80 results match your criteria: "La Paz Research Institute IdiPaz[Affiliation]"
Pediatr Infect Dis J
July 2016
Department of Pediatrics, Tropical and Infectious Diseases Unit Hospital la Paz and, La Paz Research Institute (IdiPAZ) Infectious Diseases Department, Hospital Universitario Ramón y Cajal and IRyCIS Department of Pediatrics, Tropical and Infectious Diseases Unit Hospital la Paz and La Paz Research Institute (IdiPAZ), Madrid, Spain.
Sci Rep
May 2016
Institute of Catalysis, Consejo Superior de Investigaciones Científicas (CSIC), Madrid, Spain.
Imbalances in gut bacteria have been associated with multiple diseases. However, whether there are disease-specific changes in gut microbial metabolism remains unknown. Here, we demonstrate that human immunodeficiency virus (HIV) infection (n = 33) changes, at quantifiable levels, the metabolism of gut bacteria.
View Article and Find Full Text PDFJ Oncol
April 2016
Pathology Department, Hospital Universitario La Paz, Paseo de la Castellana 261, 28046 Madrid, Spain.
As of today two types of cartilage tumors remain a challenge even for the orthopedic oncologist: enchondroma (E), a benign tumor, and chondrosarcoma (LGC), a malignant and low aggressiveness tumor. A prospective study of 133 patients with a cartilaginous tumor of low aggressiveness in the long bones of the appendicular skeleton was done to prove this difficult differential diagnosis. Parameters including medical history and radiological and nuclear imaging were collected and compared to the result of the biopsy.
View Article and Find Full Text PDFJ Allergy Clin Immunol
April 2014
Department of Immunology, School of Medicine, Complutense University and Hospital, 12 de Octubre Health Research Institute, Madrid, Spain. Electronic address:
Orphanet J Rare Dis
May 2013
Immunology Unit, Hospital Universitario La Paz and Hospital La Paz Research Institute (IdiPAZ), Madrid, Spain.
Background: Hereditary Angioedema due to C1-Inhibitor deficiency (HAE types I and II) is a monogenic disease characterized by sudden, self-limited episodes of cutaneous and mucosal swelling due to local deregulation of vascular permeability. Despite its monogenic pattern of inheritance, HAE exhibits great clinical variability and low genotype/phenotype correlation among those affected, which ultimately hinders therapeutic approach and probably underlies yet unknown genetic and environmental factors.
Methods: We studied whole-genome RNA expression of PBMCs in three HAE type-I families (accounting for 40 individuals), 24 of which carry the same R472X mutation in the C1-Inhibitor gene and show large variability in terms of disease expression.