Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Cynthia M Valerio"'
Autor:
Natália Rossin Guidorizzi, Cynthia M. Valerio, Luiz F. Viola, Victor Rezende Veras, Virgínia Oliveira Fernandes, Grayce Ellen da Cruz Paiva Lima, Amanda Caboclo Flor, Jessica Silveira Araújo, Raquel Beatriz Gonçalves Muniz, Rodrigo Oliveira Moreira, Francisco José Albuquerque De Paula, Lenita Zajdenverg, Joana R. Dantas, Amélio F. Godoy-Matos, Renan Magalhães Montenegro Júnior, Maria Cristina Foss-Freitas
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
BackgroundThere is a lack of information on the clinical and molecular presentation of familial partial lipodystrophy (FPLD), a rare genetic disorder characterized by partial subcutaneous fat loss.ObjectiveThis study aimed to provide a comprehensive
Externí odkaz:
https://doaj.org/article/428a23adc5dd4400850c68799a2ec3de
Autor:
Cynthia M. Valerio, Raquel Beatriz Gonçalves Muniz, Luiz F. Viola, Gabriela Bartzen Pereira, Rodrigo Oliveira Moreira, Marise Ribeiro de Sousa Berriel, Renan Magalhães Montenegro Júnior, Amélio F. Godoy-Matos, Lenita Zajdenverg
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
IntroductionLipodystrophies are a group of disorders characterized by selective and variable loss of adipose tissue, which can result in an increased risk of insulin resistance and its associated complications. Women with lipodystrophy often have a h
Externí odkaz:
https://doaj.org/article/2feab01f0523464c92b894280b2046d2
Autor:
Luiz F. Viola, Cynthia M. Valerio, João M. Araujo-Neto, Fabio F. Santos, Felipe Matsuura, Rodrigo O. Moreira, Amélio F. Godoy-Matos
Publikováno v:
Diabetology & Metabolic Syndrome, Vol 15, Iss 1, Pp 1-7 (2023)
Abstract Background Lipodystrophies are a heterogeneous group of diseases characterized by the selective loss of subcutaneous adipose tissue and ectopic fat deposition in different organs, including the liver. This study aimed to determine the freque
Externí odkaz:
https://doaj.org/article/f30c4f1e8f354ae88d6c845daffb15c0
Publikováno v:
Diabetology & Metabolic Syndrome, Vol 12, Iss 1, Pp 1-20 (2020)
Abstract Background The prevalence of non-alcoholic fatty liver disease (NAFLD) has been increasing rapidly. It is nowadays recognized as the most frequent liver disease, affecting a quarter of global population and regularly coexisting with metaboli
Externí odkaz:
https://doaj.org/article/a1b18818563f40a0b49f14802fdf9b4a
Autor:
Amelio F. Godoy-Matos, Cynthia M. Valerio, Rodrigo O. Moreira, Denise P. Momesso, Leonardo K. Bittencourt
Publikováno v:
Diabetology & Metabolic Syndrome, Vol 10, Iss 1, Pp 1-6 (2018)
Abstract Background To study pancreatic fat deposition and beta-cell function in familial partial lipodystrophy (FPLD) patients. Methods In a cross-sectional study, eleven patients with FPLD, and eight healthy volunteers were matched for age and body
Externí odkaz:
https://doaj.org/article/e0f9bbe042144560bb8841672345912d
Autor:
Felipe O. Matsuura, Melina Dias, Luiz Fellipe C. Viola, Fábio F. Dos Santos, Joao M. Araujo-Neto, Marcia H. Costa, Cynthia M. Valerio, Amelio F. Godoy-Matos
Publikováno v:
Diabetes. 67
Introduction: Partial lipodystrophy (PL) is a rare disease associated with insulin resistance and metabolic dysfunctions, including NAFLD. Global prevalence of NAFLD is ±25%. In PL patients NAFDL prevalence and severity remains unclear. AIMS To eval
Autor:
Patricia B. Mory, Lenita Zajdenverg, Amélio F. Godoy-Matos, Regina S Moyses, José Egídio Paulo de Oliveira, Cynthia M Valerio
Publikováno v:
Diabetology & Metabolic Syndrome
Diabetology & Metabolic Syndrome, Vol 4, Iss 1, p 40 (2012)
Diabetology & Metabolic Syndrome, Vol 4, Iss 1, p 40 (2012)
Background Familial partial lipodystrophies (FPLD) are clinically heterogeneous disorders characterized by selective loss of adipose tissue, insulin resistance and metabolic complications. Until genetic studies become available for clinical practice,
Autor:
Cynthia M Valerio, Lenita Zajdenverg, Jose Egidio P de Oliveira, Patricia B Mory, Regina S Moises, Amélio F Godoy-Matos
Publikováno v:
Diabetology & Metabolic Syndrome. 7(1):19