Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Paulo Cesar Alves da Silva"'
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:
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:
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:
Carlos A. Tonelli, Patricia N Pugliese-Pires, Mauro Czepielewski, Genoir Simoni, Alexander A. L. Jorge, José Miguel Dora, Paulo Cesar Alves da Silva, Ivo J.P. Arnhold
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
BackgroundGH insensitivity (GHI) syndrome caused by STAT5B mutations was recently reported, and it is characterized by extreme short stature and immune dysfunction. Treatment with recombinant human IGF1 (rhIGF1) is approved for patients with GHI, but
Autor:
Marilza Leal Nascimento, Masanao Ohira, Edson Cechinel, Genoir Simoni, Juliana van de Sande Lee, Tatiane de Campos, Anísia Nhelety Baptista Cristiano, Paulo Cesar Alves da Silva, Rose Marie Muller Linhares
Publikováno v:
Arquivos brasileiros de endocrinologia e metabologia. 58(7)
Objective Evaluate the Neonatal Screening Program (NSP) for congenital adrenal hyperplasia (CAH) of the Department of Health of the State of Santa Catarina (Secretaria de Estado da Saúde de Santa Catarina, SES/SC), and provide information to improve
Autor:
Giovanni S. Lobo, Genoir Simoni, Paulo Cesar Alves da Silva, Charles D. Souza, Marilza Leal Nascimento
Publikováno v:
Jornal de Pediatria. 73:176-179
OBJECTIVE The authors report early results of a screening program for Congenital Hypothyroidism in Santa Catarina, Brazil. METHODS All the assays (82.709) analysed by Laboratorio Central (LACEN) between July 1993 and December 1994 were studied. A blo
Autor:
PAULO CESAR ALVES DA SILVA
Publikováno v:
Archives of Endocrinology and Metabolism. 60:407-407
Autor:
Vinícius Nahime Brito, Angela Maria Spinola-Castro, Cristiane Kochi, Cristiane Kopacek, Paulo César Alves da Silva, Gil Guerra-Júnior
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 60, Iss 2, Pp 163-172
ABSTRACT Clinical and laboratory diagnosis and treatment of central precocious puberty (CPP) remain challenging due to lack of standardization. The aim of this revision was to address the diagnostic and therapeutic features of CPP in Brazil based on
Externí odkaz:
https://doaj.org/article/a389ff385f434983afbf79f948d87294