scholarly journals Hughes syndrome antiphospholipid syndrome

2018 ◽  
Vol 11 (4) ◽  
pp. 169 ◽  
Author(s):  
GrahamRobert Vivian Hughes
Lupus ◽  
2020 ◽  
Vol 29 (12) ◽  
pp. 1493-1502
Author(s):  
Wared Nour-Eldine ◽  
Hussein A Noureldine ◽  
Batoul A Haydar ◽  
Mariam Nour Eldine ◽  
Mohammad Hassan A Noureldine ◽  
...  

Prior to 1983, several landmark reports prepared the stage for a detailed description of the Antiphospholipid (Hughes) syndrome (APS). Formerly depicted as lupus-like, APS exhibits a wide spectrum of symptoms that overlap with Sjogren’s, Hashimoto, and other autoimmune diseases. In this review, we take a glimpse into the history of description of APS, discussing the events that led to its recognition as one of the most common autoimmune diseases and the enormous impact of that recognition in the rheumatology field.


Lupus ◽  
1998 ◽  
Vol 7 (2_suppl) ◽  
pp. 1-4 ◽  
Author(s):  
Graham RV Hughes

In the 15 years since our description of the antiphospholipid syndrome, it has become recognised as an important disease, not only in the world of lupus but in the broader areas of obstetrics, neurology and vascular disease. Although advances have been made in the understanding of the interactions of antibodies, protein co-factors, clotting molecules, endothelium and platelets, much still needs to be learnt about management where strokes, in particular, continue to cause significant morbidity.


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