Antiphospholipid Syndrome Presenting as Recurrent Pancreatitis and Renal Thrombotic Microangiopathy
Hae-Kyung LEE; Shin-Ok JEONG; Yunsuek KIM; So-Young JIN; Hyun-Sook KIM; Young-Deok CHO.
Korean Journal of Medicine
; : 598-603, 2015.
ArtÃculo en Ko | WPRIM | ID: wpr-92377
Documentos relacionados
Antiphospholipid Antibodies (aPL) and Thrombotic Microangiopathy for the Diagnosis of aPL Nephropathy: You Can't Have One Without the Other.
The estimated prevalence of antiphospholipid antibodies and criteria-antiphospholipid syndrome in subjects with renal thrombotic microangiopathy.
Update on antiphospholipid syndrome.
Increased eryptosis in patients with primary antiphospholipid syndrome (APS): a new actor in the pathogenesis of APS.
Whole blood transcriptome identifies interferon-regulated genes as key drivers in thrombotic primary antiphospholipid syndrome.
Low ectonucleotidase activity and increased neutrophil-platelet aggregates in patients with antiphospholipid syndrome.
How I diagnose and treat antiphospholipid syndrome in pregnancy.
Antiphospholipid Syndrome in Pregnancy: New and Old Pathogenetic Mechanisms.
Phenotypes in antiphospholipid syndrome: A hierarchical cluster analysis based on two independent databases.
Antiphospholipid syndrome pathogenesis in 2023: an update of new mechanisms or just a reconsideration of the old ones?