Zobrazeno 1 - 5
of 5
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6fc8a1714257c22f35c5e4a2c11f61fe
https://doi.org/10.1111/neup.12505
https://doi.org/10.1111/neup.12505
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4716b074371eafabdd81776a7efe6c28
https://doi.org/10.3233/jad-161298
https://doi.org/10.3233/jad-161298
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3dbda29c956899f8489b9d07e83000da
https://pubmed.ncbi.nlm.nih.gov/29097599
https://pubmed.ncbi.nlm.nih.gov/29097599
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56d6f879d90ba29a04ce0ff532fc532c
https://doi.org/10.1111/neup.12150
https://doi.org/10.1111/neup.12150
Autor:
Iván, Fernández-Vega, Javier, Ruiz-Ojeda, Ramon A, Juste, Maria, Geijo, Juan Jose, Zarranz, Jose Luis, Sánchez Menoyo, Ikerne, Vicente-Etxenausia, Jennifer, Mediavilla-García, Isabel, Guerra-Merino
Publikováno v:
Neuropathology : official journal of the Japanese Society of Neuropathology. 35(1)
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1d03ba450ea998a4a39f0aaed648b7c6
https://pubmed.ncbi.nlm.nih.gov/25186620
https://pubmed.ncbi.nlm.nih.gov/25186620