These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
23. Universal Germline Panel Testing for Individuals With Pheochromocytoma and Paraganglioma Produces High Diagnostic Yield. Horton C; LaDuca H; Deckman A; Durda K; Jackson M; Richardson ME; Tian Y; Yussuf A; Jasperson K; Else T J Clin Endocrinol Metab; 2022 Apr; 107(5):e1917-e1923. PubMed ID: 35026032 [TBL] [Abstract][Full Text] [Related]
24. Identification of novel SDHD mutations in patients with phaeochromocytoma and/or paraganglioma. Cascon A; Ruiz-Llorente S; Cebrian A; Telleria D; Rivero JC; Diez JJ; Lopez-Ibarra PJ; Jaunsolo MA; Benitez J; Robledo M Eur J Hum Genet; 2002 Aug; 10(8):457-61. PubMed ID: 12111639 [TBL] [Abstract][Full Text] [Related]
25. Whole exome sequencing is an efficient and sensitive method for detection of germline mutations in patients with phaeochromcytomas and paragangliomas. McInerney-Leo AM; Marshall MS; Gardiner B; Benn DE; McFarlane J; Robinson BG; Brown MA; Leo PJ; Clifton-Bligh RJ; Duncan EL Clin Endocrinol (Oxf); 2014 Jan; 80(1):25-33. PubMed ID: 24102379 [TBL] [Abstract][Full Text] [Related]
26. MAX mutations status in Swedish patients with pheochromocytoma and paraganglioma tumours. Crona J; Maharjan R; Delgado Verdugo A; Stålberg P; Granberg D; Hellman P; Björklund P Fam Cancer; 2014 Mar; 13(1):121-5. PubMed ID: 23743562 [TBL] [Abstract][Full Text] [Related]
28. Simple and rapid characterization of novel large germline deletions in SDHB, SDHC and SDHD-related paraganglioma. Hoekstra AS; van den Ende B; Julià XP; van Breemen L; Scheurwater K; Tops CM; Malinoc A; Devilee P; Neumann HP; Bayley JP Clin Genet; 2017 Apr; 91(4):536-544. PubMed ID: 27485256 [TBL] [Abstract][Full Text] [Related]
29. Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas. Benn DE; Croxson MS; Tucker K; Bambach CP; Richardson AL; Delbridge L; Pullan PT; Hammond J; Marsh DJ; Robinson BG Oncogene; 2003 Mar; 22(9):1358-64. PubMed ID: 12618761 [TBL] [Abstract][Full Text] [Related]
30. Heterogeneous genetic background of the association of pheochromocytoma/paraganglioma and pituitary adenoma: results from a large patient cohort. Dénes J; Swords F; Rattenberry E; Stals K; Owens M; Cranston T; Xekouki P; Moran L; Kumar A; Wassif C; Fersht N; Baldeweg SE; Morris D; Lightman S; Agha A; Rees A; Grieve J; Powell M; Boguszewski CL; Dutta P; Thakker RV; Srirangalingam U; Thompson CJ; Druce M; Higham C; Davis J; Eeles R; Stevenson M; O'Sullivan B; Taniere P; Skordilis K; Gabrovska P; Barlier A; Webb SM; Aulinas A; Drake WM; Bevan JS; Preda C; Dalantaeva N; Ribeiro-Oliveira A; Garcia IT; Yordanova G; Iotova V; Evanson J; Grossman AB; Trouillas J; Ellard S; Stratakis CA; Maher ER; Roncaroli F; Korbonits M J Clin Endocrinol Metab; 2015 Mar; 100(3):E531-41. PubMed ID: 25494863 [TBL] [Abstract][Full Text] [Related]
31. Case report of a man with multiple paragangliomas and pathogenic germline variants in both NF1 and SDHD. Chatzikyriakou P; Touska P; Moonim MT; Obholzer R; Afridi S; Sandison A; Oakey RJ; Izatt L Cancer Genet; 2021 Aug; 256-257():110-114. PubMed ID: 34107390 [TBL] [Abstract][Full Text] [Related]
32. Whole Exome Sequencing Identifies Novel Genetic Alterations in Patients with Pheochromocytoma/Paraganglioma. Seo SH; Kim JH; Kim MJ; Cho SI; Kim SJ; Kang H; Shin CS; Park SS; Lee KE; Seong MW Endocrinol Metab (Seoul); 2020 Dec; 35(4):909-917. PubMed ID: 33397043 [TBL] [Abstract][Full Text] [Related]
33. Cost-minimization analysis of sequential genetic testing versus targeted next-generation sequencing gene panels in patients with pheochromocytoma and paraganglioma. Pipitprapat W; Pattanaprateep O; Iemwimangsa N; Sensorn I; Panthan B; Jiaranai P; Chantratita W; Sorapipatcharoen K; Poomthavorn P; Mahachoklertwattana P; Sura T; Tunteeratum A; Srichan K; Sriphrapradang C Ann Med; 2021 Dec; 53(1):1244-1256. PubMed ID: 34309460 [TBL] [Abstract][Full Text] [Related]
34. Genetics and molecular pathogenesis of pheochromocytoma and paraganglioma. Galan SR; Kann PH Clin Endocrinol (Oxf); 2013 Feb; 78(2):165-75. PubMed ID: 23061808 [TBL] [Abstract][Full Text] [Related]