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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2014 | 2 |
2015 | 1 |
2016 | 2 |
2017 | 2 |
2019 | 2 |
2024 | 0 |
Search Results
6 results
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Page 1
Cavernous angiomas: deconstructing a neurosurgical disease.
J Neurosurg. 2019 Jul 1;131(1):1-13. doi: 10.3171/2019.3.JNS181724.
J Neurosurg. 2019.
PMID: 31261134
Free PMC article.
Review.
The pathobiology of vascular malformations: insights from human and model organism genetics.
Wetzel-Strong SE, Detter MR, Marchuk DA.
Wetzel-Strong SE, et al.
J Pathol. 2017 Jan;241(2):281-293. doi: 10.1002/path.4844. Epub 2016 Dec 4.
J Pathol. 2017.
PMID: 27859310
Free PMC article.
Review.
Item in Clipboard
RhoA Kinase Inhibition With Fasudil Versus Simvastatin in Murine Models of Cerebral Cavernous Malformations.
Shenkar R, Shi C, Austin C, Moore T, Lightle R, Cao Y, Zhang L, Wu M, Zeineddine HA, Girard R, McDonald DA, Rorrer A, Gallione C, Pytel P, Liao JK, Marchuk DA, Awad IA.
Shenkar R, et al.
Stroke. 2017 Jan;48(1):187-194. doi: 10.1161/STROKEAHA.116.015013. Epub 2016 Nov 22.
Stroke. 2017.
PMID: 27879448
Free PMC article.
Item in Clipboard
Exceptional aggressiveness of cerebral cavernous malformation disease associated with PDCD10 mutations.
Shenkar R, Shi C, Rebeiz T, Stockton RA, McDonald DA, Mikati AG, Zhang L, Austin C, Akers AL, Gallione CJ, Rorrer A, Gunel M, Min W, De Souza JM, Lee C, Marchuk DA, Awad IA.
Shenkar R, et al.
Genet Med. 2015 Mar;17(3):188-196. doi: 10.1038/gim.2014.97. Epub 2014 Aug 14.
Genet Med. 2015.
PMID: 25122144
Free PMC article.
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Rho Kinase Inhibition Blunts Lesion Development and Hemorrhage in Murine Models of Aggressive Pdcd10/Ccm3 Disease.
Shenkar R, Peiper A, Pardo H, Moore T, Lightle R, Girard R, Hobson N, Polster SP, Koskimäki J, Zhang D, Lyne SB, Cao Y, Chaudagar K, Saadat L, Gallione C, Pytel P, Liao JK, Marchuk D, Awad IA.
Shenkar R, et al.
Stroke. 2019 Mar;50(3):738-744. doi: 10.1161/STROKEAHA.118.024058.
Stroke. 2019.
PMID: 30744543
Free PMC article.
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Lesions from patients with sporadic cerebral cavernous malformations harbor somatic mutations in the CCM genes: evidence for a common biochemical pathway for CCM pathogenesis.
McDonald DA, Shi C, Shenkar R, Gallione CJ, Akers AL, Li S, De Castro N, Berg MJ, Corcoran DL, Awad IA, Marchuk DA.
McDonald DA, et al.
Hum Mol Genet. 2014 Aug 15;23(16):4357-70. doi: 10.1093/hmg/ddu153. Epub 2014 Apr 3.
Hum Mol Genet. 2014.
PMID: 24698976
Free PMC article.
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