Personas / Equipo Humano

Pedro Arango Sancho

Buscador de publicaciones

Publicaciones

  • Saraff, V, Pedro Arango Sancho, Bacchetta, J, Boot, AM, Burren, C, Chinoy, A, Dharmaraj, P, Llorente, MAG, Rodríguez, JDG, Gueorguieva, I, Davies, EH, Hayes, W, Komarzynski, S, Duro, HR, Rylands, AJ, Sandilands, K, Williams, A, Hardie, E, Ishii, H, Schnabel, D, Selveindran, SM and Linglart, A.

    The lived experience of adolescents with X-linked hypophosphataemia treated with burosumab at end of skeletal growth: a mixed-methods analysis

    PLoS One . 21(3): . Nº de citas: 1

    [doi:10.1371/journal.pone.0344902]

  • Saraff, V, Pedro Arango Sancho, Bacchetta, J, Boot, AM, Burren, CP, Chinoy, A, Dharmaraj, P, Llorente, MAG, Rodríguez, JDG, Gueorguieva, I, Hayes, W, Schnabel, D, Duro, HR, Davies, EH, Komarzynski, S, Rylands, AJ, Sandilands, K, Ishii, H, Williams, A, Selveindran, S, Barlassina, A, Bowden, A and Linglart, A.

    Adolescents' experience of living with X-linked hypophosphataemia (XLH): a mixed-methods analysis of those who continued and discontinued burosumab treatment after end of skeletal growth

    Orphanet Journal of Rare Diseases . 21(1): .

    [doi:10.1186/s13023-026-04244-2]

  • Wieers, Michiel L. A. J., Allard, Lise, D'Ambrosio, Viola, Pedro Arango Sancho, de Baaij, Jeroen H. F., Becherucci, Francesca, Bertholet-Thomas, Aurelia, Besouw, Martine, Blanchard, Anne, Cacciapuoti, Martina, Carbone, Vincenza, Cornelissen, Elisabeth A., Daffara, Federico, Degenhardt, Jan, Devuyst, Olivier, Dorresteijn, Eiske, Evans, Rhys, Figueres, Lucile, Fila, Marc, Giliberti, Marica, Gillion, Valentine, Haumann, Sophie, Hawkins-van der Cingel, Gerlineke, Houillier, Pascal, Hureaux, Marguerite, Knauf, Felix, Knebelmann, Bertrand, Konrad, Martin, Kwon, Theresa, Lemoine, Sandrine, Longo, Germana, Nijenhuis, Tom, Engberink, Rik H. G. Olde, Duro, Hector Rios, Saade, Chloe, Sayer, John A., Schlingmann, Karl-Peter, Simon, Thomas, Speeckaert, Marijn M., Tan, Hai Liang, Trepiccione, Francesco, Vargas-Poussou, Rosa, Veligratti, Faidra, Walsh, Stephen B., Salih, Mahdi, Silva, Pedro H. Imenez and Hoorn, Ewout J..

    Clinical Characteristics, Symptoms, and Long-Term Outcomes in Gitelman Syndrome

    Kidney International Reports . 10(11): 3967-3983. Nº de citas: 4

    [doi:10.1016/j.ekir.2025.09.006]

  • Godoy-Molina E, Serrano NL, Jiménez-González A, Villaronga M, Marqués Pérez-Bryan RM, Varela-Fernández R, Lotz-Esquivel S, Hevia Tuñón A, Trivedi PP, Horn N, Standing JF, Mangas-Sanjuan V, Capdevila M, Mateos A, Broun D, Lutsenko S, Medina-Rivera IF, Artuch-Iriberri R, Jou-Munoz C, Roldan-Molina M, Pedro Arango Sancho, Saez-Villafañe M, Ortiz-de-Urbina JJ, Pieras-López A, Duero M, Rosa Farré Riba, Pijuan-Marquilles J, Hoenicka J, Sacchettini JC, Petris MJ, Gohil VM and Palau F.

    Elesclomol-copper therapy improves neurodevelopment in two children with Menkes disease.

    JOURNAL OF CLINICAL INVESTIGATION . 135(19): . Nº de citas: 5

    [doi:10.1172/JCI193107]

  • Adella A, Jouret F, Madariaga L, Leermakers PA, Pedro Arango Sancho, Ariceta G, Beck BB, Bjerre A, Bockenhauer D, Coccia P, Dhamija R, de Frutos F, Garcia-Castano A, van Katwijk SB, Lucas J, Möller T, Müller D, Pinto E Vairo F, Raki M, Rips J, Schlingmann KP, Venselaar H, Machado Bressan Wilke MV, Nijenhuis T, Hoenderop J and de Baaij J.

    Novel RRAGD Variants in Autosomal Dominant Kidney Hypomagnesemia and Therapeutic Perspectives.

    Kidney International Reports . 10(10): 3640-3655. Nº de citas: 1

    [doi:10.1016/j.ekir.2025.07.035]

  • Seefried L, Aliberti F, Heier CA, Pedro Arango Sancho, Biosse Duplan M, Sakka SD, Emma F, Gardiner O, Javaid MK, Ferreira-Santos RM, Raimann A, Rak K, Bubbear JS, Cheung MS, Beck-Nielsen SS, Mindler GT and Linglart A.

    XLH Matters: an evolving programme to discuss new advances and share clinical experiences to improve patient outcomes.

    Orphanet Journal of Rare Diseases . 19(Suppl 2): 497-497. Nº de citas: 2

    [doi:10.1186/s13023-024-03387-4]

  • Casado E, Gómez-Alonso C, Pintos-Morell G, Bou-Torrent R, Barreda-Bonis AC, Torregrosa JV, Broseta-Monzó JJ, Pedro Arango Sancho, Chocrón-de-Benzaquen S, Olmedilla-Ishishi Y and Soler-López B.

    Transition of patients with metabolic bone disease from paediatric to adult healthcare services: current situation and proposals for improvement

    Orphanet Journal of Rare Diseases . 18(1): 245-245. Nº de citas: 5

    [doi:10.1186/s13023-023-02856-6]

  • Calzada Y, Revuelta I, Elena Codina Sampera, Alcaraz A, López-Báez V, Paredes D, Pedro Arango Sancho, Palou E, Garcia-Herrera A, Oppenheimer F, Diekmann F and Alvaro Madrid Aris.

    Overcoming limits: First ABO incompatible living donor paired kidney transplant in an hypersensitized pediatric recipient in Spain

    PEDIATRIC TRANSPLANTATION . 26(8): . Nº de citas: 3

    [doi:10.1111/petr.14359]