Zobrazeno 1 - 9 of 9 pro vyhledávání: '"Francielle T. Oliveira"'
1
Brazilian adult individuals with untreated isolated GH deficiency do not have accelerated subclinical atherosclerosis
Autor: Francielle T. Oliveira, Viviane C. Campos, Ívina E. S. Rocha, Joselina Luzia Menezes Oliveira, Wersley A Silva, José Augusto Barreto-Filho, Roberto Salvatori, Manuel H. Aguiar-Oliveira, Carla R P Oliveira, Ursula M M Costa
Publikováno v: Endocrine Connections
GH and its principal mediator IGF1 have important effects on metabolic and cardiovascular (CV) status. While acquired GH deficiency (GHD) is often associated with increased CV risk, the consequences of congenital GHD are not known. We have described
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e1c8e23ba5f0033eff4ad4b9bc333d3
http://europepmc.org/articles/PMC4738236
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2
Older individuals heterozygous for a growth hormone-releasing hormone receptor gene mutation are shorter than normal subjects
Autor: Marco A Cardoso-Filho, Rossana M. C. Pereira, Francielle T. Oliveira, Miburge B Gois-Junior, Elenilde G. Santos, Roberto Salvatori, Viviane C. Campos, Luiz A. Oliveira-Neto, Eugênia H. O. Valença, Carla R. P. Oliveira, Anita H. O. Souza, Alécia A Oliveira-Santos, Manuel H. Aguiar-Oliveira
Publikováno v: Journal of Human Genetics. 60:335-338
Growth hormone (GH)-releasing hormone (GHRH) is the most important stimulus for GH secretion by the pituitary gland. Subjects homozygous for GHRH receptor (GHRHR) gene (GHRHR) inactivating mutations have severe GH deficiency, resulting in severe shor
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94588667cab2e3912e1cee42ed31b54f
https://doi.org/10.1038/jhg.2015.25
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5
Altered sleep patterns in patients with non-functional GHRH receptor
Autor: Alécia A Oliveira-Santos, Francielle T. Oliveira, Augusto C N Faro, Manuel H. Aguiar-Oliveira, Ursula M.M. Costa, Carla R. P. Oliveira, Roberto Salvatori, José Antonio Miguel Marcondes, Viviane C. Campos, Larissa B Macena
Publikováno v: European journal of endocrinology. 177(1)
ObjectivesGH-releasing hormone (GHRH) exerts hypnotic actions increasing the non-rapid eye movement (NREM) sleep. Conversely, GH stimulates the REM sleep. GH deficiency (GHD) often leads to sleep problems, daytime fatigue and reduced quality of life
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e5c0f1208035fef28d248af7c6d021d
https://pubmed.ncbi.nlm.nih.gov/28432269
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6
Ocular findings in adult subjects with an inactivating mutation in GH releasing hormone receptor gene
Autor: Gustavo Barreto Melo, Luis A. Oliveira-Neto, Viviane C. Campos, Carla R. P. Oliveira, Manuel H. Aguiar-Oliveira, Alécia A Oliveira-Santos, Roberto Salvatori, Ann Hellström, Virginia M. Pereira-Gurgel, Augusto C N Faro, Francielle T. Oliveira, Eugênia H. O. Valença, Francisco de Assis Pereira
Publikováno v: Growth hormoneIGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society. 34
Objective Ocular function is fundamental for environmental adaptation and survival capacity. Growth factors are necessary for a mature eyeball, needed for adequate vision. However, the consequences of the deficiency of circulating growth hormone (GH)
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5a133ca4c940723ad58dd75881fffb6
https://pubmed.ncbi.nlm.nih.gov/28456063
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8
Heterozygosity for a Mutation in the Growth Hormone-Releasing Hormone Receptor Gene Does Not Influence Adult Stature, But Affects Body Composition
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
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ed90b2ced0d35d47314bfd8a0a262c6
https://doi.org/10.1210/jc.2007-0092
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