Bilateral dacryoadenitis and central nervous system involvement in a child with kimura disease (2022)
- Authors:
- USP affiliated authors: CHAHUD, FERNANDO - FMRP ; OLIVEIRA, RICARDO SANTOS DE - FMRP ; ROXO JÚNIOR, PÉRSIO - FMRP ; CRUZ, ANTONIO AUGUSTO VELASCO E - FMRP
- Unidade: FMRP
- DOI: 10.1097/IOP.0000000000002150
- Subjects: SISTEMA NERVOSO CENTRAL; DOENÇA CRÔNICA; LINFONODOS
- Language: Inglês
- Imprenta:
- Publisher place: Philadelphia
- Date published: 2022
- Source:
- Título: Ophthalmic Plastic and Reconstructive Surgery
- ISSN: 0740-9303
- Volume/Número/Paginação/Ano: v. 38, n. 4, p. e106-e108, 2022
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
CAMACHO, Maria Belen et al. Bilateral dacryoadenitis and central nervous system involvement in a child with kimura disease. Ophthalmic Plastic and Reconstructive Surgery, v. 38, n. 4, p. e106-e108, 2022Tradução . . Disponível em: https://doi.org/10.1097/IOP.0000000000002150. Acesso em: 20 jan. 2026. -
APA
Camacho, M. B., Chahud, F., Boasquevisques, G., Oliveira, R. S. de, Roxo Júnior, P., & Cruz, A. A. V. e. (2022). Bilateral dacryoadenitis and central nervous system involvement in a child with kimura disease. Ophthalmic Plastic and Reconstructive Surgery, 38( 4), e106-e108. doi:10.1097/IOP.0000000000002150 -
NLM
Camacho MB, Chahud F, Boasquevisques G, Oliveira RS de, Roxo Júnior P, Cruz AAV e. Bilateral dacryoadenitis and central nervous system involvement in a child with kimura disease [Internet]. Ophthalmic Plastic and Reconstructive Surgery. 2022 ; 38( 4): e106-e108.[citado 2026 jan. 20 ] Available from: https://doi.org/10.1097/IOP.0000000000002150 -
Vancouver
Camacho MB, Chahud F, Boasquevisques G, Oliveira RS de, Roxo Júnior P, Cruz AAV e. Bilateral dacryoadenitis and central nervous system involvement in a child with kimura disease [Internet]. Ophthalmic Plastic and Reconstructive Surgery. 2022 ; 38( 4): e106-e108.[citado 2026 jan. 20 ] Available from: https://doi.org/10.1097/IOP.0000000000002150 - Oculomotor disturbances due to granular cell tumor
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Informações sobre o DOI: 10.1097/IOP.0000000000002150 (Fonte: oaDOI API)
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