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.
169 related articles for article (PubMed ID: 33973836)
1. Hereditary Hemorrhagic Telangiectasia: The Convergence of Genotype, Phenotype, and Imaging in Modern Diagnosis and Management of a Multisystem Disease. Hetts SW; Shieh JT; Ohliger MA; Conrad MB Radiology; 2021 Jul; 300(1):17-30. PubMed ID: 33973836 [TBL] [Abstract][Full Text] [Related]
3. The role of interventional radiology in treatment of patients with hereditary hemorrhagic telangiectasia. Szmygin M; Szmygin P; Drelich K; Pustelniak O; Pech M; Jargiełło T Eur J Radiol; 2023 May; 162():110769. PubMed ID: 36933496 [TBL] [Abstract][Full Text] [Related]
5. Neurovascular manifestations in hereditary hemorrhagic telangiectasia: imaging features and genotype-phenotype correlations. Krings T; Kim H; Power S; Nelson J; Faughnan ME; Young WL; terBrugge KG; AJNR Am J Neuroradiol; 2015 May; 36(5):863-70. PubMed ID: 25572952 [TBL] [Abstract][Full Text] [Related]
6. Gastrointestinal Manifestations of Hereditary Hemorrhagic Telangiectasia (HHT): A Systematic Review of the Literature. Jackson SB; Villano NP; Benhammou JN; Lewis M; Pisegna JR; Padua D Dig Dis Sci; 2017 Oct; 62(10):2623-2630. PubMed ID: 28836046 [TBL] [Abstract][Full Text] [Related]
7. Liver involvement in hereditary hemorrhagic telangiectasia. Buscarini E; Gandolfi S; Alicante S; Londoni C; Manfredi G Abdom Radiol (NY); 2018 Aug; 43(8):1920-1930. PubMed ID: 29987403 [TBL] [Abstract][Full Text] [Related]
8. Association of common candidate variants with vascular malformations and intracranial hemorrhage in hereditary hemorrhagic telangiectasia. Pawlikowska L; Nelson J; Guo DE; McCulloch CE; Lawton MT; Kim H; Faughnan ME; Mol Genet Genomic Med; 2018 May; 6(3):350-356. PubMed ID: 29932521 [TBL] [Abstract][Full Text] [Related]
11. Somatic Mutations in Vascular Malformations of Hereditary Hemorrhagic Telangiectasia Result in Bi-allelic Loss of ENG or ACVRL1. Snellings DA; Gallione CJ; Clark DS; Vozoris NT; Faughnan ME; Marchuk DA Am J Hum Genet; 2019 Nov; 105(5):894-906. PubMed ID: 31630786 [TBL] [Abstract][Full Text] [Related]
12. Hereditary hemorrhagic telangiectasia patient presenting with brain abscess due to silent pulmonary arteriovenous malformation. Themistocleous M; Giakoumettis D; Mitsios A; Anagnostopoulos C; Kalyvas A; Koutsarnakis C Pan Afr Med J; 2016; 25():145. PubMed ID: 28292107 [TBL] [Abstract][Full Text] [Related]
13. The ACVRL1 c.314-35A>G polymorphism is associated with organ vascular malformations in hereditary hemorrhagic telangiectasia patients with ENG mutations, but not in patients with ACVRL1 mutations. Pawlikowska L; Nelson J; Guo DE; McCulloch CE; Lawton MT; Young WL; Kim H; Faughnan ME; Am J Med Genet A; 2015 Jun; 167(6):1262-7. PubMed ID: 25847705 [TBL] [Abstract][Full Text] [Related]