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 *

221 related articles for article (PubMed ID: 24079843)

  • 1. The prevalence and genetics of Parkinson's disease in sub-Saharan Africans.
    Blanckenberg J; Bardien S; Glanzmann B; Okubadejo NU; Carr JA
    J Neurol Sci; 2013 Dec; 335(1-2):22-5. PubMed ID: 24079843
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Analysis of LRRK2, SNCA, Parkin, PINK1, and DJ-1 in Zambian patients with Parkinson's disease.
    Yonova-Doing E; Atadzhanov M; Quadri M; Kelly P; Shawa N; Musonda ST; Simons EJ; Breedveld GJ; Oostra BA; Bonifati V
    Parkinsonism Relat Disord; 2012 Jun; 18(5):567-71. PubMed ID: 22445250
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. An analysis of genetic studies of Parkinson's disease in Africa.
    Okubadejo NU
    Parkinsonism Relat Disord; 2008; 14(3):177-82. PubMed ID: 17881276
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Targeted next-generation sequencing identifies novel variants in candidate genes for Parkinson's disease in Black South African and Nigerian patients.
    Oluwole OG; Kuivaniemi H; Abrahams S; Haylett WL; Vorster AA; van Heerden CJ; Kenyon CP; Tabb DL; Fawale MB; Sunmonu TA; Ajose A; Olaogun MO; Rossouw AC; van Hillegondsberg LS; Carr J; Ross OA; Komolafe MA; Tromp G; Bardien S
    BMC Med Genet; 2020 Feb; 21(1):23. PubMed ID: 32019516
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Etiology and pathogenesis of Parkinson's disease: from mitochondrial dysfunctions to familial Parkinson's disease].
    Hattori N
    Rinsho Shinkeigaku; 2004; 44(4-5):241-62. PubMed ID: 15287506
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Parkinson's disease in Africa: A systematic review of epidemiologic and genetic studies.
    Okubadejo NU; Bower JH; Rocca WA; Maraganore DM
    Mov Disord; 2006 Dec; 21(12):2150-6. PubMed ID: 17044056
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Exonic rearrangements in the known Parkinson's disease-causing genes are a rare cause of the disease in South African patients.
    van der Merwe C; Carr J; Glanzmann B; Bardien S
    Neurosci Lett; 2016 Apr; 619():168-71. PubMed ID: 27001088
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetics of Parkinson's disease.
    Lill CM
    Mol Cell Probes; 2016 Dec; 30(6):386-396. PubMed ID: 27818248
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Evaluating intra-genetic variants of DJ-1 among Parkinson's disease patients of eastern India.
    Sanyal J; Sarkar B; Banerjee TK; Mukherjee SC; Ray BC; Raghavendra Rao V
    Neurol Res; 2011 May; 33(4):349-53. PubMed ID: 21535932
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetics in Parkinson disease: Mendelian versus non-Mendelian inheritance.
    Hernandez DG; Reed X; Singleton AB
    J Neurochem; 2016 Oct; 139 Suppl 1(Suppl 1):59-74. PubMed ID: 27090875
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular analysis of the parkin gene in South African patients diagnosed with Parkinson's disease.
    Bardien S; Keyser R; Yako Y; Lombard D; Carr J
    Parkinsonism Relat Disord; 2009 Feb; 15(2):116-21. PubMed ID: 18514563
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene.
    Clark LN; Haamer E; Mejia-Santana H; Harris J; Lesage S; Durr A; Bs SJ; Hedrich K; Louis ED; Cote LJ; Andrews H; Fahn S; Waters C; Ford B; Frucht S; Scott W; Klein C; Brice A; Roomere H; Ottman R; Marder K
    Mov Disord; 2007 May; 22(7):932-7. PubMed ID: 17415800
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [The genetics of Parkinson disease].
    Toft M; Aasly J
    Tidsskr Nor Laegeforen; 2004 Apr; 124(7):922-4. PubMed ID: 15060636
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prevalence of parkin gene mutations and variations in idiopathic Parkinson's disease.
    Sinha R; Racette B; Perlmutter JS; Parsian A
    Parkinsonism Relat Disord; 2005 Sep; 11(6):341-7. PubMed ID: 16019250
    [TBL] [Abstract][Full Text] [Related]  

  • 17. PRKN-related familial Parkinson's disease: First molecular confirmation from East Africa.
    Dekker MCJ; Suleiman JM; Bhwana D; Howlett WP; Rashid SM; van Minkelen R; Hamel BC
    Parkinsonism Relat Disord; 2020 Apr; 73():14-15. PubMed ID: 32193156
    [No Abstract]   [Full Text] [Related]  

  • 18. Role of mendelian genes in "sporadic" Parkinson's disease.
    Lesage S; Brice A
    Parkinsonism Relat Disord; 2012 Jan; 18 Suppl 1():S66-70. PubMed ID: 22166458
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetics of Parkinson's disease.
    Kumar KR; Djarmati-Westenberger A; Grünewald A
    Semin Neurol; 2011 Nov; 31(5):433-40. PubMed ID: 22266881
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.