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Items: 1 to 20 of 126

1.

7 T MRI reveals diffuse iron deposition in putamen and caudate nucleus in CADASIL.

Liem MK, Lesnik Oberstein SA, Versluis MJ, Maat-Schieman ML, Haan J, Webb AG, Ferrari MD, van Buchem MA, van der Grond J.

J Neurol Neurosurg Psychiatry. 2012 Dec;83(12):1180-5. doi: 10.1136/jnnp-2012-302545. Epub 2012 Aug 25.

PMID:
22923513
2.

Lenticulostriate arterial lumina are normal in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a high-field in vivo MRI study.

Liem MK, van der Grond J, Versluis MJ, Haan J, Webb AG, Ferrari MD, van Buchem MA, Lesnik Oberstein SA.

Stroke. 2010 Dec;41(12):2812-6. doi: 10.1161/STROKEAHA.110.586883. Epub 2010 Oct 21.

3.

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.

4.

Cerebral microbleeds in CADASIL: a gradient-echo magnetic resonance imaging and autopsy study.

Dichgans M, Holtmannspötter M, Herzog J, Peters N, Bergmann M, Yousry TA.

Stroke. 2002 Jan;33(1):67-71.

5.

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

Monet-Leprêtre 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.

6.

Elevated brain iron is independent from atrophy in Huntington's Disease.

Dumas EM, Versluis MJ, van den Bogaard SJ, van Osch MJ, Hart EP, van Roon-Mom WM, van Buchem MA, Webb AG, van der Grond J, Roos RA; TRACK-HD investigators.

Neuroimage. 2012 Jul 2;61(3):558-64. doi: 10.1016/j.neuroimage.2012.03.056. Epub 2012 Mar 28.

PMID:
22480728
7.

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
8.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: progression of MR abnormalities in prospective 7-year follow-up study.

Liem MK, Lesnik Oberstein SA, Haan J, van der Neut IL, van den Boom R, Ferrari MD, van Buchem MA, van der Grond J.

Radiology. 2008 Dec;249(3):964-71. doi: 10.1148/radiol.2492080357. Epub 2008 Oct 7.

PMID:
18840792
9.

MRI correlates of cognitive decline in CADASIL: a 7-year follow-up study.

Liem MK, Lesnik Oberstein SA, Haan J, van der Neut IL, Ferrari MD, van Buchem MA, Middelkoop HA, van der Grond J.

Neurology. 2009 Jan 13;72(2):143-8. doi: 10.1212/01.wnl.0000339038.65508.96.

PMID:
19139365
10.

Adaptive metabolic changes in CADASIL white matter.

Akhvlediani T, Henning A, Sándor PS, Boesiger P, Jung HH.

J Neurol. 2010 Feb;257(2):171-7. doi: 10.1007/s00415-009-5281-5. Epub 2009 Aug 19.

PMID:
19690906
11.

A novel cysteine-sparing NOTCH3 mutation in a Chinese family with CADASIL.

Ge W, Kuang H, Wei B, Bo L, Xu Z, Xu X, Geng D, Sun M.

PLoS One. 2014 Aug 6;9(8):e104533. doi: 10.1371/journal.pone.0104533. eCollection 2014.

12.

Archetypal Arg169Cys mutation in NOTCH3 does not drive the pathogenesis in cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy via a loss-of-function mechanism.

Cognat E, Baron-Menguy C, Domenga-Denier V, Cleophax S, Fouillade C, Monet-Leprêtre M, Dewerchin M, Joutel A.

Stroke. 2014 Mar;45(3):842-9. doi: 10.1161/STROKEAHA.113.003339. Epub 2014 Jan 14. Erratum in: Stroke. 2014 Mar;45(3):e51.

13.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) associated with a novel C82R mutation in the NOTCH3 gene.

Zea-Sevilla MA, Bermejo-Velasco P, Serrano-Heranz R, Calero M.

J Alzheimers Dis. 2015;43(2):363-7. doi: 10.3233/JAD-141218.

PMID:
25096610
14.

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

Chen YC, Hsiao CT, Soong BW, Lee YC.

Acta Neurol Taiwan. 2014 Jun;23(2):64-74. Review. Chinese.

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.

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
17.

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
18.

New mutations in the Notch3 gene in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL).

Abramycheva N, Stepanova M, Kalashnikova L, Zakharova M, Maximova M, Tanashyan M, Lagoda O, Fedotova E, Klyushnikov S, Konovalov R, Sakharova A, Illarioshkin S.

J Neurol Sci. 2015 Feb 15;349(1-2):196-201. doi: 10.1016/j.jns.2015.01.018. Epub 2015 Jan 17.

PMID:
25623805
19.

[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
20.

Loss of venous integrity in cerebral small vessel disease: a 7-T MRI study in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

De Guio F, Vignaud A, Ropele S, Duering M, Duchesnay E, Chabriat H, Jouvent E.

Stroke. 2014 Jul;45(7):2124-6. doi: 10.1161/STROKEAHA.114.005726. Epub 2014 May 27.

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