Zobrazeno 1 - 7 of 7 pro vyhledávání: '"Lia Beatriz de Azevedo Souza Karbage"'
1
Akademický článek
Early commitment of cardiovascular autonomic modulation in Brazilian patients with congenital generalized lipodystrophy
Autor: Clarisse Mourão Melo Ponte, Virgínia Oliveira Fernandes, Maria Helane Costa Gurgel, Izabella Tamira Galdino Farias Vasconcelos, Lia Beatriz de Azevedo Souza Karbage, Christiane Bezerra Rocha Liberato, Carlos Antônio Negrato, Marília de Brito Gomes, Ana Paula Dias Rangel Montenegro, Renan Magalhães Montenegro Júnior
Publikováno v: BMC Cardiovascular Disorders, Vol 18, Iss 1, Pp 1-12 (2018)
Abstract Background Metabolic abnormalities in congenital generalized lipodystrophy (CGL) are associated with microvascular complications. However, the evaluation of different types of neuropathy in these patients, including the commitment of cardiov
Externí odkaz: https://doaj.org/article/7c7f4736f6dd4000b18cd0648f6d659f
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2
Akademický článek
Homozygous and Heterozygous Nuclear Lamin A p.R582C Mutation: Different Lipodystrophic Phenotypes in the Same Kindred
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
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3
Association between cardiovascular autonomic neuropathy and left ventricular hypertrophy in young patients with congenital generalized lipodystrophy
Autor: Ana Paula Dias Rangel Montenegro, Izabella Tamira Galdino Farias Vasconcelos, Christiane Bezerra Rocha Liberato, Virgínia Oliveira Fernandes, Clarisse Mourão Melo Ponte, Lia Beatriz de Azevedo Souza Karbage, Maria Helane Costa Gurgel, Catarina Brasil d’Alva, Renan Magalhães Montenegro Júnior, Lívia Aline de Araújo Batista
Publikováno v: Diabetology & Metabolic Syndrome, Vol 11, Iss 1, Pp 1-10 (2019)
Diabetology & Metabolic Syndrome
Repositório Institucional da Universidade Federal do Ceará (UFC)
Universidade Federal do Ceará (UFC)
instacron:UFC
Background Congenital generalized lipodystrophy (CGL) is a rare disorder characterized by the absence of subcutaneous adipose tissue, severe insulin resistance, diabetes mellitus, and cardiovascular complications, including cardiac autonomic neuropat
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b943168bb3328f0928aa63e53571aa9
http://link.springer.com/article/10.1186/s13098-019-0444-8
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4
Early commitment of cardiovascular autonomic modulation in Brazilian patients with congenital generalized lipodystrophy
Autor: Lia Beatriz de Azevedo Souza Karbage, Virgínia Oliveira Fernandes, Renan Magalhães Montenegro Júnior, Clarisse Mourão Melo Ponte, Maria Helane Costa Gurgel, Carlos Antonio Negrato, Ana Paula Dias Rangel Montenegro, Izabella Tamira Galdino Farias Vasconcelos, Christiane Bezerra Rocha Liberato, Marília B. Gomes
Publikováno v: Repositório Institucional da Universidade Federal do Ceará (UFC)
Universidade Federal do Ceará (UFC)
instacron:UFC
BMC Cardiovascular Disorders, Vol 18, Iss 1, Pp 1-12 (2018)
BMC Cardiovascular Disorders
Background Metabolic abnormalities in congenital generalized lipodystrophy (CGL) are associated with microvascular complications. However, the evaluation of different types of neuropathy in these patients, including the commitment of cardiovascular a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93e5cbd7a58a28651bf30f0f15a370eb
http://www.repositorio.ufc.br/handle/riufc/30476
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5
Homozygous and Heterozygous Nuclear Lamin A p.R582C Mutation: Different Lipodystrophic Phenotypes in the Same Kindred
Autor: Francisco Herlânio Costa Carvalho, Milena Gurgel Teles, Lia Beatriz de Azevedo Souza Karbage, Catarina Brasil d’Alva, Alexander A. L. Jorge, Lindenberg Barbosa Aguiar, Lucas Santos de Santana, Renan Magalhães Montenegro, Aline Dantas Costa-Riquetto, Ana Paula Dias Rangel Montenegro, Virgínia Oliveira Fernandes
Publikováno v: Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Repositório Institucional da Universidade Federal do Ceará (UFC)
Universidade Federal do Ceará (UFC)
instacron:UFC
Frontiers in Endocrinology, Vol 9 (2018)
Frontiers in Endocrinology
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6900e730e2655d2fe0fddef770a78ae
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