Publicacions
-
Lambruschini N, Pérez-Dueñas B, Vilaseca MA, Mas A, Artuch-Iriberri R, Gassió-Subirachs R, Gomez-Lopez L, Gutiérrez A and Campistol-Plana J.
Clinical and nutritional evaluation of phenylketonuric patients on tetrahydrobiopterin monotherapy
MOLECULAR GENETICS AND METABOLISM . 86: 54-60. Nº de cites: 81
-
Millet P, Vilaseca MA, Valls C, Pérez-Dueñas B, Artuch-Iriberri R, Gomez-Lopez L, Lambruschini N and Campistol-Plana J.
Is deoxypyridinoline a good resorption marker to detect osteopenia in phenylketonuria?
CLINICAL BIOCHEMISTRY . 38(12): 1127-1132. Nº de cites: 26
-
Pérez-Dueñas B, Valls-Solé J, Fernández-Alvarez E, Conill J, Vilaseca MA, Artuch-Iriberri R and Campistol-Plana J.
Characterization of tremor in phenylketonuric patients
JOURNAL OF NEUROLOGY . 252(11): 1328-1334. Nº de cites: 25
-
Gassió-Subirachs R, Fusté E, López-Sala A, Artuch-Iriberri R, Vilaseca MA and Campistol-Plana J.
School performance in early and continuously treated phenylketonuria
PEDIATRIC NEUROLOGY . 33(4): 267-271. Nº de cites: 55
-
Garcia-Cazorla A, Ormazabal-Herrero A, Artuch-Iriberri R, Pérez-Dueñas B, López-Casas J, Fernández-Alvarez E and Campistol-Plana J.
Inborn errors of neurotransmitters in neuropaediatrics
REVISTA DE NEUROLOGIA . 41(2): 99-108. Nº de cites: 5
-
Gassió-Subirachs R, Artuch-Iriberri R, Vilaseca MA, Fusté E, Boix Lluch C, Sans A and Campistol-Plana J.
Cognitive functions in classic phenylketonuria and mild hyperphenyl-alaninaemia:: experience in a paediatric population
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY . 47(7): 443-448. Nº de cites: 78
-
Gutiérrez-Aguilar G, Abenia-Usón P, Vilaseca MA and Campistol-Plana J.
Encephalopathy with methylmalonic aciduria and homocystinuria secondary to a deficient exogenous supply of vitamin B-12
REVISTA DE NEUROLOGIA . 40(10): 605-608. Nº de cites: 6
-
Campistol-Plana J, Malaga-Dieguez, I, Garcia-Cazorla A, Krauel-Vidal, X and Vilaseca MA.
Inborn errors of metabolism with neurological symptomathology in the neonatal period
REVISTA DE NEUROLOGIA . 40(6): 321-326. Nº de cites: 2
-
Ormazabal-Herrero A, Garcia-Cazorla A, Fernández Y, Fernández-Alvarez E, Campistol-Plana J and Artuch-Iriberri R.
HPLC with electrochemical and fluorescence detection procedures for the diagnosis of inborn errors of biogenic amines and pterins
JOURNAL OF NEUROSCIENCE METHODS . 142(1): 153-158. Nº de cites: 104
-
Galván-Manso M, Campistol-Plana J, Conill J and Sanmarti FX.
Analysis of the characteristics of epilepsy in 37 patients with the molecular diagnosis of Angelman syndrome
EPILEPTIC DISORDERS . 7(1): 19-25. Nº de cites: 37