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156 related items for PubMed ID: 9795529

  • 21. Genetic analysis of seven Mediterranean families with multiple endocrine neoplasia type 2A.
    Oriola J, Hernandez C, Simo R, Barcelo A, Casamitjana R, Vilardell E, Rivera-Fillat F.
    Clin Endocrinol (Oxf); 1996 Feb; 44(2):207-12. PubMed ID: 8849576
    [Abstract] [Full Text] [Related]

  • 22. RET oligonucleotide microarray for the detection of RET mutations in multiple endocrine neoplasia type 2 syndromes.
    Kim IJ, Kang HC, Park JH, Ku JL, Lee JS, Kwon HJ, Yoon KA, Heo SC, Yang HY, Cho BY, Kim SY, Oh SK, Youn YK, Park DJ, Lee MS, Lee KW, Park JG.
    Clin Cancer Res; 2002 Feb; 8(2):457-63. PubMed ID: 11839664
    [Abstract] [Full Text] [Related]

  • 23. A family of multiple endocrine neoplasia type 2A with the RET proto-oncogene mutation in codon 618 (Cys-->Arg).
    Nakao A, Naomoto Y, Kataoka M, Haisa M, Kataoka K, Saitoh S, Fujiwara T, Yamatsuji T, Shigemitsu K, Umeoka T, Isozaki H, Futami H, Yamaguchi K, Tanaka N.
    Jpn J Clin Oncol; 2001 Apr; 31(4):157-61. PubMed ID: 11386462
    [Abstract] [Full Text] [Related]

  • 24. Germline mutations of the RET proto-oncogene in eight Japanese patients with multiple endocrine neoplasia type 2A (MEN2A).
    Takiguchi-Shirahama S, Koyama K, Miyauchi A, Wakasugi T, Oishi S, Takami H, Hikiji K, Nakamura Y.
    Hum Genet; 1995 Feb; 95(2):187-90. PubMed ID: 7860065
    [Abstract] [Full Text] [Related]

  • 25. Somatic and MEN 2A de novo mutations identified in the RET proto-oncogene by screening of sporadic MTC:s.
    Zedenius J, Wallin G, Hamberger B, Nordenskjöld M, Weber G, Larsson C.
    Hum Mol Genet; 1994 Aug; 3(8):1259-62. PubMed ID: 7987299
    [Abstract] [Full Text] [Related]

  • 26. RET mutation profile and variable clinical manifestations in a family with multiple endocrine neoplasia type 2A and Hirschsprung's disease.
    Pasini B, Rossi R, Ambrosio MR, Zatelli MC, Gullo M, Gobbo M, Collini P, Aiello A, Pansini G, Trasforini G, degli Uberti EC.
    Surgery; 2002 Apr; 131(4):373-81. PubMed ID: 11935126
    [Abstract] [Full Text] [Related]

  • 27. The RET protooncogene in sporadic pheochromocytomas: frequent MEN 2-like mutations and new molecular defects.
    Beldjord C, Desclaux-Arramond F, Raffin-Sanson M, Corvol JC, De Keyzer Y, Luton JP, Plouin PF, Bertagna X.
    J Clin Endocrinol Metab; 1995 Jul; 80(7):2063-8. PubMed ID: 7608256
    [Abstract] [Full Text] [Related]

  • 28. Mutations of codon 918 in the RET proto-oncogene correlate to poor prognosis in sporadic medullary thyroid carcinomas.
    Zedenius J, Larsson C, Bergholm U, Bovée J, Svensson A, Hallengren B, Grimelius L, Bäckdahl M, Weber G, Wallin G.
    J Clin Endocrinol Metab; 1995 Oct; 80(10):3088-90. PubMed ID: 7559902
    [Abstract] [Full Text] [Related]

  • 29. Noncardiogenic pulmonary edema as the chief manifestation of a pheochromocytoma: a case report of MEN 2A with pedigree analysis of the RET proto-oncogene.
    Okada Y, Suchi M, Takeyama H, Hodgson ME, Kato T, Manabe T.
    Tohoku J Exp Med; 1999 Jun; 188(2):177-87. PubMed ID: 10526879
    [Abstract] [Full Text] [Related]

  • 30. Risk and penetrance of primary hyperparathyroidism in multiple endocrine neoplasia type 2A families with mutations at codon 634 of the RET proto-oncogene. Groupe D'etude des Tumeurs à Calcitonine.
    Schuffenecker I, Virally-Monod M, Brohet R, Goldgar D, Conte-Devolx B, Leclerc L, Chabre O, Boneu A, Caron J, Houdent C, Modigliani E, Rohmer V, Schlumberger M, Eng C, Guillausseau PJ, Lenoir GM.
    J Clin Endocrinol Metab; 1998 Feb; 83(2):487-91. PubMed ID: 9467562
    [Abstract] [Full Text] [Related]

  • 31. Diagnosis of multiple endocrine neoplasia [MEN] 2A, 2B and familial medullary thyroid cancer [FMTC] by multiplex PCR and heteroduplex analyses of RET proto-oncogene mutations.
    Kambouris M, Jackson CE, Feldman GL.
    Hum Mutat; 1996 Feb; 8(1):64-70. PubMed ID: 8807338
    [Abstract] [Full Text] [Related]

  • 32. Cancers connected with mutations in RET proto-oncogene.
    Altanerová V.
    Neoplasma; 2001 Feb; 48(5):325-31. PubMed ID: 11845976
    [Abstract] [Full Text] [Related]

  • 33. Germline mutations of the RET proto-oncogene in pedigree with MEN type 2A: DNA analysis and its implications for pediatric surgery.
    Shimotake T, Iwai N, Inoue K, Inazawa J, Nishisho I.
    J Pediatr Surg; 1996 Jun; 31(6):779-81. PubMed ID: 8783101
    [Abstract] [Full Text] [Related]

  • 34. Germline RET 634 mutation positive MEN 2A-related C-cell hyperplasias have genetic features consistent with intraepithelial neoplasia.
    Diaz-Cano SJ, de Miguel M, Blanes A, Tashjian R, Wolfe HJ.
    J Clin Endocrinol Metab; 2001 Aug; 86(8):3948-57. PubMed ID: 11502837
    [Abstract] [Full Text] [Related]

  • 35. Role of the RET proto-oncogene in sporadic hyperparathyroidism and in hyperparathyroidism of multiple endocrine neoplasia type 2.
    Pausova Z, Soliman E, Amizuka N, Janicic N, Konrad EM, Arnold A, Goltzman D, Hendy GN.
    J Clin Endocrinol Metab; 1996 Jul; 81(7):2711-8. PubMed ID: 8675600
    [Abstract] [Full Text] [Related]

  • 36.
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  • 37. A patient with MEN 2 and multiple mutations of RET in the germline.
    Koch CA, Huang SC, Vortmeyer AO, Zhuang Z, Chrousos GP, Pacak K.
    Exp Clin Endocrinol Diabetes; 2000 Jul; 108(8):493. PubMed ID: 11149622
    [No Abstract] [Full Text] [Related]

  • 38. RET proto-oncogene mutations in inherited and sporadic medullary thyroid cancer.
    Blaugrund JE, Johns MM, Eby YJ, Ball DW, Baylin SB, Hruban RH, Sidransky D.
    Hum Mol Genet; 1994 Oct; 3(10):1895-7. PubMed ID: 7849720
    [No Abstract] [Full Text] [Related]

  • 39. [The molecular pathology of RET protooncogene in families with multiple endocrine neoplasia type 2A].
    Biarnés J, Miranda M, Corral J, Gabau E, Matías-Guiu X, Matilla A, Soler J, Estivill X, Volpini V.
    Med Clin (Barc); 1996 Sep 21; 107(9):321-5. PubMed ID: 8984233
    [Abstract] [Full Text] [Related]

  • 40. Multiple endocrine neoplasia type 2A with the identical somatic mutation in medullary thyroid carcinoma and pheochromocytoma without germline mutation at the corresponding site in the RET proto-oncogene.
    Akama H, Noshiro T, Kimura N, Shimizu K, Watanabe T, Shibukawa S, Nakai S, Miura W, Ito S, Miura Y.
    Intern Med; 1999 Feb 21; 38(2):145-9. PubMed ID: 10225670
    [Abstract] [Full Text] [Related]

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