Zobrazeno 1 - 10
of 217
pro vyhledávání: '"J Campos-Castelló"'
Autor:
J. Campos Castelló
Publikováno v:
Revista de Medicina de la Universidad de Navarra. :34-41
Autor:
Marı́a Sagrario Manzano-Palomo, Nuria Muñoz-Jareño, J Campos-Castelló, Daniel Martín Fernández-Mayoralas
Publikováno v:
European Journal of Paediatric Neurology. 8:161-164
Unlike the case in adult-onset diabetes, neurologic complications in children with type 1 diabetes are uncommon. We report a case of a 14-year-old boy with type 1 diabetes who presented at our emergency unit with acute hemiparesis and intense headach
Autor:
M. Domínguez Salgado, R. Santiago Gómez, M.aJ. Fernández de Péres Villalaín, J. Campos Castelló
Publikováno v:
Anales de Pediatría, Vol 57, Iss 5, Pp 432-443 (2002)
La cefalea es un padecimiento común en la infancia, y su frecuencia se incrementa en la adolescencia. En la valoración de la cefalea, la historia clínica ha demostrado ser el instrumento más racional y efectivo en la valoración de esta enfermeda
Publikováno v:
European Journal of Paediatric Neurology. 1:173-176
A boy with severe symptoms of biotinidase deficiency diagnosed at the age of 12 years showed a remarkable improvement of his neurological picture and normalization of brain magnetic resonance imaging abnormalities when prescribed oral biotin.
Autor:
Jaume Campistol-Plana, Patricia Smeyers-Durá, José L. Herranz-Fernández, M. Rufo-Campos, Salvador Ibáñez-Micó, A Martínez-Bermejo, C Casas-Fernández, J Campos-Castelló, Alarcón-Martínez H
Publikováno v:
Drugs in R&D
Background The safety and effectiveness of lacosamide, an antiepileptic drug (AED) that selectively enhances the slow inactivation of voltage-gated sodium channels without affecting rapid inactivation, has been demonstrated in randomized, double-blin
Autor:
Nuria Muñoz Jareño, Celia Pérez-Cerdá Silvestre, J Campos-Castelló, Magdalena Ugarte Pérez, Daniel Martín Fernández-Mayoralas, Begoña Merinero Cortés
Publikováno v:
Journal of child neurology. 22(2)
The authors report the case of a pair of siblings with 3-methylglutaconic aciduria type 4 manifesting as Leigh syndrome. Disease progression was monitored from birth until the present. Both patients fulfilled the diagnostic criteria for Leigh syndrom
Autor:
V, San Antonio-Arce, D, Martín Fernández-Mayoralas, N, Muñoz-Jareño, C, Fresneda-Machado, A, Sáiz-Ayala, J, Campos-Castelló
Publikováno v:
Revista de neurologia. 43(9)
Leukoencephalopathy with vanishing white matter is an autosomal recessive hereditary disease that was first reported in 1997. Some time later the genetic anomalies responsible for the disease were identified, these being different mutations in any of
Autor:
J, Campos-Castelló, S, Campos-Soler
Publikováno v:
Revista de neurologia. 39(2)
The epileptic child has three times more risk of presenting cognitive disorders than other children with no neurological pathology, in accordance with three essential facts: 1. The effect exerted by the actual epilepsy. 2. Any associated previously-e
Publikováno v:
Revista de neurologia. 38(2)
The purpose of this study was to determine the therapeutic approach to be used in localisation-related and generalised epilepsies and idiopathic epileptic syndromes.Recent literature on the subject was reviewed, as were the records on a total of 118
Autor:
M, Domínguez Salgado, R, Santiago Gómez, J, Campos Castelló, M J, Fernández de Péres Villalaín
Publikováno v:
Anales espanoles de pediatria. 57(5)
Headaches are common during childhood and become more frequent in adolescence. The rational, cost-effective evaluation of children with headache begins with a careful history. The first step is to identify the temporal pattern of the headache -acute,