Results 31 to 40 of about 58,978,997 (155)
, 2021 Research and Practice in Thrombosis and Haemostasis, Volume 5, Issue S2, October 2021.
wiley +1 more source
Mediators of Inflammation, Volume 2019, Issue 1, 2019., 2019 Interleukin‐10 (IL‐10) is a key anti‐inflammatory cytokine, secreted by macrophages and other immune cells to attenuate inflammation. Autocrine type I interferons (IFNs) largely mediate the delayed expression of IL‐10 by LPS‐stimulated macrophages. We have previously shown that IL‐10 is synergistically expressed in macrophages following a costimulus of
Orna Ernst +8 more
wiley +1 more source
Trombosis venosa superficial extensa y síndrome de Behçet [PDF]
, 2021 Superficial venous thrombosis is frequent; its main risk factor is variceal veins’ presence in lower limbs, although it can occur in other prothrombotic states. Behçet syndrome is a chronic disease characterized by recurrent oral and genital aphthous and
Cervilla-Muñoz, Eva +9 more
core +1 more source
Enfermedad de Behçet: estudio retrospectivo [PDF]
, 2001 Objetivo: Desde que se establecieron los criterios para el diagnóstico de la enfermedad de Behçet (EB), se han publicado numerosas manifestaciones clínicas asociadas a esta enfermedad.
Campos,C. +5 more
core
Revista Colombiana de Nefrología, 2015 El síndrome antifosfolípido (SAF)es un trastorno hematológico que cursa con un estado de hipercoagulabilidad de origen autoinmune, caracterizado por fenómenos trombóticos venosos o arteriales, pérdidas fetales recurrentes y presencia de anticuerpos ...
Carlos Olivares +7 more
doaj +1 more source
Hughes–Stovin Syndrome: A Rare Cause of Pulmonary Artery Aneurysm and Thrombosis—A Case Report
International Journal of Rheumatic Diseases, Volume 28, Issue 4, April 2025.ABSTRACT Hughes–Stovin Syndrome (HSS) is a rare, life‐threatening condition characterized by thrombophlebitis and pulmonary artery aneurysms, often viewed as a variant of Behçet's disease. Its diagnosis and management are challenging due to its rarity and overlapping symptoms with other vascular disorders.
Abdul Qadir +3 more
wiley +1 more source
VEXAS‐Defining UBA1 Somatic Variants in 245,368 Diverse Individuals in the NIH All Of Us Cohort
Arthritis &Rheumatology, Volume 76, Issue 6, Page 942-948, June 2024.Objective Somatic variants in UBA1 cause VEXAS, a recently described, systemic autoinflammatory disease. Research on VEXAS has largely focused on highly symptomatic patients. We sought to determine the prevalence of canonical, VEXAS‐associated somatic variants and their disease penetrance in a diverse, unselected population.
Robert W. Corty +5 more
wiley +1 more source
Enfermedad de Behcet: estudio clínico y tratamiento en el Hospital Arzobispo Loayza
Revista Médica Herediana, 2001 Objetivo: Determinar la frecuencia de presentación, así como, las manifestaciones clínicas, tratamiento y evolución de la Enfermedad de Behcet en el Hospital Arzobispo Loayza (HAL) durante el periodo 1992 - 2001. Material y Métodos: Se realizó un estudio
Blanca Alzamora Barrios +1 more
doaj
Clinical course of Covid-19 in a cohort of patients with Behçet disease. [PDF]
Med Clin (Engl Ed), 2022 Correa-Rodríguez M +5 more
europepmc +2 more sources