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.
84 related articles for article (PubMed ID: 15827097)
21. Multiple endocrine neoplasia 2A due to a unique C609S RET mutation presents with pheochromocytoma and reduced penetrance of medullary thyroid carcinoma. Kinlaw WB; Scott SM; Maue RA; Memoli VA; Harris RD; Daniels GH; Porter DM; Belloni DR; Spooner ET; Ernesti MM; Noll WW Clin Endocrinol (Oxf); 2005 Dec; 63(6):676-82. PubMed ID: 16343103 [TBL] [Abstract][Full Text] [Related]
22. Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease. Neumann HP; Berger DP; Sigmund G; Blum U; Schmidt D; Parmer RJ; Volk B; Kirste G N Engl J Med; 1993 Nov; 329(21):1531-8. PubMed ID: 8105382 [TBL] [Abstract][Full Text] [Related]
23. Bilateral Pheochromocytomas in MEN2A Syndrome: A Two-Institution Experience. Lang BH; Yu HW; Lo CY; Lee KE; Garcia-Barcelo MM; Woo YC; Lee PC; Wong KP; Tam PK; Lam KS World J Surg; 2015 Oct; 39(10):2484-91. PubMed ID: 26071011 [TBL] [Abstract][Full Text] [Related]
25. [Analysis of mutations in the RET proto-oncogene in patients with medullary thyroid tumor]. Amosenko FA; Brzhezovskiĭ VZh; Liubchenko LN; Shabanov MA; Kozlova VM; Vanushko VE; Kazubskaia TP; Gar'kavtseva RF; Kalinin VN Genetika; 2003 Jun; 39(6):847-54. PubMed ID: 12884527 [TBL] [Abstract][Full Text] [Related]
26. Pheochromocytoma in multiple endocrine neoplasia type II: an example of the two-hit theory of neoplasia. Cerny JC; Jackson CE; Talpos GB; Yott JB; Lee MW Surgery; 1982 Nov; 92(5):849-52. PubMed ID: 6127813 [TBL] [Abstract][Full Text] [Related]
27. Identification of a novel point mutation in the RET gene (Ala883Thr), which is associated with medullary thyroid carcinoma phenotype only in homozygous condition. Elisei R; Cosci B; Romei C; Agate L; Piampiani P; Miccoli P; Berti P; Basolo F; Ugolini C; Ciampi R; Nikiforov Y; Pinchera A J Clin Endocrinol Metab; 2004 Nov; 89(11):5823-7. PubMed ID: 15531548 [TBL] [Abstract][Full Text] [Related]
28. Clinical screening as compared with DNA analysis in families with multiple endocrine neoplasia type 2A. Lips CJ; Landsvater RM; Höppener JW; Geerdink RA; Blijham G; van Veen JM; van Gils AP; de Wit MJ; Zewald RA; Berends MJ N Engl J Med; 1994 Sep; 331(13):828-35. PubMed ID: 7915822 [TBL] [Abstract][Full Text] [Related]
29. Expression of the ret proto-oncogene in phaeochromocytoma. An in situ hybridization and northern blot study. Matias-Guiu X; Colomer A; Mato E; Cuatrecasas M; Komminoth P; Prat J; Wolfe H J Pathol; 1995 May; 176(1):63-8. PubMed ID: 7616358 [TBL] [Abstract][Full Text] [Related]
30. A rare case of juvenile hypertension: coexistence of type 2 multiple endocrine neoplasia -related bilateral pheochromocytoma and reninoma in a young patient with ACE gene polymorphism. Paragliola RM; Capoluongo E; Torino F; Minucci A; Canu G; Prete A; Pontecorvi A; Corsello SM BMC Endocr Disord; 2015 Jun; 15():30. PubMed ID: 26084817 [TBL] [Abstract][Full Text] [Related]
31. [Multiple familial pheochromocytomas: sonographic demonstration of multiple adrenal, celiac and bladder localizations in a child]. Arroja JM; Gudinchet F; Maeder P; Fournier D Praxis (Bern 1994); 1995 Oct; 84(43):1231-4. PubMed ID: 7481340 [TBL] [Abstract][Full Text] [Related]
32. G protein gene mutations in patients with multiple endocrinopathies. Williamson EA; Johnson SJ; Foster S; Kendall-Taylor P; Harris PE J Clin Endocrinol Metab; 1995 May; 80(5):1702-5. PubMed ID: 7745022 [TBL] [Abstract][Full Text] [Related]
33. Genetic and epigenetic profile of sporadic pheochromocytomas. Cascon A; Ruiz-Llorente S; Fraga MF; Leton R; Telleria D; Sastre J; Diez JJ; Martinez Diaz-Guerra G; Diaz Perez JA; Benitez J; Esteller M; Robledo M J Med Genet; 2004 Mar; 41(3):e30. PubMed ID: 14985401 [No Abstract] [Full Text] [Related]
34. The clinical and screening age-at-onset distribution for the MEN-2 syndrome. Easton DF; Ponder MA; Cummings T; Gagel RF; Hansen HH; Reichlin S; Tashjian AH; Telenius-Berg M; Ponder BA Am J Hum Genet; 1989 Feb; 44(2):208-15. PubMed ID: 2563193 [TBL] [Abstract][Full Text] [Related]
35. Penetrance of phaeochromocytoma in Maciel RMB; Bim LV; Camacho CP; Cerutti JM Endocr Relat Cancer; 2018 Sep; 25(9):L49-L51. PubMed ID: 30012587 [No Abstract] [Full Text] [Related]
36. G691S/S904S polymorphism in the RET protooncogene of a 25-year-old medical student with bilateral pheochromocytoma. Arneth B Indian J Hum Genet; 2009 Jan; 15(1):32-5. PubMed ID: 20407648 [TBL] [Abstract][Full Text] [Related]
37. Simultaneous bilateral laparoscopic cortical-sparing adrenalectomy for bilateral pheochromocytomas in multiple endocrine neoplasia type 2. Qi XP; Lian BJ; Fang XD; Dong F; Li F; Jin HY; Zhang K; Wang KE; Zhang Y Front Surg; 2022; 9():1057821. PubMed ID: 36704524 [TBL] [Abstract][Full Text] [Related]
38. Multiple endocrine adenomatosis: in support of the common origin theories. Janson KL; Roberts JA; Varela M J Urol; 1978 Feb; 119(2):161-5. PubMed ID: 24756 [TBL] [Abstract][Full Text] [Related]
39. Does Genotype-Specific Phenotype in Patients with Multiple Endocrine Neoplasia Type 2 Occur as Current Guidelines Predict? Binter T; Baumgartner-Parzer S; Schernthaner-Reiter MH; Arikan M; Hargitai L; Niederle MB; Niederle B; Scheuba C; Riss P Cancers (Basel); 2024 Jan; 16(3):. PubMed ID: 38339246 [TBL] [Abstract][Full Text] [Related]