Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Tábita A. R. Vicente"'
Autor:
Tábita A. R. Vicente, Joselina Luzia Menezes Oliveira, Ívina E. S. Rocha, José Augusto Barreto-Filho, Manuel H. Aguiar-Oliveira, Francielle T. Oliveira, Catarine T. Farias, Viviane C. Campos, Rossana M. C. Pereira, Celi Marques-Santos, Roberto Salvatori, Alessia Sagazio, Carla R. P. Oliveira, Miburge Bolivar Gois
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 92:2353-2357
Context: Biallelic mutations in the GHRH receptor (GHRHR) gene (GHRHR) are a frequent cause of isolated GH deficiency (IGHD). Although heterozygous carriers of these mutations appear normal, we hypothesized that heterozygosity for a GHRHR mutation mi
Autor:
Carla R. P. Oliveira, Catarine T. Farias, Clarisse Miranda Prado, Joselina Luzia Menezes Oliveira, Tábita A. R. Vicente, Manuel H. Aguiar-Oliveira, Roberto Ximenes Filho, Roberto Salvatori, Allan V. O. Britto, Celi Marques-Santos, Anita H. O. Souza, Rossana M. C. Pereira, José Augusto Barreto-Filho
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 91:2093-2099
GH deficiency (GHD) acquired at adult age as a result of pathological processes of the pituitary gland or the hypothalamus causes changes that are associated with worsening cardiovascular risk. They include increase in abdominal obesity, total and lo