Results 111 to 120 of about 308,468 (256)
Evans Syndrome with Brachial Plexopathy and Steroid-Induced Gastritis
Evans syndrome is a rare, autoimmune disorder characterized by autoimmune hemolytic anemia and immune thrombocytopenia. Brachial plexopathy occurs due to damage of brachial plexus which results in weakness, numbness, and pain in the arm and shoulder ...
Mushrifa Hishmath +3 more
doaj +1 more source
Australia and the Path Not Taken: The Declining Independence and Influence of Middle Powers
ABSTRACT Australian foreign policy has famously been distinguished by the search for ‘great and powerful friends’. However, Australia's relationship with its current notional protector and key ally—the United States—has generally had more costs than benefits and, I argue, has consequently not been in Australia's much‐invoked ‘national interest ...
Mark Beeson
wiley +1 more source
Unveiling Complexity: A Case Study of Evans Syndrome Secondary to Atypical Pneumonia
Evans syndrome (ES) is a combined presentation of immune thrombocytopenia along with autoimmune hemolytic anemia with a positive direct antihuman globulin test.
Rucha Sawant +3 more
doaj +1 more source
The novel E3 ligase of PPAR?? TRIM25 regulates adipocyte differentiation [PDF]
Department of Biological SciencesPeroxisome proliferator-activated receptor ?? (PPAR??) is a ligand-dependent transcription factor which regulates glucose homeostasis and adipocyte differentiation.
Lee, Jae Min
core
ABSTRACT Background Schizophrenia is characterized by positive, negative, and cognitive symptoms. Current pharmacological treatments often fail to address cognitive deficits. In this review of clinical trials, we aim to identify studies that explore neurobiological (non‐psychological) strategies to address Cognitive Impairment Associated with ...
Bahareh Peyrovian +3 more
wiley +1 more source
Background: Influenza A can trigger rare haematologic complications such as immune thrombocytopenia (ITP) and haemolytic anaemia, most commonly in paediatric or immunocompromised populations.
Haseeb Tareen +6 more
doaj +1 more source
Abstract Congenital aniridia is a rare genetic disorder primarily caused by pathogenic variants of the PAX6 gene. It leads to various panocular anomalies, including aniridia‐associated keratopathy (AAK). This review highlights recent insights into its pathogenesis, focusing on clinical staging, microstructural changes in the cornea and molecular ...
N. Szentmáry +27 more
wiley +1 more source
ABSTRACT Background People with intellectual disabilities face significant health disparities and often encounter barriers in accessing healthcare services. Although research supports the need for reasonable adjustments to improve healthcare access for this population, implementation in acute healthcare settings remains limited.
Owen Doody +5 more
wiley +1 more source
Management of autoimmune hemolytic anemia in children and adolescents: A single center experience
OBJECTIVE: To present and discuss the treatment of autoimmune hemolytic anemia (AIHA). METHODS: The medical records of all patients (n=19) diagnosed in a tertiary hematology center between 1999 and 2010 were retrospectively reviewed. RESULTS: Median age
Nazan Sarper +3 more
doaj +1 more source
rs6971 TSPO polymorphism in Parkinson's disease
Movement Disorders, EarlyView.
Bina Patel +9 more
wiley +1 more source

