BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

204 related articles for article (PubMed ID: 12728478)

  • 1. Homozygous exon 4 deletion in parkin gene in a Korean family with autosomal recessive early onset parkinsonism.
    Kim JS; Lee KS; Kim YI; Lee KH; Kim HT
    Yonsei Med J; 2003 Apr; 44(2):336-9. PubMed ID: 12728478
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 48(1):65-71. PubMed ID: 10894217
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
    Abbas N; Lücking CB; Ricard S; Dürr A; Bonifati V; De Michele G; Bouley S; Vaughan JR; Gasser T; Marconi R; Broussolle E; Brefel-Courbon C; Harhangi BS; Oostra BA; Fabrizio E; Böhme GA; Pradier L; Wood NW; Filla A; Meco G; Denefle P; Agid Y; Brice A
    Hum Mol Genet; 1999 Apr; 8(4):567-74. PubMed ID: 10072423
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 8():47. PubMed ID: 19087301
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Three parkin gene mutations in a sibship with autosomal recessive early onset parkinsonism.
    Bonifati V; Lücking CB; Fabrizio E; Periquet M; Meco G; Brice A
    J Neurol Neurosurg Psychiatry; 2001 Oct; 71(4):531-4. PubMed ID: 11561042
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: evidence for variable homozygous deletions in the Parkin gene in affected individuals.
    Hattori N; Kitada T; Matsumine H; Asakawa S; Yamamura Y; Yoshino H; Kobayashi T; Yokochi M; Wang M; Yoritaka A; Kondo T; Kuzuhara S; Nakamura S; Shimizu N; Mizuno Y
    Ann Neurol; 1998 Dec; 44(6):935-41. PubMed ID: 9851438
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Homozygous deletion mutation of the parkin gene in patients with atypical parkinsonism.
    Kuroda Y; Mitsui T; Akaike M; Azuma H; Matsumoto T
    J Neurol Neurosurg Psychiatry; 2001 Aug; 71(2):231-4. PubMed ID: 11459900
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Deletion of the parkin and PACRG gene promoter in early-onset parkinsonism.
    Lesage S; Magali P; Lohmann E; Lacomblez L; Teive H; Janin S; Cousin PY; Dürr A; Brice A;
    Hum Mutat; 2007 Jan; 28(1):27-32. PubMed ID: 17068781
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pseudo-dominant inheritance and exon 2 triplication in a family with parkin gene mutations.
    Lücking CB; Bonifati V; Periquet M; Vanacore N; Brice A; Meco G
    Neurology; 2001 Sep; 57(5):924-7. PubMed ID: 11552035
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 53(7):1602-4. PubMed ID: 10534280
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Parkin gene causing benign autosomal recessive juvenile parkinsonism.
    Nisipeanu P; Inzelberg R; Abo Mouch S; Carasso RL; Blumen SC; Zhang J; Matsumine H; Hattori N; Mizuno Y
    Neurology; 2001 Jun; 56(11):1573-5. PubMed ID: 11402119
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study.
    Gouider-Khouja N; Larnaout A; Amouri R; Sfar S; Belal S; Ben Hamida C; Ben Hamida M; Hattori N; Mizuno Y; Hentati F
    Parkinsonism Relat Disord; 2003 Jun; 9(5):247-51. PubMed ID: 12781588
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Role of parkin mutations in 111 community-based patients with early-onset parkinsonism.
    Kann M; Jacobs H; Mohrmann K; Schumacher K; Hedrich K; Garrels J; Wiegers K; Schwinger E; Pramstaller PP; Breakefield XO; Ozelius LJ; Vieregge P; Klein C
    Ann Neurol; 2002 May; 51(5):621-5. PubMed ID: 12112109
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical findings in a large family with a parkin ex3delta40 mutation.
    Munhoz RP; Sa DS; Rogaeva E; Salehi-Rad S; Sato C; Medeiros H; Farrer M; Lang AE
    Arch Neurol; 2004 May; 61(5):701-4. PubMed ID: 15148147
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Detection of compound heterozygous deletions in the parkin gene of fibroblasts in patients with autosomal recessive hereditary parkinsonism (PARK2).
    Nakaso K; Adachi Y; Yasui K; Sakuma K; Nakashima K
    Neurosci Lett; 2006 May; 400(1-2):44-7. PubMed ID: 16517073
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Autosomal recessive early onset parkinsonism is linked to three loci: PARK2, PARK6, and PARK7.
    Bonifati V; Dekker MC; Vanacore N; Fabbrini G; Squitieri F; Marconi R; Antonini A; Brustenghi P; Dalla Libera A; De Mari M; Stocchi F; Montagna P; Gallai V; Rizzu P; van Swieten JC; Oostra B; van Duijn CM; Meco G; Heutink P;
    Neurol Sci; 2002 Sep; 23 Suppl 2():S59-60. PubMed ID: 12548343
    [TBL] [Abstract][Full Text] [Related]  

  • 17. PARKIN as a pathogenic gene for autosomal recessive juvenile parkinsonism.
    Shimizu N; Asakawa S; Minoshima S; Kitada T; Hattori N; Matsumine H; Yokochi M; Yamamura Y; Mizuno Y
    J Neural Transm Suppl; 2000; (58):19-30. PubMed ID: 11128608
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Homozygous partial genomic triplication of the parkin gene in early-onset parkinsonism.
    Mata IF; Alvarez V; Coto E; Blazquez M; Guisasola LM; Salvador C; Kachergus JM; Lincoln SJ; Farrer M
    Neurosci Lett; 2005 Jun; 380(3):257-9. PubMed ID: 15862897
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Parkin mutations are frequent in patients with isolated early-onset parkinsonism.
    Periquet M; Latouche M; Lohmann E; Rawal N; De Michele G; Ricard S; Teive H; Fraix V; Vidailhet M; Nicholl D; Barone P; Wood NW; Raskin S; Deleuze JF; Agid Y; Dürr A; Brice A; ;
    Brain; 2003 Jun; 126(Pt 6):1271-8. PubMed ID: 12764050
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of alpha-synuclein, parkin, tau, and UCH-L1 in a Japanese family with autosomal dominant parkinsonism.
    Hasegawa K; Funayama M; Matsuura N; Furusawa H; Sakai F; Kowa H; Obata F
    Eur Neurol; 2001; 46(1):20-4. PubMed ID: 11455179
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.