Publicaciones
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Montero-Sanchez R, Yubero-Siles D, Salgado MC, González MJ, Campistol-Plana J, O'Callaghan-Gordo M, Pineda M, Delgadillo V, Maynou-Fernández J, Fernandez-Isern G, Montoya C, Ruiz-Pesini E, Meavilla-Olivas SM, Neergheen V, Garcia-Cazorla A, Navas P, Hargreaves I and Artuch-Iriberri R.
Plasma coenzyme Q10 status is impaired in selected genetic conditions
SCIENTIFIC REPORTS . 9: 793-793. Nº de citas: 28
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Yubero-Siles D, Montero-Sanchez R, O'Callaghan-Gordo M, Pineda M, Meavilla-Olivas SM, Delgadillo V, Sierra-March C, Altimira L, Navas P, Pope S, Oppenheim M, Neergheen V, Ghosh A, Mills P, Clayton P, Footitt E, Cleary M, Hargreaves I, Jones SA, Heales S and Artuch-Iriberri R.
Coenzyme Q10 and Pyridoxal Phosphate Deficiency Is a Common Feature in Mucopolysaccharidosis Type III
JIMD Reports . 25: 1-7. Nº de citas: 10
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Agut-Quijano T, Muchart-Lopez J, Delgadillo V and García-Alix A.
Rombencefalosinapsis, una rara alteración del desarrollo del cerebelo de fácil diagnóstico.
ANALES DE PEDIATRIA . 81(6): .
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Delgadillo V, O'Callaghan-Gordo M, Gort L, Coll MJ and Pineda M.
Natural history of Sanfilippo syndrome in Spain
ORPHANET JOURNAL OF RARE DISEASES . 8(1): 189-189. Nº de citas: 53
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Gonzalez-Quereda L, Delgadillo V, Juan-Mateu J, Verdura E, Rodriguez MJ, Baiget M, Pineda M and Gallano P.
LMNA mutation in progeroid syndrome in association with strokes
EUROPEAN JOURNAL OF MEDICAL GENETICS . 54(6): 576-579. Nº de citas: 4
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Canals I, Elalaoui S, Pineda M, Delgadillo V, Szlago M, Jaouad I, Sefiani A, Chabás A, Coll M, Grinberg D and Vilageliu L.
Molecular analysis of Sanfilippo syndrome type C in Spain: seven novel HGSNAT mutations and characterization of the mutant alleles
CLINICAL GENETICS . 80(4): 367-374. Nº de citas: 19
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Delgadillo V, O'Callaghan-Gordo M, Artuch-Iriberri R, Montero-Sanchez R and Pineda M.
Genistein supplementation in patients affected by Sanfilippo disease
JOURNAL OF INHERITED METABOLIC DISEASE . 34(5): 1039-1044. Nº de citas: 77