Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Rodrigo Neves Ferreira"'
Autor:
Laryssa Santos Metzker, Luyanne Azevedo Cabral Ferreira, Julia Caroliny Nogueira Borges, Mariana Furieri Guzzo, Rodrigo Neves Ferreira, Lucas Luciano Rocha Silva, Rodrigo Monico Cavedo, Antonio Chambô Filho
Publikováno v:
Case Reports in Obstetrics and Gynecology, Vol 2023 (2023)
Ovarian hyperthecosis or ovarian stromal hyperplasia is a non-neoplastic functional disorder resulting from the presence of luteinized thecal cells within a hyperplastic ovarian stroma. The condition is more common in postmenopausal women than in tho
Externí odkaz:
https://doaj.org/article/19e2b149f96b4b2c8169ad2a3fdd71d2
Autor:
Fernando Augusto Rozário Garcia, Vanessa Pereira Gaigher, Rodrigo Neves Ferreira, Antônio Chambô Filho
Publikováno v:
Case Reports in Obstetrics and Gynecology, Vol 2018 (2018)
Background. First described in 1945 by Morehead and Bowman, uterine tumors resembling ovarian sex-cord tumors (UTROSCT) are rare tumors of the uterine body that tend to occur in menopausal women presenting with abnormal vaginal bleeding, abdominal pa
Externí odkaz:
https://doaj.org/article/e657aa3c28254fffbaf923518c86c0f8
Autor:
Roberta Fonseca de Souza, Janaina Pereira da Silva, Bruno Vieira Balla, Rodrigo Neves Ferreira, Antônio Chambô Filho
Publikováno v:
Case Reports in Obstetrics and Gynecology, Vol 2017 (2017)
Androgen insensitivity syndrome is the most common cause of male pseudohermaphroditism and the third most common cause of primary amenorrhea. This genetic alteration is a consequence of inherited defects on the X chromosome causing total or partial d
Externí odkaz:
https://doaj.org/article/51dabcbd1f18457ab589598943941398
Autor:
Andressa Gonçalves Amorim, Brunelle Batista Fraga Mendes, Rodrigo Neves Ferreira, Antônio Chambô Filho
Publikováno v:
Case Reports in Dermatological Medicine, Vol 2015 (2015)
The objective of this paper is to report a case of extramammary Paget disease of the vulva, to describe its diagnosis, surgical treatment, and outcome, and to discuss the general characteristics of this pathology. This is a rare neoplasm, found princ
Externí odkaz:
https://doaj.org/article/7def87c1c631423ba7ff9424ae4509fb
Autor:
Andressa Gonçalves Amorim, Fernanda Alves Barbosa Pagio, Rodrigo Neves Ferreira, Antônio Chambô Filho
Publikováno v:
Case Reports in Obstetrics and Gynecology, Vol 2014 (2014)
Externí odkaz:
https://doaj.org/article/56b30a4a6ae24bc2bc9640199827191f
Autor:
Sheyla Aparecida Rio Branco De Paranhos, Bárbara Silva De Sousa, Rodrigo Neves Ferreira, Maria Das Graças Silva Mattede, Sarah Santos Gonçalves, Raphael Lubiana Zanotti, Rafael Froede Catapane
Publikováno v:
Anais do 3º Congresso Regional de Análises Clínicas do Sudeste e 4º Encontro de Análises Clínicas do ES.
Autor:
Antônio Chambô Filho, Bárbara Luchi Montebeller, Rodrigo Neves Ferreira, Arthur Andrade Alves
Publikováno v:
Journal of Medical - Clinical Research & Reviews. 2:1-3
Autor:
Antônio Chambô Filho, Rafaela de Lacerda Trajano Pinel, Luyanne Azevedo Cabral Ferreira, Rodrigo Neves Ferreira
Publikováno v:
European Journal of Gynaecological Oncology. 41:644
Autor:
Rodrigo Neves Ferreira, Vanessa Pereira Gaigher, Fernando Augusto Rozário Garcia, Antônio Chambô Filho
Publikováno v:
Case Reports in Obstetrics and Gynecology
Case Reports in Obstetrics and Gynecology, Vol 2018 (2018)
Case Reports in Obstetrics and Gynecology, Vol 2018 (2018)
Background. First described in 1945 by Morehead and Bowman, uterine tumors resembling ovarian sex-cord tumors (UTROSCT) are rare tumors of the uterine body that tend to occur in menopausal women presenting with abnormal vaginal bleeding, abdominal pa
Autor:
Antônio Chambô Filho, Rodrigo Neves Ferreira, Bruno Vieira Balla, Janaina Pereira da Silva, Roberta Fonseca de Souza
Publikováno v:
Case Reports in Obstetrics and Gynecology
Case Reports in Obstetrics and Gynecology, Vol 2017 (2017)
Case Reports in Obstetrics and Gynecology, Vol 2017 (2017)
Androgen insensitivity syndrome is the most common cause of male pseudohermaphroditism and the third most common cause of primary amenorrhea. This genetic alteration is a consequence of inherited defects on the X chromosome causing total or partial d