Výsledky vyhledávání - "Sonir R R, Antonini"

DNA methylation is a comprehensive marker for pediatric adrenocortical tumors

Autor: Ana Carolina, Bueno, Rui M P, da Silva, Mônica F, Stecchini, Junier, Marrero-Gutiérrez, Danillo C, de Almeida E Silva, Izilda, Cardinalli, Carlos Alberto, Scrideli, Thais, Junqueira, Carlos A F, Molina, Fernando Silva, Ramalho, Silvio, Tucci, Fernanda Borchers, Coeli-Lacchini, Ayrton Custodio, Moreira, Leandra N Z, Ramalho, Silvia, Brandalise, José Andres, Yunes, Margaret, de Castro, Ricardo Zorzetto Nicoliello, Vêncio, Sonir R R, Antonini

Publikováno v: Endocrine-Related Cancer.

Children diagnosed with adrenocortical tumors (pACT) have variable outcomes and, to date, the disease lacks robust prognostic biomarkers. The prognostic potential of tumor methylation has been demonstrated in several cancers. We aimed to evaluate the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b26baf4b3fd54e8e3b5eb9ddeed00073
https://doi.org/10.1530/erc-22-0145

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Akademický článek

Bone mineral density and body composition in girls with idiopathic central precocious puberty before and after treatment with a gonadotropin-releasing hormone agonist

Autor: Sandra B. Alessandri, Francisco de A. Pereira, Rosângela A. Villela, Sonir R. R. Antonini, Paula C. L. Elias, Carlos E. Martinelli Jr., Margaret de Castro, Ayrton C. Moreira, Francisco J. A. de Paula

Publikováno v: Clinics, Vol 67, Iss 6, Pp 591-596 (2012)

OBJECTIVES: Idiopathic central precocious puberty and its postponement with a (gonadotropin-releasing hormone) GnRH agonist are complex conditions, the final effects of which on bone mass are difficult to define. We evaluated bone mass, body composit

Externí odkaz: https://doaj.org/article/2ecb77c3c93e44908c885f61d5683bf9

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Outcomes of Patients with Central Precocious Puberty Due to Loss-of-Function Mutations in the MKRN3 Gene after Treatment with Gonadotropin-Releasing Hormone Analog

Autor: Carolina de Oliveira, Ramos, Delanie B, Macedo, Ana Pinheiro M, Canton, Marina, Cunha-Silva, Sonir R R, Antonini, Monica Freire, Stecchini, Carlos Eduardo, Seraphim, Tania, Rodrigues, Berenice Bilharinho, Mendonca, Ana Claudia, Latronico, Vinicius Nahime, Brito

Publikováno v: Neuroendocrinology. 110(7-8)

Loss-of-function mutation of MKRN3 represents the most frequent genetic cause of familial central precocious puberty (CPP). The outcomes of gonadotropin-releasing hormone analog (GnRHa) treatment in CPP patients with MKRN3 defects are unknown.To desc

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b4d1b0fc84c9f577cc7572c64d431f6d
https://pubmed.ncbi.nlm.nih.gov/31671431

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Low expression of HLA-DRA, HLA-DPA1, and HLA-DPB1 is associated with poor prognosis in pediatric adrenocortical tumors (ACT)

Autor: Fabíola A, Leite, Regia C P, Lira, Paola F, Fedatto, Sonir R R, Antonini, Carlos E, Martinelli, Margaret, de Castro, Luciano, Neder, Leandra N Z, Ramalho, Silvio, Tucci, Maria J, Mastelaro, Ana L, Seidinger, Izilda A, Cardinalli, José A, Yunes, Silvia R, Brandalise, Luiz G, Tone, Carlos A, Scrideli

Publikováno v: Pediatric bloodcancer. 61(11)

Low expression of HLA class II antigens has been associated with more aggressive disease in several human malignancies including adult adrenocortical tumors (ACT), but their clinical relevance in pediatric ACT needs to be investigated.This study anal

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b9ce47278b49891873f794a86d41267c
https://pubmed.ncbi.nlm.nih.gov/25156210

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[Childhood adrenocortical tumors: from a clinical to a molecular approach]

Autor: Sonir R R, Antonini, Leandro M, Colli, Leticia, Ferro, Livia, Mermejo, Margaret de, Castro

Publikováno v: Arquivos brasileiros de endocrinologia e metabologia. 55(8)

Adrenocortical tumors (ACT) are more frequent during childhood, but they can appear at any age. ACTs can be classified in functioning, nonfunctioning (mainly observed in adults) and mixed. The diagnosis is based on clinical, biochemical findings and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ae820da7f239461399350b566a54b1a0
https://pubmed.ncbi.nlm.nih.gov/22218442

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[Mineralocorticoid resistance: pseudohypoaldosteronism type 1]

Autor: Fábio L, Fernandes-Rosa, Sonir R R, Antonini

Publikováno v: Arquivos brasileiros de endocrinologia e metabologia. 51(3)

Pseudohypoaldosteronism type 1 (PHA1) is a rare genetic disease characterized by neonatal renal salt wasting, vomiting, dehydration and failure to thrive. Affected patients present hyponatremia, hyperkalemia, associated with high levels of plasma ren

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::0f1d4b1da52a65b14eb3557395e08592
https://pubmed.ncbi.nlm.nih.gov/17546235

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