X-linked thrombocytopenia (XLT) due to WAS mutations: clinical characteristics, long-term outcome, and treatment options - Albert, Michael H.; Bittner, Tanja C.; Nonoyama, Shigeaki; Notarangelo, Lucia Dora; Burns, Siobhan; Imai, Kohsuke; Espanol, Teresa; Fasth, Anders; Pellier, Isabelle; Strauss, Gabriele; Morio, Tomohiro; Gathmann, Benjamin; et al. (Blood, 2010)
Keywords: Adolescent; Adult; Aged; Autoimmune Diseases; Autoimmune Diseases - epidemiology; Autoimmune Diseases - etiology; Biological and medical sciences; Child; Child, Preschool; complications; Disease-Free Survival; epidemiology; etiology; Female; Genes; Genes, X-Linked; genetics; Hematologic and hematopoietic diseases; Hemorrhage; Hemorrhage - epidemiology; Hemorrhage - etiology; Humans; Immunologi inom det medicinska området; Immunology in the Medical Area; Incidence; Infection; Infections - epidemiology; Infections - etiology; Kaplan-Meier Estimate; Male; Medical sciences; Middle Aged; mortality; Mutation; Neoplasms; Neoplasms - epidemiology; Neoplasms - etiology; Pediatrics; Pediatrik; Phenotype; Preschool; Retrospective Studies; Thrombocytopenia; Thrombocytopenia - complications; Thrombocytopenia - genetics; Thrombocytopenia - mortality; Wiskott-Aldrich Syndrome Protein; Wiskott-Aldrich Syndrome Protein - genetics; X-Linked; Young Adult; X linked thrombocytopenia; Prognosis; Treatment; Hematology; Genetics; Mutation; Long term