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 *

98 related articles for article (PubMed ID: 11405814)

  • 1. An apparently sporadic case with parkin gene mutation in a Korean woman.
    Jeon BS; Kim JM; Lee DS; Hattori N; Mizuno Y
    Arch Neurol; 2001 Jun; 58(6):988-9. PubMed ID: 11405814
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Imaging of dopaminergic dysfunction with [123I]FP-CIT SPECT in early-onset parkin disease.
    Varrone A; Pellecchia MT; Amboni M; Sansone V; Salvatore E; Ghezzi D; Garavaglia B; Brice A; Brunetti A; Bonavita V; De Michele G; Salvatore M; Pappatà S; Barone P
    Neurology; 2004 Dec; 63(11):2097-103. PubMed ID: 15596756
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The nigrostriatal dopaminergic system in familial early onset parkinsonism with parkin mutations.
    Portman AT; Giladi N; Leenders KL; Maguire P; Veenma-van der Duin L; Swart J; Pruim J; Simon ES; Hassin-Baer S; Korczyn AD
    Neurology; 2001 Jun; 56(12):1759-62. PubMed ID: 11425950
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Positron emission tomographic analysis of the nigrostriatal dopaminergic system in familial parkinsonism associated with mutations in the parkin gene.
    Hilker R; Klein C; Ghaemi M; Kis B; Strotmann T; Ozelius LJ; Lenz O; Vieregge P; Herholz K; Heiss WD; Pramstaller PP
    Ann Neurol; 2001 Mar; 49(3):367-76. PubMed ID: 11261512
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Dopamine transporter density measured by [123I]beta-CIT single-photon emission computed tomography is normal in dopa-responsive dystonia.
    Jeon BS; Jeong JM; Park SS; Kim JM; Chang YS; Song HC; Kim KM; Yoon KY; Lee MC; Lee SB
    Ann Neurol; 1998 Jun; 43(6):792-800. PubMed ID: 9629849
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A new mutation in the parkin gene in a patient with atypical autosomal recessive juvenile parkinsonism.
    Muñoz E; Pastor P; Martí MJ; Oliva R; Tolosa E
    Neurosci Lett; 2000 Jul; 289(1):66-8. PubMed ID: 10899410
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Importance of low-range CAG expansion and CAA interruption in SCA2 Parkinsonism.
    Kim JM; Hong S; Kim GP; Choi YJ; Kim YK; Park SS; Kim SE; Jeon BS
    Arch Neurol; 2007 Oct; 64(10):1510-8. PubMed ID: 17923635
    [TBL] [Abstract][Full Text] [Related]  

  • 8. SPECT-evaluation of the monoamine uptake site ligand [123I](1R)-2-beta-carbomethoxy-3-beta-(4-iodophenyl)-tropane ([123I]beta-CIT) in untreated patients with suspicion of Parkinson disease.
    Eising EG; Müller TT; Zander C; Kuhn W; Farahati J; Reiners C; Coenen HH
    J Investig Med; 1997 Oct; 45(8):448-52. PubMed ID: 9394097
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Dopamine transporter imaging with [123I]-beta-CIT demonstrates presynaptic nigrostriatal dopaminergic damage in Wilson's disease.
    Jeon B; Kim JM; Jeong JM; Kim KM; Chang YS; Lee DS; Lee MC
    J Neurol Neurosurg Psychiatry; 1998 Jul; 65(1):60-4. PubMed ID: 9667562
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Brain perfusion abnormalities in a sibship with parkin-linked parkinsonism.
    Kobayashi Z; Miake H; Fujigasaki H
    Parkinsonism Relat Disord; 2008 Nov; 14(7):581-3. PubMed ID: 18331811
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. [18F]-Dopa positron emission tomography imaging in early-stage, non-parkin juvenile parkinsonism.
    Pal PK; Leung J; Hedrich K; Samii A; Lieberman A; Nausieda PA; Calne DB; Breakefield XO; Klein C; Stoessl AJ
    Mov Disord; 2002 Jul; 17(4):789-94. PubMed ID: 12210877
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Association between early-onset Parkinson's disease and mutations in the parkin gene.
    Lücking CB; Dürr A; Bonifati V; Vaughan J; De Michele G; Gasser T; Harhangi BS; Meco G; Denèfle P; Wood NW; Agid Y; Brice A; ;
    N Engl J Med; 2000 May; 342(21):1560-7. PubMed ID: 10824074
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [18 F]-dopa PET study in patients with juvenile-onset PD and parkin gene mutations.
    Broussolle E; Lücking CB; Ginovart N; Pollak P; Remy P; Dürr A
    Neurology; 2000 Sep; 55(6):877-9. PubMed ID: 10994015
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Parkin mutations in a patient with hemiparkinsonism-hemiatrophy: a clinical-genetic and PET study.
    Pramstaller PP; Künig G; Leenders K; Kann M; Hedrich K; Vieregge P; Goetz CG; Klein C
    Neurology; 2002 Mar; 58(5):808-10. PubMed ID: 11889248
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Differential alteration of the nigrostriatal dopaminergic system in Wilson's disease investigated with [123I]ss-CIT and high-resolution SPET.
    Barthel H; Sorger D; Kühn HJ; Wagner A; Kluge R; Hermann W
    Eur J Nucl Med; 2001 Nov; 28(11):1656-63. PubMed ID: 11702107
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Topography of dopamine transporter availability in progressive supranuclear palsy: a voxelwise [123I]beta-CIT SPECT analysis.
    Seppi K; Scherfler C; Donnemiller E; Virgolini I; Schocke MF; Goebel G; Mair KJ; Boesch S; Brenneis C; Wenning GK; Poewe W
    Arch Neurol; 2006 Aug; 63(8):1154-60. PubMed ID: 16908744
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Parkinsonism and essential tremor in a family with pseudo-dominant inheritance of PARK2: an FP-CIT SPECT study.
    Pellecchia MT; Varrone A; Annesi G; Amboni M; Cicarelli G; Sansone V; Annesi F; Rocca FE; Vitale C; Pappatà S; Quattrone A; Barone P
    Mov Disord; 2007 Mar; 22(4):559-63. PubMed ID: 17149727
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 5.