Publications
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Garcia-Cazorla A, Sans, A, Baquero, M, Garcia-Bargo, MD, Arellano, M, Poo, P, Gean, E and Campistol-Plana J.
White matter alterations associated with chromosomal disorders
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY . 46(3): 148-153. Number of citations: 19
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Artuch-Iriberri R, Colomé C, Sierra-March C, Brandi-Tarrau N, Lambruschini N, Campistol-Plana J, Ugarte D and Vilaseca MA.
A longitudinal study of antioxidant status in phenylketonuric patients
CLINICAL BIOCHEMISTRY . 37(3): 198-203. Number of citations: 58
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Lobato-Salinas Z, Cambra-Lasaosa FJ, Campistol-Plana J, Toll-Costa T, Pons-Odena M, Palomeque A and Martín JM.
Factor V Leiden mutation as a cause of venous thrombosis
REVISTA DE NEUROLOGIA . 38(2): 136-139. Number of citations: 2
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Ugalde C, Triepels RH, Coenen MJ, van den Heuvel LP, Smeets R, Uusimaa J, Briones P, Campistol-Plana J, Majamaa K, Smeitink JA and Nijtmans LG.
Impaired complex I assembly in a Leigh syndrome patient with a novel missense mutation in the ND6 gene
ANNALS OF NEUROLOGY . 54(5): 665-669. Number of citations: 89
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Campistol-Plana J and Garcia-Cazorla A.
West's syndrome.: Analysis, aetiological factors and therapeutic options
REVISTA DE NEUROLOGIA . 37(4): 345-352. Number of citations: 14
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Colomé C, Artuch-Iriberri R, Sierra-March C, Brandi-Tarrau N, Lambruschini N, Campistol-Plana J and Vilaseca MA.
Plasma thiols and their determinants in phenylketonuria
EUROPEAN JOURNAL OF CLINICAL NUTRITION . 57(8): 964-968. Number of citations: 10
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Urreizti R, Balcells S, Rodés M, Vilarinho L, Baldellou A, Couce ML, Muñoz C, Campistol-Plana J, Pintó X, Vilaseca MA and Grinberg D.
Spectrum of CBS mutations in 16 homocystinuric patients from the Iberian Peninsula: high prevalence of T191M and absence of I278T or G307S
HUMAN MUTATION . 22(1): 103-103.
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Campistol-Plana J.
Orally administered drugs in the treatment of spasticity
REVISTA DE NEUROLOGIA . 37(1): 70-74. Number of citations: 5
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Poo P, López-Casas JA, Galván-Manso M, Aquino-Fariña L, Terricabras-Carol L and Campistol-Plana J.
Botulinum toxin type A. Indications and results
REVISTA DE NEUROLOGIA . 37(1): 74-80. Number of citations: 5
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Curcoy A, Olsen RK, Ribes A, Trenchs-Sainz de la Maza V, Vilaseca MA, Campistol-Plana J, Osorio JH, Andresen BS and Gregersen N.
Late-onset form of beta-electron transfer flavoprotein deficiency
MOLECULAR GENETICS AND METABOLISM . 78(4): 247-249. Number of citations: 29