These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

244 related items for PubMed ID: 28747092

  • 1. Clinical Features of a Family with Multiple Endocrine Neoplasia Type 2A Caused by the D631Y RET Mutation.
    Ospina NS, Maraka S, Donegan D, Morris JC.
    Thyroid; 2017 Oct; 27(10):1332-1334. PubMed ID: 28747092
    [Abstract] [Full Text] [Related]

  • 2. Patients with RET D631Y mutations most commonly present with pheochromocytoma and not medullary thyroid carcinoma.
    Elston MS, Meyer-Rochow GY, Holdaway I, Conaglen JV.
    Horm Metab Res; 2012 May; 44(5):339-42. PubMed ID: 22274720
    [Abstract] [Full Text] [Related]

  • 3. Multiple endocrine neoplasia type 2A due to an exon 8 (G533C) mutation in a large North American kindred.
    Castro MR, Thomas BC, Richards ML, Zhang J, Morris JC.
    Thyroid; 2013 Dec; 23(12):1547-52. PubMed ID: 23461807
    [Abstract] [Full Text] [Related]

  • 4. A rare missense variant in RET exon 8 in a Portuguese family with atypical multiple endocrine neoplasia type 2A.
    Martins AF, Martins JM, do Vale S, Dias T, Silveira C, da Silva IR, Carmo-Fonseca M.
    Hormones (Athens); 2016 Jul; 15(3):435-440. PubMed ID: 27838608
    [Abstract] [Full Text] [Related]

  • 5. A rare extracellular D631Y germline mutation of the RET proto-oncogene in two Korean families with multiple endocrine neoplasia 2A.
    Bae SJ, Kim DJ, Kim JY, Park SY, Choi SH, Song YD, Ki CS, Chung JH.
    Thyroid; 2006 Jun; 16(6):609-14. PubMed ID: 16839264
    [Abstract] [Full Text] [Related]

  • 6. Characterization of the largest kindred with MEN2A due to a Cys609Ser RET mutation.
    Mian C, Barollo S, Zambonin L, Pennelli G, Bernante P, Pelizzo MR, Nacamulli D, Mantero F, Girelli ME, Opocher G.
    Fam Cancer; 2009 Jun; 8(4):379-82. PubMed ID: 19475497
    [Abstract] [Full Text] [Related]

  • 7. [A comparison of clinical characteristics between 2 pedigrees of multiple endocrine neoplasia type 2A with different RET mutations].
    Weng Y, Xue SN, Zhang SL, Cheng H, Yan L.
    Zhonghua Nei Ke Za Zhi; 2018 Feb 01; 57(2):134-137. PubMed ID: 29397600
    [Abstract] [Full Text] [Related]

  • 8. Clinical features and signaling effects of RET D631Y variant multiple endocrine neoplasia type 2 (MEN2).
    Lee JY, Kim SY, Jo KH, Mo EY, Kim ES, Kim HS, Han JH, Moon SD.
    Korean J Intern Med; 2022 Mar 01; 37(2):398-410. PubMed ID: 34905813
    [Abstract] [Full Text] [Related]

  • 9. Catecholamine crisis as a first manifestation of familial bilateral pheochromocytoma caused by RET proto-oncogene mutation in codon C 634R.
    Zwolak A, Rudzki G, Świrska J, Dudzińska M, Daniluk J, Tarach J.
    Endokrynol Pol; 2015 Mar 01; 66(5):462-8. PubMed ID: 26457501
    [Abstract] [Full Text] [Related]

  • 10. Nationwide French Study of RET Variants Detected from 2003 to 2013 Suggests a Possible Influence of Polymorphisms as Modifiers.
    Lebeault M, Pinson S, Guillaud-Bataille M, Gimenez-Roqueplo AP, Carrie A, Barbu V, Pigny P, Bezieau S, Rey JM, Delvincourt C, Giraud S, Veyrat-Durebex C, Saulnier P, Bouzamondo N, Chabbert M, Blin J, Mohamed A, Romanet P, Borson-Chazot F, Rohmer V, Barlier A, Mirebeau-Prunier D.
    Thyroid; 2017 Dec 01; 27(12):1511-1522. PubMed ID: 28946813
    [Abstract] [Full Text] [Related]

  • 11. The RET p.G533C mutation confers predisposition to multiple endocrine neoplasia type 2A in a Brazilian kindred and is able to induce a malignant phenotype in vitro and in vivo.
    Oliveira MN, Hemerly JP, Bastos AU, Tamanaha R, Latini FR, Camacho CP, Impellizzeri A, Maciel RM, Cerutti JM.
    Thyroid; 2011 Sep 01; 21(9):975-85. PubMed ID: 21834681
    [Abstract] [Full Text] [Related]

  • 12. [The clinical patterns and RET proto-oncogene in fifteen multiple endocrine neoplasia type 2A pedigrees].
    Zhou YL, Zhu SX, Li JJ, Liu JB, Yin M, Xiao BY, Yu CL, Wang LM, Gu LQ, Cui B, Ning G, Li XY, Zhao YJ.
    Zhonghua Nei Ke Za Zhi; 2007 Jun 01; 46(6):466-70. PubMed ID: 17663821
    [Abstract] [Full Text] [Related]

  • 13. Multiple endocrine neoplasia type 2A in two families with the familial medullary thyroid carcinoma associated G533C mutation of the RET proto-oncogene.
    Peppa M, Boutati E, Kamakari S, Pikounis V, Peros G, Panayiotides IG, Economopoulos T, Raptis SA, Hadjidakis D.
    Eur J Endocrinol; 2008 Dec 01; 159(6):767-71. PubMed ID: 18805915
    [Abstract] [Full Text] [Related]

  • 14. [A case of multiple endocrine neoplasia type 2A (MEN2A) with a mutation in the RET gene].
    Ishizu K, Shiraishi K, Kawamura H, Naito K, Takahashi T, Yoshimura K, Tangoku A, Shirahama S.
    Hinyokika Kiyo; 1999 Jun 01; 45(6):407-10. PubMed ID: 10442282
    [Abstract] [Full Text] [Related]

  • 15. Pheochromocytoma as the first manifestation of MEN2A with RET mutation S891A: report of a case.
    Hibi Y, Ohye T, Ogawa K, Shimizu Y, Shibata M, Kagawa C, Mizuno Y, Uchino S, Kosugi S, Kurahashi H, Iwase K.
    Surg Today; 2014 Nov 01; 44(11):2195-200. PubMed ID: 24449023
    [Abstract] [Full Text] [Related]

  • 16. A NOVEL DOUBLE MUTATION VAL648ILE AND VAL804LEU OF RET PROTO-ONCOGENE IN MULTIPLE ENDOCRINE NEOPLASIA TYPE 2.
    Verrienti A, Carbone A, Bellitti P, Fabiano MC, De Rose RF, Maranghi M, Lucia P, Durante C, Rosignolo F, Pecce V, Sponziello M, Puppin C, Costante G, Bruno R.
    Endocr Pract; 2015 Nov 01; 21(11):1248-54. PubMed ID: 26247112
    [Abstract] [Full Text] [Related]

  • 17. Clinical spectrum of MEN2A in a large family caused by the infrequent RET mutation Cys609Phe.
    Oriola J, Biarnes J, Hernandez C, Simó R.
    Clin Genet; 2013 Apr 01; 83(4):384-7. PubMed ID: 22734615
    [Abstract] [Full Text] [Related]

  • 18. RET proto-oncogene mutations affecting codon 790/791: A mild form of multiple endocrine neoplasia type 2A syndrome?
    Gimm O, Niederle BE, Weber T, Bockhorn M, Ukkat J, Brauckhoff M, Thanh PN, Frilling A, Klar E, Niederle B, Dralle H.
    Surgery; 2002 Dec 01; 132(6):952-9; discussion 959. PubMed ID: 12490841
    [Abstract] [Full Text] [Related]

  • 19. The clinical spectrum of multiple endocrine neoplasia type 2a caused by the rare intracellular RET mutation S891A.
    Schulte KM, Machens A, Fugazzola L, McGregor A, Diaz-Cano S, Izatt L, Aylwin S, Talat N, Beck-Peccoz P, Dralle H.
    J Clin Endocrinol Metab; 2010 Sep 01; 95(9):E92-7. PubMed ID: 20554711
    [Abstract] [Full Text] [Related]

  • 20. Multiple endocrine neoplasia type 2A: case report.
    Păun DL, Poiană C, Petriş R, Radian S, Miulescu RD, Constantinescu G, Orban C.
    Chirurgia (Bucur); 2013 Sep 01; 108(6):900-3. PubMed ID: 24331334
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 13.