Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Jose Antonio Diniz Faria Junior"'
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:
Barbara Leitao Braga, Antonio M. Lerario, Berenice B. Mendonca, Mirian Yumie Nishi, Gil Guerra-Júnior, Bruna L Freire, Nathalia Lisboa Gomes, Sorahia Domenice, Lais Cavalca Cardoso, Anna Flavia Figueredo Benedetti, Rafael Loch Batista, Mariana F A Funari, Jose Antonio Diniz Faria Junior, Alexander A. L. Jorge, Amanda de Moraes Narcizo, Elaine Maria Frade Costa
Publikováno v:
Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation. 16(1)
Hypospadias is a common congenital disorder of male genital formation. Children born small for gestational age (SGA) present a high frequency of hypospadias of undetermined etiology. No previous study investigated the molecular etiology of hypospadia
Autor:
Mirian Yumie Nishi, Thatiana Evilen Silva, Daniela Moraes Silva, Antonio M. Lerario, Luciana Ribeiro Montenegro, Anna Flavia Figueredo Benedetti, Rafael Loch Batista, Mariana F A Funari, Sorahia Domenice, Alexander A. L. Jorge, Maria Tereza Martins Ferrari, Elaine Maria Frade Costa, Jose Antonio Diniz Faria Junior, Nathalia Lisboa Gomes, Berenice B. Mendonca
Publikováno v:
Journal of the Endocrine Society
Background: It is recommended a multidisciplinary approach consisted of clinical, hormonal and genetic workups for diagnosing 46,XY DSD. However, no previous study has quantified how useful is this combined approach. Objectives: To retrospectively re
Autor:
Barbara Leitao Braga, Antonio M. Lerario, Jose Antonio Diniz Faria Junior, Berenice B. Mendonca, Elaine Maria Frade Costa, Rafael Loch Batista, Mariana F A Funari, Bruna L Freire, Mirian Yumie Nishi, L. N. Gomes, A. A. L. Jorge, Sorahia Domenice
BackgroundHypospadias is a congenital disorder of male genital formation where the urinary opening is not on the head of the penis and genetic factors play an important role in the incidence of this early developmental defect in 46,XY individuals, in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc8b7184fc46d231123af169ca59fcce
Autor:
Juliana Moreira Silva, Rafael Loch Batista, Sorahia Domenice, Leila Cristina Pedroso de Paula, Mirian Y. Nishi, Júlio César Loguercio Leite, Tatiana Prade Hemesath, Daniela A. Moraes, Nathalia Lisboa Gomes, Elaine Mf Costa, Clarissa Gutierrez Carvalho, Jose Antonio Diniz Faria Junior, Berenice B Mendonca, Antonio M. Lerario, Thatiana Evilen Silva, Guilherme Guaragna
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bfbb8649e8e1d47e29b56449faa017ce
https://doi.org/10.1111/cge.13459/v2/response1
https://doi.org/10.1111/cge.13459/v2/response1
Autor:
Berenice B. Mendonca, Leila Cristina Pedroso de Paula, Júlio César Loguercio Leite, Eduardo Castro da Costa, Thatiana Evilen da Silva, Daniela A. Moraes, Guilherme Guaragna-Filho, Sorahia Domenice, Clarissa Gutierrez Carvalho, Jose Antonio Diniz Faria Junior, Nathalia Lisboa Gomes, Tatiana Prade Hemesath, Mirian Yumie Nishi, Elaine Maria Frade Costa, Juliana M Silva, Antonio M. Lerario, Rafael Loch Batista
Publikováno v:
Clinical genetics. 95(1)
Molecular diagnosis is rarely established in 46,XX testicular (T) disorder of sex development (DSD) individuals with atypical genitalia. The Wilms' tumour factor-1 (WT1) gene is involved in early gonadal development in both sexes. Classically, WT1 de
Autor:
Marlene Inácio, Mirian Yumie Nishi, Elaine C.F.B. Costa, Berenice B. Mendonca, Nathalia Lisboa Gomes, Ivo J.P. Arnhold, Jose Antonio Diniz Faria Junior, Antonio M. Lerario, Daniela Rodrigues de Moraes, Aline Zamboni Machado, Rafael Loch Batista, Sorahia Domenice, Thatiana Evilen da Silva
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
Background Follow-up data on patients with 46,XY partial gonadal dysgenesis (PGD) until adulthood are scarce, making information on prognosis difficult. Objective To analyse the long-term outcomes of patients with 46,XY PGD regarding testosterone pro
Autor:
Jose Antonio Diniz Faria Junior, Daniela Rodrigues de Moraes, Nathalia Lisboa Gomes, Mirian Yumie Nishi, Luciani R. Carvalho, Andresa Rodrigues, Elaine Maria Frade Costa, Sorahia Domenice, Rafael Loch Batista, Berenice B. Mendonca
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
Androgen insensitivity syndrome (AIS) is the most common cause of 46,XY disorders of sex development (46,XY DSD). This syndrome is an X-linked inheritance disease and it is caused by mutations in the human androgen receptor (AR) gene. Non-synonymous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0d70e262148ef57aa436f3da6ded22d