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 *

73 related articles for article (PubMed ID: 22410449)

  • 41. A case of α-synuclein gene duplication presenting with head-shaking movements.
    Itokawa K; Sekine T; Funayama M; Tomiyama H; Fukui M; Yamamoto T; Tamura N; Matsuda H; Hattori N; Araki N
    Mov Disord; 2013 Mar; 28(3):384-7. PubMed ID: 23124679
    [TBL] [Abstract][Full Text] [Related]  

  • 42. SPG15: a cause of juvenile atypical levodopa responsive parkinsonism.
    Mallaret M; Lagha-Boukbiza O; Biskup S; Namer IJ; Rudolf G; Anheim M; Tranchant C
    J Neurol; 2014 Feb; 261(2):435-7. PubMed ID: 24366652
    [No Abstract]   [Full Text] [Related]  

  • 43. Putaminal necrosis presenting with hemidystonia.
    Kawano H; Takeuchi Y; Misawa A; Sawada T; Imahori Y
    Pediatr Neurol; 2000 Mar; 22(3):222-4. PubMed ID: 10734254
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Early-onset parkinsonism in PPP2R5D-related neurodevelopmental disorder.
    Hetzelt KLML; Kerling F; Kraus C; Rauch C; Thiel CT; Winterholler M; Reis A; Zweier C
    Eur J Med Genet; 2021 Jan; 64(1):104123. PubMed ID: 33338668
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Pediatric-Onset Epilepsy and Developmental Epileptic Encephalopathies Followed by Early-Onset Parkinsonism.
    Spagnoli C; Fusco C; Pisani F
    Int J Mol Sci; 2023 Feb; 24(4):. PubMed ID: 36835207
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Parkinsonism in Genetic Neurodevelopmental Disorders: A Systematic Review.
    von Scheibler ENMM; van Eeghen AM; de Koning TJ; Kuijf ML; Zinkstok JR; Müller AR; van Amelsvoort TAMJ; Boot E
    Mov Disord Clin Pract; 2023 Jan; 10(1):17-31. PubMed ID: 36699000
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Case Report: Phenotype-Gene Correlation in a Case of Novel Tandem 4q Microduplication With Short Stature, Speech Delay and Microcephaly.
    Umlai UI; Haris B; Hussain K; Jithesh PV
    Front Endocrinol (Lausanne); 2021; 12():783235. PubMed ID: 35185781
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Genetics of synucleins in neurodegenerative diseases.
    Brás J; Gibbons E; Guerreiro R
    Acta Neuropathol; 2021 Apr; 141(4):471-490. PubMed ID: 32740728
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Copy number variability in Parkinson's disease: assembling the puzzle through a systems biology approach.
    La Cognata V; Morello G; D'Agata V; Cavallaro S
    Hum Genet; 2017 Jan; 136(1):13-37. PubMed ID: 27896429
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Multisystem Lewy body disease and the other parkinsonian disorders.
    Langston JW; Schüle B; Rees L; Nichols RJ; Barlow C
    Nat Genet; 2015 Dec; 47(12):1378-84. PubMed ID: 26620112
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Autosomal dominant Parkinson's disease caused by SNCA duplications.
    Konno T; Ross OA; Puschmann A; Dickson DW; Wszolek ZK
    Parkinsonism Relat Disord; 2016 Jan; 22 Suppl 1(Suppl 1):S1-6. PubMed ID: 26350119
    [TBL] [Abstract][Full Text] [Related]  

  • 52. A 6.4 Mb duplication of the α-synuclein locus causing frontotemporal dementia and Parkinsonism: phenotype-genotype correlations.
    Kara E; Kiely AP; Proukakis C; Giffin N; Love S; Hehir J; Rantell K; Pandraud A; Hernandez DG; Nacheva E; Pittman AM; Nalls MA; Singleton AB; Revesz T; Bhatia KP; Quinn N; Hardy J; Holton JL; Houlden H
    JAMA Neurol; 2014 Sep; 71(9):1162-71. PubMed ID: 25003242
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Clinical heterogeneity of alpha-synuclein gene duplication in Parkinson's disease.
    Nishioka K; Hayashi S; Farrer MJ; Singleton AB; Yoshino H; Imai H; Kitami T; Sato K; Kuroda R; Tomiyama H; Mizoguchi K; Murata M; Toda T; Imoto I; Inazawa J; Mizuno Y; Hattori N
    Ann Neurol; 2006 Feb; 59(2):298-309. PubMed ID: 16358335
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [Relationship between alpha-synuclein and Parkinson's disease].
    Nishioka K; Hattori N
    Brain Nerve; 2007 Aug; 59(8):825-30. PubMed ID: 17713118
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Partial trisomy 4q associated with young-onset dopa-responsive parkinsonism.
    Garraux G; Caberg JH; Vanbellinghen JF; Jamar M; Bours V; Moonen G; Dive D
    Arch Neurol; 2012 Mar; 69(3):398-400. PubMed ID: 22410449
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Autosomal dominant dopa-responsive parkinsonism in a multigenerational Swiss family.
    Wider C; Skipper L; Solida A; Brown L; Farrer M; Dickson D; Wszolek ZK; Vingerhoets FJ
    Parkinsonism Relat Disord; 2008 Aug; 14(6):465-70. PubMed ID: 18342564
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Delay discounting of reward and caudate nucleus volume in individuals with α-synuclein gene duplication before and after the development of Parkinson's disease.
    Szamosi A; Nagy H; Kéri S
    Neurodegener Dis; 2013; 11(2):72-8. PubMed ID: 23038403
    [TBL] [Abstract][Full Text] [Related]  

  • 58.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 59.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 60.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.