Browsing by Subject Malalties de les glàndules endocrines
Showing results 1 to 5 of 5
| Issue Date | Title | Author(s) |
|---|---|---|
| 26-Jan-2016 | Genome-wide DNA methylation analysis of pseudohypoparathyroidism patients with GNAS imprinting defects | Rochtus, Anne; Martín Trujillo, Alex; Izzi, Benedetta; Elli, Francesca; Garin, Intza; Linglart, Agnès; Mantovani, Giovanna; Perez de Nanclares, Guiomar; Thiele, Suzanne; Decallonne, Brigitte; Van Geet, Chris; Monk, Dave Nicholas; Freson, Kathleen |
| 16-Sep-2019 | Mendelian randomization analysis rules out disylipidaemia as colorectal cancer cause | Ibáñez Sanz, Gemma; Díez Villanueva, Anna; Riera Ponsati, Marina; Fernández Villa, Tania; Fernández Navarro, Pablo; Bustamante, Mariona; Llorca, Javier; Amiano, Pilar; Ascunce, Nieves; Fernández Tardón, Guillermo; Salcedo Bellido, Inmaculada; Salas, Dolores; Capelo Álvarez, Rocío; Crous Bou, Marta; Ortega Valín, Luis; Pérez Gómez, Beatriz; Castaño-Vinyals, Gemma; Palazuelos-Calderón, Camilo; Altzibar, Jone M.; Ardanaz, Eva; Tardón, Adonina; Jiménez Moleón, José Juan; Olmos Juste, Valle; Aragonès Sanz, Núria; Pollán, Marina; Kogevinas, Manolis; Moreno Aguado, Víctor |
| 7-Feb-2017 | New murine Niemann-Pick type C models bearing a pseudoexongenerating mutation recapitulate the main neurobehavioural and molecular features of the disease | Gómez Grau, Marta; Albaigès, Júlia; Casas, Josefina; Auladell i Costa, M. Carme; Dierssen, Mara; Vilageliu i Arqués, Lluïsa; Grinberg Vaisman, Daniel Raúl |
| 24-Sep-2024 | Novel truncating germline variant reinforces TINF2 as a susceptibility gene for familial non-medullary thyroid cancer | Oriola Ambrós, Josep; Díez, Orland; Mora Porta, Mireia; Halperin, Irene; Martínez, Sandra; Masas, Miriam; Tenes, Anna; Bernal, Anna; Duran, Rafael; Orois, Aida |
| 23-Feb-2022 | Two Sisters with Kallmann Syndrome, Gonadal Dysgenesis, and Multiple Neuromuscular and Endocrine Disorders: Report of Two Cases with Description of an Unusual Association | Camacho, Marta; Castelo-Branco Flores, Camil |