Personas / Equipo Humano

Veronica Delgadillo Chilavert

Buscador de publicaciones

Publicaciones

  • Olivé-Cirera G, Fonseca E, Chen LW, Fetta A, Martínez-Hernández E, Guasp M, González V, Delgadillo V, Cantarín-Extremera V, Jiménez-Legido M, Monge-Galindo L, Felipe A, Beseler B, Turón-Viñas E, Fernández-Ramos J, Martínez-González MJ, Vázquez-López M, Arrabal Fernandez L, Alvarez-Molinero M, Muñoz-Cabello B, Camacho A, Nuñez-Enamorado N, Spatola M, Sabater L, Blanco Y, Saiz A, Graus F, Dalmau J and Armangue-Salvador T.

    Differential diagnosis and comparison of diagnostic algorithms in children and adolescents with autoimmune encephalitis in Spain: a prospective cohort study and retrospective analysis

    LANCET NEUROLOGY . 24(1): 54-64. Nº de citas: 2

    [doi:10.1016/S1474-4422(24)00443-5]

  • Fonseca, E, Olivé-Cirera, G, Martinez-Hernandez, E, Guasp, M, Naranjo, L, Ruiz-García, R, Caballero, E, González-Alvarez, ?á, Delgadillo V, Romeu-Cerrillo G, Del Prado-Sanchez C, Cabrera-Maqueda, JM, Benito-León, J, Iñiguez, C, Garcia-Dominguez, JM, Calles, C, Cano, A, Alvarez-Bravo, G, González-Suárez, I, Oreja-Guevara, C, Ros, M, Millan-Pascual, J, Meca-Lallana, JE, Canelo, LB, Martín-Martínez, J, Palao, M, Gracia, J, Villaverde-González, R, Llufriu, S, Blanco, Y, Saiz, A, Dalmau, J, Sepulveda, M and Armangue-Salvador T.

    Investigating the 2023 MOGAD Criteria in Children and Adults With MOG-Antibody Positivity Within and Outside Attacks

    Neurology . 103(6): . Nº de citas: 4

    [doi:10.1212/WNL.0000000000209682]

  • 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: 29

    [doi:10.1038/s41598-018-37542-2]

  • 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

    [doi:10.1007/8904_2015_421]

  • 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): .

    [doi:10.1016/j.anpedi.2013.12.017]

  • 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: 56

    [doi:10.1186/1750-1172-8-189]

  • 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: 5

    [doi:10.1016/j.ejmg.2011.06.012]

  • 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

    [doi:10.1007/s10545-011-9342-4]

  • 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

    [doi:10.1111/j.1399-0004.2010.01525.x]