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Journal Abstract Search

217 related items for PubMed ID: 17335904

  • 1. Parkin polymorphisms and environmental exposure: decrease in age at onset of Parkinson's disease.
    Ghione I, Di Fonzo A, Saladino F, Del Bo R, Bresolin N, Comi GP, Rango M.
    Neurotoxicology; 2007 May; 28(3):698-701. PubMed ID: 17335904
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  • 4. [Etiology and pathogenesis of Parkinson's disease: from mitochondrial dysfunctions to familial Parkinson's disease].
    Hattori N.
    Rinsho Shinkeigaku; 2004 May; 44(4-5):241-62. PubMed ID: 15287506
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  • 5. Association study of Parkin gene polymorphisms with idiopathic Parkinson disease.
    Oliveira SA, Scott WK, Nance MA, Watts RL, Hubble JP, Koller WC, Lyons KE, Pahwa R, Stern MB, Hiner BC, Jankovic J, Ondo WG, Allen FH, Scott BL, Goetz CG, Small GW, Mastaglia FL, Stajich JM, Zhang F, Booze MW, Reaves JA, Middleton LT, Haines JL, Pericak-Vance MA, Vance JM, Martin ER.
    Arch Neurol; 2003 Jul; 60(7):975-80. PubMed ID: 12873854
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  • 6. Genetic and environmental findings in early-onset Parkinson's disease Brazilian patients.
    Aguiar Pde C, Lessa PS, Godeiro C, Barsottini O, Felício AC, Borges V, Silva SM, Saba RA, Ferraz HB, Moreira-Filho CA, Andrade LA.
    Mov Disord; 2008 Jul 15; 23(9):1228-33. PubMed ID: 18464276
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  • 7. Case-control study of the parkin gene in early-onset Parkinson disease.
    Clark LN, Afridi S, Karlins E, Wang Y, Mejia-Santana H, Harris J, Louis ED, Cote LJ, Andrews H, Fahn S, Waters C, Ford B, Frucht S, Ottman R, Marder K.
    Arch Neurol; 2006 Apr 15; 63(4):548-52. PubMed ID: 16606767
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  • 8. Parkin mutations in familial and sporadic Parkinson's disease among Indians.
    Chaudhary S, Behari M, Dihana M, Swaminath PV, Govindappa ST, Jayaram S, Goyal V, Maitra A, Muthane UB, Juyal RC, Thelma BK.
    Parkinsonism Relat Disord; 2006 May 15; 12(4):239-45. PubMed ID: 16500134
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  • 9. A functional polymorphism in the parkin gene promoter affects the age of onset of Parkinson's disease.
    Sutherland G, Mellick G, Sue C, Chan DK, Rowe D, Silburn P, Halliday G.
    Neurosci Lett; 2007 Mar 06; 414(2):170-3. PubMed ID: 17280783
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  • 10. Parkin mutations and phenotypic features in Czech patients with early-onset Parkinson's disease.
    Fiala O, Pospisilova L, Prochazkova J, Matejckova M, Martasek P, Novakova L, Roth J, Ruzicka E.
    Neuro Endocrinol Lett; 2010 Mar 06; 31(2):187-92. PubMed ID: 20424582
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  • 11. Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study.
    Sun M, Latourelle JC, Wooten GF, Lew MF, Klein C, Shill HA, Golbe LI, Mark MH, Racette BA, Perlmutter JS, Parsian A, Guttman M, Nicholson G, Xu G, Wilk JB, Saint-Hilaire MH, DeStefano AL, Prakash R, Williamson S, Suchowersky O, Labelle N, Growdon JH, Singer C, Watts RL, Goldwurm S, Pezzoli G, Baker KB, Pramstaller PP, Burn DJ, Chinnery PF, Sherman S, Vieregge P, Litvan I, Gillis T, MacDonald ME, Myers RH, Gusella JF.
    Arch Neurol; 2006 Jun 06; 63(6):826-32. PubMed ID: 16769863
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  • 12. Evaluation of PARKIN gene variants in West Bengal Parkinson's disease patients.
    Sanyal J, Jana A, Ghosh E, Banerjee TK, Chakraborty DP, Rao VR.
    J Hum Genet; 2015 Sep 06; 60(9):485-92. PubMed ID: 26016408
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  • 13. 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 06; 134(4):271-6. PubMed ID: 26626018
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  • 14. Coding polymorphisms in the parkin gene and susceptibility to Parkinson disease.
    Lücking CB, Chesneau V, Lohmann E, Verpillat P, Dulac C, Bonnet AM, Gasparini F, Agid Y, Dürr A, Brice A.
    Arch Neurol; 2003 Sep 06; 60(9):1253-6. PubMed ID: 12975291
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  • 15. [A study on PARKIN gene in three pedigrees with autosomal recessive early-onset Parkinson's disease].
    Jin M, Jiao JS, Gu WH, Wang K, Zou HQ, Chen B, Wang GX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Oct 06; 22(5):514-7. PubMed ID: 16215938
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  • 16. Parkinson's disease in Ireland: clinical presentation and genetic heterogeneity in patients with parkin mutations.
    Wiley J, Lynch T, Lincoln S, Skipper L, Hulihan M, Gosal D, Bisceglio G, Kachergus J, Hardy J, Farrer MJ.
    Mov Disord; 2004 Jun 06; 19(6):677-81. PubMed ID: 15197707
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  • 18. Parkin mutations and susceptibility alleles in late-onset Parkinson's disease.
    Oliveira SA, Scott WK, Martin ER, Nance MA, Watts RL, Hubble JP, Koller WC, Pahwa R, Stern MB, Hiner BC, Ondo WG, Allen FH, Scott BL, Goetz CG, Small GW, Mastaglia F, Stajich JM, Zhang F, Booze MW, Winn MP, Middleton LT, Haines JL, Pericak-Vance MA, Vance JM.
    Ann Neurol; 2003 May 06; 53(5):624-9. PubMed ID: 12730996
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  • 19. Low frequency of Parkin, Tyrosine Hydroxylase, and GTP Cyclohydrolase I gene mutations in a Danish population of early-onset Parkinson's Disease.
    Hertz JM, Ostergaard K, Juncker I, Pedersen S, Romstad A, Møller LB, Güttler F, Dupont E.
    Eur J Neurol; 2006 Apr 06; 13(4):385-90. PubMed ID: 16643317
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  • 20. Mutational screening of the parkin gene among South Indians with early onset Parkinson's disease.
    Madegowda RH, Kishore A, Anand A.
    J Neurol Neurosurg Psychiatry; 2005 Nov 06; 76(11):1588-90. PubMed ID: 16227559
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