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Results: 1 to 20 of 23

Cited In for PubMed (Select 12146805)

1.

Genetics of Vascular Dementia.

Murray ME, Meschia JF, Dickson DW, Ross OA.

Minerva Psichiatr. 2010 Mar;51(1):9-25.

2.

Microvascular pathology and morphometrics of sporadic and hereditary small vessel diseases of the brain.

Craggs LJ, Yamamoto Y, Deramecourt V, Kalaria RN.

Brain Pathol. 2014 Sep;24(5):495-509. doi: 10.1111/bpa.12177. Review.

3.
4.

Embryonic origins of human vascular smooth muscle cells: implications for in vitro modeling and clinical application.

Sinha S, Iyer D, Granata A.

Cell Mol Life Sci. 2014 Jun;71(12):2271-88. doi: 10.1007/s00018-013-1554-3. Epub 2014 Jan 18. Review.

5.

NOTCH3 variants and risk of ischemic stroke.

Ross OA, Soto-Ortolaza AI, Heckman MG, Verbeeck C, Serie DJ, Rayaprolu S, Rich SS, Nalls MA, Singleton A, Guerreiro R, Kinsella E, Wszolek ZK, Brott TG, Brown RD Jr, Worrall BB, Meschia JF.

PLoS One. 2013 Sep 23;8(9):e75035. doi: 10.1371/journal.pone.0075035. eCollection 2013.

6.

Role of electron microscopy in the diagnosis of cadasil syndrome: a study of 32 patients.

Morroni M, Marzioni D, Ragno M, Di Bella P, Cartechini E, Pianese L, Lorenzi T, Castellucci M, Scarpelli M.

PLoS One. 2013 Jun 17;8(6):e65482. doi: 10.1371/journal.pone.0065482. Print 2013.

7.

notch3 is essential for oligodendrocyte development and vascular integrity in zebrafish.

Zaucker A, Mercurio S, Sternheim N, Talbot WS, Marlow FL.

Dis Model Mech. 2013 Sep;6(5):1246-59. doi: 10.1242/dmm.012005. Epub 2013 May 29.

8.

Lombardia GENS: a collaborative registry for monogenic diseases associated with stroke.

Bersano A, Baron P, Lanfranconi S, Trobia N, Sterzi R, Motto C, Comi G, Sessa M, Martinelli-Boneschi F, Micieli G, Ferrarese C, Santoro P, Parati E, Boncoraglio G, Padovani A, Pezzini A, Candelise L; Lombardia GENS Group.

Funct Neurol. 2012 Apr-Jun;27(2):107-17.

9.

Von Willebrand Factor permeates small vessels in CADASIL and inhibits smooth muscle gene expression.

Zhang X, Meng H, Blaivas M, Rushing EJ, Moore BE, Schwartz J, Lopes MB, Worrall BB, Wang MM.

Transl Stroke Res. 2012 Mar;3(1):138-45. doi: 10.1007/s12975-011-0112-2. Epub 2011 Oct 20.

10.

Bidirectional encroachment of collagen into the tunica media in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Dong H, Blaivas M, Wang MM.

Brain Res. 2012 May 25;1456:64-71. doi: 10.1016/j.brainres.2012.03.037. Epub 2012 Mar 23.

11.

The minimum prevalence of CADASIL in northeast England.

Narayan SK, Gorman G, Kalaria RN, Ford GA, Chinnery PF.

Neurology. 2012 Mar 27;78(13):1025-7. doi: 10.1212/WNL.0b013e31824d586c. Epub 2012 Mar 14. No abstract available.

12.

Grey matter volume alterations in CADASIL: a voxel-based morphometry study.

Rossi Espagnet MC, Romano A, Carducci F, Calabria LF, Fiorillo M, Orzi F, Bozzao A.

J Headache Pain. 2012 Apr;13(3):231-8. doi: 10.1007/s10194-012-0418-9. Epub 2012 Feb 3.

13.

Generation of human vascular smooth muscle subtypes provides insight into embryological origin-dependent disease susceptibility.

Cheung C, Bernardo AS, Trotter MW, Pedersen RA, Sinha S.

Nat Biotechnol. 2012 Jan 15;30(2):165-73. doi: 10.1038/nbt.2107.

14.

Signaling required for blood vessel maintenance: molecular basis and pathological manifestations.

Murakami M.

Int J Vasc Med. 2012;2012:293641. doi: 10.1155/2012/293641. Epub 2011 Dec 6.

15.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy in an Israeli family.

Shahien R, Bianchi S, Bowirrat A.

Neuropsychiatr Dis Treat. 2011;7:383-90. doi: 10.2147/NDT.S19399. Epub 2011 Jun 20.

16.

Glial Vascular Degeneration in CADASIL.

Brennan-Krohn T, Salloway S, Correia S, Dong M, de la Monte SM.

J Alzheimers Dis. 2010 Jan 1;21(4):1393-1402.

17.

Small vessel disease and subcortical vascular dementia.

Kalaria RN, Erkinjuntti T.

J Clin Neurol. 2006 Mar;2(1):1-11. doi: 10.3988/jcn.2006.2.1.1. Epub 2006 Mar 20.

18.

Valproate activates the Notch3/c-FLIP signaling cascade: a strategy to attenuate white matter hyperintensities in bipolar disorder in late life?

Yuan P, Salvadore G, Li X, Zhang L, Du J, Chen G, Manji HK.

Bipolar Disord. 2009 May;11(3):256-69. doi: 10.1111/j.1399-5618.2009.00675.x.

19.

Neuropathological correlates of temporal pole white matter hyperintensities in CADASIL.

Yamamoto Y, Ihara M, Tham C, Low RW, Slade JY, Moss T, Oakley AE, Polvikoski T, Kalaria RN.

Stroke. 2009 Jun;40(6):2004-11. doi: 10.1161/STROKEAHA.108.528299. Epub 2009 Apr 9.

20.

Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domain.

Monet-LeprĂȘtre M, Bardot B, Lemaire B, Domenga V, Godin O, Dichgans M, Tournier-Lasserve E, Cohen-Tannoudji M, Chabriat H, Joutel A.

Brain. 2009 Jun;132(Pt 6):1601-12. doi: 10.1093/brain/awp049. Epub 2009 Mar 17.

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