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Volumn 127, Issue 2, 2002, Pages 289-292

Anti-platelet antibodies associated with the Canale-Smith syndrome bind to the same platelet glycoprotein complexes as those of idiopathic thrombocytopenic purpura patients

Author keywords

Anti platelet; Antibodies; Autoimmune lymphoproliferative syndrome; Canale Smith syndrome; Fas mutations; Human lymphoproliferative; Idiopathic; Platelet glycoprotein complexes; Purpura autoimmune disease; Syndrome; Thrombocytopenic

Indexed keywords

FIBRINOGEN RECEPTOR; GLYCOPROTEIN IB; IMMUNOGLOBULIN; THROMBOCYTE ANTIBODY; VERY LATE ACTIVATION ANTIGEN 2;

EID: 0036126466     PISSN: 00099104     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2249.2002.01750.x     Document Type: Article
Times cited : (9)

References (31)
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  • 17
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    • Deficiency of the Fas apoptosis pathway without fas gene mutations in pediatric patients with autoimmunity/lymphoproliferation
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  • 18
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    • Inherited human caspase-10 mutations underlie defective lymphocyte and dendritic cell apoptosis in Autoimmune Lymphoproliferative Syndrome Type II
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.