344 related articles for article (PubMed ID: 18499773)
1. Phaeochromocytoma in children.
Armstrong R; Sridhar M; Greenhalgh KL; Howell L; Jones C; Landes C; McPartland JL; Moores C; Losty PD; Didi M
Arch Dis Child; 2008 Oct; 93(10):899-904. PubMed ID: 18499773
[TBL] [Abstract][Full Text] [Related]
2. Hereditary pheochromocytoma and paraganglioma.
Mazzaglia PJ
J Surg Oncol; 2012 Oct; 106(5):580-5. PubMed ID: 22648936
[TBL] [Abstract][Full Text] [Related]
3. Childhood phaeochromocytoma and paraganglioma: 100% incidence of genetic mutations and 100% survival.
Hammond PJ; Murphy D; Carachi R; Davidson DF; McIntosh D
J Pediatr Surg; 2010 Feb; 45(2):383-6. PubMed ID: 20152357
[TBL] [Abstract][Full Text] [Related]
4. Phaeochromocytoma, new genes and screening strategies.
Gimenez-Roqueplo AP; Lehnert H; Mannelli M; Neumann H; Opocher G; Maher ER; Plouin PF;
Clin Endocrinol (Oxf); 2006 Dec; 65(6):699-705. PubMed ID: 17121518
[TBL] [Abstract][Full Text] [Related]
5. Pediatric paraganglioma: an early manifestation of an adult disease secondary to germline mutations.
Mora J; Cascón A; Robledo M; Catala A
Pediatr Blood Cancer; 2006 Nov; 47(6):785-9. PubMed ID: 16304664
[TBL] [Abstract][Full Text] [Related]
6. Pheochromocytoma: an update on genetics and management.
Karagiannis A; Mikhailidis DP; Athyros VG; Harsoulis F
Endocr Relat Cancer; 2007 Dec; 14(4):935-56. PubMed ID: 18045948
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Diagnosis and Management of Hereditary Phaeochromocytoma and Paraganglioma.
Lalloo F
Recent Results Cancer Res; 2016; 205():105-24. PubMed ID: 27075351
[TBL] [Abstract][Full Text] [Related]
9. Identification of novel SDHD mutations in patients with phaeochromocytoma and/or paraganglioma.
Cascon A; Ruiz-Llorente S; Cebrian A; Telleria D; Rivero JC; Diez JJ; Lopez-Ibarra PJ; Jaunsolo MA; Benitez J; Robledo M
Eur J Hum Genet; 2002 Aug; 10(8):457-61. PubMed ID: 12111639
[TBL] [Abstract][Full Text] [Related]
10. Genetic testing in pheochromocytoma: increasing importance for clinical decision making.
Bornstein SR; Gimenez-Roqueplo AP
Ann N Y Acad Sci; 2006 Aug; 1073():94-103. PubMed ID: 17102076
[TBL] [Abstract][Full Text] [Related]
11. Genetic basis of phaeochromocytoma and paraganglioma.
Benn DE; Robinson BG
Best Pract Res Clin Endocrinol Metab; 2006 Sep; 20(3):435-50. PubMed ID: 16980204
[TBL] [Abstract][Full Text] [Related]
12. Genetics of phaeochromocytoma.
Maher ER
Br Med Bull; 2006; 79-80():141-51. PubMed ID: 17339275
[TBL] [Abstract][Full Text] [Related]
13. Molecular genetic diagnosis of von Hippel-Lindau disease in familial phaeochromocytoma.
Crossey PA; Eng C; Ginalska-Malinowska M; Lennard TW; Wheeler DC; Ponder BA; Maher ER
J Med Genet; 1995 Nov; 32(11):885-6. PubMed ID: 8592333
[TBL] [Abstract][Full Text] [Related]
14. Genetic predisposition to phaeochromocytoma: analysis of candidate genes GDNF, RET and VHL.
Woodward ER; Eng C; McMahon R; Voutilainen R; Affara NA; Ponder BA; Maher ER
Hum Mol Genet; 1997 Jul; 6(7):1051-6. PubMed ID: 9215674
[TBL] [Abstract][Full Text] [Related]
15. [Diagnostic and therapeutic procedures in pheochromocytoma: current trends].
Widimský J; Zelinka T; Petrák O; Strauch B; Safarík L; Kasalický M; Vranková A; Holaj R
Vnitr Lek; 2007 Apr; 53(4):428-33. PubMed ID: 17578179
[TBL] [Abstract][Full Text] [Related]
16. New insights in the genetics of adrenocortical tumors, pheochromocytomas and paragangliomas.
Bertherat J; Gimenez-Roqueplo AP
Horm Metab Res; 2005 Jun; 37(6):384-90. PubMed ID: 16001332
[TBL] [Abstract][Full Text] [Related]
17. Paediatric bilateral adrenal phaeochromocytomas in association with a novel mutation in the von Hippel Lindau gene.
Kim L; Holland AJ; Srinivasan S; Cowell CT; Benn DE; Robinson BG
J Paediatr Child Health; 2008 Sep; 44(9):514-6. PubMed ID: 18928468
[TBL] [Abstract][Full Text] [Related]
18. Familial paraganglioma syndromes.
Chetty R
J Clin Pathol; 2010 Jun; 63(6):488-91. PubMed ID: 20498024
[TBL] [Abstract][Full Text] [Related]
19. SDH mutations in tumorigenesis and inherited endocrine tumours: lesson from the phaeochromocytoma-paraganglioma syndromes.
Pasini B; Stratakis CA
J Intern Med; 2009 Jul; 266(1):19-42. PubMed ID: 19522823
[TBL] [Abstract][Full Text] [Related]
20. Novel mutation in the TMEM127 gene associated with phaeochromocytoma.
Elston MS; Meyer-Rochow GY; Prosser D; Love DR; Conaglen JV
Intern Med J; 2013 Apr; 43(4):449-51. PubMed ID: 23551308
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
