Artigo de periodico

Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10 (2011)

• Authors:
  • Frank-Raue, Karin
  • Rybicki, Lisa A.
  • Erlic, Zoran
  • Schweizer, Heiko
  • Winter, Aurelia
  • Milos, Ioana
  • Toledo, Sergio Pereira de Almeida
  • Toledo, Rodrigo A.
  • Tavares, Marcos R.
  • Alevizaki, Maria
  • Mian, Caterina
  • Siggelkow, Heide
  • Hüfner, Michael
  • Wohllk, Nelson
  • Opocher, Giuseppe
  • Dvořáková, Šárka
  • Bendlova, Bela
  • Czetwertynska, Małgorzata
  • Skasko, Elżbieta
  • Barontini, Marta
  • Sanso, Gabriela
  • Vorländer, Christian
  • Maia, Ana Luiza
  • Patocs, Attila
  • Links, Thera P.
  • de Groot, Jan Willem
  • Kerstens, Michiel N.
  • Valk, Gerlof D.
  • Miehle, Konstanze
  • Musholt, Thomas J.
  • Biarnes, Josefina
  • Damjanovic, Svetozar
  • Muresan, Mihaela
  • Wüster, Christian
  • Fassnacht, Martin
  • Peczkowska, Mariola
  • Fauth, Christine
  • Golcher, Henriette
  • Walter, Martin A.
  • Pichl, Josef
  • Raue, Friedhelm
  • Eng, Charis
  • Neumann, Hartmut P. H.
• Autor USP: TOLEDO, SERGIO PEREIRA DE ALMEIDA - FM
• Unidade: FM
• DOI: 10.1002/humu.21385
• Subjects: NEOPLASIA ENDÓCRINA MÚLTIPLA (GENÉTICA); FATORES DE CRESCIMENTO; NEOPLASIAS DA TIREOIDE; GENÓTIPOS; CARCINOMA MEDULAR; FENÓTIPOS; METÁSTASE NEOPLÁSICA
• Language: Inglês
• Imprenta:
  • Publisher place: New York
  • Date published: 2011
• Source:
  • Título: Human mutation
  • ISSN: 1059-7794
  • Volume/Número/Paginação/Ano: v. 32, n. 1, p. 51-58, 2011

Informações sobre o DOI: 10.1002/humu.21385 (Fonte: oaDOI API)
• Este periódico é de acesso aberto
• Este artigo NÃO é de acesso aberto
  

---

How to cite

A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas

• ABNT

  FRANK-RAUE, Karin et al. Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10. Human mutation, v. 32, n. 1, p. 51-58, 2011Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1002/humu.21385/pdf. Acesso em: 23 jan. 2026.

• APA

  Frank-Raue, K., Rybicki, L. A., Erlic, Z., Schweizer, H., Winter, A., Milos, I., et al. (2011). Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10. Human mutation, 32( 1), 51-58. doi:10.1002/humu.21385

• NLM

  Frank-Raue K, Rybicki LA, Erlic Z, Schweizer H, Winter A, Milos I, Toledo SP de A, Toledo RA, Tavares MR, Alevizaki M, Mian C, Siggelkow H, Hüfner M, Wohllk N, Opocher G, Dvořáková Š, Bendlova B, Czetwertynska M, Skasko E, Barontini M, Sanso G, Vorländer C, Maia AL, Patocs A, Links TP, de Groot JW, Kerstens MN, Valk GD, Miehle K, Musholt TJ, Biarnes J, Damjanovic S, Muresan M, Wüster C, Fassnacht M, Peczkowska M, Fauth C, Golcher H, Walter MA, Pichl J, Raue F, Eng C, Neumann HPH. Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10 [Internet]. Human mutation. 2011 ; 32( 1): 51-58.[citado 2026 jan. 23 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/humu.21385/pdf

• Vancouver

  Frank-Raue K, Rybicki LA, Erlic Z, Schweizer H, Winter A, Milos I, Toledo SP de A, Toledo RA, Tavares MR, Alevizaki M, Mian C, Siggelkow H, Hüfner M, Wohllk N, Opocher G, Dvořáková Š, Bendlova B, Czetwertynska M, Skasko E, Barontini M, Sanso G, Vorländer C, Maia AL, Patocs A, Links TP, de Groot JW, Kerstens MN, Valk GD, Miehle K, Musholt TJ, Biarnes J, Damjanovic S, Muresan M, Wüster C, Fassnacht M, Peczkowska M, Fauth C, Golcher H, Walter MA, Pichl J, Raue F, Eng C, Neumann HPH. Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10 [Internet]. Human mutation. 2011 ; 32( 1): 51-58.[citado 2026 jan. 23 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/humu.21385/pdf

Últimas obras dos mesmos autores vinculados com a USP cadastradas na BDPI:

• Tumores neuroendócrinos
• Post-surgical follow-up of primary hyperparathyroidism associated with multiple endocrine neoplasia type 1
• Detection of ret proto-oncogene germline mutations in apparently sporadic cases with medullary thyroid carcinoma
• Narrowing the gap of personalized medicine in emerging countries: the case of multiple endocrine neoplasias in Brazil
• Male pseudohermaproditisms resulting from leydig cell hypoplasia
• Bone mineral density analysis in patients with primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 after total parathyroidectomy
• Deletion analysis of the p16 tumour suppressor gene in phaeochromocytomas
• Impaired adrenocorticotropin-adrenal axis in combined pituytary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene
• A new multiple endocrine neoplasia type 1 (men1) phenotype: Double pituitary adenoma secreting prolactin, LH and alpha subunit glycoprotein
• Tumor secretor de LH: um novo fenótipo na neoplasia endócrina múltipla tipo 1 (NEM-1)