Results 131 to 140 of about 45,158 (283)

Systemic Lupus Erythematosus With Catastrophic APS and Libman–Sacks Endocarditis in a Patient With Autoimmune Hemolytic Anemia: A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Systemic lupus erythematosus (SLE) can lead to antiphospholipid syndrome (APS) and catastrophic APS (CAPS), causing severe thrombotic events. This case of autoimmune hemolytic anemia (AIHA) with stroke and Libman–Sacks endocarditis highlights the need for APS evaluation and shows that prompt anticoagulation and immunosuppressive therapy are ...
Soroush Ehsan   +4 more
wiley   +1 more source

Outcomes of Cerebral Venous Thrombosis in Patients With Myeloproliferative Neoplasms from a U.S. Nationwide Hospitalization Study

open access: yes
eJHaem, Volume 7, Issue 1, February 2026.
Nikhil Vojjala   +6 more
wiley   +1 more source

Unusual Etiology of Budd‐Chiari Syndrome in an Adolescent: A Case of Combined Thrombophilic Disorder

open access: yesClinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Budd‐Chiari syndrome (BCS) is an uncommon but potentially life‐threatening hepatic vascular disorder resulting from obstruction of the hepatic venous outflow. While it predominantly affects adults, pediatric and adolescent presentations are rare, particularly those associated with inherited thrombophilia.
Santosh Sah   +5 more
wiley   +1 more source

La Sindrome Antifosfolipidi: revisione critica degli attuali aspetti diagnostici, patogenetici e terapeutici [PDF]

open access: yes, 2012
La sindrome antifosfolipidi (aPS) identifica una condizione ad aumentato rischio di occlusione vascolare e/o complicanze gravidiche, la cui definizione è stata stabilita nel 2005 sulla base di un consenso internazionale.
PARENTI, MADDALENA
core  

Atypical Manifestation of Primary Antiphospholipid Syndrome: Conservative Management of Celiac Trunk Thrombosis Case Report and Literature Review

open access: yesClinical Case Reports, Volume 13, Issue 12, December 2025.
Atypical manifestation of primary antiphospholipid syndrome: Celiac trunk thrombosis. ABSTRACT Aortic and celiac trunk thrombosis is an exceptional manifestation of antiphospholipid syndrome (APS). A 36‐year‐old woman with triple‐positive APS, prior ischemic strokes, and chronic hypertension discontinued her anticoagulation therapy with acenocoumarin 1
Alejandra Albarrán‐Sánchez   +7 more
wiley   +1 more source

Антифосфолипидные антитела: современные представления о патогенетическом действии и лабораторной диагностике [PDF]

open access: yes, 2015
антифосфолипидные антителаантитела антифосфолипидныеантифосфолипидный синдромиммуноферментный анализэнзимоиммунный линейный ...
Волкова, М. В.   +3 more
core  

Autoimmune Thrombocytopenia Treated by Low‐Dose Splenic Irradiation Followed by Splenectomy in a Patient With Systemic Lupus Erythematosus

open access: yesClinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Severe autoimmune thrombocytopenia (ATP) in systemic lupus erythematosus (SLE) patients can be life‐threatening when refractory to standard treatments. Low‐dose splenic irradiation (LDSI) can provide temporary platelet recovery before definitive splenectomy.
Ryosuke Hanaoka
wiley   +1 more source

Single‐cell transcriptome analyses reveal disturbed decidual microenvironment in women of advanced maternal age

open access: yesClinical and Translational Medicine, Volume 15, Issue 12, December 2025.
We provide the first single‐cell atlas of the human decidua in advanced maternal age (AMA). A novel PRR15‐TGF‐β axis is identified, where PRR15 loss drives stromal fibrosis and decidualisation failure. This study reveals that AMA‐associated uterine fibrosis begins in the first trimester, shifting focus to maternal factors.
Hongliang Xie   +13 more
wiley   +1 more source

Prevention of spontaneous diabetes in BB rats with FK 506 [PDF]

open access: yes, 1990
A.L. Drash   +15 more
core   +1 more source

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