Publicacions
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Pérez-Dueñas B, Cambra-Lasaosa FJ, Vilaseca MA, Lambruschini N, Campistol-Plana J and Camacho Díaz JA.
New approach to osteopenia in phenylketonuric patients
ACTA PAEDIATRICA . 91(8): 899-904. Nº de cites: 48
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Galván Manso M, Arellano M, Sans A, Sanmarti FX, Gomez-Lopez L, Vernet A and Campistol-Plana J.
A ketogenic diet: Is this a valid alternative in refractory epilepsy?
REVISTA DE NEUROLOGIA . 33(11): 1010-1014. Nº de cites: 5
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Vilaseca MA, Kobayashi K, Briones P, Lambruschini N, Campistol-Plana J, Tabata A, Alomar A, Rodès M, Lluch M and Saheki T.
Phenotype and genotype heterogeneity in Mediterranean citrullinemia
MOLECULAR GENETICS AND METABOLISM . 74(3): 396-398. Nº de cites: 20
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Serrano, M, Campistol-Plana J, Chávez B, Caritg Bosch J, Fortuny-Guasch C and Costa-Clara JM.
Multiple intracranial tuberculomas in infancy
REVISTA DE NEUROLOGIA . 33(1): 44-46. Nº de cites: 6
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Colomé C, Artuch-Iriberri R, Lambruschini N, Cambra-Lasaosa FJ, Campistol-Plana J and Vilaseca MA.
Is there a relationship between plasma phenylalanine and cholesterol in phenylketonuric patients under dietary treatment?
CLINICAL BIOCHEMISTRY . 34(5): 373-376. Nº de cites: 23
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Gudiño M, Campistol-Plana J, Poo P and Iriondo-Sanz M.
Cerebellar hemorrhage in full-term newborn babies
REVISTA DE NEUROLOGIA . 32(7): 624-627.
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García-Koerner MC, Campistol-Plana J, Agut-Quijano T, Alcorta I, Caritg Bosch J, Estella J and Mateo M.
Neurological form of onset in haemophagocytic lymphohistiocytosis
REVISTA DE NEUROLOGIA . 32(4): 333-335.
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Mallolas J, Vilaseca MA, Pavia C, Lambruschini N, Cambra-Lasaosa FJ, Campistol-Plana J, Gómez D, Carrió A, Estivill X and Milà M.
Large de novo deletion in chromosome 12 affecting the PAH, IGF1, ASCL1, and TRA1 genes
JOURNAL OF MOLECULAR MEDICINE-JMM . 78(12): 721-724. Nº de cites: 4
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Artuch-Iriberri R, Colomé C, Vilaseca MA, Sierra-March C, Cambra-Lasaosa FJ, Lambruschini N and Campistol-Plana J.
Plasma phenylalanine is associated with decreased serum ubiquinone-10 concentrations in phenylketonuria
JOURNAL OF INHERITED METABOLIC DISEASE . 24(3): 359-366. Nº de cites: 27
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Mallolas J, Vilaseca MA, Campistol-Plana J, Lambruschini N, Cambra-Lasaosa FJ, Fusté ME and Milà M.
Clinical, biochemical, neurological and molecular studies of 11 patients with novel mutations of the PAH gene
REVISTA DE NEUROLOGIA . 31(10): 907-910. Nº de cites: 7