Zobrazeno 1 - 10
of 10
pro vyhledávání: '"S H V Lemos-Marini"'
Autor:
Maria Tereza Matias Baptista, S. H. V. Lemos-Marini, Alexandre Duarte Baldin, Angela Maria Spinola-Castro, Gil Guerra-Júnior, Lília D'Souza-Li, Tatiana Fabbri, Adriana Aparecida Siviero-Miachon, Andréa Trevas Maciel-Guerra
Publikováno v:
Journal of Endocrinological Investigation. 33:691-695
Background: The majority of anthropometric assessments in Turner syndrome (TS) patients has focused on height. AIM: To analyze body proportions in young adult TS patients either treated or not treated with rhGH, and to compare them with a group of ag
Autor:
S. H. V. Lemos-Marini, Svetlana Lajic, Michela Barbaro, Maria Tereza Matias Baptista, Fernanda Caroline Soardi, M. P. De Mello, Anna Wedell, Gil Guerra-Júnior, I. F. Lau
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 93:2416-2420
Background: Most patients with 21-hydroxylase deficiency carry CYP21A1P-derived mutations, but an increasing number of novel and rare mutations have been reported in disease-causing alleles. Objective: Functional effects of three novel (p.G56R, p.L10
Autor:
C Watanabe, Ayrton Custódio Moreira, M B Melo, Luis Eduardo Calliari, Ana Claudia Latronico, Lourenço Sbragia-Neto, Gil Guerra-Júnior, R Liberatore, Osmar Monte, C L P Lancellotti, A Nigri, Carlos Alberto Longui, Maria Tereza Matias Baptista, Constantine A. Stratakis, Susan E. Taymans, M N Rocha, S. H. V. Lemos-Marini, Margaret de Castro, Berenice Bilharinho Mendonca, Bonald C. Figueiredo, A M D Tardelli
Publikováno v:
Journal of Medical Genetics. 41:354-359
The R337H TP53 mutation is a low-penetrance molecular defect that predisposes to adrenocortical tumour (ACT) formation in Brazilian and possibly other populations. Additional genetic defects may be responsible for the variable expression of ACTs in t
Autor:
L C, Kaupert, S H V, Lemos-Marini, M P, De Mello, R P, Moreira, V N, Brito, A A L, Jorge, C A, Longui, G, Guerra, B B, Mendonca, T A, Bachega
Publikováno v:
Clinical genetics. 84(5)
The 21-hydroxylase deficiency (21OHD) is caused by CYP21A2 mutations resulting in severe or moderate enzymatic impairments. 21OHD females carrying similar genotypes present different degrees of external genitalia virilization, suggesting the influenc
Autor:
Társis Paiva Vieira, S.G. Moraes, Eliane Maria Ingrid Amstalden, Beatriz Amstalden Barros, Gil Guerra-Júnior, Fernanda Borchers Coeli, Annelise Barreto de Carvalho, Juliana Godoy Assumpção, Adriana Mangue Esquiaveto-Aun, Nilma Lúcia Viguetti-Campos, Antonia Paula Marques-de-Faria, M. P. De Mello, Juliana Gabriel Ribeiro de Andrade, Lília D'Souza-Li, Andréa Trevas Maciel-Guerra, S. H. V. Lemos-Marini
Publikováno v:
Human reproduction (Oxford, England). 26(12)
The aim of this study was to investigate the frequency of gonadal tumors among patients with Turner syndrome (TS) carrying Y-derivative sequences in their chromosomal constitution.Six out of 260 patients with TS were selected based on mosaicism of th
Autor:
L C Kaupert, R P P Moreira, M P de Mello, S H V Lemos-Marini, G Guerra-Junior, V N Brito, L G Gomes, M de Castro, B B Mendonca, T A S S Bachega
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a3abcc8ddf487cd2075f5190e4388dd
https://doi.org/10.1210/endo-meetings.2010.part1.p13.p1-651
https://doi.org/10.1210/endo-meetings.2010.part1.p13.p1-651
Autor:
Milton Bricola Filho, Gil Guerra Júnior, Andréa Trevas Maciel-Guerra, Luis Alberto Magna, S. H. V. Lemos-Marini, Edwaldo E. Camargo, Carla C.M. Medeiros, Allan O. Santos, Maria Tereza Matias Baptista
Publikováno v:
Arquivos Brasileiros de Endocrinologia & Metabologia v.51 n.3 2007
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
O seguimento de pacientes com síndrome de Turner (ST) freqüentemente revela alterações transitórias, recorrentes e assintomáticas de TSH e/ou hormônios tireóideos (HT). Neste trabalho foram avaliadas estrutura e função da tireóide em porta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d58aacba5c7c26b3f411892967aef15b
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302007000300007
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302007000300007
Autor:
C, Kochi, C A, Longui, S H V, Lemos-Marini, G, Guerra-Junior, M B, Melo, L E P, Calliari, O, Monte
Publikováno v:
Genetics and molecular research : GMR. 6(1)
Thirty-seven 45 X Turner syndrome patients with confirmed peripheral blood lymphocyte karyotype were initially selected to determine the origin of the retained X chromosome and to correlate it with their parents' stature. Blood samples were available
Autor:
S. H. V. Lemos-Marini, André Moreno Morcillo, Gil Guerra-Júnior, Andréa Trevas Maciel-Guerra, Maria Tereza Matias Baptista, Luciana de Oliveira Silva
Publikováno v:
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, Volume: 49, Issue: 6, Pages: 902-907, Published: DEC 2005
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Arquivos Brasileiros de Endocrinologia & Metabologia, Volume: 49, Issue: 6, Pages: 902-907, Published: DEC 2005
OBJETIVO: Determinar a altura final (AF) de pacientes com hiperplasia supra-renal congênita e investigar fatores de melhor prognóstico de altura. METODOLOGIA: Estudamos 13 pacientes perdedores de sal (PS) e 14 virilizantes simples (VS). AF e altura
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::411b5f45b868cd3ad455a677d1739509
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302005000600008
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302005000600008
Autor:
S. H. V. Lemos-Marini, Maria C. de A. Armani, Andréa Trevas Maciel-Guerra, Alexandre Duarte Baldin, Maria Tereza Matias Baptista, Gil Guerra-Júnior
Publikováno v:
Arquivos Brasileiros de Endocrinologia & Metabologia v.49 n.2 2005
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Arquivos Brasileiros de Endocrinologia & Metabologia, Volume: 49, Issue: 2, Pages: 278-285, Published: APR 2005
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Arquivos Brasileiros de Endocrinologia & Metabologia, Volume: 49, Issue: 2, Pages: 278-285, Published: APR 2005
OBJETIVO: Avaliar a presença de resistência insulínica (RI) e alterações lipídicas na síndrome de Turner (ST), correlacionando com idade, cariótipo, pressão arterial (PA), estatura, peso, índice de massa corporal (IMC) e desenvolvimento pub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae757b656dd7f509d468b0840906c162
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302005000200015
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302005000200015