Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Borja Esteso Orduña"'
Autor:
Noelia Martínez Menéndez, Silvia Cámara Barrio, Borja Esteso Orduña, María de la Concepción Fournier del Castillo
Publikováno v:
Psicosomática y Psiquiatría, Iss 15 (2021)
Externí odkaz:
https://doaj.org/article/c7426b88ae7b4b3f9e80447c6d70057d
Autor:
Marcelo Budke, María de la Concepción Fournier Del Castillo, Borja Esteso Orduña, Maria Angeles Perez Jiménez, Marta García Fernández, Silvia Cámara Barrio, María Jesús Maldonado Belmonte, Juan Álvarez-Linera Prado, Javier González Marqués, Eva María Andrés Esteban
Publikováno v:
Epilepsybehavior : EB. 117
Background We aimed to prospectively analyze memory and executive and social cognitive functioning in patients with drug-resistant frontal lobe epilepsy (FLE) and temporal lobe epilepsy (TLE) with focal lesions and isolate the impact of intellectual
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0e81a505c24958e713a7496b6a8692f
https://pubmed.ncbi.nlm.nih.gov/33640566
https://pubmed.ncbi.nlm.nih.gov/33640566
Autor:
Laura López Marín, Silvia Cámara Barrio, María de la Concepción Fournier Del Castillo, Luis González Gutiérrez-Solana, Borja Esteso Orduña, Verónica Cantarín Extremera, Izaskun Basterra Jiménez
Publikováno v:
Neurodegenerative disease management. 10(2)
Niemann–Pick type C (NP-C) disease is a neurovisceral atypical lysosomal lipid storage disorder with a poor prognosis. We present the 5-year neuropsychological follow-up of a patient with juvenile onset NP-C, spanning the pre-diagnostic stage to th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e8f3d98b8230215a7c7e16442043fa9
https://pubmed.ncbi.nlm.nih.gov/32351165
https://pubmed.ncbi.nlm.nih.gov/32351165
Autor:
Emily M. Briceño, Borja Esteso Orduña, Javier Melero Llorente, María de la Concepción Fournier Del Castillo, Raquel Seijas Gómez, Elena García Esparza
Publikováno v:
Journal of clinical and experimental neuropsychology. 40(1)
Congenital central hypoventilation syndrome (CCHS) is a rare genetic disorder due to paired-like homeobox gene (PHOX2B) mutations. CCHS patients suffer from dysregulation of the autonomic nervous system characterized by the absence of or extremely re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d20c9b22c40cf30b661a945a3e33500
https://pubmed.ncbi.nlm.nih.gov/28708033
https://pubmed.ncbi.nlm.nih.gov/28708033