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Journal Abstract Search

245 related items for PubMed ID: 23459986

  • 21. Significance of the parkin and PINK1 gene in Jordanian families with incidences of young-onset and juvenile parkinsonism.
    Myhre R, Steinkjer S, Stormyr A, Nilsen GL, Abu Zayyad H, Horany K, Nusier MK, Klungland H.
    BMC Neurol; 2008 Dec 16; 8():47. PubMed ID: 19087301
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  • 22. Importance of familial Parkinson's disease and parkinsonism to the understanding of nigral degeneration in sporadic Parkinson's disease.
    Hattori N, Shimura H, Kubo S, Wang M, Shimizu N, Tanaka K, Mizuno Y.
    J Neural Transm Suppl; 2000 Dec 16; (60):101-16. PubMed ID: 11205133
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  • 23. Relative high frequency of the c.255delA parkin gene mutation in Spanish patients with autosomal recessive parkinsonism.
    Muñoz E, Tolosa E, Pastor P, Martí MJ, Valldeoriola F, Campdelacreu J, Oliva R.
    J Neurol Neurosurg Psychiatry; 2002 Nov 16; 73(5):582-4. PubMed ID: 12397156
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  • 24. [Parkin gene and its function; a key to understand nigral degeneration].
    Hattori N, Mizuno Y.
    Rinsho Shinkeigaku; 1999 Dec 16; 39(12):1259-61. PubMed ID: 10791092
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  • 25. Nigral degeneration and striatal dopaminergic dysfunction in idiopathic and Parkin-linked Parkinson's disease.
    Hu MT, Scherfler C, Khan NL, Hajnal JV, Lees AJ, Quinn N, Wood NW, Brooks DJ.
    Mov Disord; 2006 Mar 16; 21(3):299-305. PubMed ID: 16211589
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  • 26. Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: expanding the phenotype.
    Klein C, Pramstaller PP, Kis B, Page CC, Kann M, Leung J, Woodward H, Castellan CC, Scherer M, Vieregge P, Breakefield XO, Kramer PL, Ozelius LJ.
    Ann Neurol; 2000 Jul 16; 48(1):65-71. PubMed ID: 10894217
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  • 27. Predictors of parkin mutations in early-onset Parkinson disease: the consortium on risk for early-onset Parkinson disease study.
    Marder KS, Tang MX, Mejia-Santana H, Rosado L, Louis ED, Comella CL, Colcher A, Siderowf AD, Jennings D, Nance MA, Bressman S, Scott WK, Tanner CM, Mickel SF, Andrews HF, Waters C, Fahn S, Ross BM, Cote LJ, Frucht S, Ford B, Alcalay RN, Rezak M, Novak K, Friedman JH, Pfeiffer RF, Marsh L, Hiner B, Neils GD, Verbitsky M, Kisselev S, Caccappolo E, Ottman R, Clark LN.
    Arch Neurol; 2010 Jun 16; 67(6):731-8. PubMed ID: 20558392
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  • 28. An autopsy case of PARK2 due to a homozygous exon 2 deletion of parkin and associated with α-synucleinopathy.
    Sakuwa M, Adachi T, Yoshida K, Adachi Y, Nakano T, Hanajima R.
    Neuropathology; 2021 Aug 16; 41(4):293-300. PubMed ID: 34121225
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  • 30. Early-onset Parkinson's disease caused by a novel parkin mutation in a genetic isolate from north-eastern Brazil.
    Chien HF, Rohé CF, Costa MD, Breedveld GJ, Oostra BA, Barbosa ER, Bonifati V.
    Neurogenetics; 2006 Mar 16; 7(1):13-9. PubMed ID: 16328510
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  • 31. The parkin gene and its phenotype. Italian PD Genetics Study Group, French PD Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
    Bonifati V, De Michele G, Lücking CB, Dürr A, Fabrizio E, Ambrosio G, Vanacore N, De Mari M, Marconi R, Capus L, Breteler MM, Gasser T, Oostra B, Wood N, Agid Y, Filla A, Meco G, Brice A, Italian PD Genetics Study Group, French PD Genetics Study Group, European Consortium on Genetic Susceptibility in PD.
    Neurol Sci; 2001 Feb 16; 22(1):51-2. PubMed ID: 11487197
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  • 34. The long journey to the discovery of PARK2: The 50th Anniversary of Japanese Society of Neuropathology.
    Yamamura Y.
    Neuropathology; 2010 Oct 16; 30(5):495-500. PubMed ID: 20667007
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  • 35. An autopsy case of autosomal-recessive juvenile parkinsonism with a homozygous exon 4 deletion in the parkin gene.
    Hayashi S, Wakabayashi K, Ishikawa A, Nagai H, Saito M, Maruyama M, Takahashi T, Ozawa T, Tsuji S, Takahashi H.
    Mov Disord; 2000 Sep 16; 15(5):884-8. PubMed ID: 11009195
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  • 36. Lack of Parkin Anticipates the Phenotype and Affects Mitochondrial Morphology and mtDNA Levels in a Mouse Model of Parkinson's Disease.
    Pinto M, Nissanka N, Moraes CT.
    J Neurosci; 2018 Jan 24; 38(4):1042-1053. PubMed ID: 29222404
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  • 37. Surprising behavioral and neurochemical enhancements in mice with combined mutations linked to Parkinson's disease.
    Hennis MR, Marvin MA, Taylor CM, Goldberg MS.
    Neurobiol Dis; 2014 Feb 24; 62():113-23. PubMed ID: 24075852
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  • 38. Olfaction in Parkin single and compound heterozygotes in a cohort of young onset Parkinson's disease patients.
    Malek N, Swallow DM, Grosset KA, Lawton MA, Smith CR, Bajaj NP, Barker RA, Ben-Shlomo Y, Bresner C, Burn DJ, Foltynie T, Morris HR, Williams N, Wood NW, Grosset DG, PRoBaND Investigators.
    Acta Neurol Scand; 2016 Oct 24; 134(4):271-6. PubMed ID: 26626018
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  • 39. Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy.
    Lesage S, Drouet V, Majounie E, Deramecourt V, Jacoupy M, Nicolas A, Cormier-Dequaire F, Hassoun SM, Pujol C, Ciura S, Erpapazoglou Z, Usenko T, Maurage CA, Sahbatou M, Liebau S, Ding J, Bilgic B, Emre M, Erginel-Unaltuna N, Guven G, Tison F, Tranchant C, Vidailhet M, Corvol JC, Krack P, Leutenegger AL, Nalls MA, Hernandez DG, Heutink P, Gibbs JR, Hardy J, Wood NW, Gasser T, Durr A, Deleuze JF, Tazir M, Destée A, Lohmann E, Kabashi E, Singleton A, Corti O, Brice A, French Parkinson's Disease Genetics Study (PDG), International Parkinson's Disease Genomics Consortium (IPDGC).
    Am J Hum Genet; 2016 Mar 03; 98(3):500-513. PubMed ID: 26942284
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  • 40. Parkin mutation dosage and the phenomenon of anticipation: a molecular genetic study of familial parkinsonism.
    Poorkaj P, Moses L, Montimurro JS, Nutt JG, Schellenberg GD, Payami H.
    BMC Neurol; 2005 Feb 22; 5(1):4. PubMed ID: 15725358
    [Abstract] [Full Text] [Related]

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