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Items: 1 to 20 of 121

1.

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy.

Rovelet-Lecrux A, Hannequin D, Raux G, Le Meur N, Laquerrière A, Vital A, Dumanchin C, Feuillette S, Brice A, Vercelletto M, Dubas F, Frebourg T, Campion D.

Nat Genet. 2006 Jan;38(1):24-6. Epub 2005 Dec 20.

PMID:
16369530
2.

APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy.

Sleegers K, Brouwers N, Gijselinck I, Theuns J, Goossens D, Wauters J, Del-Favero J, Cruts M, van Duijn CM, Van Broeckhoven C.

Brain. 2006 Nov;129(Pt 11):2977-83. Epub 2006 Aug 18.

PMID:
16921174
3.

Phenotype associated with APP duplication in five families.

Cabrejo L, Guyant-Maréchal L, Laquerrière A, Vercelletto M, De la Fournière F, Thomas-Antérion C, Verny C, Letournel F, Pasquier F, Vital A, Checler F, Frebourg T, Campion D, Hannequin D.

Brain. 2006 Nov;129(Pt 11):2966-76. Epub 2006 Sep 7.

PMID:
16959815
4.

Low prevalence of APP duplications in Swedish and Finnish patients with early-onset Alzheimer's disease.

Blom ES, Viswanathan J, Kilander L, Helisalmi S, Soininen H, Lannfelt L, Ingelsson M, Glaser A, Hiltunen M.

Eur J Hum Genet. 2008 Feb;16(2):171-5. Epub 2007 Nov 28.

5.

[APP duplication causes autosomal dominant Alzheimer disease with cerebral amyloid angiopathy].

Campion D, Hannequin D.

Med Sci (Paris). 2006 May;22(5):468-9. French. No abstract available.

6.

A family with Alzheimer disease and strokes associated with A713T mutation of the APP gene.

Rossi G, Giaccone G, Maletta R, Morbin M, Capobianco R, Mangieri M, Giovagnoli AR, Bizzi A, Tomaino C, Perri M, Di Natale M, Tagliavini F, Bugiani O, Bruni AC.

Neurology. 2004 Sep 14;63(5):910-2.

PMID:
15365148
7.

Cerebral amyloid angiopathy: pathogenetic mechanisms and link to dense amyloid plaques.

Kumar-Singh S.

Genes Brain Behav. 2008 Feb;7 Suppl 1:67-82. doi: 10.1111/j.1601-183X.2007.00380.x. Review.

8.

Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum.

Campion D, Dumanchin C, Hannequin D, Dubois B, Belliard S, Puel M, Thomas-Anterion C, Michon A, Martin C, Charbonnier F, Raux G, Camuzat A, Penet C, Mesnage V, Martinez M, Clerget-Darpoux F, Brice A, Frebourg T.

Am J Hum Genet. 1999 Sep;65(3):664-70.

9.

Breakpoint sequence analysis of an AβPP locus duplication associated with autosomal dominant Alzheimer's disease and severe cerebral amyloid angiopathy.

Antonell A, Gelpi E, Sánchez-Valle R, Martínez R, Molinuevo JL, Lladó A.

J Alzheimers Dis. 2012;28(2):303-8. doi: 10.3233/JAD-2011-110911.

PMID:
22008262
10.

The cerebral beta-amyloid angiopathies: hereditary and sporadic.

Zhang-Nunes SX, Maat-Schieman ML, van Duinen SG, Roos RA, Frosch MP, Greenberg SM.

Brain Pathol. 2006 Jan;16(1):30-9. Review.

PMID:
16612980
11.

Cerebral amyloid angiopathy: an overview.

Yamada M.

Neuropathology. 2000 Mar;20(1):8-22. Review.

PMID:
10935432
12.

Experimental induction of beta-amyloid plaques and cerebral angiopathy in primates.

Baker HF, Ridley RM, Duchen LW, Crow TJ, Bruton CJ.

Ann N Y Acad Sci. 1993 Sep 24;695:228-31.

PMID:
8239287
13.

[Genetic factors for cerebral amyloid angiopathy].

Hamaguchi T, Yamada M.

Brain Nerve. 2008 Nov;60(11):1275-83. Review. Japanese.

PMID:
19069161
14.

Progression of cerebral amyloid angiopathy in transgenic mouse models of Alzheimer disease.

Domnitz SB, Robbins EM, Hoang AW, Garcia-Alloza M, Hyman BT, Rebeck GW, Greenberg SM, Bacskai BJ, Frosch MP.

J Neuropathol Exp Neurol. 2005 Jul;64(7):588-94.

PMID:
16042310
15.

Kinetics of cerebral amyloid angiopathy progression in a transgenic mouse model of Alzheimer disease.

Robbins EM, Betensky RA, Domnitz SB, Purcell SM, Garcia-Alloza M, Greenberg C, Rebeck GW, Hyman BT, Greenberg SM, Frosch MP, Bacskai BJ.

J Neurosci. 2006 Jan 11;26(2):365-71.

16.

Amyloid beta/A4 peptide associated with Alzheimer's disease and cerebral amyloid angiopathy.

Hirai S, Okamoto K.

Intern Med. 1993 Dec;32(12):923-5. Review. No abstract available.

17.

Cerebral amyloid angiopathy in the brains of patients with Alzheimer's disease: the CERAD experience, Part XV.

Ellis RJ, Olichney JM, Thal LJ, Mirra SS, Morris JC, Beekly D, Heyman A.

Neurology. 1996 Jun;46(6):1592-6.

PMID:
8649554
18.

Intrafamilial diversity of phenotype associated with app duplication.

Guyant-Marechal I, Berger E, Laquerrière A, Rovelet-Lecrux A, Viennet G, Frebourg T, Rumbach L, Campion D, Hannequin D.

Neurology. 2008 Dec 2;71(23):1925-6. doi: 10.1212/01.wnl.0000339400.64213.56. No abstract available.

PMID:
19047566
19.

No evidence of APP point mutation and locus duplication in individuals with cerebral amyloid angiopathy.

Domingues-Montanari S, Parés M, Hernández-Guillamon M, Fernández-Cadenas I, Mendioroz M, Ortega G, Boada M, Masjuan J, Huertas N, Alvarez-Sabín J, Delgado P, Montaner J; Stroke Project of Cerebrovascular Diseases Study Group, Spanish Society of Neurology.

Eur J Neurol. 2011 Oct;18(10):1279-81. doi: 10.1111/j.1468-1331.2011.03401.x. Epub 2011 Apr 4.

PMID:
21463452
20.

Cerebral amyloid angiopathy and its relationship to Alzheimer's disease.

Thal DR, Griffin WS, de Vos RA, Ghebremedhin E.

Acta Neuropathol. 2008 Jun;115(6):599-609. doi: 10.1007/s00401-008-0366-2. Epub 2008 Mar 28. Review.

PMID:
18369648

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