Publicacions
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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 cites: 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 cites: 18
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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 cites: 47
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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 cites: 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 cites: 52
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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 cites: 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 cites: 35
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Serrano M, Ormazabal-Herrero A, Pérez-Dueñas B, Artuch-Iriberri R, Coroleu W, Krauel Vidal X, Campistol-Plana J and Garcia-Cazorla A.
Perinatal asphyxia may cause reduction in csf dopamine metabolite concentrations
Neurology . 69(3): 311-313. Nº de cites: 5
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Madruga-Garrido M, Garcia-Villoria J, Ruiz-Del Portal L, Delgado-Pecellin C, Garcia-Valdecasas MS, Blanco-Martinez B, Perez-Perez M, Ribes A, Campistol-Plana J and Rufo-Campos M.
Glutaric aciduria type I with a low-excretion biochemical phenotype associated to a new mutation
REVISTA DE NEUROLOGIA . 45(2): 127-128. Nº de cites: 2
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Sempere-Pérez A, Campistol-Plana J, Garcia-Cazorla A, Guillen-Quesada A and Pérez-Muñoz N.
Multiple familial cerebral cavernomatosis
REVISTA DE NEUROLOGIA . 44(11): 657-660. Nº de cites: 9