157 related articles for article (PubMed ID: 24509376)
1. SDHB gene mutation in a carotid body paraganglioma: case report and review of the paraganglioma syndromes.
Peterson LA; Litzendorf M; Ringel MD; Vaccaro PS
Ann Vasc Surg; 2014 Jul; 28(5):1321.e9-12. PubMed ID: 24509376
[TBL] [Abstract][Full Text] [Related]
2. The presence of SDHB mutations should modify surgical indications for carotid body paragangliomas.
Ellis RJ; Patel D; Prodanov T; Nilubol N; Pacak K; Kebebew E
Ann Surg; 2014 Jul; 260(1):158-62. PubMed ID: 24169168
[TBL] [Abstract][Full Text] [Related]
3. Recurrent familial malignant carotid body tumour presenting with lymph node metastasis: case report, and review of diagnosis and management of familial carotid body tumours.
Hall TC; Renwick P; Stafford ND
J Laryngol Otol; 2010 Dec; 124(12):1344-6. PubMed ID: 20573294
[TBL] [Abstract][Full Text] [Related]
4. Head and Neck Paraganglioma Atypically Carrying a Succinate Dehydrogenase Subunit B Mutation (L157X).
Takeshima K; Ariyasu H; Uraki S; Kitahara C; Morita S; Inaba H; Iwakura H; Warigaya K; Murata SI; Yamazaki Y; Sasano H; Akamizu T
Intern Med; 2020 May; 59(9):1167-1171. PubMed ID: 32023584
[TBL] [Abstract][Full Text] [Related]
5. A novel SDHB mutation associated with hereditary head and neck paraganglioma.
Peck BW; Rich TA; Jimenez C; Kupferman ME
Laryngoscope; 2011 Dec; 121(12):2572-5. PubMed ID: 22109755
[TBL] [Abstract][Full Text] [Related]
6. Case Report: Genetic Alterations Associated with the Progression of Carotid Paraganglioma.
Pavlov V; Snezhkina A; Kalinin D; Golovyuk A; Kobelyatskaya A; Bakhtogarimov I; Volchenko N; Krasnov G; Kudryavtseva A
Curr Issues Mol Biol; 2021 Dec; 43(3):2266-2275. PubMed ID: 34940133
[TBL] [Abstract][Full Text] [Related]
7. The genetics of paragangliomas: a review.
Martin TP; Irving RM; Maher ER
Clin Otolaryngol; 2007 Feb; 32(1):7-11. PubMed ID: 17298303
[TBL] [Abstract][Full Text] [Related]
8. Contiguous bilateral head and neck paragangliomas in a carrier of the SDHB germline mutation.
Collins N; Dietzek A
J Vasc Surg; 2012 Jan; 55(1):216-9. PubMed ID: 21820839
[TBL] [Abstract][Full Text] [Related]
9. SDH deficiency is very common in carotid body paragangliomas: Genetic counseling and testing should be offered to all patients.
Sarkis LM; Clifton-Bligh R; Veivers D; Gill AJ
Head Neck; 2023 Jun; 45(6):1497-1502. PubMed ID: 37010365
[TBL] [Abstract][Full Text] [Related]
10. High prevalence of occult paragangliomas in asymptomatic carriers of SDHD and SDHB gene mutations.
Heesterman BL; Bayley JP; Tops CM; Hes FJ; van Brussel BT; Corssmit EP; Hamming JF; van der Mey AG; Jansen JC
Eur J Hum Genet; 2013 Apr; 21(4):469-70. PubMed ID: 22948026
[TBL] [Abstract][Full Text] [Related]
11. [The carotid body paraganglioma: a rare swelling of the neck].
den Brave PS; Balm AJ; Balm R
Ned Tijdschr Geneeskd; 2015; 159():A9230. PubMed ID: 26629601
[TBL] [Abstract][Full Text] [Related]
12. [Paragangliomas and paraganglioma syndromes].
Boedeker CC
Laryngorhinootologie; 2011 Mar; 90 Suppl 1():S56-82. PubMed ID: 21523634
[TBL] [Abstract][Full Text] [Related]
13. A novel G106D alteration of the SDHD gene in a pedigree with familial paraganglioma.
Ogawa K; Shiga K; Saijo S; Ogawa T; Kimura N; Horii A
Am J Med Genet A; 2006 Nov; 140(22):2441-6. PubMed ID: 17041923
[TBL] [Abstract][Full Text] [Related]
14. [Uncommon case of paraganglioma syndrome in combination with malignant paraganglioma].
Schmahl K; Atamna N; Schönijahn T; Lülsdorf P; Göller T; Jacob R
Laryngorhinootologie; 2008 Feb; 87(2):112-7. PubMed ID: 18345539
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Head and neck paragangliomas: clinical and molecular genetic classification.
Offergeld C; Brase C; Yaremchuk S; Mader I; Rischke HC; Gläsker S; Schmid KW; Wiech T; Preuss SF; Suárez C; Kopeć T; Patocs A; Wohllk N; Malekpour M; Boedeker CC; Neumann HP
Clinics (Sao Paulo); 2012; 67 Suppl 1(Suppl 1):19-28. PubMed ID: 22584701
[TBL] [Abstract][Full Text] [Related]
17. Identification of a novel SDHB c.563 T > C mutation responsible for Paraganglioma syndrome and genetic analysis of the SDHB gene in China: a case report.
Chen H; Yao W; He Q; Yu X; Bian B
BMC Med Genet; 2020 May; 21(1):116. PubMed ID: 32460727
[TBL] [Abstract][Full Text] [Related]
18. An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis.
van Nederveen FH; Gaal J; Favier J; Korpershoek E; Oldenburg RA; de Bruyn EM; Sleddens HF; Derkx P; Rivière J; Dannenberg H; Petri BJ; Komminoth P; Pacak K; Hop WC; Pollard PJ; Mannelli M; Bayley JP; Perren A; Niemann S; Verhofstad AA; de Bruïne AP; Maher ER; Tissier F; Méatchi T; Badoual C; Bertherat J; Amar L; Alataki D; Van Marck E; Ferrau F; François J; de Herder WW; Peeters MP; van Linge A; Lenders JW; Gimenez-Roqueplo AP; de Krijger RR; Dinjens WN
Lancet Oncol; 2009 Aug; 10(8):764-71. PubMed ID: 19576851
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. A novel succinate dehydrogenase subunit B germline variant associated with head and neck paraganglioma in a Dutch kindred: A family-based study.
de Vos B; Rijken JA; Adank MA; Hoksbergen AWJ; Bayley JP; Leemans CR; Hensen EF
Clin Otolaryngol; 2018 Jun; 43(3):841-845. PubMed ID: 29292578
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
