Publicaciones
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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
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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): .
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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
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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
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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
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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
