Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Luciana Mattos Barros Oliveira"'
Autor:
Arthur Machado Geiger Dias de Moraes, Caren Nariel Pereira Santos Souza, Luiza Taddeo Marques, João Fernando Nascimento de Barcelos, Felipe Barros Oliveira, Rafaela Góes Bispo, Rodrigo Gomes Santos, Ailton da Silva Santos, José Antônio Diniz Faria Júnior, Luciana Mattos Barros Oliveira
Publikováno v:
Revista de Saúde Pública, Vol 58 (2024)
ABSTRACT OBJECTIVE The transgender population in Brazil faces marginalization and difficulties in accessing education and health, leading many individuals to self-medicate. This study aimed to evaluate the impact of the implementation of Specialized
Externí odkaz:
https://doaj.org/article/adcc7b2fe5af4ca7a9d1fcdc172076b1
Autor:
Júlia Brito Vieira Thimmig, Miralba Freire de Carvalho Ribeiro da Silva, Patrícia Maria Almeida Silva, Ailton da Silva Santos, Monaliza Cardozo Rebouças, Luciana Mattos Barros Oliveira, Leila Regina Amorim Araújo de Azevedo
Publikováno v:
Brazilian Journal of Infectious Diseases, Vol 27, Iss , Pp 103220- (2023)
Introdução/Objetivo: Segundo o Ministério da Saúde, em 2021, foram registrados no Brasil mais de 167 mil novos casos de sífilis adquirida, e até junho de 2022, somaram-se mais 79.587 casos. Em 2018 foi relatado prevalência de sífilis de 26,9%
Externí odkaz:
https://doaj.org/article/e6f58bf7bc4149469fbbf5884c863ec6
Autor:
Bianca Costa Mota, Luciana Mattos Barros Oliveira, Renata Lago, Paula Brito, Ana Karina Canguçú-Campinho, Ubirajara Barroso, Maria Betânia Pereira Toralles
Publikováno v:
International Brazilian Journal of Urology, Vol 41, Iss 5, Pp 975-981 (2015)
ABSTRACT The term DSD refers to disorders that affect the normal process of sexual development causing disagreement between chromosomal, gonadal and phenotypic sex, and this study aimed to describe the clinical profile of a group with DSD 46, XY join
Externí odkaz:
https://doaj.org/article/5fb3292577114fe2bfe7e8985ca59214
Autor:
Luciana Mattos Barros Oliveira, Maria Betania Toralles, Ana Carolina S. Costa, Ubirajara Barroso, Robson Augusto Cardoso Apóstolos, Renata Lago, Ana Karina Canguçu-Campinho
Publikováno v:
Archives of Sexual Behavior. 47:2491-2496
In individuals with congenital adrenal hyperplasia (CAH) and 46,XX karyotype, androgens produced by the adrenal glands during the intrauterine development promote virilization of the genitals, which may even result in the development of a well-formed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eaaee967aa05ff6720ba7ef5ea4cdd68
https://doi.org/10.1007/s10508-018-1299-z
https://doi.org/10.1007/s10508-018-1299-z
Autor:
Lorena Moura Pontes Araujo, Paula Hayasi Pinho, Helena Moraes Cortes, Marcos Venicius Gomes de Sá, Luciana Mattos Barros Oliveira
Publikováno v:
Revista Eletrônica Acervo Saúde. 13:e9116
Objetivo: Analisar o itinerário terapêutico percorrido por homens transgêneros ao processo transexualizador pelo Sistema Único de Saúde (SUS) ofertado num serviço de cuidado a pessoas trans no nordeste brasileiro. Métodos: Estudo qualitativo,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::818de8e0d4975e99cb2033fbb944036e
https://doi.org/10.25248/reas.e9116.2021
https://doi.org/10.25248/reas.e9116.2021
Autor:
Lacey Plummer, Ravikumar Balasubramanian, Kimberly H. Cox, Luciana Mattos Barros Oliveira, William F. Crowley, Braden Corbin, Thomas J. Gardella
Publikováno v:
Human Molecular Genetics. 27:338-350
A major challenge in human genetics is the validation of pathogenicity of heterozygous missense variants. This problem is well-illustrated by PROKR2 variants associated with Isolated GnRH Deficiency (IGD). Homozygous, loss of function variants in PRO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22d2e33ffb52d692060a14172a63a6bb
https://doi.org/10.1093/hmg/ddx404
https://doi.org/10.1093/hmg/ddx404
Autor:
Francisco Buriti, Rodrigo Lessa, Ubirajara Barroso, Vinicius Menezes Jesus, Luciana Mattos Barros Oliveira, Maria Betânia Pereira Toralles
Publikováno v:
Journal of pediatric surgery. 53(4)
Introduction Genital ambiguity is a very common phenomenon in disorders of sex development (DSD). According to the Chicago Consensus 2006, feminizing genitoplasty, when indicated, should be performed in the most virilized cases (Prader III to V). Adv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77eff7d56e617d1cc13d078f441d6902
https://pubmed.ncbi.nlm.nih.gov/28917585
https://pubmed.ncbi.nlm.nih.gov/28917585
Autor:
Luciana Mattos Barros Oliveira, Maria Betânia Pereira Toralles, José Antônio Diniz Faria Junior, Daniela Nunes-Silva, Renata Lago
Publikováno v:
Arquivos Brasileiros de Endocrinologia & Metabologia, Volume: 57, Issue: 5, Pages: 354-359, Published: JUL 2013
Arquivos Brasileiros de Endocrinologia & Metabologia v.57 n.5 2013
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Repositório Institucional da UFBA
Universidade Federal da Bahia (UFBA)
instacron:UFBA
Arquivos Brasileiros de Endocrinologia & Metabologia v.57 n.5 2013
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Repositório Institucional da UFBA
Universidade Federal da Bahia (UFBA)
instacron:UFBA
OBJETIVO: O objetivo deste estudo foi avaliar pacientes com HAC clássica antes e após tratamento com glicocorticoides e/ou mineralocorticoides e comparar o perfil metabólico entre o grupo bem controlado (BC) e mal controlado (MC). SUJEITOS E MÉTO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cb9a0c7482bafc0c1bde01d8368c95a
https://doi.org/10.1590/s0004-27302013000500004
https://doi.org/10.1590/s0004-27302013000500004
Autor:
Milena Beranova, Frances J. Hayes, Luciana Mattos Barros Oliveira, Sarah B. Valkenburgh, William F. Crowley, Ernestina Schipani, Stephanie B. Seminara, Elaine Maria Frade Costa, Mario Vallejo, Ana Claudia Latronico
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 86:1532-1538
Kallmann syndrome (KS) consists of congenital, isolated, idiopathic hypogonadotropic hypogonadism (IHH) and anosmia. The gene responsible for the X-linked form of KS, KAL, encodes a protein, anosmin, that plays a key role in the migration of GnRH neu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e9599796cad21c7aabea2bfdbdbab8e
https://doi.org/10.1210/jcem.86.4.7420
https://doi.org/10.1210/jcem.86.4.7420
Autor:
Frances J. Hayes, Kathryn A. Martin, Luciana Mattos Barros Oliveira, Mario Vallejo, Stephanie B. Seminara, Nelly Pitteloud, Jose Bernardo Quintos, Grégoy Y. Bédécarrats, Ursula B. Kaiser, William F. Crowley, Ariachery C. Ammini, Ernestina Schipani, Janet E. Hall, Milena Beranova
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 86:1580-1588
Mutations in the GnRH receptor (GNRHR) have been described as a cause of reproductive failure in a subset of patients with idiopathic hypogonadotropic hypogonadism (IHH). Given the apparent rarity of these mutations, we set out to determine the frequ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::550e9ba24f3829c790c1ce4ccde4bf0c
https://doi.org/10.1210/jcem.86.4.7395
https://doi.org/10.1210/jcem.86.4.7395