Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Beatriz Amstalden, Barros"'
Autor:
Beatriz Amstalden Barros, Letícia Ribeiro de Oliveira, Cíntia Regina Crocetti Surur, Antonio de Azevedo Barros-Filho, Andrea Trevas Maciel-Guerra, Gil Guerra-Junior
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 26, Iss 1, Pp 19-23 (2021)
Complete androgen insensitivity syndrome (CAIS) is a rare condition characterized by 46,XY karyotype, female external genitalia, absence of uterus, and testes located intra-abdominally, in the inguinal ring or in the labia majora. In the present stud
Externí odkaz:
https://doaj.org/article/406c7ada877a44208d71918e19692501
Autor:
Flávia Marcorin de Oliveira, Beatriz Amstalden Barros, Ana Paula dos Santos, Nilma Lúcia Viguetti Campos, Taís Nitsch Mazzola, Paulo Latuf Filho, Liliana Aparecida Lucci De Angelo Andrade, Mara Sanches Guaragna, Maricilda Palandi de Mello, Gil Guerra‐Junior, Társis Antonio Paiva Vieira, Andréa Trevas Maciel‐Guerra
Publikováno v:
American Journal of Medical Genetics Part A. 191:592-598
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c0176a49ca5aeb9ab46481e7d9059ae
https://doi.org/10.1002/ajmg.a.63051
https://doi.org/10.1002/ajmg.a.63051
Autor:
Beatriz Amstalden Barros, Mara Sanches Guaragna, Helena Fabbri-Scallet, Maricilda Palandi de Mello, Gil Guerra-Júnior, Andréa Trevas Maciel-Guerra
Publikováno v:
Sexual Development. 16:242-251
Introduction: Ovotesticular disorder of sex development (OT-DSD) is a rare condition defined by concomitance of testicular tissue and ovarian tissue (containing follicles) in the same individual. In SRY-negative 46,XX OT-DSD, the presence of testicul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cde5738b5588d90af4b0b74edba2f200
https://doi.org/10.1159/000526036
https://doi.org/10.1159/000526036
Autor:
Georgette Beatriz De Paula, Beatriz Amstalden Barros, Stela Carpini, Bruna Jordan Tincani, Tais Nitsch Mazzola, Mara Sanches Guaragna, Cristiane Santos da Cruz Piveta, Laurione Candido de Oliveira, Juliana Gabriel Ribeiro Andrade, Guilherme Guaragna-Filho, Pedro Perez Barbieri, Nathalia Montibeler Ferreira, Marcio Lopes Miranda, Ezequiel Moreira Gonçalves, Andre Moreno Morcillo, Nilma Lucia Viguetti-Campos, Sofia Helena Valente Lemos-Marini, Roberto Benedito de Paiva Silva, Antonia Paula Marques-de-Faria, Maricilda Palandi De Mello, Andrea Trevas Maciel-Guerra, Gil Guerra-Junior
Publikováno v:
International Journal of Endocrinology, Vol 2016 (2016)
Objective. To evaluate diagnosis, age of referral, karyotype, and sex of rearing of cases with disorders of sex development (DSD) with ambiguous genitalia. Methods. Retrospective study during 23 years at outpatient clinic of a referral center. Result
Externí odkaz:
https://doaj.org/article/30ead1c5129f4ee9a6bd38be2f250503
Autor:
Maricilda Palandi de Mello, Nilma Lúcia Viguetti-Campos, Olaf Hiort, Tais Nitsch Mazzola, Helena Fabbri-Scallet, Sofia Helena Valente de Lemos-Marini, Mara Sanches Guaragna, Antonia Paula Marques-de-Faria, Társis Paiva Vieira, André Moreno Morcillo, Gil Guerra-Júnior, Debora Stabile Romero Amais, Andréa Trevas Maciel-Guerra, Tainara Emilia Rodrigues da Silva, Beatriz Amstalden Barros, Juliana Gabriel Ribeiro de Andrade
The aim of this study was to verify the influence of Y chromosome and intrauterine androgens production/action on birth weight and length of children with Disorders/Differences of Sex Development (DSD). This was a cross-sectional and retrospective st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2a25c933c23490f3f904061a56a4e11
https://doi.org/10.21203/rs.3.rs-508679/v1
https://doi.org/10.21203/rs.3.rs-508679/v1
Autor:
Márcio Lopes Miranda, Andréa Trevas Maciel-Guerra, Carlos Wustemberg Germano, Mayra de Souza El Beck, Sofia Helena Valente de Lemos-Marini, Juliana Gabriel Ribeiro de Andrade, Maricilda Palandi de Mello, Beatriz Amstalden Barros, Mara Sanches Guaragna, Nilma Lúcia Viguetti-Campos, Helena Fabbri-Scallet, Tais Nitsch Mazzola, Guilherme Guaragna-Filho, Társis Paiva Vieira, Georgette Beatriz De Paula, Antonia Paula Marques-de-Faria, Roberto B. Paiva e Silva, Gil Guerra-Júnior
Publikováno v:
Jornal de Pediatria v.96 n.5 2020
Jornal de Pediatria
Sociedade Brasileira de Pediatria (SBP)
instacron:SBPE
Jornal de Pediatria (Versão em Português), Vol 96, Iss 5, Pp 607-613 (2020)
Jornal de Pediatria, Vol 96, Iss 5, Pp 607-613 (2020)
Jornal de Pediatria, Volume: 96, Issue: 5, Pages: 607-613, Published: 11 NOV 2020
Jornal de Pediatria
Sociedade Brasileira de Pediatria (SBP)
instacron:SBPE
Jornal de Pediatria (Versão em Português), Vol 96, Iss 5, Pp 607-613 (2020)
Jornal de Pediatria, Vol 96, Iss 5, Pp 607-613 (2020)
Jornal de Pediatria, Volume: 96, Issue: 5, Pages: 607-613, Published: 11 NOV 2020
Objective: To evaluate, in a sample of patients with disorders of sex development (DSD), data related to the age at referral and their correlation with the initial complaints, gender at referral, defined gender after diagnosis and etiological diagnos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5179e1e37f741394d4ce4648edccf7fb
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572020000500607
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572020000500607
Autor:
Cíntia Regina Crocetti Surur, Andréa Trevas Maciel-Guerra, Leticia Ribeiro Oliveira, Gil Guerra-Júnior, Beatriz Amstalden Barros, Antonio de Azevedo Barros-Filho
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism
Annals of Pediatric Endocrinology & Metabolism, Vol 26, Iss 1, Pp 19-23 (2021)
Annals of Pediatric Endocrinology & Metabolism, Vol 26, Iss 1, Pp 19-23 (2021)
Complete androgen insensitivity syndrome (CAIS) is a rare condition characterized by 46,XY karyotype, female external genitalia, absence of uterus, and testes located intra-abdominally, in the inguinal ring or in the labia majora. In the present stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08d5ff4e7baa6e7f0d4008f8070c018d
https://pubmed.ncbi.nlm.nih.gov/33819955
https://pubmed.ncbi.nlm.nih.gov/33819955
Autor:
Stela Carpini, Juliana Gabriel Ribeiro de Andrade, Tais Nitsch Mazzola, Guilherme Guaragna-Filho, Maricilda Palandi de Mello, Sofia Helena Valente de Lemos-Marini, Georgette Beatriz De Paula, Antonia Paula Marques-de-Faria, Roberto Benedito de Paiva e Silva, Cristiane S C Piveta, Andréa Trevas Maciel-Guerra, Nathalia Montibeler Ferreira, Nilma Lúcia Viguetti-Campos, Márcio Lopes Miranda, Bruna J. Tincani, Ezequiel Moreira Gonçalves, Mara Sanches Guaragna, Laurione Candido de Oliveira, Gil Guerra-Júnior, André Moreno Morcillo, Pedro Perez Barbieri, Beatriz Amstalden Barros
Publikováno v:
International Journal of Endocrinology
International Journal of Endocrinology, Vol 2016 (2016)
International Journal of Endocrinology, Vol 2016 (2016)
Objective. To evaluate diagnosis, age of referral, karyotype, and sex of rearing of cases with disorders of sex development (DSD) with ambiguous genitalia.Methods. Retrospective study during 23 years at outpatient clinic of a referral center.Results.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32fe144a5e94566a2b5a35fff733aede
https://pubmed.ncbi.nlm.nih.gov/28018429
https://pubmed.ncbi.nlm.nih.gov/28018429
Autor:
Társis Paiva Vieira, S.G. Moraes, Eliane Maria Ingrid Amstalden, Beatriz Amstalden Barros, Gil Guerra-Júnior, Fernanda Borchers Coeli, Annelise Barreto de Carvalho, Juliana Godoy Assumpção, Adriana Mangue Esquiaveto-Aun, Nilma Lúcia Viguetti-Campos, Antonia Paula Marques-de-Faria, M. P. De Mello, Juliana Gabriel Ribeiro de Andrade, Lília D'Souza-Li, Andréa Trevas Maciel-Guerra, S. H. V. Lemos-Marini
Publikováno v:
Human reproduction (Oxford, England). 26(12)
The aim of this study was to investigate the frequency of gonadal tumors among patients with Turner syndrome (TS) carrying Y-derivative sequences in their chromosomal constitution.Six out of 260 patients with TS were selected based on mosaicism of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ed787c8f69057adf741e978c9e32699
https://pubmed.ncbi.nlm.nih.gov/21930534
https://pubmed.ncbi.nlm.nih.gov/21930534
Autor:
Maricilda Palandi de Mello, Gil Guerra-Júnior, Sofia Helena Valente de Lemos-Marini, Antonia Paula Marques-de-Faria, Beatriz Amstalden Barros, Annelise Barreto de Carvalho, Fernanda Borchers Coeli, Andréa Trevas Maciel-Guerra, Juliana Godoy Assumpção, Nilma Lúcia Viguetti-Campos
Publikováno v:
Arquivos Brasileiros de Endocrinologia & Metabologia v.53 n.9 2009
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
OBJETIVO: Avaliar o efeito do aprimoramento da análise cromossômica sobre os achados citogenéticos de pacientes com síndrome de Turner (ST). MÉTODOS: Estudo retrospectivo dos resultados de cariótipo de 260 pacientes com ST, com análise das té
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c67494107b8c97873e149e9d1042fec
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302009000900010
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302009000900010