Results 31 to 40 of about 36,875 (192)
Exosomes originating from human umbilical cord mesenchymal stem cells (hucMSC-exos) have become a novel strategy for treating various diseases owing to their ability to regulate intercellular signal communication. However, the potential of hucMSC-exos to
Qingfeng Lv +10 more
doaj +1 more source
Background Antiphospholipid syndrome is an autoimmune disorder characterized by the presence of antiphospholipid antibodies and commonly presents with vascular thromboembolic phenomena, thrombocytopenia, and obstetric complications.
Yogesh Sharma +2 more
doaj +1 more source
Background Antiphospholipid syndrome causes systemic arterial and venous thromboses due to the presence of antiphospholipid antibodies. Adrenal insufficiency is a rare complication of antiphospholipid syndrome that may result in fatal outcomes if left ...
Yoshihito Iijima +3 more
doaj +1 more source
A case of primary antiphospholipid syndrome under the mask of systemic lupus erythematosus
A case of late diagnosis of primary antiphospholipid syndrome in a patient with recurrent miscarriage is presented. The pronounced immunological activity of the antiphospholipid syndrome with severe arthritis, fibrosing alveolitis mimicked systemic lupus
N. S. Pozhilenko, T. V. Moiseeva
doaj +1 more source
What nephrolopathologists need to know about antiphospholipid syndrome-associated nephropathy: Is it time for formulating a classification for renal morphologic lesions? [PDF]
Context: Antiphospholipid syndrome (APS) is a systemic autoimmune disorder which commonly affects kidneys. Evidence Acquisitions: Directory of Open Access Journals (DOAJ), Google Scholar, PubMed (NLM), LISTA (EBSCO) and Web of Science have been searched.
Muhammed Mubarak, Hamid Nasri
doaj +1 more source
A significant proportion of patients with Essential Thrombocythaemia (ET) have thrombotic complications which have an important impact upon the quality, and duration of their life.
Machin, S.J. +11 more
core +1 more source
In this clinical vignette, we present a case of a 59-year-old woman with catastrophic antiphospholipid syndrome likely triggered by polymicrobial sepsis.
Shanna Ariane Tucker +2 more
doaj +1 more source
Ten years ago we described a group of patients with a combination of clinical features associated with the presence of antiphospholipid antibodies. These features included a tendency to both arterial and venous thrombosis, livedo reticularis, recurrent abortions and occasional thrombocytopenia.
G R, Hughes, M A, Khamashta
openaire +2 more sources
Antiphospholipid Syndrome: Expanding the Spectrum of Autoimmune Thrombosis [PDF]
[eng] The antiphospholipid syndrome (APS) is an acquired prothrombotic syndrome characterized by venous or arterial thromboses and pregnancy morbidity.
Gómez-Puerta, José Alfredo +1 more
core
Catastrophic Antiphospholipid Syndrome: A Case Series
Catastrophic antiphospholipid syndrome (CAPS) is the rare but most severe form of antiphospholipid syndrome with multiple organ ischemia developing over a short period of time.
Navya Christopher +5 more
doaj +1 more source

