Publications
-
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. Number of citations: 5
-
López-Laso E, Camino R, Mateos ME, Pérez-Navero JL, Ochoa JJ, Lao-Villadóniga JI, Ormazabal-Herrero A and Artuch-Iriberri R.
Dopa-responsive infantile hypokinetic rigid syndrome due to dominant guanosine triphosphate cyclohydrolase 1 deficiency
JOURNAL OF THE NEUROLOGICAL SCIENCES . 256(1-2): 90-93. Number of citations: 13
-
Campistol-Plana J, Arias-Dimas A, Poo P, Pineda M, Hoffman M, Vilaseca MA, Artuch-Iriberri R and Ribes A.
Cerebral creatine transporter deficiency:: An infradiagnosed neurometabolic disease
REVISTA DE NEUROLOGIA . 44(6): 343-347. Number of citations: 8
-
García-Vicente S, Yraola F, Marti L, González-Muñoz E, García-Barrado MJ, Cantó C, Abella A, Bour S, Artuch-Iriberri R, Sierra-March C, Brandi-Tarrau N, Carpéné C, Moratinos J, Camps M, Palacín M, Testar X, Gumà A, Albericio F, Royo M, Mian A and Zorzano A.
Oral insulin-mimetic compounds that act independently of insulin
Diabetes . 56(2): 486-493. Number of citations: 61
-
Vilaseca MA, Artuch-Iriberri R, Bauzá, FR, Pineda M, García, A and Campistol-Plana J.
Diagnóstico diferencial de la hiperhomocisteinemia en pediatría
Química Clínica . 26(4): 191-195.
-
Montero-Sanchez R, Pineda M, Aracil A, Vilaseca MA, Briones P, Sánchez-Alcázar JA, Navas P and Artuch-Iriberri R.
Clinical, biochemical and molecular aspects of cerebellar ataxia and Coenzyme Q10 deficiency
Cerebellum . 6(2): 118-122. Number of citations: 46
-
Garcia-Cazorla A, Pérez-Dueñas B, Pineda M, Artuch-Iriberri R, Vilaseca MA and Campistol-Plana J.
[Orientation of mental retardation from neurometabolic diseases].
REVISTA DE NEUROLOGIA . 43 Suppl 1: 187-92. Number of citations: 3
-
Gömez L, Garcia-Cazorla A, Gutiérrez A, Artuch-Iriberri R, Varea V, Martín J, Pinillos S and Vilaseca MA.
Treatment of severe osteoporosis with alendronate in a patient with lysinuric protein intolerance
JOURNAL OF INHERITED METABOLIC DISEASE . 29(5): 687-687. Number of citations: 9
-
Arias A, Ormazabal-Herrero A, Moreno J, González B, Vilaseca MA, García-Villoria J, Pàmpols T, Briones P, Artuch-Iriberri R and Ribes A.
Methods for the diagnosis of creatine deficiency syndromes:: A comparative study
JOURNAL OF NEUROSCIENCE METHODS . 156(1-2): 305-309. Number of citations: 31
-
López-Laso E, Ormazabal-Herrero A, Camino R, Gascón FJ, Ochoa JJ, Mateos ME, Muñoz MJ, Pérez-Navero JL, Lao JI, Vilaseca MA and Artuch-Iriberri R.
Oral phenylalanine loading test for the diagnosis of dominant guanosine triphosphate cyclohydrolase 1 deficiency
CLINICAL BIOCHEMISTRY . 39(9): 893-897. Number of citations: 7