Zobrazeno 1 - 10
of 156
pro vyhledávání: '"Maricilda Palandi de-Mello"'
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:
Reinaldo Luna de Omena Filho, Reginaldo José Petroli, Fernanda Caroline Soardi, Débora de Paula Michelatto, Taís Nitsch Mazzola, Helena Fabbri-Scallet, Maricilda Palandi de Mello, Susane Vasconcelos Zanotti, Ida Cristina Gubert, Isabella Monlleo
Publikováno v:
Italian Journal of Pediatrics, Vol 48, Iss 1, Pp 1-6 (2022)
Abstract Background The Congenital Adrenal Hyperplasia due to 21 hydroxylase deficiency is the most common cause of genital ambiguity in persons with XX sexual chromosomes. Genital ambiguity among persons with XY sexual chromosomes comprises diverse
Externí odkaz:
https://doaj.org/article/d59a302f2a2d4581a58aa32ae25e35e3
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:
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:
Osmar Henrique Della Torre, Lúcia Arisaka Paes, Taciane Barbosa Henriques, Maricilda Palandi de Mello, Eloisa Helena Rubello Valler Celeri, Paulo Dalgalarrondo, Gil Guerra-Júnior, Amilton dos Santos-Júnior
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-9 (2018)
Abstract Background Dopamine is involved in several cerebral physiological processes, and single nucleotide polymorphisms (SNP) in the dopamine D2 receptor gene (DRD2) have been associated with numerous neurological and mental disorders, including th
Externí odkaz:
https://doaj.org/article/ae6c72ab21c34507900b829fd6dc665f
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:
Mara Sanches Guaragna, Felipe Lourenço Ledesma, Victoria Zavanelli Manzano, Andréa Trevas Maciel-Guerra, Gil Guerra-Júnior, Marcelo Milone Silva, Pedro Luiz de Brito, Maricilda Palandi de Mello
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 35:837-843
Objectives Wilm’s Tumor (WT) is the most common pediatric kidney cancer. Whereas most WTs are isolated, approximately 5% are associated with syndromes such as Denys-Drash (DDS), characterized by early onset nephropathy, disorders of sex development
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7bb5dc9fe4a46b1ad90ef0a6a53b966a
https://doi.org/10.1515/jpem-2021-0673
https://doi.org/10.1515/jpem-2021-0673
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