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26. [Nonfortuitous association of endocrine diseases in 2 sisters: pheochromocytoma in one, medullary tumor of the thyroid in the other]. Decoulx M; Mesmacque R; Leduc M; Dayras M; Linquette M Lille Med; 1971 Jan; 16(1):187-91. PubMed ID: 5554688 [No Abstract] [Full Text] [Related]
27. Molecular characterization of a pediatric pheochromocytoma with suspected bilateral disease. Mircescu H; Wilkin F; Paquette J; Oligny LL; Decaluwe H; Gaboury L; Nolet S; Van Vliet G; Deal C J Pediatr; 2001 Feb; 138(2):269-73. PubMed ID: 11174629 [TBL] [Abstract][Full Text] [Related]
28. Familial concurrence of carotid body tumor and pheochromocytoma. Pritchett JW Cancer; 1982 Jun; 49(12):2578-9. PubMed ID: 7074575 [No Abstract] [Full Text] [Related]
30. DNA flow cytometry in pheochromocytoma and paraganglioma. Jung WH; Yang WI; Park C; Choi IJ Yonsei Med J; 1992 Sep; 33(3):249-57. PubMed ID: 1292249 [TBL] [Abstract][Full Text] [Related]
31. Multiple endocrine neoplasia type IIb: a description of several patients and review of the literature. Montgomery TB; Mandelstam P; Tachman ML; Miller RE; Powell DE; Flueck JA; Kotchen TA J Clin Hypertens; 1987 Mar; 3(1):31-49. PubMed ID: 2883264 [TBL] [Abstract][Full Text] [Related]
32. Characteristics of a family with the MEN-2A syndrome. Haak HR; Nieuwenhuijzen Kruseman AC Henry Ford Hosp Med J; 1987; 35(2-3):104-6. PubMed ID: 2891639 [No Abstract] [Full Text] [Related]
33. [A case of pheochromocytoma (author's transl)]. Nakamura T; Naito T; Suzuki H; Kasai K; Shiina H Horumon To Rinsho; 1980 Sep; 28(9):1051-7. PubMed ID: 7460356 [No Abstract] [Full Text] [Related]
34. Familial pheochromocytoma associated with a novel mutation in the von Hippel-Lindau gene. Gross DJ; Avishai N; Meiner V; Filon D; Zbar B; Abeliovich D J Clin Endocrinol Metab; 1996 Jan; 81(1):147-9. PubMed ID: 8550742 [TBL] [Abstract][Full Text] [Related]
35. [3 cases of pheochromocytoma associated with diabetes mellitus]. Horiuchi N; Akagami H; Ito T; Ito S; Mori Y Nihon Rinsho; 1975 Feb; 33(2):478-83. PubMed ID: 1170397 [No Abstract] [Full Text] [Related]
36. [Pheochromocytoma. Various genetic aspects]. Bicho MP Acta Med Port; 1989; 2(2):57-8. PubMed ID: 2618799 [No Abstract] [Full Text] [Related]
37. Germline SDHD mutation in familial phaeochromocytoma. Astuti D; Douglas F; Lennard TW; Aligianis IA; Woodward ER; Evans DG; Eng C; Latif F; Maher ER Lancet; 2001 Apr; 357(9263):1181-2. PubMed ID: 11323050 [TBL] [Abstract][Full Text] [Related]
38. Surgical management of hereditary pheochromocytoma. Yip L; Lee JE; Shapiro SE; Waguespack SG; Sherman SI; Hoff AO; Gagel RF; Arens JF; Evans DB J Am Coll Surg; 2004 Apr; 198(4):525-34; discussion 534-5. PubMed ID: 15051000 [TBL] [Abstract][Full Text] [Related]
39. Clinical characteristics of pheochromocytoma patients with germline mutations in SDHD. Dannenberg H; van Nederveen FH; Abbou M; Verhofstad AA; Komminoth P; de Krijger RR; Dinjens WN J Clin Oncol; 2005 Mar; 23(9):1894-901. PubMed ID: 15774781 [TBL] [Abstract][Full Text] [Related]
40. [A family with 4 cases of pheochromocytoma and 2 cases of Hippel-Lindau disease]. Matsubara T; Koyama M; Yoshida S; Itoh T; Horiuchi N; Tateishi R; Wada A; Bito S Nihon Rinsho; 1978 Sep; 36(9):3248-53. PubMed ID: 722921 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]