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Items: 1 to 20 of 116

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
2.

Immunolocalization of platelet-derived growth factor receptor-β (PDGFR-β) and pericytes in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

Craggs LJ, Fenwick R, Oakley AE, Ihara M, Kalaria RN.

Neuropathol Appl Neurobiol. 2015 Jun;41(4):557-70. doi: 10.1111/nan.12188. Epub 2015 Apr 23.

3.

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
4.

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.

5.

[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
6.
7.
8.

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
9.

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
10.

[CADASIL].

Uchino M.

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

PMID:
19069156
11.

Are granular osmiophilic material deposits an epiphenomenon in CADASIL?

Erro R, Moccia M, Cervasio M, Penco S, De Caro Mdel B, Barone P.

Folia Neuropathol. 2015;53(2):168-71.

12.

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.

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.

14.

Clusterin/Apolipoprotein J immunoreactivity is associated with white matter damage in cerebral small vessel diseases.

Craggs L, Taylor J, Slade JY, Chen A, Hagel C, Kuhlenbaeumer G, Borjesson-Hanson A, Viitanen M, Kalimo H, Deramecourt V, Oakley AE, Kalaria RN.

Neuropathol Appl Neurobiol. 2016 Feb;42(2):194-209. doi: 10.1111/nan.12248. Epub 2015 Jun 17.

15.
16.

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
17.

CADASIL: Ultrastructural insights into the morphology of granular osmiophilic material.

Lorenzi T, Ragno M, Paolinelli F, Castellucci C, Scarpelli M, Morroni M.

Brain Behav. 2017 Feb 22;7(3):e00624. doi: 10.1002/brb3.624. eCollection 2017 Mar.

18.

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. doi: 10.14670/HH-27.1307.

PMID:
22936449
19.

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.

20.

Hypomorphic Notch 3 alleles link Notch signaling to ischemic cerebral small-vessel disease.

Arboleda-Velasquez JF, Manent J, Lee JH, Tikka S, Ospina C, Vanderburg CR, Frosch MP, Rodríguez-Falcón M, Villen J, Gygi S, Lopera F, Kalimo H, Moskowitz MA, Ayata C, Louvi A, Artavanis-Tsakonas S.

Proc Natl Acad Sci U S A. 2011 May 24;108(21):E128-35. doi: 10.1073/pnas.1101964108. Epub 2011 May 9.

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