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Results: 1 to 20 of 118

1.

Brain microvascular accumulation and distribution of the NOTCH3 ectodomain and granular osmiophilic material in CADASIL.

Yamamoto Y, Craggs LJ, Watanabe A, Booth T, Attems J, Low RW, Oakley AE, Kalaria RN.

J Neuropathol Exp Neurol. 2013 May;72(5):416-31. doi: 10.1097/NEN.0b013e31829020b5.

PMID:
23584202
[PubMed - indexed for MEDLINE]
2.

Notch3 ectodomain is a major component of granular osmiophilic material (GOM) in CADASIL.

Ishiko A, Shimizu A, Nagata E, Takahashi K, Tabira T, Suzuki N.

Acta Neuropathol. 2006 Sep;112(3):333-9. Epub 2006 Jul 27.

PMID:
16871402
[PubMed - indexed for MEDLINE]
3.

Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients.

Tikka S, Mykkänen K, Ruchoux MM, Bergholm R, Junna M, Pöyhönen M, Yki-Järvinen H, Joutel A, Viitanen M, Baumann M, Kalimo H.

Brain. 2009 Apr;132(Pt 4):933-9. doi: 10.1093/brain/awn364. Epub 2009 Jan 27.

PMID:
19174371
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

[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
[PubMed - indexed for MEDLINE]
5.

Fibrosis and stenosis of the long penetrating cerebral arteries: the cause of the white matter pathology in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Miao Q, Paloneva T, Tuominen S, Pöyhönen M, Tuisku S, Viitanen M, Kalimo H.

Brain Pathol. 2004 Oct;14(4):358-64.

PMID:
15605982
[PubMed - indexed for MEDLINE]
6.

Genetic, clinical and pathological studies of CADASIL in Japan: a partial contribution of Notch3 mutations and implications of smooth muscle cell degeneration for the pathogenesis.

Santa Y, Uyama E, Chui DH, Arima M, Kotorii S, Takahashi K, Tabira T.

J Neurol Sci. 2003 Aug 15;212(1-2):79-84.

PMID:
12810003
[PubMed - indexed for MEDLINE]
7.

Renal involvement in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

Kusaba T, Hatta T, Kimura T, Sonomura K, Tanda S, Kishimoto N, Kameyama H, Okigaki M, Mori Y, Ishigami N, Mizuno T, Nakagawa M, Matsubara H.

Clin Nephrol. 2007 Mar;67(3):182-7.

PMID:
17390743
[PubMed - indexed for MEDLINE]
8.

Nephroangiosclerosis in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: is NOTCH3 mutation the common culprit?

Guerrot D, François A, Boffa JJ, Boulos N, Hanoy M, Legallicier B, Triquenot-Bagan A, Guyant-Marechal L, Laquerriere A, Freguin-Bouilland C, Ronco P, Godin M.

Am J Kidney Dis. 2008 Aug;52(2):340-5. doi: 10.1053/j.ajkd.2008.04.017. Epub 2008 Jun 24.

PMID:
18572291
[PubMed - indexed for MEDLINE]
9.

Ultrastructure of granular osmiophilic material deposits (GOM) in arterioles of CADASIL patients.

Lewandowska E, Dziewulska D, Parys M, Pasennik E.

Folia Neuropathol. 2011;49(3):174-80.

PMID:
22101950
[PubMed - indexed for MEDLINE]
10.

[CADASIL].

Uchino M.

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

PMID:
19069156
[PubMed - indexed for MEDLINE]
11.

Small cerebral vessel disease in familial amyloid and non-amyloid angiopathies: FAD-PS-1 (P117L) mutation and CADASIL. Immunohistochemical and ultrastructural studies.

Szpak GM, Lewandowska E, Wierzba-Bobrowicz T, Bertrand E, Pasennik E, Mendel T, Stepień T, Leszczyńska A, Rafałowska J.

Folia Neuropathol. 2007;45(4):192-204. Erratum in: Folia Neuropathol. 2008;46(1):92.

PMID:
18176893
[PubMed - indexed for MEDLINE]
12.

Transgenic mice expressing mutant Notch3 develop vascular alterations characteristic of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Ruchoux MM, Domenga V, Brulin P, Maciazek J, Limol S, Tournier-Lasserve E, Joutel A.

Am J Pathol. 2003 Jan;162(1):329-42.

PMID:
12507916
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Role of electron microscopy in the diagnosis of cadasil syndrome: a study of 32 patients.

Morroni M, Marzioni D, Ragno M, Di Bella P, Cartechini E, Pianese L, Lorenzi T, Castellucci M, Scarpelli M.

PLoS One. 2013 Jun 17;8(6):e65482. doi: 10.1371/journal.pone.0065482. Print 2013.

PMID:
23799017
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Hereditary multi-infarct dementia of the Swedish type is a novel disorder different from NOTCH3 causing CADASIL.

Low WC, Junna M, Börjesson-Hanson A, Morris CM, Moss TH, Stevens DL, St Clair D, Mizuno T, Zhang WW, Mykkänen K, Wahlstrom J, Andersen O, Kalimo H, Viitanen M, Kalaria RN.

Brain. 2007 Feb;130(Pt 2):357-67.

PMID:
17235124
[PubMed - indexed for MEDLINE]
Free Article
15.

Renal involvement in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): report of a case with a six-year follow-up.

Ragno M, Trojano L, Pianese L, Boni MV, Silvestri S, Mambelli V, Lorenzi T, Scarpelli M, Morroni M.

Histol Histopathol. 2012 Oct;27(10):1307-14.

PMID:
22936449
[PubMed - indexed for MEDLINE]
16.

CADASIL: intracytoplasmic granular osmiophilic material deposits are pseudoinclusions.

Morroni M, Lorenzi T.

J Neuropathol Exp Neurol. 2013 Aug;72(8):801. doi: 10.1097/NEN.0b013e31829ecd60. No abstract available.

PMID:
23877249
[PubMed - indexed for MEDLINE]
17.

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.

PMID:
19293235
[PubMed - indexed for MEDLINE]
Free PMC Article
18.
19.

The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients.

Joutel A, Andreux F, Gaulis S, Domenga V, Cecillon M, Battail N, Piga N, Chapon F, Godfrain C, Tournier-Lasserve E.

J Clin Invest. 2000 Mar;105(5):597-605.

PMID:
10712431
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Bidirectional encroachment of collagen into the tunica media in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Dong H, Blaivas M, Wang MM.

Brain Res. 2012 May 25;1456:64-71. doi: 10.1016/j.brainres.2012.03.037. Epub 2012 Mar 23.

PMID:
22503071
[PubMed - indexed for MEDLINE]
Free PMC Article

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