210 related articles for article (PubMed ID: 11391796)
21. Genomic imprinting and environment in hereditary paraganglioma.
Baysal BE
Am J Med Genet C Semin Med Genet; 2004 Aug; 129C(1):85-90. PubMed ID: 15264276
[TBL] [Abstract][Full Text] [Related]
22. Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families.
Hensen EF; Jordanova ES; van Minderhout IJ; Hogendoorn PC; Taschner PE; van der Mey AG; Devilee P; Cornelisse CJ
Oncogene; 2004 May; 23(23):4076-83. PubMed ID: 15064708
[TBL] [Abstract][Full Text] [Related]
23. Phenotype variability of neural crest derived tumours in six Italian families segregating the same founder SDHD mutation Q109X.
Simi L; Sestini R; Ferruzzi P; Gaglianò MS; Gensini F; Mascalchi M; Guerrini L; Pratesi C; Pinzani P; Nesi G; Ercolino T; Genuardi M; Mannelli M
J Med Genet; 2005 Aug; 42(8):e52. PubMed ID: 16061558
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma.
Bayley JP; van Minderhout I; Weiss MM; Jansen JC; Oomen PH; Menko FH; Pasini B; Ferrando B; Wong N; Alpert LC; Williams R; Blair E; Devilee P; Taschner PE
BMC Med Genet; 2006 Jan; 7():1. PubMed ID: 16405730
[TBL] [Abstract][Full Text] [Related]
26. Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas.
Baysal BE; Willett-Brozick JE; Lawrence EC; Drovdlic CM; Savul SA; McLeod DR; Yee HA; Brackmann DE; Slattery WH; Myers EN; Ferrell RE; Rubinstein WS
J Med Genet; 2002 Mar; 39(3):178-83. PubMed ID: 11897817
[TBL] [Abstract][Full Text] [Related]
27. [From gene to disease; from SDHD, a defect in the respiratory chain, to paragangliomas and pheochromocytomas].
Taschner PE; Bröcker-Vriends AH; van der Mey AG
Ned Tijdschr Geneeskd; 2002 Nov; 146(46):2188-90. PubMed ID: 12467161
[TBL] [Abstract][Full Text] [Related]
28. Malignant head and neck paragangliomas in SDHB mutation carriers.
Boedeker CC; Neumann HP; Maier W; Bausch B; Schipper J; Ridder GJ
Otolaryngol Head Neck Surg; 2007 Jul; 137(1):126-9. PubMed ID: 17599579
[TBL] [Abstract][Full Text] [Related]
29. Mutations in SDHC cause autosomal dominant paraganglioma, type 3.
Niemann S; Müller U
Nat Genet; 2000 Nov; 26(3):268-70. PubMed ID: 11062460
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Carotid body paraganglioma and SDHD mutation in a Greek family.
Liapis CD; Bellos JK; Halapas A; Lembessis P; Koutsilieris M; Kostakis A
Anticancer Res; 2005; 25(3c):2449-52. PubMed ID: 16080474
[TBL] [Abstract][Full Text] [Related]
32. A novel mutation of POU3F4 causes congenital profound sensorineural hearing loss in a large Chinese family.
Wang QJ; Li QZ; Rao SQ; Zhao YL; Yuan H; Yang WY; Han DY; Shen Y
Laryngoscope; 2006 Jun; 116(6):944-50. PubMed ID: 16735904
[TBL] [Abstract][Full Text] [Related]
33. SDH mutations in patients affected by paraganglioma syndromes: a personal experience.
Mannelli M; Simi L; Ercolino T; Gaglianò MS; Becherini L; Vinci S; Sestini R; Gensini F; Pinzani P; Mascalchi M; Guerrini L; Pratesi C; Nesi G; Torti F; Cipollini F; Bernini GP; Genuardi M
Ann N Y Acad Sci; 2006 Aug; 1073():183-9. PubMed ID: 17102085
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Spectrum of mutations in USH2A in British patients with Usher syndrome type II.
Leroy BP; Aragon-Martin JA; Weston MD; Bessant DA; Willis C; Webster AR; Bird AC; Kimberling WJ; Payne AM; Bhattacharya SS
Exp Eye Res; 2001 May; 72(5):503-9. PubMed ID: 11311042
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Hereditary paraganglioma-pheochromocytoma syndromes associated with SDHD and RET mutations.
Choi Jdo W; Tucker KM; Lee TT; Chong GC
Head Neck; 2014 Oct; 36(10):E99-E102. PubMed ID: 24375508
[TBL] [Abstract][Full Text] [Related]
38. Analysis of the SLC26A4 gene in patients with Pendred syndrome in Taiwan.
Lai CC; Chiu CY; Shiao AS; Tso YC; Wu YC; Tu TY; Jap TS
Metabolism; 2007 Sep; 56(9):1279-84. PubMed ID: 17697873
[TBL] [Abstract][Full Text] [Related]
39. A novel locus for autosomal dominant nonsyndromic hearing loss identified at 5q31.1-32 in a Chinese pedigree.
Xia J; Deng H; Feng Y; Zhang H; Pan Q; Dai H; Long Z; Tang B; Deng H; Chen Y; Zhang R; Zheng D; He Y; Xia K
J Hum Genet; 2002; 47(12):635-40. PubMed ID: 12522684
[TBL] [Abstract][Full Text] [Related]
40. A novel SDHD mutation associated with neck paraganglioma.
Reboll R; Martínez-Leon J; Zapater E; Juez M; Garcia-Planells J; Martinez-Cadenas C; Basterra J
Acta Otolaryngol; 2011 Oct; 131(10):1110-6. PubMed ID: 21619495
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]