122 related articles for article (PubMed ID: 25783443)
1. Necessity for lifelong follow-up of patients with familial paraganglioma syndrome: A case report.
Persky MJ; Adelman M; Zias E; Myssiorek D
Head Neck; 2015 Dec; 37(12):E174-8. PubMed ID: 25783443
[TBL] [Abstract][Full Text] [Related]
2. Mandibular Lytic Lesion in Familial Paraganglioma Syndrome Type I: A Clinical Conundrum.
Sinha P; Yuen SN; Chernock RD; Haughey BH
Ann Otol Rhinol Laryngol; 2017 Aug; 126(8):615-618. PubMed ID: 28670912
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Synchronous carotid body and thoracic paraganglioma associated with a germline SDHC mutation.
Vandy FC; Sisk G; Berguer R
J Vasc Surg; 2011 Mar; 53(3):805-7. PubMed ID: 21106325
[TBL] [Abstract][Full Text] [Related]
5. A novel mutation in the SDHD gene responsible for familial paraganglioma. Medical and psychological implications.
Prontera P; Ferrando B; Giuliani V; Falcinelli F; Mencarelli A; Rogaia D; Pasini B; Donti E
Genet Couns; 2008; 19(4):413-8. PubMed ID: 19239085
[TBL] [Abstract][Full Text] [Related]
6. Frequent germ-line succinate dehydrogenase subunit D gene mutations in patients with apparently sporadic parasympathetic paraganglioma.
Dannenberg H; Dinjens WN; Abbou M; Van Urk H; Pauw BK; Mouwen D; Mooi WJ; de Krijger RR
Clin Cancer Res; 2002 Jul; 8(7):2061-6. PubMed ID: 12114404
[TBL] [Abstract][Full Text] [Related]
7. Management of carotid body tumors and familial paragangliomas: review of 30 years' experience.
Unlü Y; Becit N; Ceviz M; Koçak H
Ann Vasc Surg; 2009; 23(5):616-20. PubMed ID: 19747612
[TBL] [Abstract][Full Text] [Related]
8. Paraganglioma of the carotid body: treatment strategy and SDH-gene mutations.
Fruhmann J; Geigl JB; Konstantiniuk P; Cohnert TU
Eur J Vasc Endovasc Surg; 2013 May; 45(5):431-6. PubMed ID: 23433498
[TBL] [Abstract][Full Text] [Related]
9. Novel germline SDHD deletion associated with an unusual sympathetic head and neck paraganglioma.
Cadiñanos J; Llorente JL; de la Rosa J; Villameytide JA; Illán R; Durán NS; Murias E; Cabanillas R
Head Neck; 2011 Aug; 33(8):1233-40. PubMed ID: 20310044
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. [Carotid body and glomus vagale tumours (author's transl)].
Rose KG; Jahnke K; Galanski M
HNO; 1979 Jun; 27(6):192-200. PubMed ID: 222718
[TBL] [Abstract][Full Text] [Related]
12. Novel germline SDHD mutation in a patient with recurrent familial carotid body tumor and concomitant pheochromocytoma.
Kim ES; Kim SY; Mo EY; Jang DK; Moon SD; Han JH
Head Neck; 2014 Dec; 36(12):E131-5. PubMed ID: 24599702
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. [Carotid body tumors and familial glomic disease].
Ribet M; Deminatti M; Desaulty-Cousin A; Meignié P
Presse Med (1893); 1969 Jun; 77(29):1043-6. PubMed ID: 4307286
[No Abstract] [Full Text] [Related]
15. [Chemodectomas of the glomus caroticum].
Mazzilli G; Lievore R; Perbellini A; Rossi M; Candiani P
Chir Ital; 1986 Jun; 38(3):269-75. PubMed ID: 3024857
[TBL] [Abstract][Full Text] [Related]
16. Diagnosis and management of hereditary paraganglioma syndrome due to the F933>X67 SDHD mutation.
Marvin ML; Bradford CR; Sisson JC; Gruber SB
Head Neck; 2009 May; 31(5):689-94. PubMed ID: 19072999
[TBL] [Abstract][Full Text] [Related]
17. Biochemically silent abdominal paragangliomas in patients with mutations in the succinate dehydrogenase subunit B gene.
Timmers HJ; Pacak K; Huynh TT; Abu-Asab M; Tsokos M; Merino MJ; Baysal BE; Adams KT; Eisenhofer G
J Clin Endocrinol Metab; 2008 Dec; 93(12):4826-32. PubMed ID: 18840642
[TBL] [Abstract][Full Text] [Related]
18. Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss.
Badenhop RF; Cherian S; Lord RS; Baysal BE; Taschner PE; Schofield PR
Genes Chromosomes Cancer; 2001 Jul; 31(3):255-63. PubMed ID: 11391796
[TBL] [Abstract][Full Text] [Related]
19. Brotherly lumps. Familial occurrence of chemodectoma.
Beard M; McQuarrie DG
Minn Med; 1968 Jan; 51(1):79-82. PubMed ID: 4295142
[No Abstract] [Full Text] [Related]
20. Familial multicentric non-chromaffin paragangliomas: a case report on a patient with glomus jugulare and bilateral carotid body tumours.
Pereira DT; Hunter RD
Clin Oncol; 1980 Sep; 6(3):273-5. PubMed ID: 6253111
[No Abstract] [Full Text] [Related]
[Next] [New Search]