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    Results: 1 to 20 of 339

    1.

    Evaluation of brain apoptosis in a CADASIL postmortem case.

    Battisti C, Formichi P, Radi E, Malandrini A, Federico A.

    Clin Neuropathol. 2009 Sep-Oct;28(5):358-61.PMID: 19788051 [PubMed - indexed for MEDLINE]Related articles

    2.

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

    Retief C, Schutte CM, Baker MK.

    S Afr Med J. 2009 Jun;99(6):461-5.PMID: 19736850 [PubMed - indexed for MEDLINE]Related articles

    3.

    Notch signaling and CADASIL.

    Tang SC, Jeng JS, Lee MJ, Yip PK.

    Acta Neurol Taiwan. 2009 Jun;18(2):81-90. Review.PMID: 19673359 [PubMed - indexed for MEDLINE]Related articles

    4.

    High recurrence of the R1006C NOTCH3 mutation in central Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

    Cappelli A, Ragno M, Cacchiò G, Scarcella M, Staffolani P, Pianese L.

    Neurosci Lett. 2009 Sep 22;462(2):176-8. Epub 2009 Jul 2.PMID: 19576955 [PubMed - indexed for MEDLINE]Related articles

    5.

    Cadasil.

    Chabriat H, Joutel A, Dichgans M, Tournier-Lasserve E, Bousser MG.

    Lancet Neurol. 2009 Jul;8(7):643-53. Review.PMID: 19539236 [PubMed - indexed for MEDLINE]Related articles

    6.

    Cysteine-sparing notch3 mutations: cadasil or cadasil variants?

    Quattrone A, Mazzei R.

    Neurology. 2009 Jun 16;72(24):2135-6; author reply 2136. No abstract available. PMID: 19528524 [PubMed - indexed for MEDLINE]Related articles

    7.

    Cognitive impairment and cerebral hypoperfusion in a CADASIL patient improved during administration of lomerizine.

    Mizuno T, Kondo M, Ishigami N, Tamura A, Itsukage M, Koizumi H, Isayama R, Hosomi A, Nagakane Y, Tokuda T, Sugimoto E, Ushijima Y, Nakagawa M.

    Clin Neuropharmacol. 2009 Mar-Apr;32(2):113-6.PMID: 19512965 [PubMed - indexed for MEDLINE]Related articles

    8.

    Methodological issues in right-to-left shunt detection in CADASIL patients.

    Mazzucco S, Anzola GP, Rizzuto N.

    Stroke. 2009 Jul;40(7):e509; author reply e510. Epub 2009 May 28. No abstract available. PMID: 19478217 [PubMed - indexed for MEDLINE]Related articles

    9.

    CADASIL mutations enhance spontaneous multimerization of NOTCH3.

    Opherk C, Duering M, Peters N, Karpinska A, Rosner S, Schneider E, Bader B, Giese A, Dichgans M.

    Hum Mol Genet. 2009 Aug 1;18(15):2761-7. Epub 2009 May 5.PMID: 19417009 [PubMed - indexed for MEDLINE]Related articles

    10.

    Different clinical phenotypes in monozygotic CADASIL twins with a novel NOTCH3 mutation.

    Mykkänen K, Junna M, Amberla K, Bronge L, Kääriäinen H, Pöyhönen M, Kalimo H, Viitanen M.

    Stroke. 2009 Jun;40(6):2215-8. Epub 2009 Apr 16.PMID: 19372454 [PubMed - indexed for MEDLINE]Related articles

    11.

    Neuropathological correlates of temporal pole white matter hyperintensities in CADASIL.

    Yamamoto Y, Ihara M, Tham C, Low RW, Slade JY, Moss T, Oakley AE, Polvikoski T, Kalaria RN.

    Stroke. 2009 Jun;40(6):2004-11. Epub 2009 Apr 9.PMID: 19359623 [PubMed - indexed for MEDLINE]Related articles

    12.

    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. Epub 2009 Mar 18.PMID: 19299137 [PubMed - indexed for MEDLINE]Related articles

    13.

    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. Epub 2009 Mar 17.PMID: 19293235 [PubMed - indexed for MEDLINE]Related articles

    14.

    Apathy: a major symptom in CADASIL.

    Reyes S, Viswanathan A, Godin O, Dufouil C, Benisty S, Hernandez K, Kurtz A, Jouvent E, O'Sullivan M, Czernecki V, Bousser MG, Dichgans M, Chabriat H.

    Neurology. 2009 Mar 10;72(10):905-10.PMID: 19273824 [PubMed - indexed for MEDLINE]Related articles

    15.

    Cerebrovascular reactivity is a main determinant of white matter hyperintensity progression in CADASIL.

    Liem MK, Lesnik Oberstein SA, Haan J, Boom R, Ferrari MD, Buchem MA, Grond J.

    AJNR Am J Neuroradiol. 2009 Jun;30(6):1244-7. Epub 2009 Mar 6.PMID: 19270103 [PubMed - indexed for MEDLINE]Related articles

    16.

    A pathogenic rare mutation on exon 22 of the NOTCH3 gene disclosed in an Italian patient affected by CADASIL.

    Ungaro C, Servillo P, Mazzei R, Consoli D, Conforti FL, Sprovieri T, Lanza PL, Quattrone A.

    Neurol Sci. 2009 Jun;30(3):269-71. Epub 2009 Mar 4. No abstract available. PMID: 19259619 [PubMed - indexed for MEDLINE]Related articles

    17.

    The remarkably variable expressivity of CADASIL: report of a minimally symptomatic man at an advanced age.

    Lee YC, Yang AH, Soong BW.

    J Neurol. 2009 Jun;256(6):1026-7. Epub 2009 Mar 1. No abstract available. PMID: 19252787 [PubMed - indexed for MEDLINE]Related articles

    18.

    Acute confusional migraine may be a presenting feature of CADASIL.

    Sathe S, DePeralta E, Pastores G, Kolodny EH.

    Headache. 2009 Apr;49(4):590-6. Epub 2009 Feb 25.PMID: 19245392 [PubMed - indexed for MEDLINE]Related articles

    19.

    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. Epub 2009 Feb 26.PMID: 19242647 [PubMed - indexed for MEDLINE]Related articles

    20.

    CADASIL management or what to do when there is little one can do.

    del Río-Espínola A, Mendióroz M, Domingues-Montanari S, Pozo-Rosich P, Solé E, Fernández-Morales J, Fernández-Cadenas I, Montaner J.

    Expert Rev Neurother. 2009 Feb;9(2):197-210. Review.PMID: 19210195 [PubMed - indexed for MEDLINE]Related articles

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