U54NS065705/NS/NINDS NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2011	1
2012	5
2013	6
2014	2
2015	4
2016	1
2020	1
2024	0

1

Comi AM. Comi AM. Handb Clin Neurol. 2015;132:157-68. doi: 10.1016/B978-0-444-62702-5.00011-1. Handb Clin Neurol. 2015. PMID: 26564078 Review.

2

Current Therapeutic Options in Sturge-Weber Syndrome.

Comi A. Comi A. Semin Pediatr Neurol. 2015 Dec;22(4):295-301. doi: 10.1016/j.spen.2015.10.005. Epub 2015 Nov 11. Semin Pediatr Neurol. 2015. PMID: 26706016 Free PMC article. Review.

3

Genetics of cerebral cavernous malformations: current status and future prospects.

Choquet H, Pawlikowska L, Lawton MT, Kim H. Choquet H, et al. J Neurosurg Sci. 2015 Sep;59(3):211-20. Epub 2015 Apr 22. J Neurosurg Sci. 2015. PMID: 25900426 Free PMC article. Review.

4

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.

5

Updates and future horizons on the understanding, diagnosis, and treatment of Sturge-Weber syndrome brain involvement.

Lo W, Marchuk DA, Ball KL, Juhász C, Jordan LC, Ewen JB, Comi A; Brain Vascular Malformation Consortium National Sturge-Weber Syndrome Workgroup. Lo W, et al. Dev Med Child Neurol. 2012 Mar;54(3):214-23. doi: 10.1111/j.1469-8749.2011.04169.x. Epub 2011 Dec 23. Dev Med Child Neurol. 2012. PMID: 22191476 Free PMC article. Review.

6

Urine vascular biomarkers in Sturge-Weber syndrome.

Sreenivasan AK, Bachur CD, Lanier KE, Curatolo AS, Connors SM, Moses MA, Comi AM. Sreenivasan AK, et al. Vasc Med. 2013 Jun;18(3):122-8. doi: 10.1177/1358863X13486312. Vasc Med. 2013. PMID: 23720035

7

Cytochrome P450 and matrix metalloproteinase genetic modifiers of disease severity in Cerebral Cavernous Malformation type 1.

Choquet H, Trapani E, Goitre L, Trabalzini L, Akers A, Fontanella M, Hart BL, Morrison LA, Pawlikowska L, Kim H, Retta SF. Choquet H, et al. Free Radic Biol Med. 2016 Mar;92:100-109. doi: 10.1016/j.freeradbiomed.2016.01.008. Epub 2016 Jan 19. Free Radic Biol Med. 2016. PMID: 26795600 Free PMC article.

8

Case report of subdural hematoma in a patient with Sturge-Weber syndrome and literature review: questions and implications for therapy.

Lopez J, Yeom KW, Comi A, Van Haren K. Lopez J, et al. J Child Neurol. 2013 May;28(5):672-5. doi: 10.1177/0883073812449514. Epub 2012 Jul 17. J Child Neurol. 2013. PMID: 22805242 Review.

9

Sturge-Weber syndrome and port-wine stains caused by somatic mutation in GNAQ.

Shirley MD, Tang H, Gallione CJ, Baugher JD, Frelin LP, Cohen B, North PE, Marchuk DA, Comi AM, Pevsner J. Shirley MD, et al. N Engl J Med. 2013 May 23;368(21):1971-9. doi: 10.1056/NEJMoa1213507. Epub 2013 May 8. N Engl J Med. 2013. PMID: 23656586 Free PMC article.

10

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; Brain Vascular Malformation Consortium HHT Investigator Group. Krings T, et al. AJNR Am J Neuroradiol. 2015 May;36(5):863-70. doi: 10.3174/ajnr.A4210. Epub 2015 Jan 8. AJNR Am J Neuroradiol. 2015. PMID: 25572952 Free PMC article.

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