TY  - JOUR
AU  - Martínez de LaPiscina, Idoia
AU  - Hernández-Ramírez, Laura C
AU  - Portillo, Nancy
AU  - Gómez-Gila, Ana L
AU  - Urrutia, Inés
AU  - Martínez-Salazar, Rosa
AU  - García-Castaño, Alejandro
AU  - Aguayo, Aníbal
AU  - Rica, Itxaso
AU  - Gaztambide, Sonia
AU  - Faucz, Fabio R
AU  - Keil, Margaret F
AU  - Lodish, Maya B
AU  - Quezado, Martha
AU  - Pankratz, Nathan
AU  - Chittiboina, Prashant
AU  - Lane, John
AU  - Kay, Denise M
AU  - Mills, James L
AU  - Castaño, Luis
AU  - Stratakis, Constantine A
PY  - 2020
DO  - 10.3389/fendo.2020.00433
SN  - 1664-2392
UR  - https://hdl.handle.net/10668/27352
T2  - Frontiers in endocrinology
AB  - Context: The DICER1 syndrome is a multiple neoplasia disorder caused by germline mutations in the DICER1 gene. In DICER1 patients, aggressive congenital pituitary tumors lead to neonatal Cushing's disease (CD). The role of DICER1 in other...
LA  - en
KW  - Cushing's disease
KW  - DICER1
KW  - corticotropinoma
KW  - disease-modifying gene
KW  - pituitary neuroendocrine tumor
KW  - Adolescent
KW  - Adult
KW  - Child
KW  - Cohort Studies
KW  - DEAD-box RNA Helicases
KW  - Female
KW  - Genetic Testing
KW  - Germ-Line Mutation
KW  - Humans
KW  - Male
KW  - Pituitary ACTH Hypersecretion
KW  - Ribonuclease III
KW  - Young Adult
TI  - Rare Germline DICER1 Variants in Pediatric Patients With Cushing's Disease: What Is Their Role?
TY  - research article
VL  - 11
ER  -