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Journal Abstract Search

189 related items for PubMed ID: 11009195

  • 21. Identification and characterization of the human parkin gene promoter.
    West A, Farrer M, Petrucelli L, Cookson M, Lockhart P, Hardy J.
    J Neurochem; 2001 Sep; 78(5):1146-52. PubMed ID: 11553688
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  • 22. Parkin is linked to the ubiquitin pathway.
    Tanaka K, Suzuki T, Chiba T, Shimura H, Hattori N, Mizuno Y.
    J Mol Med (Berl); 2001 Sep; 79(9):482-94. PubMed ID: 11692161
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  • 25. Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations.
    van de Warrenburg BP, Lammens M, Lücking CB, Denèfle P, Wesseling P, Booij J, Praamstra P, Quinn N, Brice A, Horstink MW.
    Neurology; 2001 Feb 27; 56(4):555-7. PubMed ID: 11222808
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  • 27. Restricted occurrence of Lewy bodies in the dorsal vagal nucleus in a patient with late-onset parkinsonism.
    Wakabayashi K, Toyoshima Y, Awamori K, Anezaki T, Yoshimoto M, Tsuji S, Takahashi H.
    J Neurol Sci; 1999 Jun 01; 165(2):188-91. PubMed ID: 10450807
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  • 28. [Two cases of sporadic juvenile Parkinson's disease caused by homozygous deletion of Parkin gene].
    Ujike H, Yamamoto M, Yamaguchi K, Kanzaki A, Takagi M, Kuroda S.
    No To Shinkei; 1999 Dec 01; 51(12):1061-4. PubMed ID: 10654303
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  • 29. DJ-1 linked parkinsonism (PARK7) is associated with Lewy body pathology.
    Taipa R, Pereira C, Reis I, Alonso I, Bastos-Lima A, Melo-Pires M, Magalhães M.
    Brain; 2016 Jun 01; 139(Pt 6):1680-7. PubMed ID: 27085187
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  • 32. [An 80-year-old woman with parkinsonism and progressive dementia].
    Hattori N, Sumino S, Takanashi M, Mori H, Wakiya M, Shirai T, Sugita H, Mizuno Y.
    No To Shinkei; 1999 Jun 01; 51(6):541-50. PubMed ID: 10423759
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  • 36. Genetic Variations and Neuropathologic Features of Patients with PRKN Mutations.
    Seike N, Yokoseki A, Takeuchi R, Saito K, Miyahara H, Miyashita A, Ikeda T, Aida I, Nakajima T, Kanazawa M, Wakabayashi M, Toyoshima Y, Takahashi H, Matsumoto R, Toda T, Onodera O, Ishikawa A, Ikeuchi T, Kakita A.
    Mov Disord; 2021 Jul 01; 36(7):1634-1643. PubMed ID: 33570211
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  • 37. Autosomal-recessive juvenile parkinsonism in a Jewish Yemenite kindred: mutation of Parkin gene.
    Nisipeanu P, Inzelberg R, Blumen SC, Carasso RL, Hattori N, Matsumine H, Mizuno Y.
    Neurology; 1999 Oct 22; 53(7):1602-4. PubMed ID: 10534280
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  • 38. 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 22; 42(4):638-43. PubMed ID: 9382476
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  • 39. Parkin disease: a clinicopathologic entity?
    Doherty KM, Silveira-Moriyama L, Parkkinen L, Healy DG, Farrell M, Mencacci NE, Ahmed Z, Brett FM, Hardy J, Quinn N, Counihan TJ, Lynch T, Fox ZV, Revesz T, Lees AJ, Holton JL.
    JAMA Neurol; 2013 May 22; 70(5):571-9. PubMed ID: 23459986
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  • 40. Point mutations (Thr240Arg and Gln311Stop) [correction of Thr240Arg and Ala311Stop] in the Parkin gene.
    Hattori N, Matsumine H, Asakawa S, Kitada T, Yoshino H, Elibol B, Brookes AJ, Yamamura Y, Kobayashi T, Wang M, Yoritaka A, Minoshima S, Shimizu N, Mizuno Y.
    Biochem Biophys Res Commun; 1998 Aug 28; 249(3):754-8. PubMed ID: 9731209
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