Results 1 to 10 of about 94 (80)
Emergence, spread, and impact of high-pathogenicity avian influenza H5 in wild birds and mammals of South America and Antarctica. [PDF]
Conserv BiolAbstract The currently circulating high‐pathogenicity avian influenza (HPAI) virus of the subtype H5 causes variable illness and death in wild and domestic birds and mammals, as well as in humans. This virus evolved from the Goose/Guangdong lineage of the HPAI H5 virus, which emerged in commercial poultry in China in 1996, spilled over into wild birds,
Kuiken T +9 more
europepmc +2 more sources
UEG Week 2025 Oral Presentations [PDF]
United European Gastroenterol JUnited European Gastroenterology Journal, Volume 13, Issue S8, Page S7-S188, October 2025.
europepmc +2 more sources
J Extracell VesiclesJournal of Extracellular Vesicles, Volume 14, Issue S1, October 2025.
europepmc +2 more sources
UEG Week 2025 Poster Presentations [PDF]
United European Gastroenterol JUnited European Gastroenterology Journal, Volume 13, Issue S8, Page S803-S1476, October 2025.
europepmc +2 more sources
Neurodegeneration and epigenetics: A review
Neurología, 2023 Neuronal function and differentiation are tightly regulated by both genome and epigenome. Based on the environmental information the epigenetic changes occur. Neurodegeneration is the consequence of dysregulation of both the genome and epigenome. In this
P. Ghosh, A. Saadat
doaj +3 more sources
Creutzfeldt-Jakob disease in Peru: report of eleven cases
Revista Peruana de Medicina Experimental y Salud Pública, 2014 Creutzfeldt-Jakob disease (CJD) is a fatal neurological disease caused by pathological isoform of the human prion protein. Clinical features of six cases of the sporadic form of CJD with definitive diagnosis by histopathology, and five cases with ...
Luis Torres-Ramírez +7 more
doaj +1 more source
Revista de la Facultad de Ciencias Médicas de Córdoba, 2004 La encefalopatía de Creutzfeldt Jakob (ECJ), es la de mayor incidencia dentro del grupo de las encefalopatías espongiformes transmisibles o enfermedades por priones, las que tienen como característica única entre todas las patologías, la de poder ...
Rolando Cosacov +6 more
doaj +1 more source
Structural and functional neuroimaging in human prion diseases
Neurología (English Edition), 2013 Introduction: Prion diseases are neurodegenerative disorders resulting from the accumulation of a misfolded isoform of the cellular prion protein (PrPC). They can occur as acquired, sporadic, or hereditary forms. Although prion diseases show a wide range
S. Ortega-Cubero +6 more
doaj +1 more source
Galicia Clínica, 2020 Las demencias rápidamente progresivas (DRP) engloban un grupo muy heterogéneo de entidades caracterizadas por la aparición de trastornos cognitivos y conductuales relevantes que evolucionan en pocas semanas o meses. La triada clínica habitual consiste en
Miguel Angel Nuñez Viejo +1 more
doaj +1 more source
Neuroimagen estructural y funcional en las enfermedades priónicas humanas
Neurología, 2013 Resumen: Introducción: Las prionopatías son un conjunto de enfermedades neurodegenerativas producidas por el acúmulo de una isoforma anormal de la proteína priónica celular (PrPc). Se clasifican en adquiridas, hereditarias y esporádicas.
S. Ortega-Cubero +6 more
doaj +1 more source