Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Artigo
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Multiple endocrine neoplasia type 1 in Brazil: MEN1 founding mutation, clinical features, and bone mineral density profileD. M. Lourenço Jr R. A Toledo; I. I Mackowiak; F. L Coutinho; M. G Cavalcanti; J. E. M Correia-Deur; F Montenegro; S. A. C Siqueira; L. C Margarido; M. C Machado; S. P. A ToledoEuropean Journal of Endocrinology Oslo v. 159, n. 3, p. 259-274, 2008Oslo 2008Acesso online. A biblioteca também possui exemplares impressos. |
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2 |
Material Type: Artigo
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A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reducd GH1 expression in siblings with isolated GH deficiency (IGHD)João L. O. Madeira Alexander Augusto de Lima Jorge; Regina M Martin; Luciana Ribeiro Montenegro; Marcela M Franca; Everlayny F Costalong; Fernanda A Correa; Aline P Otto; Ivo J. P Arnhold; Helayne S Freitas; Ubiratan Fabres Machado; Berenice Bilharinho de Mendonça; Luciani R CarvalhoEuropean journal of endocrinology Oslo v. 175, n. 02, p. K7-K15, 2016Oslo 2016Acesso online |
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3 |
Material Type: Artigo
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Post-receptor IGF1 insensitivity restricted to the MAPK pathway in a Silver–Russell syndrome patient with hypomethylation at the imprinting control region on chromosome 11Luciana R. Montenegro Andrea C Leal; Debora C Coutinho; Helena P. L Valassi; Mirian Y Nishi; Ivo J. P Arnhold; Berenice B Mendonca; Alexander A. L JorgeEuropean Journal of Endocrinology Oslo v. 166, n. 3, p. 543-550, 2012Oslo 2012Acesso online. A biblioteca também possui exemplares impressos. |