Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Luciana Ribeiro Montenegro"'
Autor:
Helena Panteliou Lima Valassi, Mirian Yumie Nishi, Berenice B. Mendonca, Alexander A. L. Jorge, I J P Arnhold, Debora Cabral Coutinho, Andrea de Castro Leal, Luciana Ribeiro Montenegro
Publikováno v:
European Journal of Endocrinology. 166:543-550
BackgroundHypomethylation of the paternal imprinting center region 1 (ICR1) is the most frequent molecular cause of Silver–Russell syndrome (SRS). Clinical evidence suggests that patients with this epimutation have mild IGF1 insensitivity.Objective
Autor:
Alexander A. L. Jorge, Andrea de Castro Leal, Debora Cabral Coutinho, Luciana Ribeiro Montenegro, Ana Pinheiro Machado Canton, Ivo J.P. Arnhold
Publikováno v:
Arquivos Brasileiros de Endocrinologia & Metabologia v.55 n.8 2011
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Aproximadamente 10% das crianças nascidas pequenas para a idade gestacional (PIGs) não apresentam recuperação espontânea do crescimento. As causas desse déficit de crescimento pré-natal e sua manutenção após o nascimento ainda não são com
Autor:
Jana Jovanovska, Velibor B. Tasic, Luciana Ribeiro Montenegro, Zoran Gucev, Daiane Beneduzzi, Leticia Ferreira Gontijo Silveira, Marina Krstevska-Konstantinova
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 27
AIM The genetic background of idiopathic central precocious puberty (ICPP) is not well understood. The genetic activation of pubertal onset is thought to arise from the effect of multiple genes. Familial ICPP has been reported suggesting the existenc
Autor:
Luciana Ribeiro Montenegro, Frederico G. Marchisotti, Ivo J.P. Arnhold, Luciani R. Carvalho, Alexander A. L. Jorge, Karina Berger, Berenice B. Mendonca
Publikováno v:
Growth hormoneIGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society. 19(2)
Compare the most frequently used weight-based GH dosing with an IGF-I level-based strategy in the treatment of children with severe GH deficiency. Additionally, analyse the influence of the GH receptor exon 3 polymorphism on IGF-I levels during GH th
Autor:
Ivo J.P. Arnhold, Alexander A. L. Jorge, Luciana Ribeiro Montenegro, Frederico G. Marchisotti, Berenice B. Mendonca, Luciani R. Carvalho
Publikováno v:
The Journal of clinical endocrinology and metabolism. 91(3)
A polymorphism in GHR gene, the presence or absence of exon 3, has been shown to influence the 1- and 2-yr growth responses to human recombinant GH (hGH) therapy in children without GH deficiency (GHD).The objective of this study was to assess the in