Zobrazeno 1 - 10
of 18
pro vyhledávání: '"AndrÈa Trevas Maciel-Guerra"'
Autor:
Luísa Riccetto, Tarsis Paiva Vieira, Nilma Lucia Viguetti-Campos, Tais Nitsch Mazzola, Mara Sanches Guaragna, Helena Fabbri-Scallet, Maricilda Palandi de Mello, Antonia Paula Marques-de-Faria, Andrea Trevas Maciel-Guerra, Gil Guerra Junior
Publikováno v:
São Paulo Medical Journal (2022)
ABSTRACT BACKGROUND: Knowledge of clinical and laboratory differences between chromosomal and undefined causes aids etiological research on non-obstructive azoospermia. OBJECTIVE: Compare clinical and laboratory differences between men with non-obstr
Externí odkaz:
https://doaj.org/article/43cb5aac28cd44e196b1b2b76f0d93da
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:
Felipe Rodrigues de Oliveira, Taís Nitsch Mazzola, Maricilda Palandi de Mello, Ana Paula Francese-Santos, Sofia Helena V. de Lemos-Marini, Andrea Trevas Maciel-Guerra, Olaf Hiort, Ralf Werner, Gil Guerra-Junior, Helena Fabbri-Scallet
Publikováno v:
Life, Vol 13, Iss 5, p 1093 (2023)
The group of disorders known as 46,XY gonadal dysgenesis (GD) is characterized by anomalies in testis determination, including complete and partial GD (PGD) and testicular regression syndrome (TRS). Several genes are known to be involved in sex devel
Externí odkaz:
https://doaj.org/article/c7ac1de1023e4cebaa36d633c47c12ee
Autor:
Letícia Ribeiro Oliveira, Carlos Alberto Longui, Guilherme Guaragna-Filho, José Luiz Costa, Rafael Lanaro, David Antônio Silva, Maria Izabel Chiamolera, Maricilda Palandi de Mello, André Moreno Morcillo, Andrea Trevas Maciel-Guerra, Gil Guerra-Junior
Publikováno v:
Endocrine Connections, Vol 9, Iss 11, Pp 1085-1094 (2020)
Objective: Steroid measurement is a challenge in pediatric endocrinology. Currently, liquid chromatography with tandem mass spectrometry (LC-MS/MS) is considered a gold standard for this purpose. The aim of this study was to co mpare both LC-MS/MS
Externí odkaz:
https://doaj.org/article/9fe49c78dc1442e79c4a079f727a6441
Autor:
Guilherme Guaragna-Filho, Antônio Ramos Calixto, Anna Beatriz Lima do Valle Astur, Georgette Beatriz de Paula, Laurione Cândido de Oliveira, André Moreno Morcillo, Ezequiel Moreira Gonçalves, Maricilda Palandi de Mello, Andrea Trevas Maciel-Guerra, Gil Guerra-Junior
Publikováno v:
São Paulo Medical Journal (2022)
Abstract BACKGROUND: Because normal male sexual differentiation is more complex than normal female sexual differentiation, there are more cases of disorders of sex development (DSDs) with 46,XY karyotype that have unclear etiology. However, Leydig an
Externí odkaz:
https://doaj.org/article/4bfacdf32ec54db19ea35d2847541e0a
Autor:
Stela Carpini, Annelise Barreto Carvalho, Sofia Helena Valente de Lemos-Marini, Gil Guerra-Junior, Andréa Trevas Maciel-Guerra
Publikováno v:
BMC Endocrine Disorders, Vol 18, Iss 1, Pp 1-7 (2018)
Abstract Background Ultrasensitive assays to measure pre-pubertal gonadotropins levels could help identify patients with Turner syndrome (TS) in mid-childhood, but studies in this field are scarce. The aim of this study was to analyze gonadotropins l
Externí odkaz:
https://doaj.org/article/9f11d7b3f9ef4434b5011ba8e8e077ff
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:
Adriano Morad Bley, Egberto Ribeiro Turato, Carlos Roberto Soares Freire de Rivorêdo, Roberto Benedito de Paiva e Silva, Andrea Trevas Maciel-Guerra, Antonia Paula Marques-de-Faria, Gil Guerra-Junior, Maria Tereza Matias Baptista
Publikováno v:
Revista Latinoamericana de Psicopatologia Fundamental, Vol 15, Iss 3, Pp 464-481 (2012)
OBJECTIVE: To investigate how sexual identity is structured and also to investigate the relationship between sexual identity, choice of sex object and sexual difference. METHOD: Semi-structured interviews were held with seven adult patients who were
Externí odkaz:
https://doaj.org/article/30c6aa3fa92d464fad190d5591f2cbe1
Autor:
Flavia Maria Rodrigues Hoffmann, Patrícia Fernandes Rodrigues, Teresa Maria Momensohn dos Santos, Edi Lucia Sartorato, Andréa Trevas Maciel-Guerra, Carla Gentile Matas, Vanessa Cristine Sousa de Moraes
Publikováno v:
Brazilian Journal of Otorhinolaryngology, Vol 74, Iss 5, Pp 698-702 (2008)
Summary: Hearing loss is a multifaceted condition with many etiologies, among which genetic mutation is. Therefore, it is important to connect audiological investigation to etiological diagnosis. Aim: this study aims to establish the audiological and
Externí odkaz:
https://doaj.org/article/d75e4949ac844c3abe2166ba9a1367ce
Autor:
Renata de Lima, Cristina Forti Iamada, Luciana Oliveira Silva, Maricilda Palandi de Mello, Andréa Trevas Maciel-Guerra
Publikováno v:
Genetics and Molecular Biology, Vol 31, Iss 4, Pp 839-842 (2008)
We report on a girl presenting Léri-Weill dyschondrosteosis (LWD) due to deletion of the SHOX gene. Her family included individuals with short stature alone or with both short stature and mesomelia or Madelung's deformity. The deletion was demonstra
Externí odkaz:
https://doaj.org/article/61422cb2a536496d84d3d78b879a492d