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Journal Abstract Search

115 related items for PubMed ID: 1751863

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  • 25. [Clinical presentation of Moroccan cases with Alzheimer's disease].
    El Kadmiri N, Zaid Y, Hamzi K, Nadifi S, Slassi I, El Moutawakil B.
    Encephale; 2014 Dec; 40(6):481-6. PubMed ID: 25127896
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  • 28. A multigenerational pedigree of late-onset Alzheimer's disease implies new genetic causes.
    Jimenez-Escrig A, Gomez-Tortosa E, Baron M, Rabano A, Arcos-Burgos M, Palacios LG, Yusta A, Anta P, Perez I, Hierro M, Munoz DG, Barquero S.
    Brain; 2005 Jul; 128(Pt 7):1707-15. PubMed ID: 15843424
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  • 29. The R269H mutation in presenilin-1 presenting as late-onset autosomal dominant Alzheimer's disease.
    Larner AJ, Ray PS, Doran M.
    J Neurol Sci; 2007 Jan 31; 252(2):173-6. PubMed ID: 17188713
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  • 31. Familial Alzheimer's disease.
    Sadovnick AD, Tuokko H, Horton A, Baird PA, Beattie BL.
    Can J Neurol Sci; 1988 May 31; 15(2):142-6. PubMed ID: 3383026
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  • 32. Clinical features of early-onset Alzheimer disease in a large kindred with an E280A presenilin-1 mutation.
    Lopera F, Ardilla A, Martínez A, Madrigal L, Arango-Viana JC, Lemere CA, Arango-Lasprilla JC, Hincapíe L, Arcos-Burgos M, Ossa JE, Behrens IM, Norton J, Lendon C, Goate AM, Ruiz-Linares A, Rosselli M, Kosik KS.
    JAMA; 1997 Mar 12; 277(10):793-9. PubMed ID: 9052708
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  • 33. The novel PSEN1 M84V mutation associated to frontal dysexecutive syndrome, spastic paraparesis, and cerebellar atrophy in a dominant Alzheimer's disease family.
    Gallo M, Frangipane F, Cupidi C, De Bartolo M, Turone S, Ferrari C, Nacmias B, Grimaldi G, Laganà V, Colao R, Bernardi L, Anfossi M, Conidi ME, Vasso F, Curcio SAM, Mirabelli M, Smirne N, Torchia G, Muraca MG, Puccio G, Di Lorenzo R, Piccininni M, Tedde A, Maletta RG, Sorbi S, Bruni AC.
    Neurobiol Aging; 2017 Aug 12; 56():213.e7-213.e12. PubMed ID: 28532646
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  • 34. Cerebral arteriovenous malformation in three successive generations.
    Larsen PD, Hellbusch LC, Lefkowitz DM, Schaefer GB.
    Pediatr Neurol; 1997 Jul 12; 17(1):74-6. PubMed ID: 9308982
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  • 37. [Autosomal dominant transmission in retinitis pigmentosa].
    Ghenoiu R.
    Oftalmologia; 1993 Jul 12; 37(4):339-41. PubMed ID: 8286320
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  • 38. Genetic heterogeneity in Alzheimer's disease: a grade of membership analysis.
    Corder EH, Woodbury MA.
    Genet Epidemiol; 1993 Jul 12; 10(6):495-9. PubMed ID: 8314050
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  • 39. Molecular diagnosis of autosomal dominant early onset Alzheimer's disease: an update.
    Raux G, Guyant-Maréchal L, Martin C, Bou J, Penet C, Brice A, Hannequin D, Frebourg T, Campion D.
    J Med Genet; 2005 Oct 12; 42(10):793-5. PubMed ID: 16033913
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