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42. Relapsing pheochromocytoma in a Chinese women caused by a novel mutation in exon 6 of the SDHB gene: a case report. Reusch J; Haag C; Raue F; Badenhoop K Exp Clin Endocrinol Diabetes; 2007 Oct; 115(9):616-8. PubMed ID: 17943698 [TBL] [Abstract][Full Text] [Related]
43. [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]
47. Gene probe analysis in an informative family with multiple endocrine neoplasia syndrome type 2A (MEN 2A). Improvement in carrier risk estimation. Morrison PJ; Hadden DR; Hughes AE; Kennedy L; Russell CJ; Nevin NC Q J Med; 1991 Jul; 80(291):597-603. PubMed ID: 1682970 [TBL] [Abstract][Full Text] [Related]
48. Catechol amine metabolism: peripheral plasma levels of epinephrine (E) and norepinephrine (NE) during laparotomy under different types of anesthesia in dogs, during operation in man (including adrenal vein sampling), and before and following resection of a pheochromocytoma associated with von Recklinghausen's neurofibromatosis. HARDY JD; CARTER T; TURNER MD Ann Surg; 1959 Oct; 150(4):666-83. PubMed ID: 14399750 [No Abstract] [Full Text] [Related]
50. [The pheochromocytoma as a dominant hereditary dysgenetic tumor]. von DOEPP C Virchows Arch Pathol Anat Physiol Klin Med; 1962; 335():231-9. PubMed ID: 13886916 [No Abstract] [Full Text] [Related]
51. Hypertension and excretion of 1-Oxygenated steroids. Edwards RW; Harvey DR; Knight-Jones E Arch Dis Child; 1968 Oct; 43(231):611-5. PubMed ID: 5696471 [No Abstract] [Full Text] [Related]
52. [Familial pheochromocytoma in a daughter (extra-adrenal) and her mother]. Nakagawa S; Kojima M; Nakao M; Ohnishi K; Watanabe H Hinyokika Kiyo; 1987 Jul; 33(7):985-92. PubMed ID: 3318335 [TBL] [Abstract][Full Text] [Related]
53. [Familial pheochromocytoma: four cases in one kindred (author's transl)]. Mori Y; Kiyohara H; Miki T; Horiuchi N; Kotake T Nihon Hinyokika Gakkai Zasshi; 1977 Apr; 68(4):398-406. PubMed ID: 559872 [No Abstract] [Full Text] [Related]
54. A decade (2001-2010) of genetic testing for pheochromocytoma and paraganglioma. Buffet A; Venisse A; Nau V; Roncellin I; Boccio V; Le Pottier N; Boussion M; Travers C; Simian C; Burnichon N; Abermil N; Favier J; Jeunemaitre X; Gimenez-Roqueplo AP Horm Metab Res; 2012 May; 44(5):359-66. PubMed ID: 22517557 [TBL] [Abstract][Full Text] [Related]
55. Pheochromocytoma in father and son: report of the eighth known affected kindred. GREENBERG RE; GARDNER LI J Clin Endocrinol Metab; 1959 Mar; 19(3):351-62. PubMed ID: 13631052 [No Abstract] [Full Text] [Related]
56. Phaeochromocytoma in father and son. Clezy JK; Barker J; Patel P; Richens JE P N G Med J; 1986 Jun; 29(2):157-60. PubMed ID: 3465100 [No Abstract] [Full Text] [Related]
57. 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]