Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Salomão Cury-Rad Oka"'
Autor:
Damião Edgleys Porto, Francisco Jadson Lima, Gustavo Pina Godoy, Josuel Raimundo Cavalcante, Salomão Cury-Rad Oka
Publikováno v:
The Open Dentistry Journal
Epithelial-myoepithelial carcinoma was first described by Danath et al. in 1972 and is classified as a rare low-grade biphasic neoplasm of the salivary glands. This case report presents a male patient who had a lesion in the oral mucosa with a histor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f906e5e5181071502258043daa6df42d
http://europepmc.org/articles/PMC3434468
http://europepmc.org/articles/PMC3434468
Autor:
Josuel Raimundo Cavalcante, Thiago de Santana Santos, Salomão Cury-Rad Oka, Emanuel Dias de Oliveira e Silva, Ana Cláudia Amorim Gomes, Edwaldo Dourado
Publikováno v:
Journal of Craniofacial Surgery. 23:982-985
OBJECTIVE: The objective of this research was to study the influence of the use of helmet in facial trauma victims of motorcycle accidents with moderate traumatic brain injury. METHODS: We retrospectively reviewed the incidence of facial injuries in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10fc41b5192577e68dda3d2c7045f01d
https://doi.org/10.1097/scs.0b013e31824e5b04
https://doi.org/10.1097/scs.0b013e31824e5b04
Autor:
Josuel Raimundo Cavalcante, Salomão Cury-Rad Oka, Gustavo Pina Godoy, Heládio Neiva de Castro, Sara Cury-Rad Oka
Publikováno v:
Northeast Brazilian Health Journal (Revista Piauiense de Saúde). 2
As fissuras labio-palatinas sao patologias biopsicossociais graves que se situam entre o 3o ou 4o defeito congenito mais frequente. Um bebe em cada 650 nascidos vivos apresenta o problema em algum estadiamento, de modo que, no Brasil, existem, aproxi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b375f562d81ae6b779b1fee79264fc2
https://doi.org/10.13046/rps.v2i1.19
https://doi.org/10.13046/rps.v2i1.19
Autor:
Renata Quirino, de Almeida-Barros, Salomão Cury-Rad, Oka, Ana Carolina Barbosa, Pordeus, Paula Frassinetti Vasconcelos, de Medeiros, Patricia Meira, Bento, Gustavo Pina, Godoy
Publikováno v:
Quintessence international (Berlin, Germany : 1985). 43(3)
Mucopolysaccharidosis (MPS) is a group of rare metabolic diseases characterized by intralysosomal accumulation of glycosaminoglycans. MPS type VI or Maroteaux-Lamy syndrome is an autosomal-recessive syndrome caused by mutations in the lysosomal enzym
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::15c96dd97b5e45523befbefa72729fe4
https://pubmed.ncbi.nlm.nih.gov/22299127
https://pubmed.ncbi.nlm.nih.gov/22299127