122 related articles for article (PubMed ID: 20583550)
1. Early presentation of familial paraganglioma with SDHB mutation in a 13 year old child and its mother.
Santiago AH; Campbell BT; Estrada DE
J Pediatr Endocrinol Metab; 2010 Apr; 23(4):419-22. PubMed ID: 20583550
[TBL] [Abstract][Full Text] [Related]
2. De novo SDHB gene mutation in a family with extra-adrenal paraganglioma.
Mauer CB; Reys B; Wickiser J
Fam Cancer; 2020 Jul; 19(3):269-271. PubMed ID: 32200538
[TBL] [Abstract][Full Text] [Related]
3. Identification of succinate dehydrogenase-deficient bladder paragangliomas.
Mason EF; Sadow PM; Wagner AJ; Remillard SP; Flood TA; Belanger EC; Hornick JL; Barletta JA
Am J Surg Pathol; 2013 Oct; 37(10):1612-8. PubMed ID: 23797725
[TBL] [Abstract][Full Text] [Related]
4. R46Q mutation in the succinate dehydrogenase B gene (SDHB) in a Japanese family with both abdominal and thoracic paraganglioma following metastasis.
Takekoshi K; Isobe K; Suzuki H; Nissato S; Kawakami Y; Kawai K; Yamada N
Endocr J; 2008 May; 55(2):299-303. PubMed ID: 18362451
[TBL] [Abstract][Full Text] [Related]
5. Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations.
Neumann HP; Pawlu C; Peczkowska M; Bausch B; McWhinney SR; Muresan M; Buchta M; Franke G; Klisch J; Bley TA; Hoegerle S; Boedeker CC; Opocher G; Schipper J; Januszewicz A; Eng C;
JAMA; 2004 Aug; 292(8):943-51. PubMed ID: 15328326
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Bronchial Paraganglioma with SDHB Deficiency.
Ghigna MR; Dorfmuller P; Crutu A; Fadel E; de Montpréville VT
Endocr Pathol; 2016 Dec; 27(4):332-337. PubMed ID: 26895210
[TBL] [Abstract][Full Text] [Related]
8. Four generations of SDHB-related disease: complexities in management.
Srirangalingam U; LeCain M; Tufton N; Akker SA; Drake WM; Metcalfe K
Fam Cancer; 2017 Apr; 16(2):279-282. PubMed ID: 27896548
[TBL] [Abstract][Full Text] [Related]
9. High frequency of SDHB germline mutations in patients with malignant catecholamine-producing paragangliomas: implications for genetic testing.
Brouwers FM; Eisenhofer G; Tao JJ; Kant JA; Adams KT; Linehan WM; Pacak K
J Clin Endocrinol Metab; 2006 Nov; 91(11):4505-9. PubMed ID: 16912137
[TBL] [Abstract][Full Text] [Related]
10. Cervical paragangliomas: is SDH genetic analysis systematically required?
Fakhry N; Niccoli-Sire P; Barlier-Seti A; Giorgi R; Giovanni A; Zanaret M
Eur Arch Otorhinolaryngol; 2008 May; 265(5):557-63. PubMed ID: 17987308
[TBL] [Abstract][Full Text] [Related]
11. A large deletion in the succinate dehydrogenase B gene (SDHB) in a Japanese patient with abdominal paraganglioma and concomitant metastasis.
Kodama H; Iihara M; Nissato S; Isobe K; Kawakami Y; Okamoto T; Takekoshi K
Endocr J; 2010; 57(4):351-6. PubMed ID: 20379037
[TBL] [Abstract][Full Text] [Related]
12. A Novel SDHB IVS2-2A>C Mutation Is Responsible for Hereditary Pheochromocytoma/Paraganglioma Syndrome.
Yamanaka M; Shiga K; Fujiwara S; Mizuguchi Y; Yasuda S; Ishizawa K; Saiki Y; Higashi K; Ogawa T; Kimura N; Horii A
Tohoku J Exp Med; 2018 Jun; 245(2):99-105. PubMed ID: 29925701
[TBL] [Abstract][Full Text] [Related]
13. Malignant paraganglioma associated with succinate dehydrogenase subunit B in an 8-year-old child: the age of first screening?
Prodanov T; Havekes B; Nathanson KL; Adams KT; Pacak K
Pediatr Nephrol; 2009 Jun; 24(6):1239-42. PubMed ID: 19189136
[TBL] [Abstract][Full Text] [Related]
14. Sporadic paraganglioma caused by de novo SDHB mutations in a 6-year-old girl.
Imamura H; Muroya K; Tanaka E; Konomoto T; Moritake H; Sato T; Kimura N; Takekoshi K; Nunoi H
Eur J Pediatr; 2016 Jan; 175(1):137-41. PubMed ID: 26283294
[TBL] [Abstract][Full Text] [Related]
15. Cardiac Paraganglioma Arising From the Right Atrioventricular Groove in a Paraganglioma-Pheochromocytoma Family Syndrome With Evidence of SDHB Gene Mutation: An Unusual Presentation.
Del Forno B; Zingaro C; Di Palma E; Capestro F; Rescigno G; Torracca L
Ann Thorac Surg; 2016 Sep; 102(3):e215-e216. PubMed ID: 27549546
[TBL] [Abstract][Full Text] [Related]
16. The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas.
Burnichon N; Rohmer V; Amar L; Herman P; Leboulleux S; Darrouzet V; Niccoli P; Gaillard D; Chabrier G; Chabolle F; Coupier I; Thieblot P; Lecomte P; Bertherat J; Wion-Barbot N; Murat A; Venisse A; Plouin PF; Jeunemaitre X; Gimenez-Roqueplo AP;
J Clin Endocrinol Metab; 2009 Aug; 94(8):2817-27. PubMed ID: 19454582
[TBL] [Abstract][Full Text] [Related]
17. Low penetrance of a SDHB mutation in a large Dutch paraganglioma family.
Hes FJ; Weiss MM; Woortman SA; de Miranda NF; van Bunderen PA; Bonsing BA; Stokkel MP; Morreau H; Romijn JA; Jansen JC; Vriends AH; Bayley JP; Corssmit EP
BMC Med Genet; 2010 Jun; 11():92. PubMed ID: 20540712
[TBL] [Abstract][Full Text] [Related]
18. High prevalence of SDHB mutations in head and neck paraganglioma in Belgium.
Persu A; Hamoir M; Grégoire V; Garin P; Duvivier E; Reychler H; Chantrain G; Mortier G; Mourad M; Maiter D; Vikkula M
J Hypertens; 2008 Jul; 26(7):1395-401. PubMed ID: 18551016
[TBL] [Abstract][Full Text] [Related]
19. A case of familial paraganglioma syndrome type 4 caused by a mutation in the SDHB gene.
Drucker AM; Houlden RL
Nat Clin Pract Endocrinol Metab; 2006 Dec; 2(12):702-6; quiz following 706. PubMed ID: 17143317
[TBL] [Abstract][Full Text] [Related]
20. Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes.
Benn DE; Gimenez-Roqueplo AP; Reilly JR; Bertherat J; Burgess J; Byth K; Croxson M; Dahia PL; Elston M; Gimm O; Henley D; Herman P; Murday V; Niccoli-Sire P; Pasieka JL; Rohmer V; Tucker K; Jeunemaitre X; Marsh DJ; Plouin PF; Robinson BG
J Clin Endocrinol Metab; 2006 Mar; 91(3):827-36. PubMed ID: 16317055
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]