Zobrazeno 1 - 10
of 65
pro vyhledávání: '"Milena, Gurgel Teles"'
Autor:
Vinícius Vigliazzi Peghinelli, Maria Teresa De Sibio, Igor de Carvalho Depra, Milena Gurgel Teles Bezerra, Marna Eliana Sakalem, Adriano Francisco De Marchi Júnior, Paula Barreto da Rocha, Helena Paim Tilli, Bianca Mariani Gonçalves, Ester Mariane Vieira, Mariana Menezes Lourenço, Célia Regina Nogueira
Publikováno v:
Heliyon, Vol 10, Iss 16, Pp e36006- (2024)
Aim: This study aimed to evaluate the mean post-test probability (PTP) of the Maturity-onset diabetes of the young (MODY) calculator in a multiethnic cohort of patients previously diagnosed with type 1 diabetes (T1DM). Materials and methods: The MODY
Externí odkaz:
https://doaj.org/article/9bf662171e9f426783d2787411823760
Akademický článek
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Autor:
Renata P. Dotto, Lucas Santos de Santana, Susan C. Lindsey, Lilian Araújo Caetano, Luciana F. Franco, Regina Célia M. S. Moisés, João R. Sa, José Luiz Nishiura, Milena Gurgel Teles, Ita P. Heilberg, Magnus R. Dias-da-Silva, Fernando M. A. Giuffrida, André F. Reis
Publikováno v:
Archives of Endocrinology and Metabolism, Iss 0 (2019)
ABSTRACT Objective To verify the presence of variants in HNF1B in a sample of the Brazilian population selected according to the presence of renal cysts associated with hyperglycemia. Subjects and methods We evaluated 28 unrelated patients with clini
Externí odkaz:
https://doaj.org/article/ab4eb53cfd9d44968e33d297e58012cc
Autor:
Renan Magalhães Montenegro, Aline Dantas Costa-Riquetto, Virgínia Oliveira Fernandes, Ana Paula Dias Rangel Montenegro, Lucas Santos de Santana, Alexander Augusto de Lima Jorge, Lia Beatriz de Azevedo Souza Karbage, Lindenberg Barbosa Aguiar, Francisco Herlânio Costa Carvalho, Milena Gurgel Teles, Catarina Brasil d'Alva
Publikováno v:
Frontiers in Endocrinology, Vol 9 (2018)
Background: Dunnigan-type familial partial lipodystrophy (FPLD2) is a rare autosomal dominant disease caused by heterozygous mutations in the LMNA gene that results in regional loss of subcutaneous adipose tissue with onset in puberty. However, a gen
Externí odkaz:
https://doaj.org/article/127372d3b46c4b9c8268f408815b0046
Autor:
Joya E. M. Correia-Deur, Lucas Santos de Santana, Lílian Araújo Caetano, Antonio M. Lerario, Milena Gurgel Teles, Chong Ae Kim, Débora Romeo Bertola, Marcia Nery, Aline Dantas Costa-Riquetto, Alexander A. L. Jorge
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 64, Iss 5, Pp 559-566 (2020)
Archives of Endocrinology and Metabolism v.64 n.5 2020
Arquivos de Endocrinologia e Metabolismo
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Archives of Endocrinology and Metabolism, Issue: ahead, Published: 28 AUG 2020
Archives of Endocrinology and Metabolism, Volume: 64, Issue: 5, Pages: 559-566, Published: 28 AUG 2020
Archives of Endocrinology and Metabolism v.64 n.5 2020
Arquivos de Endocrinologia e Metabolismo
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Archives of Endocrinology and Metabolism, Issue: ahead, Published: 28 AUG 2020
Archives of Endocrinology and Metabolism, Volume: 64, Issue: 5, Pages: 559-566, Published: 28 AUG 2020
Objective: Our aim is to establish genetic diagnosis of congenital generalized lipodystrophy (CGL) using targeted massively parallel sequencing (MPS), also known as next-generation sequencing (NGS). Subjects and methods: Nine unrelated individuals wi
Autor:
Melanie Rodacki, Marcello Casaccia Bertoluci, Renan Magalhães Montenegro Junior, Monica Andrade Lima Gabbay, Milena Gurgel Teles Bezerra
Publikováno v:
Diretriz da Sociedade Brasileira de Diabetes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5aa433358e500f03ee1817a89c53c37
https://doi.org/10.29327/557753.2022-1
https://doi.org/10.29327/557753.2022-1
Autor:
Thais Della Manna, Simone Sakura Ito, Tiago Jeronimo Dos Santos, Caroline Gouvêa Buff Passone, Durval Damiani, Marina Ybarra, Milena Gurgel Teles
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 32:421-428
Background Insulin autoimmune syndrome (IAS) is a rare cause of hyperinsulinemic hypoglycemia (HH) not addressed as a potential differential diagnosis in current pediatric guidelines. We present a case of IAS in a child with no previous history of au
Autor:
Pedro, Campos Franco, Lucas, Santos de Santana, Aline, Dantas Costa-Riquetto, Augusto Cezar, Santomauro Junior, Alexander A L, Jorge, Milena, Gurgel Teles
Publikováno v:
Diabetes Research and Clinical Practice. 187:109875
To describe the clinical and genetic characteristics and long-term follow-up of a cohort with maturity-onset diabetes of the young (MODY), and to evaluate how molecular diagnosis impacted on treatment.A large observational, retrospective, cohort stud
Publikováno v:
J Diabetes Sci Technol
Autor:
Lílian Araújo Caetano, Leticia E. Sewaybricker, Elisangela P S Quedas, Margaret C. S. Boguszewski, Zuleica Isabel Zarabia, Milena Gurgel Teles, Flavia Osmo Floh, Lindiane Gomes Crisostomo, Marcio F Vendramini, Marcia Nery, Alexander A. L. Jorge, Aline Dantas Costa-Riquetto, Paulo Ferrez Collett-Solberg, Leila Guastapaglia, Suely Keiko Kohara, Caroline Passone, Lucas Santos de Santana
Publikováno v:
Clinical Genetics. 92:388-396
Maturity-onset diabetes of the young (MODY) is a form of monogenic diabetes with autosomal dominant inheritance. GCK -MODY and HNF1A -MODY are the prevalent subtypes. Currently, there is growing concern regarding the correct interpretation of molecul