Têmis Maria Félix (Têmis M Félix, Temis Maria Felix)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 16

Top Venues

International journal for equity in health

American journal of medical genetics. Part A

International archives of otorhinolaryngology

Journal of medical Internet research

Hospital de Clinicas de Porto Alegre

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Hospital de Clinicas de Porto Alegre Oct 10 1993

Brazil

Médica :: Serviço de Genética Médica

Publications

Arthur Cherem Netto Fernandes, Têmis Maria Félix
Evaluation of functioning and associated factors in children and adolescents with osteogenesis imperfecta. Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo 43 (2024)
Amaro Freire de Queiroz Júnior, Maria Teresa Vieira Sanseverino, Marcus Vinicius Martins Collares, Adriana Fornari, Luiza Amaral do Virmond, João Oliveira Bosco Filho, Osvaldo Artigalás, Têmis Maria Félix
CNOT1 p.Arg535Cys variant in holoprosencephaly with late onset diabetes mellitus. American journal of medical genetics. Part A (2024)
Filipe Andrade Bernardi, Bibiana Mello de Oliveira, Diego Bettiol Yamada, Milena Artifon, Amanda Maria Schmidt, Victória Machado Scheibe, Domingos Alves, Têmis Maria Félix
The Minimum Data Set for Rare Diseases: Systematic Review. Journal of medical Internet research 25 (2023)
Têmis Maria Félix, Carolina Fischinger Moura de Souza, João Bosco Oliveira, Mariana Rico-Restrepo, Edmar Zanoteli, Mayana Zatz, Roberto Giugliani
Challenges and recommendations to increasing the use of exome sequencing and whole genome sequencing for diagnosing rare diseases in Brazil: an expert perspective. International journal for equity in health 22 (1) (2023)
Têmis Maria Félix, Carolina Fischinger Moura de Souza, João Bosco Oliveira, Mariana Rico-Restrepo, Edmar Zanoteli, Mayana Zatz, Roberto Giugliani
Challenges and recommendations to increasing the use of exome sequencing and whole genome sequencing for diagnosing rare diseases in Brazil: an expert perspective. International journal for equity in health 22 (1) (2023)
Têmis Maria Félix, Carolina Fischinger Moura de Souza, João Bosco Oliveira, Mariana Rico-Restrepo, Edmar Zanoteli, Mayana Zatz, Roberto Giugliani
Challenges and recommendations to increasing the use of exome sequencing and whole genome sequencing for diagnosing rare diseases in Brazil: an expert perspective. International journal for equity in health 22 (1) (2023)
Têmis Maria Félix, Carolina Fischinger Moura de Souza, João Bosco Oliveira, Mariana Rico-Restrepo, Edmar Zanoteli, Mayana Zatz, Roberto Giugliani
Challenges and recommendations to increasing the use of exome sequencing and whole genome sequencing for diagnosing rare diseases in Brazil: an expert perspective. International journal for equity in health 22 (1) (2023)
Rowena Rubim Couto, Francyne Kubaski, Marina Siebert, Têmis Maria Félix, Ana Carolina Brusius Facchin, Sandra Leistner-Segal
Increased Serum Levels of miR-125b and miR-132 in Fragile X Syndrome: A Preliminary Study. Neurology. Genetics 8 (6) (2022)
Têmis Maria Félix, Bibiana Mello de Oliveira, Milena Artifon, Isabelle Carvalho, Filipe Andrade Bernardi, Ida V D Schwartz, Jonas A Saute, Victor E F Ferraz, Angelina X Acosta, Ney Boa Sorte, Domingos Alves, null null
Epidemiology of rare diseases in Brazil: protocol of the Brazilian Rare Diseases Network (RARAS-BRDN). Orphanet journal of rare diseases 17 (1) (2022)
Domingos Alves, Diego Bettiol Yamada, Filipe Andrade Bernardi, Isabelle Carvalho, Márcio Eloi Colombo Filho, Mariane Barros Neiva, Vinícius Costa Lima, Têmis Maria Félix
Mapping, Infrastructure, and Data Analysis for the Brazilian Network of Rare Diseases: Protocol for the RARASnet Observational Cohort Study. JMIR research protocols 10 (1) (2021)
Augusto César Cardoso Dos Santos, Ana Cláudia Medeiros-de-Souza, João Matheus Bremm, Ronaldo Fernandes Santos Alves, Valdelaine Etelvina Miranda de Araujo, Júlio Cesar Loguercio Leite, Lavínia Schuler Faccini, Maria Teresa Vieira Sanseverino, Simone de Menezes Karam, Têmis Maria Félix, Mariana Bertol Leal, Eduardo Marques Macario, Arnaldo Correia de Medeiros, Giovanny Vinicius Araújo de França
List of priority congenital anomalies for surveillance under the Brazilian Live Birth Information System. Epidemiologia e servicos de saude : revista do Sistema Unico de Saude do Brasil 30 (1) (2021)
Bruna S Pinheiro, Patrícia M Barrios, Liliane T Souza, Têmis Maria Félix
Echocardiographic study in children with osteogenesis imperfecta. Cardiology in the young 30 (10) (2020)
Samira Spineli-Silva, Ilária Cristina Sgardioli, Ana P Dos Santos, Luna L Bergamini, Isabella L Monlleó, Marshall I B Fontes, Têmis Maria Félix, Erlane M Ribeiro, Ana C Xavier, Elaine Lustosa-Mendes, Vera Lúcia Gil-da-Silva-Lopes, Társis Antonio Paiva Vieira
Genomic imbalances in craniofacial microsomia. American journal of medical genetics. Part C, Seminars in medical genetics 184 (4) (2020)
Marcelo Wierzynski Oliveira, Joel Lavinsky, Marcel Machado Valerio, Têmis Maria Félix, Luiz Lavinsky
Tympanic Membrane Retractions in patients with Williams Syndrome: A Controlled Study. International archives of otorhinolaryngology 25 (3) (2020)
Liliane Todeschini de Souza, Ricardo Rodrigues Nunes, Otavio de Azevedo Magalhães, Têmis Maria Félix
A new case of osteogenesis imperfecta type VIII and retinal detachment. American journal of medical genetics. Part A 185 (1) (2020)
Bruna Pinheiro, Marina B Zambrano, Ana Paula Vanz, Evelise Brizola, Liliane Todeschini de Souza, Têmis Maria Félix
Cyclic pamidronate treatment for osteogenesis imperfecta: Report from a Brazilian reference center. Genetics and molecular biology 42 (1 suppl 1) (2019)

Têmis Maria Félix.css-eqlu8i{font-size:small;padding-left:4px;} (Têmis M Félix, Temis Maria Felix)

Publication Activity (10 Years)

Top Topics

Top Venues

Têmis Maria Félix (Têmis M Félix, Temis Maria Felix)