Publicacions
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Mallolas, J, Mila, M, Lambruschini N, Cambra-Lasaosa FJ, Campistol-Plana J and Vilaseca MA.
Biochemical phenotype and its relationship with genotype in hyperphenylalaninemia heterozygotes
MOLECULAR GENETICS AND METABOLISM . 67(2): 156-161. Nº de cites: 13
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Cardo E, Campistol-Plana J, Caritg J, Ruiz S, Vilaseca MA, Kirkham F and Blom HJ.
Fatal haemorrhagic infarct in an infant with homocystinuria
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY . 41(2): 132-135. Nº de cites: 19
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Campistol-Plana J.
Reaching a diagnosis in congenital metabolic disorders using neuroimaging
REVISTA DE NEUROLOGIA . 28(1): 16-23. Nº de cites: 11
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Pineda M, Aracil A, Vernet A, Espada M, Cobo E, Arteaga R, Artigas J, Barrionuevo C, Bautista-González L, Berenguer-Molla R, Caballero J, Cabrera J, Campistol-Plana J, Campos J, Casas-Fernández C, Castelló M, Castro-Gago M, Castroviejo P, Colomer J, Delgado P, Domingo R, Domínguez-Jiménez A, Fernández-Alvarez E, García-Aymerich J and Vidal R.
A study of Rett syndrome in the Spanish population
REVISTA DE NEUROLOGIA . 28(1): 105-109. Nº de cites: 7
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Pineda Sánchez J, Palomeque A, Cambra-Lasaosa FJ, Caritg Bosch J, Martín Rodrigo JM, Campistol-Plana J and Fernández-Alvarez E.
Enfermedad de Moya-Moya. Una causa de oclusin vascular en la infancia.
ANALES DE PEDIATRIA . 50(1): 44-48.
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Campistol-Plana J, Arellano, M, Poo P, Escofet, C, Pérez Olarte, P and Vilaseca MA.
Embriopatía por fenilcetonuria materna. Una causa de retardo mental poco diagnosticada. Revision de ocho observaciones
ANALES DE PEDIATRIA . 51(2): 139-142.
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Cardo E, Vilaseca MA, Campistol-Plana J, Artuch-Iriberri R, Colomé C and Pineda M.
Evaluation of hyperhomocysteinaemia in children with stroke.
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY . 3(3): 113-7. Nº de cites: 38
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Campistol-Plana J, Gassió-Subirachs R, Pineda M and Fernández-Alvarez E.
Acute necrotizing encephalopathy of childhood (infantile bilateral thalamic necrosis): two non-Japanese cases
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY . 40(11): 771-774. Nº de cites: 41
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Sierra C, Vilaseca MA, Moyano D, Brandi N, Campistol-Plana J, Lambruschini N, Cambra-Lasaosa FJ, Deulofeu R and AUREA MIRA VALLET.
Antioxidant status in hyperphenylalaninemia
CLINICA CHIMICA ACTA . 276(1): 1-9. Nº de cites: 57
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Busquets C, Coll MJ, Christensen E, Campistol-Plana J, Clusellas N, Vilaseca MA and Ribes A.
Feasibility of molecular prenatal diagnosis of glutaric aciduria type I in chorionic villi
JOURNAL OF INHERITED METABOLIC DISEASE . 21(3): 243-246. Nº de cites: 6