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Akademický článek

Case report: Insulinomatosis: description of four sporadic cases and review of the literature

Autor: Delmar Muniz Lourenço, Maria Lucia Corrêa-Giannella, Sheila Aparecida Coelho Siqueira, Marcia Nery, Flavio Galvão Ribeiro, Elizangela Pereira de Souza Quedas, Manoel de Souza Rocha, Ramon Marcelino do Nascimento, Maria Adelaide Albergaria Pereira

Publikováno v: Frontiers in Endocrinology, Vol 14 (2024)

The best-known etiologies of hyperinsulinemic hypoglycemia are insulinoma, non-insulinoma pancreatogenous hypoglycemic syndrome, autoimmune processes, and factitious hypoglycemia. In 2009, a disease not associated with classic genetic syndromes and c

Externí odkaz: https://doaj.org/article/c4bff7e8323245fbb077be2b075027fe

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Akademický článek

Epidemiology and risk factors of hypoglycemia in subjects with type 1 diabetes in Brazil: a cross-sectional, multicenter study

Autor: Alexandre Barbosa Câmara de Souza, Maria Lúcia Cardillo Correa-Giannella, Marilia Brito Gomes, Carlos Antonio Negrato, Marcia Nery

Publikováno v: Archives of Endocrinology and Metabolism (2022)

ABSTRACT Objective: The aim of this study was to investigate the factors associated with hypoglycemia and severe hypoglycemia (SH) in individuals with type 1 diabetes mellitus (T1D) in Brazil. Materials and methods: This multicenter, cross-sectional

Externí odkaz: https://doaj.org/article/0e5f4e4d212c4f0e9ba5cb8c6b657f5e

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Akademický článek

InsulinAPP application protocol for the inpatient management of type 2 diabetes on a hospitalist-managed ward: a retrospective study

Autor: Marcos Tadashi Kakitani Toyoshima, Pedro Henrique Ribeiro Brandes, Gerhard da Paz Lauterbach, Jéssica Ribeiro Andrade Moraes, Edison Ferreira de Paiva, Guillermo E. Umpierrez, Marcia Nery, Rodrigo Hidd Kondo

Publikováno v: Archives of Endocrinology and Metabolism (2022)

ABSTRACT Objective: We assessed metrics related to inpatient glycemic control using InsulinAPP, an application available for free in Brazil, on the hospitalist-managed ward of our hospital. Subjects and methods: We performed a retrospective study of

Externí odkaz: https://doaj.org/article/5519aff745f54ffab420cebf6169ce25

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Akademický článek

Effects of glucocorticoids on interstitial glucose concentrations in individuals with hematologic cancer and without known diagnosis of diabetes: a pilot study

Autor: Marcos Tadashi Kakitani Toyoshima, Priscilla Cukier, Alexandre Barbosa Câmara de Souza, Juliana Pereira, Ana Oliveira Hoff, Marcia Nery

Publikováno v: Einstein (São Paulo), Vol 20 (2022)

ABSTRACT Objective To analyze interstitial glucose behavior during glucocorticoid use in non-diabetic patients receiving chemotherapy for hematologic malignancies. Methods Prospective pilot study carried out to assess interstitial glucose levels in 1

Externí odkaz: https://doaj.org/article/a933f1d0330841ffb8f3dfde69959145

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Akademický článek

Targeted sequencing identifies novel variants in common and rare MODY genes

Autor: Lucas S. deSantana, Lilian A. Caetano, Aline D. Costa‐Riquetto, Pedro C. Franco, Renata P. Dotto, André F. Reis, Letícia S. Weinert, Sandra P. Silveiro, Marcio F. Vendramini, Flaviene A. doPrado, Giovanna C. P. Abrahão, Ana Gregória F. P. deAlmeida, Maria da G. Rodrigues Tavares, Wagner Rodrigo B. Gonçalves, Augusto C. Santomauro Junior, Bruno Halpern, Alexander A. L. Jorge, Marcia Nery, Milena G. Teles

Publikováno v: Molecular Genetics & Genomic Medicine, Vol 7, Iss 12, Pp n/a-n/a (2019)

Abstract Background Maturity‐onset diabetes of the young (MODY) is a form of monogenic diabetes with autosomal dominant inheritance. To date, mutations in 11 genes have been frequently associated with this phenotype. In Brazil, few cohorts have bee

Externí odkaz: https://doaj.org/article/f6853023510c4840b9ed6cfc0e72d576

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Akademický článek

Diabetic foot screening: study of a 3000 times cheaper instrument

Autor: Maria Candida Ribeiro Parisi, Daniel Giannella, Tulio Diniz Fernandes, Karla Freire Rezende, Marcia Nery

Publikováno v: Clinics, Vol 66, Iss 6, Pp 1105-1107 (2011)

Externí odkaz: https://doaj.org/article/6eddcea8d6f64b82bdb12a5b0559a6ac

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Akademický článek

Apoplexia pituitária seguida de remissão endócrina: relato de dois casos Pituitary apoplexy followed by endocrine remission: report of two cases

Autor: MARCELO MIRANDA, LUCIANA BARROS, MIRTA KNOPFELMACHER, ELIANA C. AUGUSTO, ANGELO JACOMOSSI, ARTHUR CUKIERT, LUIS R. SALGADO, MARCIA NERY, JAYME GOLDMAN, BERNARDO LIBERMAN

Publikováno v: Arquivos de Neuro-Psiquiatria, Vol 56, Iss 3A, Pp 449-452 (1998)

A apoplexia pituitária é evento raro e a ocorrência de remissão endócrina em pacientes portadores de tumores secretores é ainda mais incomum. O presente estudo relata os casos de dois pacientes portadores de macroadenomas (um com doença de Cus

Externí odkaz: https://doaj.org/article/01de136c99ab4e5a9c2e4a14d6dd6637

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Akademický článek

Gêmeas idênticas discordantes para a doença de Cushing: relato de caso Identical twins discordant for Cushing's disease: case report

Autor: MARCELO MAIA PINHEIRO, BERNARDO LIBERMAN, LUIS ROBERTO SALGADO, JAYME GOLDMAN, MARCIA NERY, ARTHUR CUKIERT

Publikováno v: Arquivos de Neuro-Psiquiatria, Vol 57, Iss 3A, Pp 686-688 (1999)

A doença de Cushing é rara em crianças e sua ocorrência em gêmeos é ainda mais rara. O presente estudo relata a ocorrência de gêmeas idênticas discordantes quanto à doença de Cushing. Uma das gêmeas, desenvolveu síndrome de Cushing aos 1

Externí odkaz: https://doaj.org/article/0f4a24fcbede48aeb699253c9f7f766c

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Genetics, clinical features and outcomes of non-syndromic pituitary gigantism: experience of a single center from Sao Paulo, Brazil

Autor: Raquel S. Jallad, Marcello D. Bronstein, Marcia Nery, Isabella P. P. Grande, Alexander A. L. Jorge, Heraldo Mendes Garmes, Constantine A. Stratakis, Berenice B. Mendonca, Giampaolo Trivellin, Ericka B. Trarbach, Felipe Barjud Pereira do Nascimento, Felipe Henning Gaia Duarte

Publikováno v: Pituitary. 24:252-261

Non-syndromic pituitary gigantism (PG) is a very rare disease. Aryl hydrocarbon receptor-interacting protein (AIP) and G protein-coupled receptor 101 (GPR101) genetic abnormalities represent important etiologic causes of PG and may account for up to

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::324682b83219d188653e015c6c98b770
https://doi.org/10.1007/s11102-020-01105-4

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Targeted massively parallel sequencing for congenital generalized lipodystrophy

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

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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76a27175df56b59f2c7121ba28bcc555
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972020000500559&tlng=en

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