Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1971 1
1974 1
1996 1
1998 1
2004 4
2005 2
2006 6
2007 7
2008 8
2009 13
2010 7
2011 9
2012 9
2013 4
2014 7
2015 8
2016 3
2017 1
2018 3
2019 1
2020 1
2021 7
2022 3
2023 1
2024 2

Text availability

Article attribute

Article type

Publication date

Search Results

96 results

Results by year

Filters applied: . Clear all
Page 1
Arteriovenous malformation.
Young WL, Kwok PY, Pawlikowska L, Lawton MT, Kim H, Hysi PG, Marchuk DA. Young WL, et al. Among authors: pawlikowska l. J Neurosurg. 2007 Apr;106(4):731-2; author reply 732-3. doi: 10.3171/jns.2007.106.4.731. J Neurosurg. 2007. PMID: 17432733 No abstract available.
Molecular basis of intrahepatic cholestasis.
Carlton VE, Pawlikowska L, Bull LN. Carlton VE, et al. Among authors: pawlikowska l. Ann Med. 2004;36(8):606-17. doi: 10.1080/07853890410018916. Ann Med. 2004. PMID: 15768832 Review.
Genotype-Phenotype Correlations in Children with HHT.
Kilian A, Latino GA, White AJ, Clark D, Chakinala MM, Ratjen F, McDonald J, Whitehead K, Gossage JR, Lin D, Henderson K, Pollak J, McWilliams JP, Kim H, Lawton MT, Faughnan ME; the Brain Vascular Malformation Consortium HHT Investigator Group. Kilian A, et al. J Clin Med. 2020 Aug 22;9(9):2714. doi: 10.3390/jcm9092714. J Clin Med. 2020. PMID: 32842615 Free PMC article.
Intracranial Hemorrhage Rate and Lesion Burden in Patients With Familial Cerebral Cavernous Malformation.
Weinsheimer S, Nelson J, Abla AA, Ko NU, Tsang C, Okoye O, Zabramski JM, Akers A, Zafar A, Mabray MC, Hart BL, Morrison L, McCulloch CE, Kim H; Brain Vascular Malformation Consortium Cerebral Cavernous Malformation Investigator Group *. Weinsheimer S, et al. J Am Heart Assoc. 2023 Feb 7;12(3):e027572. doi: 10.1161/JAHA.122.027572. Epub 2023 Jan 25. J Am Heart Assoc. 2023. PMID: 36695309 Free PMC article.
Neurovascular Complications and Pulmonary Arteriovenous Malformation Feeding Artery Size.
Ananiadis T, Faughnan ME, Clark D, Prabhudesai V, Kim H, Lawton MT, Vozoris NT; Brain Vascular Malformation Consortium HHT Investigator Group. Ananiadis T, et al. Ann Am Thorac Soc. 2022 Aug;19(8):1432-1435. doi: 10.1513/AnnalsATS.202202-130RL. Ann Am Thorac Soc. 2022. PMID: 35442860 Free PMC article. No abstract available.
Biology of vascular malformations of the brain.
Leblanc GG, Golanov E, Awad IA, Young WL; Biology of Vascular Malformations of the Brain NINDS Workshop Collaborators. Leblanc GG, et al. Stroke. 2009 Dec;40(12):e694-702. doi: 10.1161/STROKEAHA.109.563692. Epub 2009 Oct 15. Stroke. 2009. PMID: 19834013 Free PMC article. Review.
Quantification metrics for telangiectasia using optical coherence tomography.
Cardinell JL, Ramjist JM, Chen C, Shi W, Nguyen NQ, Yeretsian T, Choi M, Chen D, Clark DS, Curtis A, Kim H, Faughnan ME, Yang VXD; Brain Vascular Malformation Consortium HHT Investigator Group. Cardinell JL, et al. Sci Rep. 2022 Feb 2;12(1):1805. doi: 10.1038/s41598-022-05272-1. Sci Rep. 2022. PMID: 35110554 Free PMC article.
Contemporary human genetic strategies in aging research.
Bloss CS, Pawlikowska L, Schork NJ. Bloss CS, et al. Among authors: pawlikowska l. Ageing Res Rev. 2011 Apr;10(2):191-200. doi: 10.1016/j.arr.2010.07.005. Epub 2010 Aug 10. Ageing Res Rev. 2011. PMID: 20709627 Free PMC article. Review.
Predictors of mortality in patients with hereditary hemorrhagic telangiectasia.
Thompson KP, Nelson J, Kim H, Pawlikowska L, Marchuk DA, Lawton MT, Faughnan ME; Brain Vascular Malformation Consortium HHT Investigator Group. Thompson KP, et al. Among authors: pawlikowska l. Orphanet J Rare Dis. 2021 Jan 6;16(1):12. doi: 10.1186/s13023-020-01579-2. Orphanet J Rare Dis. 2021. PMID: 33407668 Free PMC article.
96 results