Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Marilza Leal Nascimento"'
Autor:
Jéssica Mallmann Erbes Schaefer Martins, Barbara Leitao Braga, Klevia Nunes Feitosa Sampaio, Tamires de Souza Garcia, Juliana Van de Sande Lee, Edson Cechinel, Genoir Simoni, Marilza Leal Nascimento, Paulo Cesar Alves da Silva, Maria C. V. Fragoso, Tania A. A. S. Bachega, Mirian Y. Nishi, Berenice B. Mendonca
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 68 (2024)
SUMMARY Beckwith-Wiedemann syndrome (BWS) is a common genetic congenital disease characterized by somatic overgrowth and its broad clinical spectrum includes pre- and post-natal macrosomia, macroglossia, visceromegaly, increased risk of neonatal hypo
Externí odkaz:
https://doaj.org/article/53542a5606084650927adb2dcee6a9e7
Autor:
Marilza Leal Nascimento, Andre Leal Nascimento, Patricia Dornbusch, Masanao Ohira, Genoir Simoni, Edson Cechinel, Rose Marie Mueller Linhares, Juliana van De Sande Lee, Paulo Cesar Alves Silva
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 64, Iss 6, Pp 816-823 (2020)
ABSTRACT Oubjective: To assess the implications of changing the cutoff level of TSH from 10 to 6 mIU/L. Subjects and methods: The study population was constituted by 74.123 children screened for congenital hypothyroidism by the National Screening Pro
Externí odkaz:
https://doaj.org/article/9f99c72b79854a979a5a7c844b47793d
Autor:
Marilza Leal Nascimento, Guiomar Madureira, Berenice B. Mendonca, Delanie B. Macedo, Ana Claudia Latronico, Carolina Ramos, Vinicius Nahime Brito, Tania A. S. S. Bachega
Publikováno v:
Hormone Research in Paediatrics. 91:411-415
Background/Aims: Premature pubarche is associated with conditions such as virilizing congenital adrenal hyperplasia, androgen-secreting tumors, and exogenous exposure to androgen products. We describe the clinical and hormonal features of a series of
Autor:
Edson Cechinel, Jéssica M E S Martins, Genoir Simoni, Paulo Cesar Alves da Silva, Juliana S Lee, Tamires S Garcia, Marilza Leal Nascimento
Publikováno v:
Journal of the Endocrine Society
Introduction: Beckwith-Wiedemann syndrome (BWS) is characterized by variable phenotypes that might include overgrowth, macroglossia, abdominal wall defects, neonatal hypoglycemia, hemihypertrophy and predisposition to embryonal tumours. Some features
Autor:
Ivy Zortéa S, Parise, Guilherme A, Parise, Lúcia, Noronha, Mirvat, Surakhy, Thiago Demetrius, Woiski, Denise B, Silva, Tatiana Ei-Jaick B, Costa, Maria Helena C P, Del-Valle, Heloisa, Komechen, Roberto, Rosati, Melyssa Grignet, Ribeiro, Marilza Leal, Nascimento, José Antônio de, Souza, Diancarlos P, Andrade, Mariana M, Paraizo, Marjorana Martini R, Galvão, José Renato S, Barbosa, Miriam Lacerda, Barbosa, Gislaine C, Custódio, Mirna M O, Figueiredo, Ana Luiza M R, Fabro, Gareth, Bond, Marco, Volante, Enzo, Lalli, Bonald C, Figueiredo
Publikováno v:
Cancers
Adrenocortical carcinoma (ACC) is a rare disease among children. Our goal was to identify prognostic biomarkers in 48 primary ACCs from children (2.83 ± 2.3 y; mean age ± SD) by evaluating the tumor stage and outcome for an age of diagnosis before
Autor:
Mariana M Paraizo, Diancarlos P. Andrade, Ivy Zortéa S Parise, Enzo Lalli, Marco Volante, Heloisa Komechen, Mirvat Surakhy, Bonald C. Figueiredo, Marjorana Martini R Galvão, Marilza Leal Nascimento, Miriam L. Barbosa, Tatiana Ei-Jaick B Costa, Thiago Demetrius Woiski, Ana Luiza M. R. Fabro, Denise B Silva, José Antônio de Souza, Maria Helena C P Del-Valle, José Renato S. Barbosa, Mirna M O Figueiredo, Gislaine Custódio, Roberto Rosati, Melyssa Grignet Ribeiro, Lucia de Noronha, Gareth L. Bond, Guilherme A Parise
Publikováno v:
Cancers
Cancers, MDPI, 2019, 11 (11), pp.1730. ⟨10.3390/cancers11111730⟩
Cancers, 2019, 11 (11), pp.1730. ⟨10.3390/cancers11111730⟩
Cancers, Vol 11, Iss 11, p 1730 (2019)
Volume 11
Issue 11
Cancers, MDPI, 2019, 11 (11), pp.1730. ⟨10.3390/cancers11111730⟩
Cancers, 2019, 11 (11), pp.1730. ⟨10.3390/cancers11111730⟩
Cancers, Vol 11, Iss 11, p 1730 (2019)
Volume 11
Issue 11
Adrenocortical carcinoma (ACC) is a rare disease among children. Our goal was to identify prognostic biomarkers in 48 primary ACCs from children (2.83 ±
2.3 y
mean age ±
SD) by evaluating the tumor stage and outcome for an
2.3 y
mean age ±
SD) by evaluating the tumor stage and outcome for an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3356c3e7c8163df88cd589ec427fb338
https://www.hal.inserm.fr/inserm-02437545/document
https://www.hal.inserm.fr/inserm-02437545/document
Publikováno v:
Blucher Chemical Engineering Proceedings.
Autor:
Suzana Nesi-França, Edna Teruko Kimura, Léa Maria Zanini Maciel, Célia Regina Nogueira, Sandra Elisabete Vieira, Gláucia Maria Ferreira da Silva Mazeto, Patrícia Künzle Ribeiro Magalhães, Marilza Leal Nascimento
Publikováno v:
Arquivos Brasileiros de Endocrinologia & Metabologia, Volume: 57, Issue: 3, Pages: 184-192, Published: APR 2013
Arquivos Brasileiros de Endocrinologia & Metabologia v.57 n.3 2013
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
SciELO
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Arquivos Brasileiros de Endocrinologia & Metabologia v.57 n.3 2013
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
SciELO
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Submitted by Guilherme Lemeszenski (guilherme@nead.unesp.br) on 2013-08-22T19:04:17Z No. of bitstreams: 1 S0004-27302013000300004.pdf: 141374 bytes, checksum: c57e14da8d45c97e5a8b0b82a2b58905 (MD5) Made available in DSpace on 2013-08-22T19:04:17Z (GM
Autor:
Masanao Ohira, Rose Marie Muller Linhares, Paulo Cesar Alves da Silva, Genoir Simoni, Edson Cechinel, Fernanda Hostim Rabello, Marilza Leal Nascimento
Publikováno v:
Arquivos Brasileiros de Endocrinologia & Metabologia v.56 n.9 2012
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Arquivos Brasileiros de Endocrinologia & Metabologia, Volume: 56, Issue: 9, Pages: 627-632, Published: DEC 2012
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Arquivos Brasileiros de Endocrinologia & Metabologia, Volume: 56, Issue: 9, Pages: 627-632, Published: DEC 2012
OBJETIVO: Avaliar a etiologia, no primeiro atendimento, dos casos de hipotireoidismo congênito primário (HCP) identificados pelo Programa de Triagem Neonatal de Santa Catarina entre julho de 2007 e junho de 2009. SUJEITOS E MÉTODOS: Estudo prospec
Autor:
Marilza Leal Nascimento
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
O hipotireoidismo congênito (HC) é uma das causas mais frequentes de deficiência mental passível de prevenção. Esforços devem ser utilizados na sua detecção e no tratamento precoces. O atraso no diagnóstico e no tratamento resultará em seq