Publications
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Campistol-Plana J.
Neonatal neurological advances
REVISTA DE NEUROLOGIA . 31(7): 601-604. Number of citations: 2
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Campistol-Plana J.
Seizures and epileptic syndromes in the newborn. Forms of presentation, protocol for investigation and treatment
REVISTA DE NEUROLOGIA . 31(7): 624-631. Number of citations: 7
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Busquets C, Merinero B, Christensen E, Gelpí JL, Campistol-Plana J, Pineda M, Fernández-Alvarez E, Prats JM, Sans A, Arteaga R, Martí M, Campos J, Martínez-Pardo M, Martínez-Bermejo A, Ruiz-Falcó ML, Vaquerizo J, Orozco M, Ugarte M, Coll MJ and Ribes A.
Glutaryl-CoA dehydrogenase deficiency in Spain: Evidence of two groups of patients, genetically, and biochemically distinct
PEDIATRIC RESEARCH . 48(3): 315-322. Number of citations: 114
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Campistol-Plana J.
Epileptic syndromes in the first year of life and congenital errors of metabolism
REVISTA DE NEUROLOGIA . 30: 60-74. Number of citations: 14
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Campistol-Plana J, Chávez B, Vilaseca MA and Artuch-Iriberri R.
Antiepileptic drugs and carnitine
REVISTA DE NEUROLOGIA . 30: 105-109. Number of citations: 12
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Cardo E, Monrós E, Colomé C, Artuch-Iriberri R, Campistol-Plana J, Pineda M and Vilaseca MA.
Children with stroke:: Polymorphism of the MTHFR gene, mild hyperhomocysteinemia, and vitamin status
JOURNAL OF CHILD NEUROLOGY . 15(5): 295-298. Number of citations: 63
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Pérez-Cerdá C, Merinero B, Rodríguez-Pombo P, Pérez-Dueñas B, Desviat LR, Muro S, Richard E, García MJ, Gangoiti J, Ruiz Sala P, Sanz P, Briones P, Ribes A, Martínez-Pardo M, Campistol-Plana J, Pérez M, Lama R, Murga ML, Lema-Garrett T, Verdú A and Ugarte M.
Potential relationship between genotype and clinical outcome in propionic acidaemia patients
EUROPEAN JOURNAL OF HUMAN GENETICS . 8(3): 187-194. Number of citations: 55
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Cardo E, Pineda M, Vilaseca MA, Artuch-Iriberri R and Campistol-Plana J.
Risk factors in cerebrovascular disease in childhood
REVISTA DE NEUROLOGIA . 30(1): 21-27. Number of citations: 11
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Cardo, E, Pineda M, Artuch-Iriberri R, Vilaseca MA and Campistol-Plana J.
Propuesta de protocolo de estudio de las enfermedades cerebrovasculares de la infancia
ANALES DE PEDIATRIA . 52(5): 435-442.
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Quintillá-Martínez JM, Campistol-Plana J, Boleda Vall-Llobera, MD, Vilaseca MA, Artuch-Iriberri R, Palomeque A, Briones, P and Ribes Rubió, A.
Síndrome de Reye-like como manifestacion inicial de enfermedad mitocondrial
ANALES DE PEDIATRIA . 52(5): 479-482.