Glanzmann thrombasthenia in children from Argentina

Purpose: Glanzmann thrombasthenia is a well-defined inherited disorder of platelet function characterized by a decrease or absence of functional platelet glycoprotein (GP) GPIIbIIIa. The diagnosis must be considered in patients presenting with mucocutaneous bleeding, purpura, a normal platelet count...

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Autores principales:	Sassetti, B., Lajmanovich, A., Vázquez, A., Vizcarguénaga, M.I., Berthier, R., Aversa, L., Bustelo, P., Kordich, L.
Formato:	JOUR
Materias:	Bleeding disorder GPIIbIIIa GT Pediatrics fibrinogen receptor adolescent argentina article autosomal recessive disorder bleeding bleeding time child clinical article disease classification female glanzmann disease human male priority journal purpura thrombocyte aggregation Adolescent Argentina Blotting, Southern Child Child, Preschool Female Humans Immunoenzyme Techniques Infant Male Megakaryocytes Platelet Glycoprotein GPIIb-IIIa Complex Thrombasthenia
Acceso en línea:	http://hdl.handle.net/20.500.12110/paper_10774114_v18_n1_p23_Sassetti
Aporte de:	Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires

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