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 *

244 related articles for article (PubMed ID: 23459986)

  • 1. Parkin disease: a clinicopathologic entity?
    Doherty KM; Silveira-Moriyama L; Parkkinen L; Healy DG; Farrell M; Mencacci NE; Ahmed Z; Brett FM; Hardy J; Quinn N; Counihan TJ; Lynch T; Fox ZV; Revesz T; Lees AJ; Holton JL
    JAMA Neurol; 2013 May; 70(5):571-9. PubMed ID: 23459986
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Parkin-positive autosomal recessive juvenile Parkinsonism with alpha-synuclein-positive inclusions.
    Sasaki S; Shirata A; Yamane K; Iwata M
    Neurology; 2004 Aug; 63(4):678-82. PubMed ID: 15326242
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A multidisciplinary study of patients with early-onset PD with and without parkin mutations.
    Lohmann E; Thobois S; Lesage S; Broussolle E; du Montcel ST; Ribeiro MJ; Remy P; Pelissolo A; Dubois B; Mallet L; Pollak P; Agid Y; Brice A;
    Neurology; 2009 Jan; 72(2):110-6. PubMed ID: 18987353
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations.
    van de Warrenburg BP; Lammens M; Lücking CB; Denèfle P; Wesseling P; Booij J; Praamstra P; Quinn N; Brice A; Horstink MW
    Neurology; 2001 Feb; 56(4):555-7. PubMed ID: 11222808
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. A homozygous parkin p.G284R mutation in a Chinese family with autosomal recessive juvenile parkinsonism.
    Chen H; Huang X; Yuan L; Xia H; Xu H; Yang Y; Zheng W; Deng H
    Neurosci Lett; 2016 Jun; 624():100-4. PubMed ID: 27177722
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Autosomal recessive early-onset parkinsonism with diurnal fluctuation: clinicopathologic characteristics and molecular genetic identification.
    Yamamura Y; Hattori N; Matsumine H; Kuzuhara S; Mizuno Y
    Brain Dev; 2000 Sep; 22 Suppl 1():S87-91. PubMed ID: 10984666
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Morphological substrates of mental dysfunction in Lewy body disease: an update.
    Jellinger KA
    J Neural Transm Suppl; 2000; 59():185-212. PubMed ID: 10961431
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. A Peruvian family with a novel PARK2 mutation: Clinical and pathological characteristics.
    Cornejo-Olivas MR; Torres L; Mata IF; Mazzetti P; Rivas D; Cosentino C; Inca-Martinez M; Cuba JM; Zabetian CP; Leverenz JB
    Parkinsonism Relat Disord; 2015 May; 21(5):444-8. PubMed ID: 25817512
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Significance of the parkin gene and protein in understanding Parkinson's disease.
    Fishman PS; Oyler GA
    Curr Neurol Neurosci Rep; 2002 Jul; 2(4):296-302. PubMed ID: 12044248
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Autosomal recessive juvenile parkinsonism: a key to understanding nigral degeneration in sporadic Parkinson's disease.
    Hattori N; Shimura H; Kubo S; Kitada T; Wang M; Asakawa S; Minashima S; Shimizu N; Suzuki T; Tanaka K; Mizuno Y
    Neuropathology; 2000 Sep; 20 Suppl():S85-90. PubMed ID: 11037196
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Parkinson's disease with Lewy bodies associated with a heterozygous PARKIN dosage mutation.
    Sharp ME; Marder KS; Côté L; Clark LN; Nichols WC; Vonsattel JP; Alcalay RN
    Mov Disord; 2014 Apr; 29(4):566-8. PubMed ID: 24375549
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Parkin and PINK1 parkinsonism may represent nigral mitochondrial cytopathies distinct from Lewy body Parkinson's disease.
    Ahlskog JE
    Parkinsonism Relat Disord; 2009 Dec; 15(10):721-7. PubMed ID: 19815446
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Lewy body pathology in a patient with a homozygous parkin deletion.
    Miyakawa S; Ogino M; Funabe S; Uchino A; Shimo Y; Hattori N; Ichinoe M; Mikami T; Saegusa M; Nishiyama K; Mori H; Mizuno Y; Murayama S; Mochizuki H
    Mov Disord; 2013 Mar; 28(3):388-91. PubMed ID: 23401296
    [TBL] [Abstract][Full Text] [Related]  

  • 18. PINK1-linked parkinsonism is associated with Lewy body pathology.
    Samaranch L; Lorenzo-Betancor O; Arbelo JM; Ferrer I; Lorenzo E; Irigoyen J; Pastor MA; Marrero C; Isla C; Herrera-Henriquez J; Pastor P
    Brain; 2010 Apr; 133(Pt 4):1128-42. PubMed ID: 20356854
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic screening reveals high frequency of PARK2 mutations and reduced Parkin expression conferring risk for Parkinsonism in North West India.
    Vinish M; Prabhakar S; Khullar M; Verma I; Anand A
    J Neurol Neurosurg Psychiatry; 2010 Feb; 81(2):166-70. PubMed ID: 19734163
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 13.