Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Tatiana Prade Hemesath"'
Autor:
Tatiana Prade Hemesath, Leila Cristina Pedroso de Paula, Clarissa Gutierrez Carvalho, Julio Cesar Loguercio Leite, Guilherme Guaragna-Filho, Eduardo Corrêa Costa
Publikováno v:
Frontiers in Pediatrics, Vol 6 (2019)
Appropriate management of disorders of sex development (DSD) has been a matter of discussion since the first guidelines were published in the 1950s. In the last decade, with the advent of the 2006 consensus, the classical methods, especially regardin
Externí odkaz:
https://doaj.org/article/0265ca95607c4c90bc99a88bd77e04b5
Autor:
Tatiana Prade Hemesath
Publikováno v:
Psicologia: Reflexão e Crítica, Vol 26, Iss 3, Pp 583-590 (2013)
O estudo investigou as representações de mães e pais sobre a constituição de identidade de gênero em crianças nascidas com diagnóstico de Anomalias da Diferenciação Sexual (ADS). As ADS são distúrbios da diferenciação sexual que resulta
Externí odkaz:
https://doaj.org/article/a73e722312a94e87bcda970ed90dbdea
Autor:
Tatiana Prade Hemesath, Eduardo Corrêa Costa, Guilherme Guaragna-Filho, Júlio César Loguercio Leite, Marcelo Costamilan Rombaldi, Clarissa Gutierrez Carvalho
Publikováno v:
Asian Journal of Endoscopic Surgery. 15:356-358
Laparoscopy was introduced more than 100 years ago. However, in some fields its use still meets resistance. Technology such as laparoscopy may help to identify rare and complex disorders, even in very ordinary procedures, such as inguinal hernia repa
Autor:
Tatiana Prade Hemesath, Mariluce Riegel, Matheus Vernet Machado Bressan Wilke, Clarissa Gutierrez Carvalho, Júlio César Loguercio Leite, Guilherme Guaragna-Filho, Eduardo Corrêa Costa, Iara Regina Siqueira Lucena
Publikováno v:
Urology. 158
This report describes an adolescent with Mixed Gonadal Dysgenesis and unexpected mosaicism [karyotype 46,X,mar(Y)/ 47,X, mar(Y),+mar(Y)].). Diagnosis with 1 month of age due to atypical genitalia. He presented a right streak gonad, which was removed
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