Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Grayce Ellen da Cruz Paiva"'
Autor:
Victor Rezende Veras, Grayce Ellen da Cruz Paiva Lima, Ivana da Ponte Melo, Virginia Oliveira Fernandes, Fabia Karine de Moura Lopes, Camila Lopes do Amaral, Maria Helane Gurgel Castelo, Larissa Luna Queiroz, Jessica Silveira Araújo, Cynthia Melissa Valerio, Renan Magalhães Montenegro Junior
Publikováno v:
Diabetology & Metabolic Syndrome, Vol 16, Iss 1, Pp 1-8 (2024)
Abstract Background Familial Partial Lipodystrophy (FPLD) is a disease with wide clinical and genetic variation, with seven different subtypes described. Until genetic testing becomes feasible in clinical practice, non-invasive tools are used to eval
Externí odkaz:
https://doaj.org/article/e8fdd7cf89324f76a75294dc6f70bd33
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:
Erika Bastos Lima Freire, Catarina Brasil d’Alva, Mayara Ponte Madeira, Grayce Ellen da Cruz Paiva Lima, Virginia Oliveira Fernandes, Lindenberg Barbosa Aguiar, Leonardo Barreira Portella, Renan Galvão Ozório, Clarisse Mourão Melo Ponte, Ana Paula Dias Rangel Montenegro, Renan Magalhães Montenegro Junior
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
IntroductionCongenital Generalized Lipodystrophy (CGL) is a rare autosomal recessive disease caused by mutations in genes responsible for the formation and development of adipocytes. Bone abnormalities are described. However, there is a scarcity of d
Externí odkaz:
https://doaj.org/article/6362b76f54e14f088ed97b7afe6de44b
Autor:
Natália Bitar da Cunha Olegario, Joel Sotero da Cunha Neto, Paulo Cirillo Souza Barbosa, Plácido Rogério Pinheiro, Pedro Lino Azevêdo Landim, Ana Paula Dias Rangel Montenegro, Virginia Oliveira Fernandes, Victor Hugo Costa de Albuquerque, João Batista Furlan Duarte, Grayce Ellen da Cruz Paiva Lima, Renan Magalhães Montenegro Junior
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-6 (2023)
Abstract Congenital Generalized Lipodystrophy (CGL) is a rare autosomal recessive disease characterized by near complete absence of functional adipose tissue from birth. CGL diagnosis can be based on clinical data including acromegaloid features, aca
Externí odkaz:
https://doaj.org/article/bc7dd10b74c04cd887f43adcae313313
Autor:
Renan Magalhães Montenegro Junior, Clarisse Mourão Melo Ponte, Maria Helane Costa Gurgel Castelo, Alessandro Conrado de Oliveira Silveira, Virgínia Oliveira Fernandes, Catarina Brasil D’Alva, Luiz Felipe Valter Oliveira, Angélica Domingues Hristov, Silviane Praciano Bandeira, Grayce Ellen da Cruz Paiva, José Eduardo Levi
Publikováno v:
Diabetology & Metabolic Syndrome, Vol 14, Iss 1, Pp 1-12 (2022)
Abstract Background Previous studies suggest intestinal dysbiosis is associated with metabolic diseases. However, the causal relationship between them is not fully elucidated. Gut microbiota evaluation of patients with congenital generalized lipodyst
Externí odkaz:
https://doaj.org/article/7a73fe888ce04d58afb2cc684fe9b0dc
Autor:
Mayara Ponte Madeira, Erika Bastos Lima Freire, Virginia Oliveira Fernandes, Grayce Ellen da Cruz Paiva Lima, Ivana da Ponte Melo, Ana Paula Dias Rangel Montenegro, José Ednésio da Cruz Freire, Caroline de Fátima Aquino Moreira-Nunes, Raquel Carvalho Montenegro, Jeová Keny Baima Colares, Renan Magalhães Montenegro Junior, Brazilian Group for the Study of Inherited and Acquired Lipodystrophies (BRAZLIPO)
Publikováno v:
Diabetology & Metabolic Syndrome, Vol 13, Iss 1, Pp 1-9 (2021)
Abstract Background A new strain of human coronavirus (HCoV) spread rapidly around the world. Diabetes and obesity are associated with a worse prognosis in these patients. Congenital Generalized Lipodystrophy (CGL) patients generally have poorly cont
Externí odkaz:
https://doaj.org/article/ab762307fc244b7594e31f0b7309d5dd
Autor:
Renan Magalhães Montenegro Junior, Grayce Ellen da Cruz Paiva Lima, Virgínia Oliveira Fernandes, Ana Paula Dias Rangel Montenegro, Clarisse Mourão Melo Ponte, Lívia Vasconcelos Martins, Daniel Pascoalino Pinheiro, Maria Elisabete Amaral de Moraes, Manoel Odorico de Moraes Filho, Catarina Brasil d’Alva
Publikováno v:
Diabetology & Metabolic Syndrome, Vol 12, Iss 1, Pp 1-9 (2020)
Abstract Background Congenital generalized lipodystrophy (CGL) is a rare autosomal recessive disorder characterized by the near-total loss of subcutaneous adipose tissue soon after birth, resulting in ectopic fat deposition and severe metabolic distu
Externí odkaz:
https://doaj.org/article/cfeb4e703baa435a877312f57a1db0c8
Autor:
Erika Bastos Lima Freire, Mayara Ponte Madeira, Grayce Ellen da Cruz Paiva Lima, Virginia Oliveira Fernandes, Lindenberg Barbosa Aguiar, João Paulo Uchoa Fontenele, Ana Paula Dias Rangel Montenegro, Thyciara Fontenele Marques, Renan Galvão Ozório, Catarina Brasil d’Alva, Renan Magalhães Montenegro
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
Paget’s disease of bone (PDB) is a common skeleton disorder in which the diagnosis is suggested by radiological analyses. Congenital generalized lipodystrophy (CGL) is a rare, but a radiologic differential diagnosis of Paget’s disease. Patients p
Externí odkaz:
https://doaj.org/article/eb5a44f060d44843a0791f29ccad0506
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