Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Milena Garcia, Abrão"'
Autor:
Natalino Hajime Yoshinari, Milena Garcia Abrão, Virginia Lúcia Nazário Bonoldi, Cleber Oliveira Soares, Claudio Roberto Madruga, Alessandra Scofield, Carlos Luis Massard, Adivaldo Henrique da Fonseca
Publikováno v:
Memorias do Instituto Oswaldo Cruz, Vol 98, Iss 3, Pp 311-318 (2003)
This paper reports a case of coinfection caused by pathogens of Lyme disease and babesiosis in brothers. This was the first case of borreliosis in Brazil, acquired in Cotia County, State of São Paulo, Brazil. Both children had tick bite history, pre
Externí odkaz:
https://doaj.org/article/766c4cc994bb43f39577ca4a8e569f61
Autor:
Marilena Nakaguma, Alexander A. L. Jorge, Luciani R. Carvalho, Fernanda A. Correa, Berenice B. Mendonca, Milena Garcia Abrão, Ivo J.P. Arnhold, João Luiz de Oliveira Madeira, Mirian Yumie Nishi
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 63, Iss 2, Pp 167-174 (2019)
Archives of Endocrinology and Metabolism, Volume: 63, Issue: 2, Pages: 167-174, Published: 13 MAY 2019
Archives of Endocrinology and Metabolism v.63 n.2 2019
Arquivos de Endocrinologia e Metabolismo
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Archives of Endocrinology and Metabolism, Volume: 63, Issue: 2, Pages: 167-174, Published: 13 MAY 2019
Archives of Endocrinology and Metabolism v.63 n.2 2019
Arquivos de Endocrinologia e Metabolismo
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
The first description of patients with combined pituitary hormone deficiencies (CPHD) caused by PROP1 mutations was made 20 years ago. Here we updated the clinical and genetic characteristics of patients with PROP1 mutations and summarized the phenot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb821cce1018092795060a5e4a61ed31
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972019000200167&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972019000200167&lng=en&tlng=en
Autor:
Fernanda A. Correa, Isabela Peixoto Biscotto, Everlayny F. Costalonga, Mirian Yumie Nishi, Marilena Nakaguma, João L o m Madeira, Anna Flavia Figueredo Benedetti, Thiago Pequeno, Milena Garcia Abrão, Silvana Santos, Luciani R. Carvalho, Marcela M. França, Berenice B. Mendonca, Ivo J.P. Arnhold, Thamiris Fernandes, Mirta Miras, Thalita Figueiredo, Aline P. Otto, Alexander A. L. Jorge
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
SummaryBackground Mutations in PROP1, HESX1 and LHX3 are associated with combined pituitary hormone deficiency (CPHD) and orthotopic posterior pituitary lobe (OPP). Objective To identify mutations in PROP1, HESX1 and LHX3 in a large cohort of patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34f019222228626ff8b81c61577d89f0
https://pubmed.ncbi.nlm.nih.gov/28734020
https://pubmed.ncbi.nlm.nih.gov/28734020
Autor:
Milena Garcia Abrão
Publikováno v:
Biblioteca Digital de Teses e Dissertações da USP
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
As mutações no gene PROP1 são a causa genética mais comum da deficiência combinada de hormônios hipofisários. Até o momento, diversas mutações missense e pequenas deleções foram descritas sendo a mutação 301-302 delAG a mais freqüente.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9f56f6a6f2af446bd20175d11edce49
https://doi.org/10.11606/t.5.2005.tde-15022006-203659
https://doi.org/10.11606/t.5.2005.tde-15022006-203659
Autor:
Ana Elisa C. Billerbeck, Berenice B. Mendonca, Luciani R. Carvalho, Angela Silva Barbosa, Mirian Yumie Nishi, Regina Matsunaga Martin, Ivo J.P. Arnhold, Maristela V. Leite, Milena Garcia Abrão
Publikováno v:
Clinical Endocrinology. 65:294-300
Summary Objective PROP1 mutations are the most common cause of genetic combined pituitary hormone deficiency (CPHD). The aim of this study was to investigate the PROP1 gene in two siblings with CPHD. Design Pituitary function and imaging assessment a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::842f6ce97107a34fca05621214011580
https://doi.org/10.1111/j.1365-2265.2006.02592.x
https://doi.org/10.1111/j.1365-2265.2006.02592.x
Autor:
Carlos L Massard, Milena Garcia Abrão, Alessandra Scofield, Cláudio R. Madruga, Adivaldo Henrique da Fonseca, Virginia Lucia Nazario Bonoldi, Natalino Hajime Yoshinari, Cleber O. Soares
Publikováno v:
Memórias do Instituto Oswaldo Cruz., Vol 98, Iss 3, Pp 311-318 (2003)
Memórias do Instituto Oswaldo Cruz, Volume: 98, Issue: 3, Pages: 311-318, Published: APR 2003
Memórias do Instituto Oswaldo Cruz, Volume: 98, Issue: 3, Pages: 311-318, Published: APR 2003
This paper reports a case of coinfection caused by pathogens of Lyme disease and babesiosis in brothers. This was the first case of borreliosis in Brazil, acquired in Cotia County, State of São Paulo, Brazil. Both children had tick bite history, pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50b1b65ccec778ca160845fa15a33c87
https://doi.org/10.1590/s0074-02762003000300004
https://doi.org/10.1590/s0074-02762003000300004
Autor:
Milena Garcia, Abrão, Ana Elisa C, Billerbeck, Mirian Yumie, Nishi, Suemi, Marui, Berenice B de, Mendonça
Publikováno v:
Arquivos brasileiros de endocrinologia e metabologia. 49(6)
DNA extraction of peripheral leukocytes is the most broadly used technique to obtain DNA. However, cell collection from an oral swab, frequently used in forensics, is useful to obtain DNA samples, mainly in newborns, children and patients who live fa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a919c09f79ed5bb03665cfe858522fe9
https://pubmed.ncbi.nlm.nih.gov/16544023
https://pubmed.ncbi.nlm.nih.gov/16544023
Autor:
Berenice B. Mendonca, Mirian Yumie Nishi, Ana Elisa C. Billerbeck, Milena Garcia Abrão, Suemi Marui
Publikováno v:
Arquivos Brasileiros de Endocrinologia & Metabologia, Volume: 49, Issue: 6, Pages: 978-982, Published: DEC 2005
Arquivos Brasileiros de Endocrinologia & Metabologia v.49 n.6 2005
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Arquivos Brasileiros de Endocrinologia & Metabologia v.49 n.6 2005
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
A extração de DNA de leucócitos periféricos é o meio de obtenção de DNA mais amplamente utilizado. Entretanto, a coleta de células a partir de swab oral, geralmente utilizada em medicina forense, é útil para obtenção de amostras de DNA de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::299be26b5024dd8ff0408affd582c67e
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302005000600019&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302005000600019&lng=en&tlng=en
Autor:
Milena Garcia Abrão
Publikováno v:
Biblioteca Digital de Teses e Dissertações da USPUniversidade de São PauloUSP.
As mutações no gene PROP1 são a causa genética mais comum da deficiência combinada de hormônios hipofisários. Até o momento, diversas mutações missense e pequenas deleções foram descritas sendo a mutação 301-302 delAG a mais freqüente.