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Items: 1 to 20 of 320

1.

Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): from discovery to gene identification.

Fukutake T.

J Stroke Cerebrovasc Dis. 2011 Mar-Apr;20(2):85-93. doi: 10.1016/j.jstrokecerebrovasdis.2010.11.008. Epub 2011 Jan 7. Review.

PMID:
21215656
2.

[Carasil].

Fukutake T.

Brain Nerve. 2011 Feb;63(2):99-108. Review. Japanese.

PMID:
21301034
3.

Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease.

Hara K, Shiga A, Fukutake T, Nozaki H, Miyashita A, Yokoseki A, Kawata H, Koyama A, Arima K, Takahashi T, Ikeda M, Shiota H, Tamura M, Shimoe Y, Hirayama M, Arisato T, Yanagawa S, Tanaka A, Nakano I, Ikeda S, Yoshida Y, Yamamoto T, Ikeuchi T, Kuwano R, Nishizawa M, Tsuji S, Onodera O.

N Engl J Med. 2009 Apr 23;360(17):1729-39. doi: 10.1056/NEJMoa0801560.

5.

[Molecular pathogenesis of cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy].

Shiga A, Nozaki H, Nishizawa M, Onodera O.

Brain Nerve. 2010 Jun;62(6):595-9. Review. Japanese.

PMID:
20548119
6.
7.

Cerebral arterial pathology of CADASIL and CARASIL (Maeda syndrome).

Arima K, Yanagawa S, Ito N, Ikeda S.

Neuropathology. 2003 Dec;23(4):327-34. Review.

PMID:
14719550
8.

["CADASIL"--a newly discovered hereditary cerebrovascular disease].

Søndergaard H, Jørgensen HS, Olsen TS.

Ugeskr Laeger. 1998 Mar 9;160(11):1617-20. Review. Danish.

PMID:
9522653
9.
10.

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

Chabriat H, Joutel A, Vahedi K, Iba-Zizen MT, Tournier-Lasserve E, Bousser MG.

J Mal Vasc. 1996;21(5):277-82. Review. French.

PMID:
9026542
11.

[Dominant autosomal cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). A review].

Navarro E, Díaz F, Muñoz L, Giménez-Roldán S.

Neurologia. 2002 Oct;17(8):410-7. Review. Spanish.

PMID:
12396971
12.

Mutation of the Notch 3 gene in a Thai cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy family.

Suwanwela N, Srikiatkhachorn A, Tangwongchai S, Phanthumchina K, Suwanwela N.

J Med Assoc Thai. 2003 Feb;86(2):178-82.

PMID:
12678157
14.

Cerebral small-vessel disease protein HTRA1 controls the amount of TGF-β1 via cleavage of proTGF-β1.

Shiga A, Nozaki H, Yokoseki A, Nihonmatsu M, Kawata H, Kato T, Koyama A, Arima K, Ikeda M, Katada S, Toyoshima Y, Takahashi H, Tanaka A, Nakano I, Ikeuchi T, Nishizawa M, Onodera O.

Hum Mol Genet. 2011 May 1;20(9):1800-10. doi: 10.1093/hmg/ddr063. Epub 2011 Feb 14.

PMID:
21320870
15.

[Report of a patient with CADASIL having a novel missense mutation of the Notch 3 gene--association with alopecia and lumbar herniated disk].

Yamada H, Yasuda T, Kotorii S, Takahashi K, Tabira T, Sunada Y.

Rinsho Shinkeigaku. 2001 Feb-Mar;41(2-3):144-6. Japanese.

PMID:
11481859
16.

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

LaPoint SF, Patel U, Rubio A.

Adv Anat Pathol. 2000 Sep;7(5):307-21. Review.

PMID:
10976909
17.

A Chinese pedigree of cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): clinical and radiological features.

Zheng DM, Xu FF, Gao Y, Zhang H, Han SC, Bi GR.

J Clin Neurosci. 2009 Jun;16(6):847-9. doi: 10.1016/j.jocn.2008.08.031. Epub 2009 Mar 18.

PMID:
19299137
18.

[CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy): clinical features and neuroimaging].

Chabriat H, Joutel A, Vahedi K, Iba-Zizen MT, Tournier-Lasserve E, Bousser MG.

Bull Acad Natl Med. 2000;184(7):1523-31; discussion 1531-3. Review. French.

PMID:
11261256
20.

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