Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ikerne Vicente Etxenausia"'
Autor:
Juan Jose Zarranz Imirizaldu, María V. Geijo, Isidro Ferrer, Daniela Diaz-Lucena, Franc Llorens, Itxaso Azkune Calle, Ikerne Vicente Etxenausia, Jorge Santos-Juanes, Iván Fernández-Vega, Ramón A. Juste
Publikováno v:
Neuropathology. 38:561-567
Proteinase K-resistant prion protein (PrPRes ) nuclear and perinuclear immunoreactivity in oligodendrocytes of the frontal cortex is found in one case of otherwise typical sporadic Creutzfeldt-Jakob disease (sCJD) type VV2a. The PrP nature of the inc
Autor:
Carla Martín, Jesus Merayo-Lloves, Iván Fernández-Vega, Luis M. Quirós, Laura Lorente-Gea, Irune Ruiz-Diaz, Helena Ordiales, Beatriz García, María Cristina Caballero-Martínez, Isabel Guerra-Merino, Kelvin Piña Batista, Jorge Santos-Juanes, Ikerne Vicente-Etxenausia, Sonia Castañón, Bárbara Muñiz-Alonso, Olivia García-Suárez, Santiago Fernández-Menéndez
Publikováno v:
Journal of Alzheimer's Disease. 58:185-192
BACKGROUND Heparan sulfate proteoglycans (HSPGs) promote amyloid-β peptide and tau fibrillization in Alzheimer's disease (AD) and provide resistance against proteolytic breakdown. Heparanase (HPSE) is the only enzyme that cleaves heparan sulfate (HS
Autor:
Isabel Guerra-Merino, Aitzol Miguelez-Rodriguez, Ikerne Vicente-Etxenausia, Katty Perez de Heredia-Goñi, Jorge Santos-Juanes, Luis M. Quirós, Laura Lorente-Gea, José Javier Aguirre, Beatriz García, Iván Fernández-Vega
Publikováno v:
Journal of clinical pathology. 71(5)
AimsTo investigate the expression of major proteins related to primary neurodegenerative diseases and their prognostic significance in brains with Creutzfeldt-Jakob disease (CJD).Materials and methodsThirty consecutive cases of confirmed CJD during t
Autor:
Iván Fernández-Vega, Javier Ruiz-Ojeda, Ikerne Vicente-Etxenausia, María V. Geijo, Ramón A. Juste, Jose Luis Sánchez Menoyo, Isabel Guerra-Merino, Juan J. Zarranz, Jennifer Mediavilla-García
Publikováno v:
Neuropathology. 35:56-63
We report hereby an autopsy case of sporadic mixed phenotype CJD without hereditary burden and a long-term clinical course. An 80-year old man was diagnosed with mild cognitive impairment 27 months before death, caused by bronchopneumonia and severe
Autor:
Fernández‐Vega, Ivan1,2, Díaz‐Lucena, Daniela3,4, Azkune Calle, Itxaso5, Geijo, Maria6, Juste, Ramon A.6, Llorens, Franc3,4, Vicente Etxenausia, Ikerne2, Santos‐Juanes, Jorge7, Zarranz Imirizaldu, Juan Jose8, Ferrer, Isidro3,4,9,10 8082ifa@gmail.com
Publikováno v:
Neuropathology. Oct2018, Vol. 38 Issue 5, p561-567. 7p.
Autor:
Fernández‐Vega, Iván1,2, Ruiz‐Ojeda, Javier3, Juste, Ramon A.4, Geijo, Maria4, Zarranz, Juan Jose5, Sánchez Menoyo, Jose Luis3, Vicente‐Etxenausia, Ikerne2, Mediavilla‐García, Jennifer2, Guerra‐Merino, Isabel1,2
Publikováno v:
Neuropathology. Feb2015, Vol. 35 Issue 1, p56-63. 8p.
Autor:
Miguelez-Rodriguez, Aitzol, Santos-Juanes, Jorge, Vicente-Etxenausia, Ikerne, de Heredia-Goñi, Katty Perez, Garcia, Beatriz, Quiros, Luis M., Lorente-Gea, Laura, Guerra-Merino, Isabel, Aguirre, Jose J., Fernandez-Vega, Ivan
Publikováno v:
Journal of Clinical Pathology; May2018, Vol. 71 Issue 5, p446-450, 5p