Publicaciones
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Fons-Estupina C, Campistol-Plana J, Narbona J, Velázquez R, Eiris J and García Peñas JJ.
Alternating hemiplegia of childhood in Spanish population. Study of a series of 17 patients
MEDICINA CLINICA . 130(15): 577-579. Nº de citas: 4
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González-Rabelino, G, Campistol-Plana J, Navarro, R, Capdevila-Cirera A and Solá, T.
Moyamoya en la población infantil: análisis de una serie occidental y revisión de la bibliografía.
REVISTA DE NEUROLOGIA . 46(7): 385-391.
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Campistol-Plana J and García, MA.
Epilepsias refractarias a fármacos antiepilépticos con respuesta a otros fármacos
NEUROLOGIA . 4(3): 35-40.
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Gutiérrez-Mata AP, López-Casas J, Ortez-González CI, Sempere-Pérez A, Casartelli MJ and Campistol-Plana J.
Clinical characteristics and progress of patients with migrainous headaches monitored in the headache unit in a paediatric referral hospital
REVISTA DE NEUROLOGIA . 46(6): 331-336. Nº de citas: 7
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Duarte S, Sanmarti F, Gonzalez V, Pérez-Dueñas B, Ormazabal-Herrero A, Artuch-Iriberri R, Campistol-Plana J and Garcia-Cazorla A.
Cerebrospinal fluid pterins and neurotransmitters in early severe epileptic encephalopathies
BRAIN & DEVELOPMENT . 30(2): 106-111. Nº de citas: 19
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Donati F, Gobbi G, Campistol-Plana J, Rapatz G, Daehler M, Sturm Y and Aldenkamp AP.
The cognitive effects of oxcarbazepine versus carbamazepine or valproate in newly diagnosed children with partial seizures
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY . 16(8): 670-679. Nº de citas: 48
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Ribasés M, Serrano M, Fernández-Alvarez E, Pahisa S, Ormazabal-Herrero A, Garcia-Cazorla A, Pérez-Dueñas B, Campistol-Plana J, Artuch-Iriberri R and Cormand B.
A homozygous tyrosine hydroxylase gene promoter mutation in a patient with dopa-responsive encephalopathy:: Clinical, biochemical and genetic analysis
MOLECULAR GENETICS AND METABOLISM . 92(3): 274-277. Nº de citas: 28
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Arias A, Corbella M, Fons-Estupina C, Sempere A, García-Villoria J, Ormazabal-Herrero A, Poo P, Pineda M, Vilaseca MA, Campistol-Plana J, Briones P, Pàmpols T, Salomons GS, Ribes A and Artuch-Iriberri R.
Creatine transporter deficiency:: Prevalence among patients with mental retardation and pitfalls in metabolite screening
CLINICAL BIOCHEMISTRY . 40(16-17): 1328-1331. Nº de citas: 53
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Serrano M, Lizarraga I, Reiss J, Dias AP, Pérez-Dueñas B, Vilaseca MA, Artuch-Iriberri R, Campistol-Plana J and Garcia-Cazorla A.
Cranial ultrasound and chronological changes in molybdenum cofactor deficiency
PEDIATRIC RADIOLOGY . 37(10): 1043-1046. Nº de citas: 11
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Garcia-Cazorla A, Serrano M, Pérez-Dueñas B, González V, Ormazabal-Herrero A, Pineda M, Fernández-Alvarez E, Campistol-Plana J and Artuch-Iriberri R.
Secondary abnormalities of neurotransmitters in infants with neurological disorders
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY . 49(10): 740-744. Nº de citas: 37