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  • Povo-Retana A, Landauro-Vera R, Fariñas M, Sánchez-García S, Alvarez-Lucena C, Marín-del Barrio S, Cascante M and Boscá L.

    Defining the metabolic signatures associated with human macrophage polarisation.

    BIOCHEMICAL SOCIETY TRANSACTIONS . 51(4): 1429-1436. Number of citations: 1

    [doi:10.1042/BST20220504]

  • Povo-Retana A, Fariñas M, Landauro-Vera R, Mojena M, Alvarez-Lucena C, Fernández-Moreno MA, Castrillo A, de la Rosa Medina JV, Sánchez-García S, Foguet C, Mas F, Marín-del Barrio S, Cascante M and Boscá L.

    Immunometabolic actions of trabectedin and lurbinectedin on human macrophages: relevance for their anti-tumor activity.

    FRONTIERS IN IMMUNOLOGY . 14: 1211068-1211068. Number of citations: 1

    [doi:10.3389/fimmu.2023.1211068]

  • Miñones-Suarez L, Pérez de Nanclares G, Marín-del Barrio S, Alcázar Villar MJ, de Sotto-Esteban D, Mogas E, Rey Cordo L, Riaño-Galán I, Lumbreras Fernández J and Leis R.

    Nutrition recommendations for patients with pseudohypoparathyroidism.

    anales de pediatria . 99(2): 129-135.

    [doi:10.1016/j.anpede.2023.05.007]

  • González-Lamuño D, Lorente Rodríguez A, Luis Yanes MI, Marín-del Barrio S, Martínez Díaz-Guerra G and Peris P.

    Clinical practice recommendations for the diagnosis and treatment of X-linked hypophosphatemia: A consensus based on the ADAPTE method

    MEDICINA CLINICA . 159(3): . Number of citations: 2

    [doi:10.1016/j.medcli.2021.07.0290025-7753]

  • Yanes MIL, Diaz-Curiel M, Peris P, Vicente C, Marín-del Barrio S, Ramon-Krauel M, Hernandez J, Broseta JJ, Espinosa L, Mendizabal S, Perez-Sukia L, Martínez V, Palazón C, Piñero JA, Calleja MA, Espin J, Arborio-Pinel R and Ariceta G.

    Health-related quality of life of X-linked hypophosphatemia in Spain

    ORPHANET JOURNAL OF RARE DISEASES . 17(1): 298-298. Number of citations: 5

    [doi:10.1186/s13023-022-02452-0]

  • Marín-del Barrio S.

    Raquitismo hipofosfatémico autosómico recesivo por mutación en el gen ENPP1. Más allá del raquitismo hipofosfatémico ligado a X

    Anales de Nefrología Pediátrica . 1(1): 26-28.

  • Prado-Carro AM, Calzada-Hernández J, Marín-del Barrio S, Cardona-Hernandez R, Oriola J, Nicolás M and Ramon-Krauel M.

    Patient With iDEND Syndrome-Related Mutation

    Diabetes Care . 37(6): 123-124. Number of citations: 1

    [doi:10.2337/dc13-2877]

  • Vila-Perez D, Marín-del Barrio S, Camacho Díaz JA, Morey, M. and Loidi, L..

    Four Cases of X-Linked Hypophosphatemic Rickets, Clinical Description and GeneticTesting.

    Open Journal of Genetics . : 40-45.

  • Prado AM, Casano-Sancho P and Marín-del Barrio S.

    Diabetes insípida central idiopática ¿Qué seguimiento deberíamos hacer?

    Revista Española de Endocrinología Pediátrica . 4(1): 62-67.

  • Marín-del Barrio S, Casano-Sancho P, Villarreal-Peña N, Sebastiani G, Pinillos S, Pérez-Dueñas B, Hwa V, Rosenfeld RG and Ibañez-Toda L.

    Triple A Syndrome in a Patient with Genetic Growth Hormone Insensitivity: Phenotypic Effects of Two Genetic Disorders

    HORMONE RESEARCH IN PAEDIATRICS . 77(1): 63-68. Number of citations: 9

    [doi:10.1159/000335235]