111 related articles for article (PubMed ID: 11519521)
21. [Complex II (succinate-ubiquinone reductase) deficiency].
Nonaka I
Ryoikibetsu Shokogun Shirizu; 2001; (36):132-4. PubMed ID: 11596343
[No Abstract] [Full Text] [Related]
22. Moving Beyond "Lumpology": PET/CT Imaging of Pheochromocytoma and Paraganglioma.
Hofman MS; Hicks RJ
Clin Cancer Res; 2015 Sep; 21(17):3815-7. PubMed ID: 26152741
[TBL] [Abstract][Full Text] [Related]
23. Diagnosing patients with hereditary paraganglial tumours.
Erlic Z; Neumann HP
Lancet Oncol; 2009 Aug; 10(8):741. PubMed ID: 19647193
[No Abstract] [Full Text] [Related]
24. G12S and H50R variations are polymorphisms in the SDHD gene.
Cascón A; Ruiz-Llorente S; Cebrián A; Letón R; Tellería D; Benítez J; Robledo M
Genes Chromosomes Cancer; 2003 Jun; 37(2):220-1. PubMed ID: 12696072
[No Abstract] [Full Text] [Related]
25. Mitochondrial gene linked to rare hereditary tumour.
Senior K
Mol Med Today; 2000 May; 6(5):183. PubMed ID: 10782063
[No Abstract] [Full Text] [Related]
26. An unusual succinate dehydrogenase gene mutation C in a case of laryngeal paraganglioma.
Garrel R; Raynaud P; Raingeard I; Muyshondt C; Gardiner Q; Guerrier B; Pujol P; Coupier I
J Laryngol Otol; 2009 Jan; 123(1):141-4. PubMed ID: 18267044
[TBL] [Abstract][Full Text] [Related]
27. Where metabolism meets oncogenesis: another false lead?
Grossman AB
Lancet Oncol; 2010 Apr; 11(4):309-10. PubMed ID: 20071234
[No Abstract] [Full Text] [Related]
28. Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibility.
Astuti D; Hart-Holden N; Latif F; Lalloo F; Black GC; Lim C; Moran A; Grossman AB; Hodgson SV; Freemont A; Ramsden R; Eng C; Evans DG; Maher ER
Clin Endocrinol (Oxf); 2003 Dec; 59(6):728-33. PubMed ID: 14974914
[TBL] [Abstract][Full Text] [Related]
29. New advances in the genetics of pheochromocytoma and paraganglioma syndromes.
Gimenez-Roqueplo AP
Ann N Y Acad Sci; 2006 Aug; 1073():112-21. PubMed ID: 17102078
[TBL] [Abstract][Full Text] [Related]
30. Late-onset optic atrophy, ataxia, and myopathy associated with a mutation of a complex II gene.
Birch-Machin MA; Taylor RW; Cochran B; Ackrell BA; Turnbull DM
Ann Neurol; 2000 Sep; 48(3):330-5. PubMed ID: 10976639
[TBL] [Abstract][Full Text] [Related]
31. Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma.
Baysal BE; Ferrell RE; Willett-Brozick JE; Lawrence EC; Myssiorek D; Bosch A; van der Mey A; Taschner PE; Rubinstein WS; Myers EN; Richard CW; Cornelisse CJ; Devilee P; Devlin B
Science; 2000 Feb; 287(5454):848-51. PubMed ID: 10657297
[TBL] [Abstract][Full Text] [Related]
32. Malignant paraganglioma caused by a novel germline mutation of the succinate dehydrogenase D-gene--a case report.
Papaspyrou K; Rossmann H; Fottner C; Weber MM; Mann W; Lackner KJ; Helling K
Head Neck; 2008 Jul; 30(7):964-9. PubMed ID: 18213727
[TBL] [Abstract][Full Text] [Related]
33. Etiopathogenesis and clinical presentation of carotid body tumors.
Baysal BE; Myers EN
Microsc Res Tech; 2002 Nov; 59(3):256-61. PubMed ID: 12384970
[TBL] [Abstract][Full Text] [Related]
34. A novel mutation in the SDHD gene in a family with inherited paragangliomas--implications of genetic diagnosis for follow up and treatment.
Renard L; Godfraind C; Boon LM; Vikkula M
Head Neck; 2003 Feb; 25(2):146-51. PubMed ID: 12509798
[TBL] [Abstract][Full Text] [Related]
35. Gross SDHB deletions in patients with paraganglioma detected by multiplex PCR: a possible hot spot?
Cascón A; Montero-Conde C; Ruiz-Llorente S; Mercadillo F; Letón R; Rodríguez-Antona C; Martínez-Delgado B; Delgado M; Díez A; Rovira A; Díaz JA; Robledo M
Genes Chromosomes Cancer; 2006 Mar; 45(3):213-9. PubMed ID: 16258955
[TBL] [Abstract][Full Text] [Related]
36. K40E: a novel succinate dehydrogenase (SDH)B mutation causing familial phaeochromocytoma and paraganglioma.
McDonnell CM; Benn DE; Marsh DJ; Robinson BG; Zacharin MR
Clin Endocrinol (Oxf); 2004 Oct; 61(4):510-4. PubMed ID: 15473885
[TBL] [Abstract][Full Text] [Related]
37. Germline SDHB mutations are common in patients with apparently sporadic sympathetic paragangliomas.
Klein RD; Jin L; Rumilla K; Young WF; Lloyd RV
Diagn Mol Pathol; 2008 Jun; 17(2):94-100. PubMed ID: 18382370
[TBL] [Abstract][Full Text] [Related]
38. Molecular pathways linking the pheochromocytoma susceptibility genes.
Leow MK
Pediatr Blood Cancer; 2007 Dec; 49(7):1050-1; author reply 1052-3. PubMed ID: 17243134
[No Abstract] [Full Text] [Related]
39. [Pheochromocytomas and paragangliomas: implications of new insights for diagnosis and treatment].
van der Kleij-Corssmit EP; Havekes B; Vriends AH; Jansen JC; Romijn JA
Ned Tijdschr Geneeskd; 2008 Mar; 152(9):489-93. PubMed ID: 18389879
[TBL] [Abstract][Full Text] [Related]
40. cDNA microarray analysis assists in diagnosis of malignant intrarenal pheochromocytoma originally masquerading as a renal cell carcinoma.
Takahashi M; Yang XJ; McWhinney S; Sano N; Eng C; Kagawa S; Teh BT; Kanayama HO
J Med Genet; 2005 Aug; 42(8):e48. PubMed ID: 16061554
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
