Institution
Hospital Universitario Insular de Gran Canaria
Recent research
- Health & Medicine
Genomic and clinical landscape of RAS mutations in acute myeloid leukemia
RAS mutations are recurrent in acute myeloid leukemia (AML); yet, their genomic and clinical landscape remain poorly characterized. We analyzed centralized molecular profiling data in 8,553 patients with newly diagnosed AML. Of these, 1,775 (21%) harbored RAS mutations: NRAS in 1...
- Health & MedicineOpen access
Beyond β-amyloid: transthyretin cerebral amyloid angiopathy
Abstract Cerebral amyloid angiopathy (CAA) is most commonly associated with β-amyloid deposition, but other amyloid proteins may accumulate in leptomeningeal and superficial cortical vessels. We report a man first evaluated neurologically at 44 years of age after approximately on...
- Health & MedicineOpen access
High-voltage electrical injuries are uncommon but potentially limb- and life-threatening because the extent of deep tissue damage may be disproportionate to the visible cutaneous injury. Upper limb involvement is particularly important when the hand is affected and when acute mot...
- Health & MedicineOpen access
Abstract Background Neglected tropical diseases (NTDs) represent an increasing but often overlooked challenge for European health systems owing to international mobility, migration, travel, and climate-related changes in disease ecology. Although effective treatments exist for mo...
- Health & MedicineOpen access
Systemic lupus erythematosus (SLE) is characterized by elevated levels of various cytokines. Interleukin (IL)-13 is a pleiotropic type 2 cytokine that plays a central role in allergic inflammation and tissue fibrosis. Until recently, serum measurement of IL-13 was not feasible be...
- Health & Medicine
ABSTRACT Background Minimally invasive left pancreatectomy (MILP) has become the preferred approach to treat lesions of the pancreatic body and tail. However, the procedure may require conversion to open surgery, with reported conversion rates varying widely in the literature. Th...
- Health & MedicineOpen access
Integrated multiomics analysis reveals metabolic and microbiome alterations in Wilson disease
Wilson disease (WD) is a rare autosomal recessive disorder caused by mutations in ATP7B , which encodes a copper transporter. Abnormal ATP7B function leads to copper deposition, mainly in the liver and brain, resulting in hepatic, neurological, and psychiatric impairments. Metabo...