191 related articles for article (PubMed ID: 31773218)
1. Clinical and Biochemical Features of Pheochromocytoma Characteristic of Von Hippel-Lindau Syndrome.
Li SR; Nicholson KJ; Mccoy KL; Carty SE; Yip L
World J Surg; 2020 Feb; 44(2):570-577. PubMed ID: 31773218
[TBL] [Abstract][Full Text] [Related]
2. Genotype-phenotype correlations of pheochromocytoma in two large von Hippel-Lindau (VHL) type 2A kindreds with different missense mutations.
Nielsen SM; Rubinstein WS; Thull DL; Armstrong MJ; Feingold E; Stang MT; Gnarra JR; Carty SE
Am J Med Genet A; 2011 Jan; 155A(1):168-73. PubMed ID: 21204227
[TBL] [Abstract][Full Text] [Related]
3. Uncommon clinical presentations of pheochromocytoma and paraganglioma in two different patients affected by two distinct novel VHL germline mutations.
Ercolino T; Becherini L; Valeri A; Maiello M; Gaglianò MS; Parenti G; Ramazzotti M; Piscitelli E; Simi L; Pinzani P; Nesi G; Degl'Innocenti D; Console N; Bergamini C; Mannelli M
Clin Endocrinol (Oxf); 2008 May; 68(5):762-8. PubMed ID: 18031321
[TBL] [Abstract][Full Text] [Related]
4. Early identification of patients with von Hippel-Lindau disease at risk for pheochromocytoma.
Maranchie JK; Walther MM
Curr Urol Rep; 2001 Feb; 2(1):24-30. PubMed ID: 12084291
[TBL] [Abstract][Full Text] [Related]
5. Pheochromocytoma in von Hippel-Lindau disease and neurofibromatosis type 1.
Opocher G; Conton P; Schiavi F; Macino B; Mantero F
Fam Cancer; 2005; 4(1):13-6. PubMed ID: 15883705
[TBL] [Abstract][Full Text] [Related]
6. Laparoscopic adrenal-sparing approach for children with bilateral pheochromocytoma in Von Hippel-Lindau disease.
Rubalcava NS; Overman RE; Kartal TT; Bruch SW; Else T; Newman EA
J Pediatr Surg; 2022 Mar; 57(3):414-417. PubMed ID: 34016427
[TBL] [Abstract][Full Text] [Related]
7. [Clinical status of Von Hippel-Lindau disease associated pheochromocytoma in Japan: a national epidemiologic survey].
Shuin T; Yao M; Shinohara N; Yamasaki I; Tamura K
Nihon Hinyokika Gakkai Zasshi; 2012 May; 103(3):557-61. PubMed ID: 22876661
[TBL] [Abstract][Full Text] [Related]
8. Clinical and genetic characterization of pheochromocytoma in von Hippel-Lindau families: comparison with sporadic pheochromocytoma gives insight into natural history of pheochromocytoma.
Walther MM; Reiter R; Keiser HR; Choyke PL; Venzon D; Hurley K; Gnarra JR; Reynolds JC; Glenn GM; Zbar B; Linehan WM
J Urol; 1999 Sep; 162(3 Pt 1):659-64. PubMed ID: 10458336
[TBL] [Abstract][Full Text] [Related]
9. Role of SDHAF2 and SDHD in von Hippel-Lindau associated pheochromocytomas.
Kugelberg J; Welander J; Schiavi F; Fassina A; Bäckdahl M; Larsson C; Opocher G; Söderkvist P; Dahia PL; Neumann HP; Gimm O
World J Surg; 2014 Mar; 38(3):724-32. PubMed ID: 24322175
[TBL] [Abstract][Full Text] [Related]
10. Differential genetic alterations in von Hippel-Lindau syndrome-associated and sporadic pheochromocytomas.
Bender BU; Gutsche M; Gläsker S; Müller B; Kirste G; Eng C; Neumann HP
J Clin Endocrinol Metab; 2000 Dec; 85(12):4568-74. PubMed ID: 11134110
[TBL] [Abstract][Full Text] [Related]
11. Germline VHL gene mutations in Hungarian families with von Hippel-Lindau disease and patients with apparently sporadic unilateral pheochromocytomas.
Gergics P; Patocs A; Toth M; Igaz P; Szucs N; Liko I; Fazakas F; Szabo I; Kovacs B; Glaz E; Racz K
Eur J Endocrinol; 2009 Sep; 161(3):495-502. PubMed ID: 19574279
[TBL] [Abstract][Full Text] [Related]
12. [Pheochromocytoma, first manifestation of Von Hippel-Lindau disease: a possibility to be considered].
Richard S; Resche F; Vermesse B; Fendler JP; Francillard M; Laroche F; Luton JP; Méry JP; Proye C; Redondo A
Arch Mal Coeur Vaiss; 1992 Aug; 85(8):1153-6. PubMed ID: 1482250
[TBL] [Abstract][Full Text] [Related]
13. Pheochromocytoma and Von Hippel-Lindau in pregnancy.
Kolomeyevskaya N; Blazo M; Van den Veyver I; Strehlow S; Aagaard-Tillery KM
Am J Perinatol; 2010 Mar; 27(3):257-63. PubMed ID: 19784914
[TBL] [Abstract][Full Text] [Related]
14. Pheochromocytoma Screening Initiation and Frequency in von Hippel-Lindau Syndrome.
Aufforth RD; Ramakant P; Sadowski SM; Mehta A; Trebska-McGowan K; Nilubol N; Pacak K; Kebebew E
J Clin Endocrinol Metab; 2015 Dec; 100(12):4498-504. PubMed ID: 26451910
[TBL] [Abstract][Full Text] [Related]
15. Volatile Hypertensive Crisis Secondary to Pheochromocytoma: A Case Report of von Hippel-Lindau Syndrome.
Anderson S
J Pediatr Health Care; 2020; 34(3):264-272. PubMed ID: 32143938
[No Abstract] [Full Text] [Related]
16. Von Hippel-Lindau disease and rapidly progressing pheochromocytomas in siblings.
Fugaru I; Goudie C; Capolicchio JP
Fam Cancer; 2022 Apr; 21(2):229-233. PubMed ID: 33877494
[TBL] [Abstract][Full Text] [Related]
17. Pediatric pheochromocytoma in association with Von Hippel-Lindau disease: Focus on screening strategies.
Vérot PL; Rabattu PY; Chabre O; Gayot A; Sartelet H; Faguet R; Robert Y; Piolat C
Arch Pediatr; 2020 Nov; 27(8):497-501. PubMed ID: 33067065
[TBL] [Abstract][Full Text] [Related]
18. Case report: a synonymous VHL mutation (c.414A > G, p.Pro138Pro) causes pathogenic familial hemangioblastoma through dysregulated splicing.
Liu F; Calhoun B; Alam MS; Sun M; Wang X; Zhang C; Haldar K; Lu X
BMC Med Genet; 2020 Feb; 21(1):42. PubMed ID: 32106822
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. A family with von Hippel-Lindau disease revealed by pheochromocytoma.
Tomita N; Moriguchi A; Yamasaki K; Taniyama Y; Kotani N; Hashiya N; Yoshida M; Yao M; Higaki J; Ogihara T
Hypertens Res; 2001 Jul; 24(4):445-50. PubMed ID: 11510758
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]