Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Maricilda P. de Mello"'
Autor:
Ana Paula Francese-Santos, Jakob A. Meinel, Cristiane S. C. Piveta, Juliana G. R. Andrade, Beatriz A. Barros, Helena Fabbri-Scallet, Vera Lúcia Gil-da-Silva-Lopes, Gil Guerra-Junior, Axel Künstner, Hauke Busch, Olaf Hiort, Maricilda P. de Mello, Ralf Werner, Andréa T. Maciel-Guerra
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 1, p 494 (2022)
A region of 160 kb at Xp21.2 has been defined as dosage-sensitive sex reversal (DSS) and includes the NR0B1 gene, considered to be the candidate gene involved in XY gonadal dysgenesis if overexpressed. We describe a girl with 46,XY partial gonadal dy
Externí odkaz:
https://doaj.org/article/0bbf5b9fc89f47f798397319e474c5c5
Autor:
Isabella L. Monlleó, Susane V. Zanotti, Bárbara Priscila B. de Araújo, Erisvaldo F. Cavalcante Júnior, Paula D. Pereira, Paulo M. de Barros, Maria Deysiane P. Araújo, Ana Thaysa V. S. de Mendonça, Catarina R. S. Santos, Ylana R. dos Santos, Débora de Paula Michelatto, Maricilda P. de Mello, Andrea T. Maciel-Guerra, Gil Guerra-Júnior
Publikováno v:
Jornal de Pediatria, Vol 88, Iss 6, Pp 489-495 (2012)
OBJETIVOS: Avaliar a prevalência e descrever alterações da morfologia genital em recém-nascidos em duas maternidades-escola de gestão pública. MÉTODOS: Estudo caso/controle, descritivo, transversal. Utilizou-se protocolo clínico para avaliaç
Externí odkaz:
https://doaj.org/article/718fcbb8efbb4847bdbb78450bf27952
Autor:
Carolina Paniago Lopes, Gentil Ferreira Gonçalves Neto, Maria Fernanda Vanti Macedo Paulino, Adriana Mangue Esquiaveto-Aun, Maricilda Palandi de Mello, Elizabeth João Pavin, Ikaro Soares Santos Breder, Mariana Zorron Mei Hsia Pu, Sofia Helena Valente de Lemos-Marini, Gil Guerra Junior
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 68 (2024)
ABSTRACT Objective: Considering the rarity and clinical and molecular diversity of Wolfram syndrome (WS), the objective of this study was to identify patients with a clinical presentation suggestive of WS following up at a single Brazilian diabetes s
Externí odkaz:
https://doaj.org/article/cbf3da5adedf4723adfdf888d2ce1a13
Autor:
Maricilda P. de Mello, Henrique B. M. Gomes, Palmira Guevara, José L. Ramirez, José Franco da Silveira
Publikováno v:
Memorias do Instituto Oswaldo Cruz, Vol 83, Pp 334-336 (1988)
Externí odkaz:
https://doaj.org/article/2eab4146b40742f2a051e3ac28f8d024
Autor:
Helena Fabbri-Scallet, Ralf Werner, Mara S. Guaragna, Juliana G.R. de Andrade, Andrea T. Maciel-Guerra, Nadine C. Hornig, Olaf Hiort, Gil Guerra-Júnior, Maricilda P. de Mello
Publikováno v:
Sexual Development. 16:252-260
Introduction: NR5A1 is an essential transcription factor that regulates several target genes involved in reproduction and endocrine function. Pathogenic variants in this gene are responsible for a wide spectrum of disorders/differences of sex develop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9bf304c1bf27be93e1879ddcb724d0dc
https://doi.org/10.1159/000524956
https://doi.org/10.1159/000524956
Autor:
Leticia R. de Oliveira, Carlos A. Longui, Guilherme Guaragna-Filho, José L. da Costa, Rafael Lanaro, Maria I. Chiamolera, Maricilda P. de Mello, André M. Morcillo, Andrea T. Maciel-Guerra, Gil Guerra-Junior
Publikováno v:
Sexual Development. 16:266-269
The human chorionic gonadotropin (hCG) stimulation test that evaluates gonadal steroidogenesis is crucial in the assessment of patients with 46,XY disorders of sex development (DSD). This study aimed to determine a testosterone (T) cutoff level that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f45e21d9deb4d0297031c5da8b892cd
https://doi.org/10.1159/000519422
https://doi.org/10.1159/000519422
Corrigendum to 'Pharmacogenetics of Risperidone and Cardiovascular Risk in Children and Adolescents'
Autor:
Amilton Dos Santos-Júnior, Taciane Barbosa Henriques, Maricilda Palandi de Mello, Osmar Henrique Della Torre, Lúcia Arisaka Paes, Adriana Perez Ferreira-Neto, Letícia Esposito Sewaybricker, Thiago Salum Fontana, Eloisa Helena Rubello Valler Celeri, Gil Guerra-Júnior, Paulo Dalgalarrondo
Publikováno v:
International Journal of Endocrinology, Vol 2017 (2017)
Externí odkaz:
https://doaj.org/article/46fa639e7c914e3c8148ccaa61722458
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:
Amilton Dos Santos-Júnior, Taciane Barbosa Henriques, Maricilda Palandi de Mello, Osmar Henrique Della Torre, Lúcia Arisaka Paes, Adriana Perez Ferreira-Neto, Letícia Esposito Sewaybricker, Thiago Salum Fontana, Eloisa Helena Rubello Valler Celeri, Gil Guerra-Júnior, Paulo Dalgalarrondo
Publikováno v:
International Journal of Endocrinology, Vol 2016 (2016)
Objective. To identify the frequency of obesity and metabolic complications in child and adolescent users of risperidone. Potential associations with clinical parameters and SNPs of the HTR2C, DRD2, LEP, LEPR, MC4R, and CYP2D6 genes were analyzed. Me
Externí odkaz:
https://doaj.org/article/d7b533f9b895486ca4b4a8c5523f52cd
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