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Items: 1 to 20 of 150

1.

Cerebral hemorrhages in CADASIL: report of four cases and a brief review.

Rinnoci V, Nannucci S, Valenti R, Donnini I, Bianchi S, Pescini F, Dotti MT, Federico A, Inzitari D, Pantoni L.

J Neurol Sci. 2013 Jul 15;330(1-2):45-51. doi: 10.1016/j.jns.2013.04.002. Epub 2013 Apr 30.

PMID:
23639391
2.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy resulting in stroke in an 11-year-old male.

Granild-Jensen J, Jensen UB, Schwartz M, Hansen US.

Dev Med Child Neurol. 2009 Sep;51(9):754-7. doi: 10.1111/j.1469-8749.2008.03241.x. Epub 2009 Jan 29.

3.

Clinical significance of cerebral microbleeds locations in CADASIL with R544C NOTCH3 mutation.

Lee JS, Kang CH, Park SQ, Choi HA, Sim KB.

PLoS One. 2015 Feb 18;10(2):e0118163. doi: 10.1371/journal.pone.0118163. eCollection 2015. Erratum in: PLoS One. 2015;10(4):e0125297.

4.

Comparison of clinical, familial, and MRI features of CADASIL and NOTCH3-negative patients.

Pantoni L, Pescini F, Nannucci S, Sarti C, Bianchi S, Dotti MT, Federico A, Inzitari D.

Neurology. 2010 Jan 5;74(1):57-63. doi: 10.1212/WNL.0b013e3181c7da7c.

PMID:
20038773
5.

[Case of CADASIL showing spontaneous subcortical hemorrhage with a novel mutation of Notch3 gene].

Kotorii S, Goto H, Kondo T, Matsuo H, Takahashi K, Shibuya N.

Rinsho Shinkeigaku. 2006 Sep;46(9):644-8. Japanese.

PMID:
17260807
6.

CADASIL and autoimmunity: coexistence in a family with the R169C mutation at exon 4 of the NOTCH3 gene.

Paraskevas GP, Bougea A, Synetou M, Vassilopoulou S, Anagnostou E, Voumvourakis K, Iliopoulos A, Spengos K.

Cerebrovasc Dis. 2014;38(4):302-7. doi: 10.1159/000369000. Epub 2014 Nov 20.

PMID:
25412914
7.

[Clinical features in 4 Chinese families with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)].

Lv H, Yao S, Zhang W, Wang ZX, Huang YN, Niu XY, Zhang Z, Yuan Y.

Beijing Da Xue Xue Bao. 2004 Oct;36(5):496-500. Chinese.

8.

Population-specific spectrum of NOTCH3 mutations, MRI features and founder effect of CADASIL in Chinese.

Lee YC, Liu CS, Chang MH, Lin KP, Fuh JL, Lu YC, Liu YF, Soong BW.

J Neurol. 2009 Feb;256(2):249-55. doi: 10.1007/s00415-009-0091-3. Epub 2009 Feb 26.

PMID:
19242647
9.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: two novel mutations in the NOTCH3 gene in Chinese.

Lee YC, Yang AH, Liu HC, Wong WJ, Lu YC, Chang MH, Soong BW.

J Neurol Sci. 2006 Jul 15;246(1-2):111-5. Epub 2006 Mar 31.

PMID:
16580020
10.

Lacunar infarcts are the main correlate with cognitive dysfunction in CADASIL.

Liem MK, van der Grond J, Haan J, van den Boom R, Ferrari MD, Knaap YM, Breuning MH, van Buchem MA, Middelkoop HA, Lesnik Oberstein SA.

Stroke. 2007 Mar;38(3):923-8. Epub 2007 Feb 1.

11.

Sporadic vascular dementia as clinical presentation of a new missense mutation within exon 7 of NOTCH3 gene.

Pradotto L, Azan G, Doriguzzi C, Valentini C, Mauro A.

J Neurol Sci. 2008 Aug 15;271(1-2):207-10. doi: 10.1016/j.jns.2008.04.015. Epub 2008 May 21.

PMID:
18499132
12.

p.Arg332Cys mutation of NOTCH3 gene in two unrelated Japanese families with CADASIL.

Sano Y, Shimizu F, Kawai M, Omoto M, Negoro K, Kurokawa T, Fujisawa H, Suzuki M, Okayama N, Suehiro Y, Hinoda Y, Kanda T.

Intern Med. 2011;50(22):2833-8. Epub 2011 Nov 15.

13.

Screening for NOTCH3 gene mutations among 151 consecutive Korean patients with acute ischemic stroke.

Choi JC, Lee KH, Song SK, Lee JS, Kang SY, Kang JH.

J Stroke Cerebrovasc Dis. 2013 Jul;22(5):608-14. doi: 10.1016/j.jstrokecerebrovasdis.2011.10.013. Epub 2011 Nov 30.

PMID:
22133740
14.

The R110C mutation in Notch3 causes variable clinical features in two Turkish families with CADASIL syndrome.

Uyguner ZO, Siva A, Kayserili H, Saip S, Altintaş A, Apak MY, Albayram S, Işik N, Akman-Demir G, Taşyürekli M, Oz B, Wollnik B.

J Neurol Sci. 2006 Jul 15;246(1-2):123-30. Epub 2006 May 30.

PMID:
16730748
15.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

Lesnik Oberstein SA, Haan J.

Panminerva Med. 2004 Dec;46(4):265-76. Review.

PMID:
15876982
16.

Characteristics of CADASIL in Korea: a novel cysteine-sparing Notch3 mutation.

Kim Y, Choi EJ, Choi CG, Kim G, Choi JH, Yoo HW, Kim JS.

Neurology. 2006 May 23;66(10):1511-6.

PMID:
16717210
17.

Spontaneous intracerebral hemorrhage in CADASIL.

Lian L, Li D, Xue Z, Liang Q, Xu F, Kang H, Liu X, Zhu S.

J Headache Pain. 2013 Dec 17;14:98. doi: 10.1186/1129-2377-14-98.

18.

Report of two Chinese families and a review of Mainland Chinese CADASIL patients.

Yin XZ, Ding MP, Zhang BR, Liu JR, Zhang L, Wang PZ, Zhou FY, Zhao GH.

J Neurol Sci. 2009 Apr 15;279(1-2):88-92. doi: 10.1016/j.jns.2008.12.011. Epub 2009 Jan 23. Review.

PMID:
19167727
19.

Renal involvement in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

Kusaba T, Hatta T, Kimura T, Sonomura K, Tanda S, Kishimoto N, Kameyama H, Okigaki M, Mori Y, Ishigami N, Mizuno T, Nakagawa M, Matsubara H.

Clin Nephrol. 2007 Mar;67(3):182-7.

PMID:
17390743
20.

[A new Spanish family with CADASIL associated with 346C>T mutation of NOTCH3 gene].

Avila A, Bello J, Maho P, Gómez MI.

Neurologia. 2007 Sep;22(7):484-7. Spanish.

PMID:
17853970
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