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Journal Abstract Search

125 related items for PubMed ID: 2173372

  • 1. Autosomal dominant Lewy-body Parkinson's disease.
    Golbe LI, Miller DC, Duvoisin RC.
    Adv Neurol; 1990; 53():287-92. PubMed ID: 2173372
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  • 3. [Hereditary Parkinson disease: report of 3 families with dominant autosomal inheritance].
    Wszolek ZK, Cordes M, Calne DB, Münter MD, Cordes I, Pfeifer RF.
    Nervenarzt; 1993 May; 64(5):331-5. PubMed ID: 8321342
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  • 4. Autosomal dominant Lewy body parkinsonism in a four-generation family.
    Waters CH, Miller CA.
    Ann Neurol; 1994 Jan; 35(1):59-64. PubMed ID: 8285594
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  • 7. Variable onset of adult inherited focal dystonia: a problem for genetic studies.
    Micheli S, Fernández-Pardal M, Quesada P, Brannan T, Obeso JA.
    Mov Disord; 1994 Jan; 9(1):64-8. PubMed ID: 8139606
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  • 8. Low frequency of alpha-synuclein mutations in familial Parkinson's disease.
    Farrer M, Wavrant-De Vrieze F, Crook R, Boles L, Perez-Tur J, Hardy J, Johnson WG, Steele J, Maraganore D, Gwinn K, Lynch T.
    Ann Neurol; 1998 Mar; 43(3):394-7. PubMed ID: 9506559
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  • 9. Pure akinesia due to lewy body Parkinson's disease: a case with pathology.
    Quinn NP, Luthert P, Honavar M, Marsden CD.
    Mov Disord; 1989 Mar; 4(1):85-9. PubMed ID: 2538728
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  • 10. Esophageal Lewy bodies associated with ganglion cell loss in achalasia. Similarity to Parkinson's disease.
    Qualman SJ, Haupt HM, Yang P, Hamilton SR.
    Gastroenterology; 1984 Oct; 87(4):848-56. PubMed ID: 6088351
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  • 11. The Lewy body in Parkinson's disease.
    Forno LS.
    Adv Neurol; 1987 Oct; 45():35-43. PubMed ID: 3030070
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  • 12. Exclusion of genetic linkage to 4q21-23 and 17q21 in a family with Lewy body parkinsonism.
    Hardy J, Pérez-Tur J, Baker M, Farrer M, Crook R, Hutton M, Johnson WG, Gwinn K, Muenter M, Rocca WA, Maraganore D.
    Am J Med Genet; 1998 Mar 28; 81(2):166-71. PubMed ID: 9613857
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  • 13. A pathological study of the association between Lewy body disease and Alzheimer's disease.
    Gibb WR, Mann DM, Mountjoy CQ, Lees AJ.
    Adv Neurol; 1990 Mar 28; 53():55-9. PubMed ID: 2173375
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  • 14. The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia.
    Zarranz JJ, Alegre J, Gómez-Esteban JC, Lezcano E, Ros R, Ampuero I, Vidal L, Hoenicka J, Rodriguez O, Atarés B, Llorens V, Gomez Tortosa E, del Ser T, Muñoz DG, de Yebenes JG.
    Ann Neurol; 2004 Feb 28; 55(2):164-73. PubMed ID: 14755719
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  • 15. A susceptibility locus for Parkinson's disease maps to chromosome 2p13.
    Gasser T, Müller-Myhsok B, Wszolek ZK, Oehlmann R, Calne DB, Bonifati V, Bereznai B, Fabrizio E, Vieregge P, Horstmann RD.
    Nat Genet; 1998 Mar 28; 18(3):262-5. PubMed ID: 9500549
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  • 18. Autosomal-dominant dentatorubropallidoluysian atrophy in the United Kingdom.
    Warner TT, Lennox GG, Janota I, Harding AE.
    Mov Disord; 1994 May 28; 9(3):289-96. PubMed ID: 8041369
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  • 19. Familial parkinsonism and dementia with "ballooned neurons".
    Mizutani T, Inose T, Nakajima S, Gambetti P.
    Adv Neurol; 1993 May 28; 60():613-7. PubMed ID: 8420199
    [No Abstract] [Full Text] [Related]

  • 20. Novel alpha-synuclein-immunoreactive proteins in brain samples from the Contursi kindred, Parkinson's, and Alzheimer's disease.
    Langston JW, Sastry S, Chan P, Forno LS, Bolin LM, Di Monte DA.
    Exp Neurol; 1998 Dec 28; 154(2):684-90. PubMed ID: 9878203
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