Zobrazeno 1 - 9 of 9 pro vyhledávání: '"Paula Fernanda Silva Fonseca"'
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Akademický článek
Quality of life scores differs between genotypic groups of patients with suspected hereditary hemochromatosis
Autor: Paula Fernanda Silva Fonseca, Rodolfo Delfini Cançado, Flavio Augusto Naoum, Carla Luana Dinardo, Guilherme Henrique Hencklain Fonseca, Sandra Fatima Menosi Gualandro, José Eduardo Krieger, Alexandre Costa Pereira, Pierre Brissot, Paulo Caleb Junior Lima Santos
Publikováno v: BMC Medical Genetics, Vol 19, Iss 1, Pp 1-5 (2018)
Abstract Background Hereditary hemochromatosis (HH) encompasses a group of autosomal recessive disorders mainly characterized by enhanced intestinal absorption of iron and its accumulation in parenchymal organs. HH diagnosis is based on iron biochemi
Externí odkaz: https://doaj.org/article/43e123d81f7c4a6bb4f7d80d50b831ff
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2
Quality of Life Scores Remained Different among the Genotypic Groups of Patients with Suspected Hemochromatosis, Even after Treatment Period
Autor: Luis Alfredo Utria Acevedo, Aline Morgan Alvarenga, Paula Fernanda Silva Fonseca, Nathália Kozikas da Silva, Rodolfo Delfini Cançado, Flavio Augusto Naoum, Carla Luana Dinardo, Alexandre Costa Pereira, Pierre Brissot, Paulo Caleb Junior Lima Santos
Publikováno v: Genes
Genes, 2022, 13 (1), pp.118. ⟨10.3390/genes13010118⟩
Genes, Vol 13, Iss 118, p 118 (2022)
Genes; Volume 13; Issue 1; Pages: 118
Background: Hemochromatosis is a genetic condition of iron overload caused by deficiency of hepcidin. In a previous stage of this study, patients with suspected hemochromatosis had their quality of life (QL) measured. We observed that QL scores diffe
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02abae0cd656846cfdc08d0a42e03e17
https://hal.science/hal-03555426/document
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3
Novel mutations in the bone morphogenetic protein 6 gene in patients with iron overload and non-homozygous genotype for the HFE p.Cys282Tyr mutation
Autor: Pierre Brissot, Aline Morgan Alvarenga, Flávio Augusto Naoum, Rodolfo D. Cançado, Theo G M Oliveira, Paula Fernanda Silva Fonseca, Carla Luana Dinardo, Nathália Kozikas da Silva, Paulo Caleb Junior Lima Santos, Jacilene Barbosa da Silva Monteiro
Publikováno v: Blood Cells, Molecules and Diseases
Blood Cells, Molecules and Diseases, Elsevier, 2020, 84, pp.102444. ⟨10.1016/j.bcmd.2020.102444⟩
Blood Cells, Molecules and Diseases, 2020, 84, pp.102444. ⟨10.1016/j.bcmd.2020.102444⟩
International audience; Background - Five main genes are associated with hemochromatosis; however, current studies show that, in addition to these genes, others may be associated with primary iron overload (IO). One of these is the bone morphogenetic
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b63111d39cc76f72fac280246d05043c
https://hal-univ-rennes1.archives-ouvertes.fr/hal-02864471
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6
Quality of life scores differs between genotypic groups of patients with suspected hereditary hemochromatosis
Autor: Guilherme Henrique Hencklain Fonseca, Paula Fernanda Silva Fonseca, Carla Luana Dinardo, Alexandre C. Pereira, José Eduardo Krieger, Paulo Caleb Junior Lima Santos, Rodolfo D. Cançado, Sandra Fátima Menosi Gualandro, Pierre Brissot, Flávio Augusto Naoum
Publikováno v: Repositório Institucional da UNIFESP
Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
BMC Medical Genetics
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-5 (2018)
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES) [2013/09295-3] Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP), Brazil [2013/20614-3] Background: Hereditary hemochromatosis (HH) encompasses a group of autosomal reces
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d0251fa82c503838b1b475ad982142b
https://repositorio.unifesp.br/handle/11600/54273
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7
Assessment of quality of life and health perception in patients with hereditary hemochromatosis
Autor: Paula Fernanda Silva Fonseca
Publikováno v: Biblioteca Digital de Teses e Dissertações da USP
Universidade de São Paulo (USP)
instacron:USP
Introdução: A hemocromatose hereditária (HH) é uma doença autossômica recessiva caracterizada principalmente pelo aumento da absorção intestinal de ferro e seu acúmulo em órgãos. O diagnóstico da HH baseia-se nas avaliações de exames la
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5838054fa3f5ccb4c45a17be8b1c8a4d
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8
Impact of Caffeine and/or Estrogen Deficiency on Trabecular Bone Area and Healing: A Study in Rats
Autor: Paula Fernanda Silva Fonseca, Victor E. Arana-Chavez, Caetlin Kelmy Craneck Braz, Diogo José Barreto Menezes, Marta Ferreira Bastos, Poliana Mendes Duarte, Nilton Azambuja, Joyce Pinho Bezerra
Publikováno v: The International Journal of Oral & Maxillofacial Implants. 29:221-231
Purpose To evaluate the effects of caffeine and/or estrogen deficiency on trabecular bone area (TBA) and bone healing in rats. Materials and methods Rats were divided into groups (n=15/group) as follows: control, caffeine, ovariectomy (OVX), and caff
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bedbc382fe7242dbc53d0077353deed
https://doi.org/10.11607/jomi.3186
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