Maxillary myxomas associated with MEN1 syndrome (2014)
- Authors:
- Autor USP: TOLEDO, SERGIO PEREIRA DE ALMEIDA - FM
- Unidade: FM
- Subjects: GENES; OSSOS FACIAIS; NEOPLASIAS DO TECIDO CONJUNTIVO; MANDÍBULA
- Language: Inglês
- Imprenta:
- Source:
- Título: Wiener Klinische Wochenschrift
- ISSN: 0043-5325
- Volume/Número/Paginação/Ano: v. 126, n. 3, p. S142-S143, abst. CP4.4, 2014
- Conference titles: International workshop on multiple endocrine neoplasia and other rare endocrine tumors
-
ABNT
LOURENÇO, D. M. et al. Maxillary myxomas associated with MEN1 syndrome. Wiener Klinische Wochenschrift, v. 126, n. 3, p. S142-S143, 2014Tradução . . Disponível em: http://download.springer.com/static/pdf/98/art%253A10.1007%252Fs00508-014-0578-5.pdf?originUrl=http%3A%2F%2Flink.springer.com%2Farticle%2F10.1007%2Fs00508-014-0578-5&token2=exp=1441028215~acl=%2Fstatic%2Fpdf%2F98%2Fart%25253A10.1007%25252Fs00508-014-0578-5.pdf%3ForiginUrl%3Dhttp%253A%252F%252Flink.springer.com%252Farticle%252F10.1007%252Fs00508-014-0578-5*~hmac=73d6878165a21b41ce52406bd29e650b2d7f444eeccde0e5517495f2244945e5. Acesso em: 17 mar. 2026. -
APA
Lourenço, D. M., Toledo, R. A., Sekiya, T., Moraes, M. B., Santana, L. S., & Toledo, S. P. A. (2014). Maxillary myxomas associated with MEN1 syndrome. Wiener Klinische Wochenschrift, 126( 3), S142-S143. Recuperado de http://download.springer.com/static/pdf/98/art%253A10.1007%252Fs00508-014-0578-5.pdf?originUrl=http%3A%2F%2Flink.springer.com%2Farticle%2F10.1007%2Fs00508-014-0578-5&token2=exp=1441028215~acl=%2Fstatic%2Fpdf%2F98%2Fart%25253A10.1007%25252Fs00508-014-0578-5.pdf%3ForiginUrl%3Dhttp%253A%252F%252Flink.springer.com%252Farticle%252F10.1007%252Fs00508-014-0578-5*~hmac=73d6878165a21b41ce52406bd29e650b2d7f444eeccde0e5517495f2244945e5 -
NLM
Lourenço DM, Toledo RA, Sekiya T, Moraes MB, Santana LS, Toledo SPA. Maxillary myxomas associated with MEN1 syndrome [Internet]. Wiener Klinische Wochenschrift. 2014 ; 126( 3): S142-S143.[citado 2026 mar. 17 ] Available from: http://download.springer.com/static/pdf/98/art%253A10.1007%252Fs00508-014-0578-5.pdf?originUrl=http%3A%2F%2Flink.springer.com%2Farticle%2F10.1007%2Fs00508-014-0578-5&token2=exp=1441028215~acl=%2Fstatic%2Fpdf%2F98%2Fart%25253A10.1007%25252Fs00508-014-0578-5.pdf%3ForiginUrl%3Dhttp%253A%252F%252Flink.springer.com%252Farticle%252F10.1007%252Fs00508-014-0578-5*~hmac=73d6878165a21b41ce52406bd29e650b2d7f444eeccde0e5517495f2244945e5 -
Vancouver
Lourenço DM, Toledo RA, Sekiya T, Moraes MB, Santana LS, Toledo SPA. Maxillary myxomas associated with MEN1 syndrome [Internet]. Wiener Klinische Wochenschrift. 2014 ; 126( 3): S142-S143.[citado 2026 mar. 17 ] Available from: http://download.springer.com/static/pdf/98/art%253A10.1007%252Fs00508-014-0578-5.pdf?originUrl=http%3A%2F%2Flink.springer.com%2Farticle%2F10.1007%2Fs00508-014-0578-5&token2=exp=1441028215~acl=%2Fstatic%2Fpdf%2F98%2Fart%25253A10.1007%25252Fs00508-014-0578-5.pdf%3ForiginUrl%3Dhttp%253A%252F%252Flink.springer.com%252Farticle%252F10.1007%252Fs00508-014-0578-5*~hmac=73d6878165a21b41ce52406bd29e650b2d7f444eeccde0e5517495f2244945e5 - Primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 (HTP/Men 1): Increment of bone mineral density after parathyroidectomy
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- Sindrome hereditária caracterizada por micropênis, hipoandrogenismo e níveis séricos altos de gonadotrofinas devido a distúrbio primário nas células de leydig, associada a testículos de tamanho normal e ausência de ambiguidade genital: uma provável nova entidade clínica
- Inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, xx female
- Missense mutation in the lh receptor gene causas leydig cell hypoplasia
- A differential diagnosis of inherited endocrine tumors and their tumor counterparts
- Hugt frequency of hirschprung in a large family C620R-ret mutated family
- Peptide hormone receptor defects leading to abnormal phenotypes
- Hypercalcitoninemia is not pathognomonic of medullary thyroid carcinoma
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