Zobrazeno 1 - 10
of 84
pro vyhledávání: '"Crésio Alves"'
Autor:
Crésio Alves, Ruth Rocha Franco
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 64, Iss 3, Pp 223-234 (2020)
ABSTRACT Prader-Willi syndrome (PWS) is a genetic disorder caused by the absence of gene expression in the 15q11.2-q13 paternal chromosome. Patients with PWS develop hypothalamic dysfunction that can lead to various endocrine changes such as: obesity
Externí odkaz:
https://doaj.org/article/25ea39a0b8644d7b806c5915745cb6bc
Autor:
Maria Betânia Toralles, Bruno Meira Castro Trindade, Luiza Cavalcanti Fadul, Clóvis F. Peixoto Junior, Marco Antonio Costa Campos de Santana, Crésio Alves
Publikováno v:
Cadernos de Saúde Pública, Vol 25, Iss 1, Pp 105-110 (2009)
Agente teratogênico é definido como o agente físico, químico, biológico ou estado de deficiência que, durante a vida embrionária, leva a alteração na estrutura ou função do concepto. Informações sobre a conduta a ser tomada no caso de ex
Externí odkaz:
https://doaj.org/article/d044f70d8e1f40e480335d1c363d15fe
Publikováno v:
Cadernos de Saúde Pública, Vol 23, Iss 5, Pp 1005-1014 (2007)
A substância exógena que causa efeitos adversos na saúde de um organismo ou sua descendência, como resultado de distúrbios na função hormonal, é denominada interferente endócrino. Nos últimos anos, produtos ambientais com atividades hormona
Externí odkaz:
https://doaj.org/article/16d21847afcb4559a6480fcb001ed7f6
Publikováno v:
Acta Gastroenterológica Latinoamericana, Vol 36, Iss 2, Pp 86-93 (2006)
Los factores genéticos, inmunológicos y ambientales están envueltos en la patogénesis de las enfermedades gastrointestinales. Situado en el brazo corto del cromosoma 6, el sistema HLA se destaca por su polimorfismo y capacidad de conferir suscept
Externí odkaz:
https://doaj.org/article/bd90d393e63e42bf9214af846de16832
Autor:
Crésio Alves, Renata Arruti
Publikováno v:
Acta Ortopédica Brasileira, Vol 17, Iss 1, Pp 55-57 (2009)
OBJETIVO: Relatar uma série de casos de hiperfosfatasemia transitória benigna da infância (HTBI). DESCRIÇÃO: São descritas quatro meninas. A faixa etária variou de 11-45 meses (mediana: 13 meses). Ao diagnóstico, a fosfatase alcalina sérica
Externí odkaz:
https://doaj.org/article/bc1c9b710b5e496d871c4fed0c2029c9
Autor:
Crésio Alves, Michele Souza Dantas da Silva, Luciana Muniz Pinto, Maria Betânia Pereira Toralles, José Tavares-Neto
Publikováno v:
São Paulo Medical Journal, Vol 128, Iss 4, Pp 206-210
CONTEXT AND OBJECTIVE: The lack of a clear definition for human "race" and the importance of this topic in medical practice continue to create doubt among scholars. Here, we evaluate the use of the variable "race" by medical students in Salvador, Bra
Externí odkaz:
https://doaj.org/article/6f0d075ffd3f4ce594bee4eca6d5035c
Autor:
Josilene Luciene Duarte, Crésio Alves, Luciene da Cruz Fernandes, Iza Cristina Salles, Caio Leônidas Oliveira de Andrade, Helton Estrela Ramos, Hélida Braga
Publikováno v:
Journal of Otology, Vol 16, Iss 2, Pp 71-79 (2021)
Journal of Otology
Journal of Otology
Aim To evaluate the hearing of children with congenital hypothyroidism (CH) and to analyze the knowledge that parents’ have on the possible auditory impacts of the disease. Methods A total of 263 parents/guardians were interviewed about aspects of
Autor:
Thaís Florence, Ana Cecília Travassos Santiago, Louise Perna Martins da Cunha, Crésio Alves, Mariana Melo Costa, Hugo da Costa Ribeiro Junior, Sandra Santos Valois
Publikováno v:
Pediatric Endocrinology Diabetes and Metabolism. 27:26-31
Introduction Being born small for gestational age (SGA) implies an increase in the childhood morbidity and mortality rates, in addition to being related to changes in the pattern of growth and body composition, which may be associated with the develo
Autor:
Sonir Roberto Rauber Antonini, Leda L Ferreira, Thaisa B Moscato, Antonio Carlos dos Santos, Gildasio Carvalho da Conceicao, Paulo S. Silveira-Mattos, Crésio Alves, María B. Arriaga, Federico Costa, Juan P. Aguilar Ticona
Publikováno v:
JAMA network open. 4(5)
The Zika virus infects progenitor neuron cells, disrupts cerebral development, and, in mice, drives hypothalamic defects. Patients with microcephaly caused by congenital Zika infection present with midline cerebral defects, which may result in hypopi
Autor:
Gabriela Carvalho Machado, Crésio Alves, Helton Estrela Ramos, Luciene da Cruz Fernandes, Taíse Lima de Oliveira Cerqueira, Luan Paulo Franco Magalhães, Caio Leônidas Oliveira de Andrade
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 122:12-17
Introduction The investigation of amplitudes of otoacoustic emissions in congenital hypothyroidism can provide information on cochlear function with more sensibility, when compared to other methods of auditory evaluation. Aim To investigate cochlear