1873-3492 TI - Glanzmann thrombasthenia: An update. KW - glanzmann KW - glycoprotein KW - glycoproteins KW - gpiibiiia KW - review AU - Franchini, Massimo AU - Favaloro, Emmanuel AU - Lippi, Giuseppe PY - 2009/10/23/ UR - http://dx.doi.org/10.1016/j.cca.2009.10.016 ER -