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.
24. Germline mutations and genotype-phenotype correlations in patients with apparently sporadic pheochromocytoma/paraganglioma in Korea. Kim JH; Seong MW; Lee KE; Choi HJ; Ku EJ; Bae JH; Park SS; Choi SH; Kim SW; Shin C; Kim SY Clin Genet; 2014 Nov; 86(5):482-6. PubMed ID: 24134185 [TBL] [Abstract][Full Text] [Related]
25. Management of hereditary pheochromocytoma in von Hippel-Lindau kindreds with partial adrenalectomy. Walther MM; Keiser HR; Choyke PL; Rayford W; Lyne JC; Linehan WM J Urol; 1999 Feb; 161(2):395-8. PubMed ID: 9915410 [TBL] [Abstract][Full Text] [Related]
26. [Local recurrence of pheochromocytoma associated with von Hippel-Lindau disease 26 years after bilateral adrenalectomy : a case report]. Fujita N; Mikami J; Murasawa H; Okamoto A; Imai A; Hatakeyama S; Ishimura H; Yoneyama T; Koie T; Kamimura N; Ohyama C; Morohashi S; Kijima H Hinyokika Kiyo; 2013 Jul; 59(7):427-30. PubMed ID: 23945322 [TBL] [Abstract][Full Text] [Related]
27. A novel von Hippel-Lindau point mutation presents as apparently sporadic pheochromocytoma. Rich TA; Jonasch E; Matin S; Waguespack SG; Gombos DS; Santarpia L; Stolle C; Jimenez C Cancer Invest; 2008 Jul; 26(6):642-6. PubMed ID: 18584357 [TBL] [Abstract][Full Text] [Related]
28. The occurrence of SDHB gene mutations in pheochromocytoma. Van Nederveen FH; Dinjens WN; Korpershoek E; De Krijger RR Ann N Y Acad Sci; 2006 Aug; 1073():177-82. PubMed ID: 17102084 [TBL] [Abstract][Full Text] [Related]
30. Frequent genetic changes in childhood pheochromocytomas. De Krijger RR; Petri BJ; Van Nederveen FH; Korpershoek E; De Herder WW; De Muinck Keizer-Schrama SM; Dinjens WN Ann N Y Acad Sci; 2006 Aug; 1073():166-76. PubMed ID: 17102083 [TBL] [Abstract][Full Text] [Related]
31. Phaeochromocytoma associated with a de novo VHL mutation as form fruste of von Hippel-Lindau disease. Frenzel S; Apel TW; Heidemann PH; Zerres K; Neumann HP; Dörr HG Eur J Pediatr; 2001 Jul; 160(7):421-4. PubMed ID: 11475579 [TBL] [Abstract][Full Text] [Related]
32. Adrenal adenoma in von Hippel-Lindau syndrome: A case report with review of literature. Palui R; Kamalanathan S; Sahoo J; Dorairajan LN; Badhe B; Gochhait D J Cancer Res Ther; 2019 Mar; 15(Supplement):S163-S166. PubMed ID: 30900640 [TBL] [Abstract][Full Text] [Related]
33. Posterior mediastinal paraganglioma with bilateral adrenal pheochromocytoma. Kwon HJ; Park JH; Jin GY; Chung MJ; Lim ST; Kim MH; Kim HJ; Lee YC Respir Med; 2004 Jun; 98(6):574-6. PubMed ID: 15191044 [TBL] [Abstract][Full Text] [Related]
34. 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]
35. Concurrent heterozygous Von-Hippel-Lindau and transmembrane-protein-127 gene mutation causing an erythropoietin-secreting pheochromocytoma in a normotensive patient with severe erythrocytosis. Negro A; Graiani G; Nicoli D; Farnetti E; Casali B; Verzicco I; Tedeschi S; Ghirarduzzi A; Cannone V; Marco LDE; Filice A; Gemelli G; Giunta A; Cabassi A J Hypertens; 2020 Feb; 38(2):340-346. PubMed ID: 31568062 [TBL] [Abstract][Full Text] [Related]
36. Extra-adrenal and adrenal pheochromocytomas associated with a germline SDHC mutation. Peczkowska M; Cascon A; Prejbisz A; Kubaszek A; Cwikła BJ; Furmanek M; Erlic Z; Eng C; Januszewicz A; Neumann HP Nat Clin Pract Endocrinol Metab; 2008 Feb; 4(2):111-5. PubMed ID: 18212813 [TBL] [Abstract][Full Text] [Related]
37. Germinal mutations of RET, SDHB, SDHD, and VHL genes in patients with apparently sporadic pheochromocytomas and paragangliomas. Krawczyk A; Hasse-Lazar K; Pawlaczek A; Szpak-Ulczok S; Krajewska J; Paliczka-Cieślak E; Jurecka-Lubieniecka B; Roskosz J; Chmielik E; Ziaja J; Cierpka L; Peczkowska M; Preibisz A; Januszewicz A; Otto M; Jarzab B Endokrynol Pol; 2010; 61(1):43-8. PubMed ID: 20205103 [TBL] [Abstract][Full Text] [Related]
38. Three novel VHL germline mutations in Korean patients with von Hippel-Lindau disease and pheochromocytomas. Kang HC; Kim IJ; Park JH; Shin Y; Jang SG; Ahn SA; Park HW; Lim SK; Oh SK; Kim DJ; Lee KW; Choi YS; Park YJ; Lee MR; Kim DW; Park JG Oncol Rep; 2005 Oct; 14(4):879-83. PubMed ID: 16142346 [TBL] [Abstract][Full Text] [Related]
39. Ultrastructural findings in adrenal cortical adenomas clinically mimicking pheochromocytoma: a comparison with other adrenal tumors and tissue preparation techniques. Perrino CM; Prall DN; Calomeni EP; Nadasdy T; Zynger DL Ultrastruct Pathol; 2012 Oct; 36(5):287-93. PubMed ID: 23025647 [TBL] [Abstract][Full Text] [Related]
40. Von Hippel-Lindau disease: a single gene, several hereditary tumors. Crespigio J; Berbel LCL; Dias MA; Berbel RF; Pereira SS; Pignatelli D; Mazzuco TL J Endocrinol Invest; 2018 Jan; 41(1):21-31. PubMed ID: 28589383 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]