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 *

254 related articles for article (PubMed ID: 11971093)

  • 21. High frequency of Parkin exon rearrangements in Mexican-mestizo patients with early-onset Parkinson's disease.
    Guerrero Camacho JL; Monroy Jaramillo N; Yescas Gómez P; Rodríguez Violante M; Boll Woehrlen C; Alonso Vilatela ME; López López M
    Mov Disord; 2012 Jul; 27(8):1047-51. PubMed ID: 22777964
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Parkin mutations and early-onset parkinsonism in a Taiwanese cohort.
    Wu RM; Bounds R; Lincoln S; Hulihan M; Lin CH; Hwu WL; Chen J; Gwinn-Hardy K; Farrer M
    Arch Neurol; 2005 Jan; 62(1):82-7. PubMed ID: 15642853
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Exon dosage analysis of parkin gene in Chinese sporadic Parkinson's disease.
    Guo JF; Dong XL; Xu Q; Li N; Yan XX; Xia K; Tang BS
    Neurosci Lett; 2015 Sep; 604():47-51. PubMed ID: 26240990
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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; 67(6):731-8. PubMed ID: 20558392
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Distribution, type, and origin of Parkin mutations: review and case studies.
    Hedrich K; Eskelson C; Wilmot B; Marder K; Harris J; Garrels J; Meija-Santana H; Vieregge P; Jacobs H; Bressman SB; Lang AE; Kann M; Abbruzzese G; Martinelli P; Schwinger E; Ozelius LJ; Pramstaller PP; Klein C; Kramer P
    Mov Disord; 2004 Oct; 19(10):1146-57. PubMed ID: 15390068
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Parkin dosage mutations in patients with early-onset sporadic and familial Parkinson's disease in Chinese: an independent pathogenic role.
    Wang C; Ma H; Feng X; Xie S; Chan P
    Brain Res; 2010 Oct; 1358():30-8. PubMed ID: 20800584
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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; 7(1):13-9. PubMed ID: 16328510
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. 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]  

  • 31. Analysis of exon dosage using MLPA in South African Parkinson's disease patients.
    Keyser RJ; Lombard D; Veikondis R; Carr J; Bardien S
    Neurogenetics; 2010 Jul; 11(3):305-12. PubMed ID: 20013014
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. [A novel point mutation in parkin gene was identified in an early-onset case of Parkinson's disease].
    Wang T; Liang Z; Sun S; Cao X; Peng H; Cao F; Liu H; Tong E
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Apr; 20(2):111-3. PubMed ID: 12673578
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Lewy bodies and parkinsonism in families with parkin mutations.
    Farrer M; Chan P; Chen R; Tan L; Lincoln S; Hernandez D; Forno L; Gwinn-Hardy K; Petrucelli L; Hussey J; Singleton A; Tanner C; Hardy J; Langston JW
    Ann Neurol; 2001 Sep; 50(3):293-300. PubMed ID: 11558785
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Molecular genetic analysis of the alpha-synuclein and the parkin gene in Parkinson's disease in Finland.
    Autere JM; Hiltunen MJ; Mannermaa AJ; Jäkälä PA; Hartikainen PH; Majamaa K; Alafuzoff I; Soininen HS
    Eur J Neurol; 2002 Sep; 9(5):479-83. PubMed ID: 12220378
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Lewy body Parkinson's disease in a large pedigree with 77 Parkin mutation carriers.
    Pramstaller PP; Schlossmacher MG; Jacques TS; Scaravilli F; Eskelson C; Pepivani I; Hedrich K; Adel S; Gonzales-McNeal M; Hilker R; Kramer PL; Klein C
    Ann Neurol; 2005 Sep; 58(3):411-22. PubMed ID: 16130111
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [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; 22(5):514-7. PubMed ID: 16215938
    [TBL] [Abstract][Full Text] [Related]  

  • 39. DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease.
    Hedrich K; Djarmati A; Schäfer N; Hering R; Wellenbrock C; Weiss PH; Hilker R; Vieregge P; Ozelius LJ; Heutink P; Bonifati V; Schwinger E; Lang AE; Noth J; Bressman SB; Pramstaller PP; Riess O; Klein C
    Neurology; 2004 Feb; 62(3):389-94. PubMed ID: 14872018
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Analysis of deletion mutations in the PARK2 gene in idiopathic Parkinson's disease].
    Slominskiĭ PA; Miloserdova OV; Popova SN; Giliazova IR; Khidiiatova IV; Magzhanov RV; Khusnutdinova EK; Limborskaia SA
    Genetika; 2003 Feb; 39(2):223-8. PubMed ID: 12669418
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.