HHT Program Research Publications
We offer opportunities for research enrollment through our collaborations and participation in the Cure HHT Research Network. Here, we highlight some of our recent publications.
2024
Current Practice: Rationale for Screening Children with Hereditary Hemorrhagic Telangiectasia for Brain Vascular Malformations. Beslow LA, White AJ, Krings T, Hammill AM, Lang SS, Baba A, Clancy MS, Olitsky SE, Hetts SW. AJNR Am J Neuroradiol. 2024 Sep 9;45(9):1177-1184.
De Novo Brain Vascular Malformations in Hereditary Hemorrhagic Telangiectasia. Beslow LA, Krings T, Kim H, Hetts SW, Lawton MT, Ratjen F, Whitehead KJ, Gossage JR, McCulloch CE, Clancy M, Bagheri N, Faughnan ME; Brain Vascular Malformation Consortium HHT Investigator Group.
Pediatr Neurol. 2024 Jun;155:120-125.
Brain AVM compactness score in children with hereditary hemorrhagic telangiectasia. Beslow LA, Vossough A, Kim H, Nelson J, Lawton MT, Pollak J, Lin DDM, Ratjen F, Hammill AM, Hetts SW, Gossage JR, Whitehead KJ, Faughnan ME, Krings T; Brain Vascular Malformation Consortium HHT Investigator Group. Childs Nerv Syst. 2024 Jul;40(7):2101-2108.
Beslow L.A., Kim H., Hetts S.W., Ratjen F., Clancy M.S., Gossage J.R., Faughnan M.E. Brain and lung arteriovenous malformation rescreening practices for children and adults with hereditary hemorrhagic telangiectasia. Orphanet Journal of Rare Diseases. (in press)
2020
Cerebrovascular Malformations in a Pediatric Hereditary Hemorrhagic Telangiectasia Cohort. Beslow LA, Breimann J, Licht DJ, Waldman J, Fallacaro S, Pyeritz RE, Goldmuntz E, Vossough A. Pediatr Neurol. 2020 Sep;110:49-54.