Zobrazeno 1 - 10
of 119
pro vyhledávání: '"T, Cabada"'
Publikováno v:
Neurología, Vol 36, Iss 2, Pp 171-173 (2021)
Externí odkaz:
https://doaj.org/article/dcff02cce73f4835898922170a4b0001
Publikováno v:
Neurología (English Edition), Vol 36, Iss 2, Pp 171-173 (2021)
Externí odkaz:
https://doaj.org/article/188e0ca171164d2d9200f0a6d39436e5
Autor:
M. Iridoy, T. Cabada, B Remirez, Marisol Gómez, I. Jericó, R. Seijas, P López, J Díaz, Pablo Lecumberri
Publikováno v:
Neuroradiology. 63:1019-1029
Myotonic dystrophy type 1 (DM1) is a muscular dystrophy with neurological, cognitive, and radiological abnormalities. The developmental or degenerative nature of these abnormalities, and their progression over time, remains unclear. The aim of this s
Autor:
M.C. Bacaicoa Saralegui, M.V. Zelaya Huerta, P. López Sala, T. Cabada Giadás, N. Alberdi Aldasoro
Publikováno v:
Radiología. 62:59-66
Resumen Introduccion La leucoencefalopatia multifocal progresiva (LMP) es una enfermedad desmielinizante del sistema nervioso central causada por la reactivacion del virus JC. Esta encefalopatia oportunista se asocia mayormente a pacientes inmunodepr
Autor:
P. López Sala, T. Cabada Giadás, N. Alberdi Aldasoro, M.C. Bacaicoa Saralegui, M.V. Zelaya Huerta
Publikováno v:
Radiología (English Edition). 62:59-66
Introduction Progressive multifocal leukoencephalopathy is a demyelinating disease of the central nervous system caused by the reactivation of the JC virus. This opportunistic encephalopathy mainly affects immunodepressed patients with stage III HIV
Publikováno v:
Neurología, Vol 36, Iss 2, Pp 171-173 (2021)
[Neuropsychological profile in patients with myotonic dystrophy type 1: a four-year follow-up study]
Autor:
J, Díaz-Leiva, T, Cabada-Giadás, R, Seijas-Gómez, I, Jericó-Pascual, P, López-Sala, M, Iridoy-Zulet
Publikováno v:
Revista de neurologia. 70(11)
Myotonic dystrophy type 1 (MD1), or Steinert's disease, is a multisystemic disorder of autosomal dominant inheritance, whose adult variant usually presents with multidomain cognitive impairment and affects patients' functionality and quality of life.
Autor:
P, López Sala, N, Alberdi Aldasoro, M V, Zelaya Huerta, M C, Bacaicoa Saralegui, T, Cabada Giadás
Publikováno v:
Radiologia. 62(1)
Progressive multifocal leukoencephalopathy is a demyelinating disease of the central nervous system caused by the reactivation of the JC virus. This opportunistic encephalopathy mainly affects immunodepressed patients with stage III HIV infection, al
Autor:
P López-Sala, M Iridoy-Zulet, Raquel Seijas-Gómez, T Cabada-Giadás, J Díaz-Leiva, I Jericó-Pascual
Publikováno v:
Revista de Neurología. 70:406
Introduccion. La distrofia miotonica tipo 1 (DM1), o enfermedad de Steinert, es un trastorno multisistemico de herencia autosomica dominante, cuya variante adulta suele cursar con deterioro cognitivo multidominio y afectacion de la funcionalidad y la
Autor:
T. Cabada Giadás, M. Mendigaña Ramos
Publikováno v:
Radiología. 57:156-166
Advances in imaging studies for acute ischemic stroke are largely due to the development of new efficacious treatments carried out in the acute phase. Together with computed tomography (CT) perfusion studies, CT angiography facilitates the selection