Research

HSJD researchers

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Publications

  • Carcavilla A, Suárez L, Ramon-Krauel M, Ezquieta-Zubicaray B, Labarta JI, Quinteiro S, Rodríguez-Sánchez A, López-Siguero JP, Riaño I and González-Casado I.

    Tratamiento con hormona de crecimiento en el síndrome de Noonan: revisión de la bibliografía y recomendaciones de tratamiento

    Revista Española de Endocrinología Pediátrica . 11(1): 23-39.

    [doi:10.3266/RevEspEndocrinolPediatr.pre2020.Jul.584]

  • Bossacoma F, Cuadrado-Vilanova M, Vinent-Genestar J, Correa MG, Gavrus D, Castillo H, Català-Mora J, Mora J, Schaiquevich P, Chantada G and Carcaboso AM.

    Optimizing the storage of chemotherapeutics for ophthalmic oncology: stability of topotecan solution for intravitreal injection

    OPHTHALMIC GENETICS . 41(4): 397-400. Number of citations: 2

    [doi:10.1080/13816810.2020.1776336]

  • Cubiro, X, Rozas-Munoz, E, Castel, P, Crespo, ER, Garcia-Melendo, C, Puig, L and Baselga E.

    Clinical and genetic evaluation of six children with diffuse capillary malformation and undergrowth

    PEDIATRIC DERMATOLOGY . 37(5): 833-838. Number of citations: 9

    [doi:10.1111/pde.14252]

  • Garcia-Aparicio L, Blazquez-Ruiz FJ, Martín Solé O, Rojas-Ticona J, Moraleda I, Tarrado X and Pérez-Bertólez S.

    Our experience with laparoscopic Anderson-Hynes ureteropyeloplasty.

    Cirugia pediatrica : organo oficial de la Sociedad Espanola de Cirugia Pediatrica . 33(3): 131-136.

  • Carcavilla A, Suárez L, Rodríguez Sánchez A, Gonzalez-Casado I, Ramon-Krauel M, Labarta JI, Quinteiro Gonzalez S, Riaño Galán I and López-Siguero JP.

    Noonan syndrome: genetic and clinical update and treatment options

    ANALES DE PEDIATRIA . 93(1): . Number of citations: 23

    [doi:10.1016/j.anpedi.2020.04.008]

  • Eggermann T, Elbracht M, Kurth I, Juul A, Johannsen TH, Netchine I, Mastorakos G, Johannsson G, Musholt TJ, Zenker M, Prawitt D, Pereira AM, Hiort O and European Reference Network on Rare Endocrine Conditions (ENDO-ERN.

    Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN)

    ORPHANET JOURNAL OF RARE DISEASES . 15(1): 144-144. Number of citations: 18

    [doi:10.1186/s13023-020-01420-w]

  • Boix-Vilanova J, Baselga E, Vera A, Gonzalez-Hermosa MDR, Azaña JM and Martin-Santiago A.

    Expanding the phenotypes of congenital hemangiomas

    PEDIATRIC DERMATOLOGY . 37(5): 872-876. Number of citations: 3

    [doi:10.1111/pde.14231]

  • Peiró-García A, Corominas L, Coelho A, DeSena-DeCabo L, Torner-Rubies F and García-Fontecha CG.

    How the COVID-19 pandemic is affecting paediatric orthopaedics practice: a preliminary report

    JOURNAL OF CHILDRENS ORTHOPAEDICS . 14(3): 154-160. Number of citations: 19

    [doi:10.1302/1863-2548.14.200099]

  • Turner D, Huang Y, Martín-de-Carpi J, Aloi M, Focht G, Kang B, Zhou Y, Sanchez C, Kappelman MD, Uhlig HH, Pujol G, Ledder O, Lionetti P, Dias JA, Ruemmele FM, Russell RK and Paediatric IBD Porto group of ESPGHAN.

    Corona Virus Disease 2019 and Paediatric Inflammatory Bowel Diseases: Global Experience and Provisional Guidance (March 2020) from the Paediatric IBD Porto Group of European Society of Paediatric Gastroenterology, Hepatology, and Nutrition

    JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION . 70(6): 727-733. Number of citations: 93

    [doi:10.1097/MPG.0000000000002729]

  • Vidal M, Jansà M, Roca D, Yoldi C, Cardona-Hernandez R, Giménez M and Conget I.

    Hypoglycaemia unawareness in young people with type 1 diabetes transferred to an adult center.

    Endocrinologia, diabetes y nutricion . 67(6): 394-400. Number of citations: 4

    [doi:10.1016/j.endinu.2019.07.009]