These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

185 related articles for article (PubMed ID: 31927768)

  • 61. Parkin analysis in early onset Parkinson's disease.
    Sironi F; Primignani P; Zini M; Tunesi S; Ruffmann C; Ricca S; Brambilla T; Antonini A; Tesei S; Canesi M; Zecchinelli A; Mariani C; Meucci N; Sacilotto G; Cilia R; Isaias IU; Garavaglia B; Ghezzi D; Travi M; Decarli A; Coviello DA; Pezzoli G; Goldwurm S
    Parkinsonism Relat Disord; 2008; 14(4):326-33. PubMed ID: 18519021
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Drosophila PINK1 and parkin loss-of-function mutants display a range of non-motor Parkinson's disease phenotypes.
    Julienne H; Buhl E; Leslie DS; Hodge JJL
    Neurobiol Dis; 2017 Aug; 104():15-23. PubMed ID: 28435104
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Heterozygous parkin point mutations are as common in control subjects as in Parkinson's patients.
    Kay DM; Moran D; Moses L; Poorkaj P; Zabetian CP; Nutt J; Factor SA; Yu CE; Montimurro JS; Keefe RG; Schellenberg GD; Payami H
    Ann Neurol; 2007 Jan; 61(1):47-54. PubMed ID: 17187375
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Variability in clinical phenotypes of heterozygous and homozygous cases of Parkin-related Parkinson's disease.
    Thompson AJ; Scholz SW; Singleton AB; Hardwick A; McFarland NR; Okun MS
    Int J Neurosci; 2013 Dec; 123(12):847-9. PubMed ID: 23767969
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Parkin (PARK 2) mutations are rare in Czech patients with early-onset Parkinson's disease.
    Fiala O; Zahorakova D; Pospisilova L; Kucerova J; Matejckova M; Martasek P; Roth J; Ruzicka E
    PLoS One; 2014; 9(9):e107585. PubMed ID: 25238391
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Mutations in the parkin gene are a minor cause of Parkinson's disease in the South African population.
    Haylett WL; Keyser RJ; du Plessis MC; van der Merwe C; Blanckenberg J; Lombard D; Carr J; Bardien S
    Parkinsonism Relat Disord; 2012 Jan; 18(1):89-92. PubMed ID: 21996382
    [TBL] [Abstract][Full Text] [Related]  

  • 67. 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; 53(5):624-9. PubMed ID: 12730996
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Onset and progression of disease in familial and sporadic Parkinson's disease.
    Inzelberg R; Schecthman E; Paleacu D; Zach L; Bonwitt R; Carasso RL; Nisipeanu P
    Am J Med Genet A; 2004 Jan; 124A(3):255-8. PubMed ID: 14708097
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Parkinson's disease phenotype is influenced by the severity of the mutations in the GBA gene.
    Thaler A; Bregman N; Gurevich T; Shiner T; Dror Y; Zmira O; Gan-Or Z; Bar-Shira A; Gana-Weisz M; Orr-Urtreger A; Giladi N; Mirelman A
    Parkinsonism Relat Disord; 2018 Oct; 55():45-49. PubMed ID: 29784561
    [TBL] [Abstract][Full Text] [Related]  

  • 70. REM sleep-associated motor behaviors in Parkinson's disease patients with heterozygous Parkin mutations.
    Sixel-Döring F; Lohmann K; Klein C; Trenkwalder C; Mollenhauer B
    Mov Disord; 2015 Apr; 30(4):597-8. PubMed ID: 25771888
    [No Abstract]   [Full Text] [Related]  

  • 71. Genetic analysis of Parkin in early onset Parkinson's disease (PD): Novel intron 9 g > a single nucleotide polymorphism and risk of Taiwanese PD.
    Wu YR; Wu CH; Chao CY; Kuan CC; Zhang WL; Wang CK; Chang CY; Chang YC; Lee-Chen GJ; Chen CM
    Am J Med Genet B Neuropsychiatr Genet; 2010 Jan; 153B(1):229-34. PubMed ID: 19475582
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Mutation analysis of the PARKIN, PINK1, DJ1, and SNCA genes in Turkish early-onset Parkinson's patients and genotype-phenotype correlations.
    Erer S; Egeli U; Zarifoglu M; Tezcan G; Cecener G; Tunca B; Ak S; Demirdogen E; Kenangil G; Kaleagası H; Dogu O; Saka E; Elibol B
    Clin Neurol Neurosurg; 2016 Sep; 148():147-53. PubMed ID: 27455133
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Parkin Somatic Mutations Link Melanoma and Parkinson's Disease.
    Levin L; Srour S; Gartner J; Kapitansky O; Qutob N; Dror S; Golan T; Dayan R; Brener R; Ziv T; Khaled M; Schueler-Furman O; Samuels Y; Levy C
    J Genet Genomics; 2016 Jun; 43(6):369-79. PubMed ID: 27297116
    [TBL] [Abstract][Full Text] [Related]  

  • 74. A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson's disease.
    Nishioka K; Kefi M; Jasinska-Myga B; Wider C; Vilariño-Güell C; Ross OA; Heckman MG; Middleton LT; Ishihara-Paul L; Gibson RA; Amouri R; Ben Yahmed S; Ben Sassi S; Zouari M; El Euch G; Farrer MJ; Hentati F
    J Neurol Neurosurg Psychiatry; 2010 Apr; 81(4):391-5. PubMed ID: 19726410
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Prevalence and clinical features of LRRK2 mutations in patients with Parkinson's disease in southern Spain.
    Gao L; Gómez-Garre P; Díaz-Corrales FJ; Carrillo F; Carballo M; Palomino A; Díaz-Martín J; Mejías R; Vime PJ; López-Barneo J; Mir P
    Eur J Neurol; 2009 Aug; 16(8):957-60. PubMed ID: 19473361
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Mutation screening and association analysis of the parkin gene in Parkinson's disease patients from South-West China.
    Peng R; Gou Y; Yuan Q; Li T; Latsoudis H; Yuan G; Luo D; Liu X; Collier DA
    Eur Neurol; 2003; 49(2):85-9. PubMed ID: 12584415
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Influence of depression in mild Parkinson's disease on longitudinal motor and cognitive function.
    Ng A; Chander RJ; Tan LC; Kandiah N
    Parkinsonism Relat Disord; 2015 Sep; 21(9):1056-60. PubMed ID: 26117438
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Analysis of the parkin deletion in sporadic and familial Parkinson's disease. Short communication.
    Krüger R; Vieira-Säcker AM; Kuhn W; Müller T; Woitalla D; Schöls L; Przuntek H; Epplen JT; Riess O
    J Neural Transm (Vienna); 1999; 106(2):159-63. PubMed ID: 10226936
    [TBL] [Abstract][Full Text] [Related]  

  • 79. The sooner, the later - Delayed diagnosis in Parkinson's disease due to Parkin mutations.
    Borsche M; Balck A; Kasten M; Lohmann K; Klein C; Brüggemann N
    Parkinsonism Relat Disord; 2019 Aug; 65():284-285. PubMed ID: 31255538
    [TBL] [Abstract][Full Text] [Related]  

  • 80. 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; 76(11):1588-90. PubMed ID: 16227559
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.