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Results: 19

1.

Two novel HTRA1 mutations in a European CARASIL patient.

Bianchi S, Di Palma C, Gallus GN, Taglia I, Poggiani A, Rosini F, Rufa A, Muresanu DF, Cerase A, Dotti MT, Federico A.

Neurology. 2014 Mar 11;82(10):898-900. doi: 10.1212/WNL.0000000000000202. Epub 2014 Feb 5. No abstract available.

PMID:
24500651
[PubMed - indexed for MEDLINE]
2.

A novel mutation of the high-temperature requirement A serine peptidase 1 (HTRA1) gene in a Chinese family with cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL).

Chen Y, He Z, Meng S, Li L, Yang H, Zhang X.

J Int Med Res. 2013 Oct;41(5):1445-55. doi: 10.1177/0300060513480926. Epub 2013 Aug 20.

PMID:
23963851
[PubMed - indexed for MEDLINE]
3.

CARASIL.

Diwan AG, Bhosle DG, Vikram A, Biniwale A, Chaudhary S, Patodiya B.

J Assoc Physicians India. 2012 May;60:59-61.

PMID:
23029730
[PubMed - indexed for MEDLINE]
4.

A novel mutation in the HTRA1 gene identified in Chinese CARASIL pedigree.

Wang XL, Li CF, Guo HW, Cao BZ.

CNS Neurosci Ther. 2012 Oct;18(10):867-9. doi: 10.1111/j.1755-5949.2012.00373.x. Epub 2012 Aug 20. No abstract available.

PMID:
22900900
[PubMed - indexed for MEDLINE]
5.

Hereditary cerebral small vessel diseases: a review.

Federico A, Di Donato I, Bianchi S, Di Palma C, Taglia I, Dotti MT.

J Neurol Sci. 2012 Nov 15;322(1-2):25-30. doi: 10.1016/j.jns.2012.07.041. Epub 2012 Aug 4. Review.

PMID:
22868088
[PubMed - indexed for MEDLINE]
6.

A novel mutation in the HTRA1 gene causes CARASIL without alopecia.

Nishimoto Y, Shibata M, Nihonmatsu M, Nozaki H, Shiga A, Shirata A, Yamane K, Kosakai A, Takahashi K, Nishizawa M, Onodera O, Suzuki N.

Neurology. 2011 Apr 12;76(15):1353-5. doi: 10.1212/WNL.0b013e318215281d. No abstract available.

PMID:
21482952
[PubMed - indexed for MEDLINE]
7.

Neurological picture. Neuroaxonal integrity evaluated by MR spectroscopy in a case of CARASIL.

Nishimoto Y, Shibata M, Onodera O, Suzuki N.

J Neurol Neurosurg Psychiatry. 2011 Aug;82(8):860-1. doi: 10.1136/jnnp.2010.240051. Epub 2011 Mar 28. No abstract available.

PMID:
21444319
[PubMed - indexed for MEDLINE]
8.

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
[PubMed - indexed for MEDLINE]
Free Article
9.

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
[PubMed - indexed for MEDLINE]
10.

A missense HTRA1 mutation expands CARASIL syndrome to the Caucasian population.

Mendioroz M, Fernández-Cadenas I, Del Río-Espinola A, Rovira A, Solé E, Fernández-Figueras MT, García-Patos V, Sastre-Garriga J, Domingues-Montanari S, Alvarez-Sabín J, Montaner J.

Neurology. 2010 Nov 30;75(22):2033-5. doi: 10.1212/WNL.0b013e3181ff96ac. No abstract available.

PMID:
21115960
[PubMed - indexed for MEDLINE]
11.

Review: molecular genetics and pathology of hereditary small vessel diseases of the brain.

Yamamoto Y, Craggs L, Baumann M, Kalimo H, Kalaria RN.

Neuropathol Appl Neurobiol. 2011 Feb;37(1):94-113. doi: 10.1111/j.1365-2990.2010.01147.x. Review.

PMID:
21062344
[PubMed - indexed for MEDLINE]
12.

New information on the genetics of stroke.

Meschia JF.

Curr Neurol Neurosci Rep. 2011 Feb;11(1):35-41. doi: 10.1007/s11910-010-0155-x. Review.

PMID:
21058051
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Hereditary and non-hereditary microangiopathies in the young. An up-date.

Ringelstein EB, Kleffner I, Dittrich R, Kuhlenbäumer G, Ritter MA.

J Neurol Sci. 2010 Dec 15;299(1-2):81-5. doi: 10.1016/j.jns.2010.08.037. Epub 2010 Sep 18. Review.

PMID:
20851424
[PubMed - indexed for MEDLINE]
14.

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.

PMID:
19387015
[PubMed - indexed for MEDLINE]
Free Article
15.

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
[PubMed - indexed for MEDLINE]
16.

Extensive loss of arterial medial smooth muscle cells and mural extracellular matrix in cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL).

Oide T, Nakayama H, Yanagawa S, Ito N, Ikeda S, Arima K.

Neuropathology. 2008 Apr;28(2):132-42. Epub 2007 Nov 6.

PMID:
18021191
[PubMed - indexed for MEDLINE]
17.

Single gene disorders causing ischaemic stroke.

Razvi SS, Bone I.

J Neurol. 2006 Jun;253(6):685-700. Review.

PMID:
16807686
[PubMed - indexed for MEDLINE]
18.

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
[PubMed - indexed for MEDLINE]
19.

Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy.

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

Neurology. 2002 Mar 12;58(5):817-20.

PMID:
11889251
[PubMed - indexed for MEDLINE]

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