Zobrazeno 1 - 10
of 51
pro vyhledávání: '"J M Prats, Viñas"'
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 76(2)
Autor:
M J, Martínez-González, S, Martínez-González, A, García-Ribes, S, Mintegi-Raso, J, Benito-Fernández, J M, Prats-Viñas
Publikováno v:
Revista de neurologia. 42(6)
Acute childhood ataxia is a cause of referency to the pediatric emergency room. AIM. To characterize the etiology, clinical picture, management, and outcome of acute ataxia in our hospital.A prospective study was undertaken including 39 children with
Autor:
L, Aldamiz-Echevarría Azuar, J M, Prats Viñas, P, Sanjurjo Crespo, J A, Prieto Perera, M T, Labayru Echeverría
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 63(6)
Propionic acidemia is a disorder of branch-chain amino acids, the side chain of cholesterol and odd-chain fatty acid metabolism that leads to the accumulation of toxic acid metabolites. The clinical features typically begin shortly after birth, altho
Autor:
A, Cabrera Duro, D, Rodrigo Carbonero, J, Aramendi Gallardo, E, Pastor Menchaca, J M, Galdeano Miranda, T, Hermana Tenzanos, J M, Prats Viñas
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 62(4)
We report a 2-month old newborn with a family history of adenoma sebaceum, achromic spots and renal lithiasis. Echocardiography-magnetic resonance imaging showed a solitary pediculated rhabdomyoma in the left ventricular outlet tract causing a severe
Publikováno v:
Revista de neurologia. 40(5)
Gait apraxia is not used to be considered as a diagnostic entity in Pediatric Neurology.We present two pediatric patients that, after to have acquired normal gait and in consequence of a acute process, they lost the capacity to walk. In spite of inte
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
Publikováno v:
Revista de neurologia. 37(10)
Tourette syndrome shows a fluctuating evolution, often masked by its comorbidity.To study the clinical factors predicting the initial remission of tics in children with Tourette syndrome. Patients and methods. All patients attended during the last 5
Publikováno v:
Neurologia (Barcelona, Spain). 18(5)
Autor:
I, Rouco Axpe, C, Garaizar Axpe, M, Labairu Echevarría, P, Sanjurjo Crespo, L, Aldamiz Echevarría, J M, Prats Viñas
Publikováno v:
Neurologia (Barcelona, Spain). 18(5)
Leigh syndrome is probably the most frequent metabolic disorder in infancy and childhood. The classic form of the disease is characterized by bilateral lesions of basal ganglia and brainstem. The extensive involvement of white matter, without radiolo
Publikováno v:
Revista de neurologia. 36(4)