6 results match your criteria: "Hospital Universitario La Paz-FIBHULP[Affiliation]"
J Plast Reconstr Aesthet Surg
December 2024
Division of Plastic and Reconstructive Surgery, Hospital Universitario 'La Paz' FIBHULP-IdiPaz, Paseo de la Castellana, 261, 28046 Madrid, Spain. Electronic address:
Introduction: Despite its infrequency, 'spare-part surgery' represents a reconstructive strategy that uses segments of amputated limbs as donor tissue to preserve function in other injured anatomical regions. The purpose of this study was to review our 14-year experience in emergency microsurgical reconstruction of traumatised limbs using free fillet flaps obtained from non-salvageable amputated parts.
Materials And Methods: A retrospective observational study was conducted on patients who underwent urgent free fillet flap transfer for upper or lower limb reconstruction between 2007 and 2021.
Ticks Tick Borne Dis
November 2024
Fundación para la Investigación Biomédica del Hospital Universitario la Paz -FIBHULP-, Paseo de la Castellana, 261, 28046, Madrid, Spain. Electronic address:
Cholesterol is a molecule vital for tick physiology, but ticks cannot synthesize it and rely on dietary cholesterol. Therefore, tick proteins involved in cholesterol absorption and transport, such as the Niemann-Pick type C1 domain-containing (NPC1) proteins, are promising targets for anti-tick vaccine development. The aim of this study was to assess the structure, function, and protective efficacy of the NPC1 orthologues identified previously in the midgut transcriptomes of argasid ticks Ornithodoros erraticus and Ornithodoros moubata.
View Article and Find Full Text PDFFront Pharmacol
September 2019
Cellular Biology in Renal Diseases Laboratory, IIS-Fundación Jiménez Díaz, Universidad Autónoma de Madrid, Madrid, Spain.
Hypertension is now considered as an inflammatory disease, and the kidney is a key end-organ target. Experimental and clinical studies suggest that interleukin 17A (IL-17A) is a promising therapeutic target in immune and chronic inflammatory diseases, including hypertension and kidney disease. Elevated circulating IL-17A levels have been observed in hypertensive patients.
View Article and Find Full Text PDFNephrol Dial Transplant
September 2011
Research Unit, Hospital Universitario La Paz-FIBHULP, Madrid, Spain.
Background: Depending on the cytokine microenvironment, macrophages (Mϕ) can adopt a proinflammatory (M1) or a profibrotic (M2) phenotype characterized by the expression of cell surface proteins such as CD206 and CD163 and soluble factors such as CC chemokine ligand 18 (CCL18). A key role for Mϕ in fibrosis has been observed in diverse organ settings. We studied the Mϕ population in a human model of peritoneal dialysis in which continuous stress due to dialysis fluids and recurrent peritonitis represent a risk for peritoneal membrane dysfunction reflected as ultrafiltration failure (UFF) and peritoneal fibrosis.
View Article and Find Full Text PDFJ Allergy Clin Immunol
March 2010
Research Unit, Hospital Universitario La Paz-FIBHULP, Madrid, Spain.
Background: Toxic epidermal necrolysis (TEN) and Stevens-Johnson syndrome (SJS) are severe, bullous cutaneous diseases with uncertain pathogenesis, although cytotoxic T cells seem to be involved. Natural killer (NK)-like activity has been found in blister infiltrates. Cytotoxic T lymphocytes (CTLs) with NK-like activity (NK-CTLs) have been shown to express T-cell receptors restricted by the HLA-Ib molecule HLA-E.
View Article and Find Full Text PDFAm J Physiol Gastrointest Liver Physiol
May 2009
Research Unit, La Paz University Hospital-Fundación para la Investigación Biomédica del Hospital Universitario La Paz (FIBHULP), Madrid, Spain.
Farnesoid X receptor (FXR) is a bile acid-sensing nuclear receptor that controls bile acid homeostasis. It has been suggested that downregulation of FXR contributes to the pathogenesis of an inherited disorder of bile secretion caused by mutations in ATP8B1. We have investigated the relationship between ATP8B1 knockdown and FXR downregulation in the human hepatoblastoma cell line HepG2.
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