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Journal Abstract Search

157 related items for PubMed ID: 7668822

  • 1. A Greek-American kindred with autosomal dominant, levodopa-responsive parkinsonism and anticipation.
    Markopoulou K, Wszolek ZK, Pfeiffer RF.
    Ann Neurol; 1995 Sep; 38(3):373-8. PubMed ID: 7668822
    [Abstract] [Full Text] [Related]

  • 2. [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
    [Abstract] [Full Text] [Related]

  • 3. SCA2 may present as levodopa-responsive parkinsonism.
    Payami H, Nutt J, Gancher S, Bird T, McNeal MG, Seltzer WK, Hussey J, Lockhart P, Gwinn-Hardy K, Singleton AA, Singleton AB, Hardy J, Farrer M.
    Mov Disord; 2003 Apr; 18(4):425-9. PubMed ID: 12671950
    [Abstract] [Full Text] [Related]

  • 4. [A family of parkinsonism in which the clinical feature of constituents varied with the age of onset].
    Sasaki R, Kuzuhara S, Taniguchi A, Narita Y, Naito Y.
    Rinsho Shinkeigaku; 1994 Jul; 34(7):736-8. PubMed ID: 7955737
    [Abstract] [Full Text] [Related]

  • 5. Clinical genetic analysis of Parkinson's disease in the Contursi kindred.
    Golbe LI, Di Iorio G, Sanges G, Lazzarini AM, La Sala S, Bonavita V, Duvoisin RC.
    Ann Neurol; 1996 Nov; 40(5):767-75. PubMed ID: 8957018
    [Abstract] [Full Text] [Related]

  • 6. Familial parkinsonism, dementia, and Lewy body disease: study of family G.
    Denson MA, Wszolek ZK, Pfeiffer RF, Wszolek EK, Paschall TM, McComb RD.
    Ann Neurol; 1997 Oct; 42(4):638-43. PubMed ID: 9382476
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. A large kindred with autosomal dominant Parkinson's disease.
    Golbe LI, Di Iorio G, Bonavita V, Miller DC, Duvoisin RC.
    Ann Neurol; 1990 Mar; 27(3):276-82. PubMed ID: 2158268
    [Abstract] [Full Text] [Related]

  • 9. Genetic linkage studies in autosomal dominantly inherited L-DOPA responsive parkinsonism. Evaluation of candidate genes.
    Gasser T, Wszolek Z, Supala A, Trofatter J, Ozelius L, Uitti RJ, Pfeiffer RF, Gusella J, Calne D, Breakefield XO.
    Adv Neurol; 1996 Mar; 69():87-95. PubMed ID: 8615189
    [No Abstract] [Full Text] [Related]

  • 10. Clinical features of familial Parkinson's disease in Thai patients.
    Prueksaritanond S, Boongird P, Pulkes T, Prueksaritanond S.
    Qual Prim Care; 2009 Mar; 17(2):115-22. PubMed ID: 19416604
    [Abstract] [Full Text] [Related]

  • 11. A family with hereditary juvenile dystonia-parkinsonism.
    Ishikawa A, Miyatake T.
    Mov Disord; 1995 Jul; 10(4):482-8. PubMed ID: 7565830
    [Abstract] [Full Text] [Related]

  • 12. Neuropathology of two members of a German-American kindred (Family C) with late onset parkinsonism.
    Wszolek ZK, Gwinn-Hardy K, Wszolek EK, Muenter MD, Pfeiffer RF, Rodnitzky RL, Uitti RJ, McComb RD, Gasser T, Dickson DW.
    Acta Neuropathol; 2002 Apr; 103(4):344-50. PubMed ID: 11904753
    [Abstract] [Full Text] [Related]

  • 13. Western Nebraska family (family D) with autosomal dominant parkinsonism.
    Wszolek ZK, Pfeiffer B, Fulgham JR, Parisi JE, Thompson BM, Uitti RJ, Calne DB, Pfeiffer RF.
    Neurology; 1995 Mar; 45(3 Pt 1):502-5. PubMed ID: 7898705
    [Abstract] [Full Text] [Related]

  • 14. [Familial parkinsonism: different clinical phenotype between a mother and her daughter].
    Kanemaru K, Ishii K, Mitani K, Nagura H, Yamanouchi H.
    Rinsho Shinkeigaku; 1997 Jan; 37(1):47-9. PubMed ID: 9146074
    [Abstract] [Full Text] [Related]

  • 15. Dopa responsive dystonia and juvenile Parkinson's disease: two subtypes of the same disorder?
    Lamberti P, de Mari M, Iliceto G, Federico F.
    Acta Neurol (Napoli); 1992 Jan; 14(4-6):451-4. PubMed ID: 1293988
    [Abstract] [Full Text] [Related]

  • 16. [A 62-year-old man with familial parkinsonism with the onset at 24 years of the age].
    Takubo H, Kondo T, Mori H, Miyake T, Suda K, Yokochi M, Imai H, Mizuno Y.
    No To Shinkei; 1996 Jun; 48(6):587-97. PubMed ID: 8703564
    [Abstract] [Full Text] [Related]

  • 17. Familial Ménière's disease in five generations.
    Frykholm C, Larsen HC, Dahl N, Klar J, Rask-Andersen H, Friberg U.
    Otol Neurotol; 2006 Aug; 27(5):681-6. PubMed ID: 16868516
    [Abstract] [Full Text] [Related]

  • 18. 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; 18(3):262-5. PubMed ID: 9500549
    [Abstract] [Full Text] [Related]

  • 19. Genetic linkage studies in autosomal dominant parkinsonism: evaluation of seven candidate genes.
    Gasser T, Wszolek ZK, Trofatter J, Ozelius L, Uitti RJ, Lee CS, Gusella J, Pfeiffer RF, Calne DB, Breakefield XO.
    Ann Neurol; 1994 Sep; 36(3):387-96. PubMed ID: 7915897
    [Abstract] [Full Text] [Related]

  • 20. [Progress in the basic and clinical aspects of Parkinson's disease].
    Mizuno Y.
    Rinsho Shinkeigaku; 2004 Nov; 44(11):741-50. PubMed ID: 15651281
    [Abstract] [Full Text] [Related]

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