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.
184 related articles for article (PubMed ID: 31046099)
41. Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene. Schiavi F; Boedeker CC; Bausch B; Peçzkowska M; Gomez CF; Strassburg T; Pawlu C; Buchta M; Salzmann M; Hoffmann MM; Berlis A; Brink I; Cybulla M; Muresan M; Walter MA; Forrer F; Välimäki M; Kawecki A; Szutkowski Z; Schipper J; Walz MK; Pigny P; Bauters C; Willet-Brozick JE; Baysal BE; Januszewicz A; Eng C; Opocher G; Neumann HP; JAMA; 2005 Oct; 294(16):2057-63. PubMed ID: 16249420 [TBL] [Abstract][Full Text] [Related]
42. Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome. Panizza E; Ercolino T; Mori L; Rapizzi E; Castellano M; Opocher G; Ferrero I; Neumann HP; Mannelli M; Goffrini P Hum Mol Genet; 2013 Feb; 22(4):804-15. PubMed ID: 23175444 [TBL] [Abstract][Full Text] [Related]
43. 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]
45. Paraganglioma of the Vagina Associated With Germline SDHB Mutation: Report of a Case With Review of the Literature. Wong RW; Liu APY; Choi CKM; Chan AOK Int J Gynecol Pathol; 2020 Nov; 39(6):599-604. PubMed ID: 31851064 [TBL] [Abstract][Full Text] [Related]
46. Early-onset renal cell carcinoma as a novel extraparaganglial component of SDHB-associated heritable paraganglioma. Vanharanta S; Buchta M; McWhinney SR; Virta SK; Peçzkowska M; Morrison CD; Lehtonen R; Januszewicz A; Järvinen H; Juhola M; Mecklin JP; Pukkala E; Herva R; Kiuru M; Nupponen NN; Aaltonen LA; Neumann HP; Eng C Am J Hum Genet; 2004 Jan; 74(1):153-9. PubMed ID: 14685938 [TBL] [Abstract][Full Text] [Related]
47. Mutational profile and genotype/phenotype correlation of non-familial pheochromocytoma and paraganglioma. Albattal S; Alswailem M; Moria Y; Al-Hindi H; Dasouki M; Abouelhoda M; Alkhail HA; Alsuhaibani E; Alzahrani AS Oncotarget; 2019 Oct; 10(57):5919-5931. PubMed ID: 31666924 [TBL] [Abstract][Full Text] [Related]
48. Silent genetic alterations identified by targeted next-generation sequencing in pheochromocytoma/paraganglioma: A clinicopathological correlations. Pillai S; Gopalan V; Lo CY; Liew V; Smith RA; Lam AK Exp Mol Pathol; 2017 Feb; 102(1):41-46. PubMed ID: 27986441 [TBL] [Abstract][Full Text] [Related]
49. Chromosomal changes in sporadic and familial head and neck paragangliomas. Sevilla MA; Hermsen MA; Weiss MM; Grimbergen A; Balbín M; Llorente JL; Rodrigo JP; Suárez C Otolaryngol Head Neck Surg; 2009 May; 140(5):724-9. PubMed ID: 19393419 [TBL] [Abstract][Full Text] [Related]