Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Temis Maria Felix"'
Autor:
Marcelo Wierzynski Oliveira, Joel Lavinsky, Marcel Machado Valerio, Temis Maria Felix, Luiz Lavinsky
Publikováno v:
International Archives of Otorhinolaryngology, Vol 25, Iss 03, Pp e443-e445 (2021)
Introduction The role of elastin in tympanic retractions and chronic otitis media is not well established. Williams Syndrome (WS), a pathology related to a mutation in the elastin gene, could generate tympanic retractions. Objective To compare the pr
Externí odkaz:
https://doaj.org/article/c019a007b788482fad19a7938c45cf79
Autor:
Bibiana Mello de Oliveira, Filipe Andrade Bernardi, João Francisco Baiochi, Mariane Barros Neiva, Milena Artifon, Alberto Andrade Vergara, Ana Maria Martins, Anete Sevciovic Grumach, Angelina Xavier Acosta, Antonette Souto El Husny, Bethania de Freitas Rodrigues Ribeiro, Camila Ferreira Ramos, Carlos Eduardo Steiner, Chong Ae Kim, Denise Maria Christofolini, Diego Bettiol Yamada, Ellaine Doris Fernandes Carvalho, Erlane Marques Ribeiro, Fabíola de Arruda Bastos, Faradiba Sarquis Serpa, Flávia Reseda Brandão, Giselle Maria Araujo Felix Adjuto, Isabelle Carvalho, Jonas Alex Morales Saute, Juan Clinton Llerena Junior, Larissa Souza Mario Bueno, Luiz Carlos Santana da Silva, Mara Lucia Schmitz Ferreira Santos, Marcela Câmara Machado Costa, Marcia Maria Costa Giacon Giusti, Marcial Francis Galera, Márcio Eloi Colombo Filho, Maria Denise Fernandes Carvalho de Andrade, Maria Teresinha De Oliveira Cardoso, Marilaine Matos de Menezes Ferreira, Michelle Zeny, Milena Coelho Fernandes Caldato, Ney Boa Sorte, Nina Rosa de Castro Musolino, Paula Frassinetti Vasconcelos de Medeiros, Paulo Ricardo Gazzola Zen, Raquel Tavares Boy Da Silva, Rayana Elias Maia, Rodrigo Fock, Rosemarie Elizabeth Schimidt Almeida, Solange Oliveira Rodrigues Valle, Tatiana Amorim, Thaís Bomfim Teixeira, Vania Mesquita Gadelha Prazeres, Victor Evangelista de Faria Ferraz, Vinicius Costa Lima, Wagner José Martins Paiva, Ida Vanessa Doederlein Schwartz, Domingos Alves, Têmis Maria Félix, Raras Network Group
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-13 (2024)
Abstract Background The Brazilian Policy for Comprehensive Care for People with Rare Diseases was implemented in 2014; however, national epidemiological data on rare diseases (RDs) are scarce and mainly focused on specific disorders. To address this
Externí odkaz:
https://doaj.org/article/5b03fce23cb148d88e2d9b95dbec7a0d
Autor:
Myrianne Barbosa, Cláudia Lorea, Camila Azevedo, Luana Lopes, Alef Almeida, Temis Felix, Gabriel Ogata, Marcelo Nita, Têmis Maria Félix
Publikováno v:
Jornal de Assistência Farmacêutica e Farmacoeconomia, Vol 9, Iss s. 1 (2024)
Introdução A aderência aos Protocolos Clínicos e Diretrizes Terapêuticas (PDCTs) é fundamental para otimizar a gestão e o monitoramento da jornada do paciente. No entanto, observa-se uma lacuna na literatura científica devido à ausência
Externí odkaz:
https://doaj.org/article/7458792104d34a99a4dc4d3f0a6c132e
Autor:
Andressa Colares da Costa Otavio, Monalise Costa Batista Berbert, Hilton Justino da Silva, Erissandra Gomes, Têmis Maria Félix
Publikováno v:
Audiology: Communication Research, Vol 29 (2024)
RESUMO Objetivo Investigar e correlacionar a pressão lingual da região anterior e posterior em contração isométrica e durante deglutição de saliva de indivíduos com osteogênese imperfeita. Métodos Estudo transversal observacional, do qual p
Externí odkaz:
https://doaj.org/article/a3f63a8c3760442e89d9c8c4f2a1b2dc
Autor:
Maria Eduarda Gomes, Fernanda Kehdy, Fernanda Saloum de Neves-Manta, Dafne Dain Gandelman Horovitz, Maria Teresa Sanseverino, Gabriela Ferraz Leal, Têmis Maria Felix, Denise Pontes Cavalcanti, Juan Clinton Llerena, Sayonara Gonzalez
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-7 (2024)
Abstract Cartilage-hair hypoplasia syndrome (CHH) is an autosomal recessive disorder frequently linked to n.72A>G (previously known as n.70A>G and n.71A>G), the most common RMRP variant worldwide. More than 130 pathogenic variants in this gene have a
Externí odkaz:
https://doaj.org/article/34039a6314534692b817227cc3c278af
Publikováno v:
Revista Paulista de Pediatria, Vol 43 (2024)
ABSTRACT Objective: The aim of this study was to evaluate the functioning and associated factors in children and adolescents with osteogenesis imperfecta (OI). Methods: This is a cross-sectional study conducted on 30 children and adolescents with OI.
Externí odkaz:
https://doaj.org/article/5b3f283244d640ea939648add722563e
Publikováno v:
Annals of Nutrition and Metabolism. 72:21-29
Background/Aims: Osteogenesis Imperfecta (OI) is a bone disease characterized by bone fragility, deformities, and multiple fractures. The aim of this study was to compare the different methods of measuring the basal metabolic rate (BMR) and body comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::797b059a8e4417a468f8f82217be3d75
https://doi.org/10.1159/000481918
https://doi.org/10.1159/000481918
Publikováno v:
Journal of human nutrition and dietetics : the official journal of the British Dietetic AssociationReferences. 32(5)
Background In several bone disorders, adequate calcium intake is a coadjuvant intervention to regular treatment. Osteogenesis imperfecta (OI) is a collagen disorder with a range of symptoms, ranging from fractures to minimum trauma, and it is typical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6510cf2d12503ede6d2299ac7218e8dc
https://pubmed.ncbi.nlm.nih.gov/31037781
https://pubmed.ncbi.nlm.nih.gov/31037781
Commentary: 'Quality of Life in Caregivers of Children and Adolescents with Osteogenesis Imperfecta'
Publikováno v:
Journal of Rare Diseases Research & Treatment. 4:1-2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8083028d0fe6d2ec38ef45823ad1c2c8
https://doi.org/10.29245/2572-9411/2019/3.1175
https://doi.org/10.29245/2572-9411/2019/3.1175
Autor:
Evelise Brizola, Elza Daniel de Mello, Temis Maria Felix, Marina B. Zambrano, Ana Paula Vanz, Bruna Pinheiro
Publikováno v:
Journal of the American College of Nutrition. 35:339-345
Vitamin D is essential to the development and maintenance of the skeleton, especially for children with bone disorders such as osteogenesis imperfecta (OI). We evaluated serum 25-hydroxyvitamin D (25-OHD) levels to assess the relationship between det
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::611c0d5282ac54909e4d8badc3da6133
https://doi.org/10.1080/07315724.2015.1057776
https://doi.org/10.1080/07315724.2015.1057776