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Items: 1 to 20 of 243

1.

Prevalence of CADASIL and Fabry Disease in a Cohort of MRI Defined Younger Onset Lacunar Stroke.

Kilarski LL, Rutten-Jacobs LC, Bevan S, Baker R, Hassan A, Hughes DA, Markus HS; UK Young Lacunar Stroke DNA Study.

PLoS One. 2015 Aug 25;10(8):e0136352. doi: 10.1371/journal.pone.0136352. eCollection 2015.

2.

Acute simultaneous multiple lacunar infarcts as the initial presentation of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

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

J Chin Med Assoc. 2015 Jul;78(7):424-6. doi: 10.1016/j.jcma.2015.01.007. Epub 2015 May 7.

3.

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
4.

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
5.

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
6.

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
7.

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
8.

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.

PMID:
17272761
9.

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
10.

Yield of screening for CADASIL mutations in lacunar stroke and leukoaraiosis.

Dong Y, Hassan A, Zhang Z, Huber D, Dalageorgou C, Markus HS.

Stroke. 2003 Jan;34(1):203-5.

PMID:
12511775
11.

CADASIL with a novel NOTCH3 mutation (Cys478Tyr).

Ozaki K, Irioka T, Ishikawa K, Mizusawa H.

J Stroke Cerebrovasc Dis. 2015 Mar;24(3):e61-2. doi: 10.1016/j.jstrokecerebrovasdis.2014.11.022. Epub 2015 Jan 13.

PMID:
25595846
12.

[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
13.

Two novel mutations of the NOTCH3 gene in Korean patients with CADASIL.

Kim Y, Kim JS, Kim G, No YJ, Yoo HW.

Mutat Res. 2006 Jan 29;593(1-2):116-20. Epub 2005 Oct 26.

PMID:
16256149
14.

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

Ueda M, Nakaguma R, Ando Y.

Rinsho Byori. 2009 Mar;57(3):242-51. Review. Japanese.

PMID:
19363995
15.

[CADASIL].

Uchino M.

Brain Nerve. 2008 Nov;60(11):1224-34. Review. Japanese.

PMID:
19069156
16.

The role of clinical and neuroimaging features in the diagnosis of CADASIL.

Bersano A, Bedini G, Markus HS, Vitali P, Colli-Tibaldi E, Taroni F, Gellera C, Baratta S, Mosca L, Carrera P, Ferrari M, Cereda C, Grieco G, Lanfranconi S, Mazucchelli F, Zarcone D, De Lodovici ML, Bono G, Boncoraglio GB, Parati EA, Calloni MV, Perrone P, Bordo BM, Motto C, Agostoni E, Pezzini A, Padovani A, Micieli G, Cavallini A, Molini G, Sasanelli F, Sessa M, Comi G, Checcarelli N, Carmerlingo M, Corato M, Marcheselli S, Fusi L, Grampa G, Uccellini D, Beretta S, Ferrarese C, Incorvaia B, Tadeo CS, Adobbati L, Silani V, Faragò G, Trobia N, Grond-Ginsbach C, Candelise L; Lombardia GENS-group.

J Neurol. 2018 Dec;265(12):2934-2943. doi: 10.1007/s00415-018-9072-8. Epub 2018 Oct 11.

PMID:
30311053
17.

CADASIL in central Italy: a retrospective clinical and genetic study in 229 patients.

Bianchi S, Zicari E, Carluccio A, Di Donato I, Pescini F, Nannucci S, Valenti R, Ragno M, Inzitari D, Pantoni L, Federico A, Dotti MT.

J Neurol. 2015 Jan;262(1):134-41. doi: 10.1007/s00415-014-7533-2. Epub 2014 Oct 26.

PMID:
25344745
18.

[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.

19.

Spectrum of NOTCH3 mutations in Korean patients with clinically suspicious cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Kim YE, Yoon CW, Seo SW, Ki CS, Kim YB, Kim JW, Bang OY, Lee KH, Kim GM, Chung CS, Na DL.

Neurobiol Aging. 2014 Mar;35(3):726.e1-6. doi: 10.1016/j.neurobiolaging.2013.09.004. Epub 2013 Oct 16.

PMID:
24139282
20.

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.

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