Publications
-
Kalko SG, Paco-Mercader S, Jou-Munoz C, Rodríguez MA, Meznaric M, Rogac M, Jekovec-Vrhovsek M, Sciacco M, Moggio M, Fagiolari G, De Paepe B, De Meirleir L, Ferrer I, Roig-Quilis M, Munell F, Montoya J, López-Gallardo E, Ruiz-Pesini E, Artuch-Iriberri R, Montero-Sanchez R, Torner-Rubies F, Nascimento-Osorio A, Ortez-Gonzalez CI, Colomer J and Jimenez-Mallebrera C.
Transcriptomic profiling of TK2 deficient human skeletal muscle suggests a role for the p53 signalling pathway and identifies growth and differentiation factor-15 as a potential novel biomarker for mitochondrial myopathies
BMC Genomics . 15: 91-91. Number of citations: 108
-
Buján N, Arias A, Montero-Sanchez R, García-Villoria J, Lissens W, Seneca S, Espinós C, Navas P, De Meirleir L, Artuch-Iriberri R, Briones P and Ribes A.
Characterization of CoQ10 biosynthesis in fibroblasts of patients with primary and secondary CoQ10 deficiency
JOURNAL OF INHERITED METABOLIC DISEASE . 37(1): 53-62. Number of citations: 26
-
Molero M, Fernández-Ureña S, Jordán-García I, Serrano M, Ormazabal-Herrero A, Garcia-Cazorla A and Artuch-Iriberri R.
Cerebrospinal Fluid Neopterin Analysis in Neuropediatric Patients: Establishment of a New Cut Off-Value for the Identification of Inflammatory-Immune Mediated Processes
PLoS One . 8(12): . Number of citations: 23
-
Ortez-Gonzalez CI, Jou-Munoz C, Cortés-Saladelafont E, Moreno J, Pérez A, Ormazabal-Herrero A, Pérez-Cerdá C, Pérez B, Artuch-Iriberri R, Cusi V and Garcia-Cazorla A.
Infantile parkinsonism and gabaergic hypotransmission in a patient with pyruvate carboxylase deficiency
Gene . 532(2): 302-306. Number of citations: 12
-
Tondo M, Calpena E, Arriola G, Sanz P, Martorell-Sampol L, Ormazabal-Herrero A, Castejon E, Palacin M, Ugarte M, Espinos C, Perez B, Pérez-Dueñas B, Pérez-Cerda C and Artuch-Iriberri R.
Clinical, biochemical, molecular and therapeutic aspects of 2 new cases of 2-aminoadipic semialdehyde synthase deficiency
MOLECULAR GENETICS AND METABOLISM . 110(3): 231-236. Number of citations: 12
-
Alonso A, Merchán P, Sandoval JE, Sánchez-Arrones L, Artuch-Iriberri R, Ferrán JL, Martínez-de-la-Torre M and Puelles L.
Development of the serotonergic cells in murine raphe nuclei and their relations with rhombomeric domains
BRAIN STRUCTURE & FUNCTION . 218(5): 1229-1277. Number of citations: 102
-
Matos IV, Castejón E, Meavilla S, O'Callaghan-Gordo M, Garcia-Villoria J, López-Sala A, Ribes A, Artuch-Iriberri R and Garcia-Cazorla A.
Clinical and biochemical outcome after hydroxocobalamin dose escalation in a series of patients with cobalamin C deficiency
MOLECULAR GENETICS AND METABOLISM . 109(4): 360-365. Number of citations: 33
-
Duarte ST, Armstrong-Moron J, Roche-Martinez A, Ortez-Gonzalez CI, Pérez A, O'Callaghan-Gordo M, Pereira A, Sanmartí F, Ormazabal-Herrero A, Artuch-Iriberri R, Pineda M and Garcia-Cazorla A.
Abnormal Expression of Cerebrospinal Fluid Cation Chloride Cotransporters in Patients with Rett Syndrome
PLoS One . 8(7): . Number of citations: 60
-
Montero-Sanchez R, Grazina M, López-Gallardo E, Montoya J, Briones P, Navarro-Sastre A, Land JM, Hargreaves IP, Artuch-Iriberri R and Jimenez-Mallebrera C.
Coenzyme Q10 deficiency in mitochondrial DNA depletion syndromes
Mitochondrion . 13(4): 337-341. Number of citations: 48
-
Pons R, Syrengelas D, Youroukos S, Orfanou I, Dinopoulos A, Cormand B, Ormazabal-Herrero A, Garcia-Cazorla A, Serrano M and Artuch-Iriberri R.
Levodopa-induced dyskinesias in tyrosine hydroxylase deficiency
MOVEMENT DISORDERS . 28(8): 1058-1063. Number of citations: 60