Outcomes of adrenal-sparing surgery or total adrenalectomy in phaeochromocytoma associated with multiple endocrine neoplasia type 2: an international retrospective population-based study (2014)
- Authors:
- Castinetti, Frederic
- Qi, Xiao-Ping
- Walz, Martin K.
- Maia, Ana Luiza
- Sansó, Gabriela
- Peczkowska, Mariola
- Hasse-Lazar, Kornelia
- Links, Thera P.
- Dvorakova, Sarka
- Toledo, Rodrigo A.
- Mian, Caterina
- Bugalho, Maria Joao
- Wohllk, Nelson
- Kollyukh, Oleg
- Canu, Letizia
- Loli, Paola
- Bergmann, Simona R.
- Costa, Josefina Biarnes
- Makay, Ozer
- Patocs, Attila
- Pfeifer, Marija
- Shah, Nalini S.
- Cuny, Thomas
- Brauckhoff, Michael
- Autor USP: TOLEDO, SERGIO PEREIRA DE ALMEIDA - FM
- Unidade: FM
- DOI: 10.1016/S1470-2045(14)70154-8
- Subjects: NEOPLASIA ENDÓCRINA MÚLTIPLA (DIAGNÓSTICO;TERAPIA); CENTROS COMUNITÁRIOS DE SAÚDE; FEOCROMOCITOMA (EPIDEMIOLOGIA)
- Language: Inglês
- Imprenta:
- Source:
- Título: The Lancet Oncology
- ISSN: 1470-2045
- Volume/Número/Paginação/Ano: v. 15, n. 6, p. 648-655, 2014
- Este artigo possui versão em acesso aberto
- URL de acesso aberto
- PDF de acesso aberto
- Versão do Documento: Versão publicada (Published version)
-
Status: Artigo possui acesso gratuito no site do editor (Bronze Open Access) -
ABNT
CASTINETTI, Frederic et al. Outcomes of adrenal-sparing surgery or total adrenalectomy in phaeochromocytoma associated with multiple endocrine neoplasia type 2: an international retrospective population-based study. The Lancet Oncology, v. 15, n. 6, p. 648-655, 2014Tradução . . Disponível em: http://ac.els-cdn.com/S1470204514701548/1-s2.0-S1470204514701548-main.pdf?_tid=996753ea-2317-11e4-a1c7-00000aab0f6b&acdnat=1407954679_2dc799ef0beedd0ec92653f9a1263a3e. Acesso em: 17 mar. 2026. -
APA
Castinetti, F., Qi, X. -P., Walz, M. K., Maia, A. L., Sansó, G., Peczkowska, M., et al. (2014). Outcomes of adrenal-sparing surgery or total adrenalectomy in phaeochromocytoma associated with multiple endocrine neoplasia type 2: an international retrospective population-based study. The Lancet Oncology, 15( 6), 648-655. doi:10.1016/S1470-2045(14)70154-8 -
NLM
Castinetti F, Qi X-P, Walz MK, Maia AL, Sansó G, Peczkowska M, Hasse-Lazar K, Links TP, Dvorakova S, Toledo RA, Mian C, Bugalho MJ, Wohllk N, Kollyukh O, Canu L, Loli P, Bergmann SR, Costa JB, Makay O, Patocs A, Pfeifer M, Shah NS, Cuny T, Brauckhoff M. Outcomes of adrenal-sparing surgery or total adrenalectomy in phaeochromocytoma associated with multiple endocrine neoplasia type 2: an international retrospective population-based study [Internet]. The Lancet Oncology. 2014 ; 15( 6): 648-655.[citado 2026 mar. 17 ] Available from: http://ac.els-cdn.com/S1470204514701548/1-s2.0-S1470204514701548-main.pdf?_tid=996753ea-2317-11e4-a1c7-00000aab0f6b&acdnat=1407954679_2dc799ef0beedd0ec92653f9a1263a3e -
Vancouver
Castinetti F, Qi X-P, Walz MK, Maia AL, Sansó G, Peczkowska M, Hasse-Lazar K, Links TP, Dvorakova S, Toledo RA, Mian C, Bugalho MJ, Wohllk N, Kollyukh O, Canu L, Loli P, Bergmann SR, Costa JB, Makay O, Patocs A, Pfeifer M, Shah NS, Cuny T, Brauckhoff M. Outcomes of adrenal-sparing surgery or total adrenalectomy in phaeochromocytoma associated with multiple endocrine neoplasia type 2: an international retrospective population-based study [Internet]. The Lancet Oncology. 2014 ; 15( 6): 648-655.[citado 2026 mar. 17 ] Available from: http://ac.els-cdn.com/S1470204514701548/1-s2.0-S1470204514701548-main.pdf?_tid=996753ea-2317-11e4-a1c7-00000aab0f6b&acdnat=1407954679_2dc799ef0beedd0ec92653f9a1263a3e - Primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 (HTP/Men 1): Increment of bone mineral density after parathyroidectomy
- Somatotroph pituitary adenoma with acromegaly and autosomal dominant polycystic kidney disease: SSTR5 polymorphism and PKD1 mutation
- AIP ad P27/KIP1 gne vriants are not associated ptuitary aenoma penotypes in a large MEN1 family
- 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
Informações sobre a disponibilidade de versões do artigo em acesso aberto coletadas automaticamente via oaDOI API (Unpaywall).
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas