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Pubmed for Handhelds

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Journal Abstract Search

378 related items for PubMed ID: 24993959

  • 1.
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  • 2. GCH1 mutations in dopa-responsive dystonia and Parkinson's disease.
    Yoshino H, Nishioka K, Li Y, Oji Y, Oyama G, Hatano T, Machida Y, Shimo Y, Hayashida A, Ikeda A, Mogushi K, Shibagaki Y, Hosaka A, Iwanaga H, Fujitake J, Ohi T, Miyazaki D, Sekijima Y, Oki M, Kusaka H, Fujimoto KI, Ugawa Y, Funayama M, Hattori N.
    J Neurol; 2018 Aug; 265(8):1860-1870. PubMed ID: 29948246
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  • 5. Common and rare GCH1 variants are associated with Parkinson's disease.
    Rudakou U, Ouled Amar Bencheikh B, Ruskey JA, Krohn L, Laurent SB, Spiegelman D, Liong C, Fahn S, Waters C, Monchi O, Fon EA, Dauvilliers Y, Alcalay RN, Dupré N, Gan-Or Z.
    Neurobiol Aging; 2019 Jan; 73():231.e1-231.e6. PubMed ID: 30314816
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  • 6. Novel GCH1 variant in Dopa-responsive dystonia and Parkinson's disease.
    Lewthwaite AJ, Lambert TD, Rolfe EB, Olgiati S, Quadri M, Simons EJ, Morrison KE, Bonifati V, Nicholl DJ.
    Parkinsonism Relat Disord; 2015 Apr; 21(4):394-7. PubMed ID: 25634433
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  • 7. A Compound Heterozygote for GCH1 Mutation Represents a Case of Atypical Dopa-Responsive Dystonia.
    Giri S, Naiya T, Roy S, Das G, Wali GM, Das SK, Ray K, Ray J.
    J Mol Neurosci; 2019 Jun; 68(2):214-220. PubMed ID: 30911941
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  • 8. Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia.
    Clot F, Grabli D, Cazeneuve C, Roze E, Castelnau P, Chabrol B, Landrieu P, Nguyen K, Ponsot G, Abada M, Doummar D, Damier P, Gil R, Thobois S, Ward AJ, Hutchinson M, Toutain A, Picard F, Camuzat A, Fedirko E, Sân C, Bouteiller D, LeGuern E, Durr A, Vidailhet M, Brice A, French Dystonia Network.
    Brain; 2009 Jul; 132(Pt 7):1753-63. PubMed ID: 19491146
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  • 9. Dopa-responsive dystonia and early-onset Parkinson's disease in a patient with GTP cyclohydrolase I deficiency?
    Hjermind LE, Johannsen LG, Blau N, Wevers RA, Lucking CB, Hertz JM, Friberg L, Regeur L, Nielsen JE, Sørensen SA.
    Mov Disord; 2006 May; 21(5):679-82. PubMed ID: 16267845
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  • 11. Catecholamines and Parkinson's disease: tyrosine hydroxylase (TH) over tetrahydrobiopterin (BH4) and GTP cyclohydrolase I (GCH1) to cytokines, neuromelanin, and gene therapy: a historical overview.
    Nagatsu T.
    J Neural Transm (Vienna); 2024 Jun; 131(6):617-630. PubMed ID: 37638996
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  • 12. GCH1 in early-onset Parkinson's disease.
    Cobb SA, Wider C, Ross OA, Mata IF, Adler CH, Rajput A, Rajput AH, Wu RM, Hauser R, Josephs KA, Carr J, Gwinn K, Heckman MG, Aasly JO, Lynch T, Uitti RJ, Wszolek ZK, Kapatos G, Farrer MJ.
    Mov Disord; 2009 Oct 30; 24(14):2070-5. PubMed ID: 19735094
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  • 14. Study of GCH1 and TH genes in Chinese patients with Parkinson's disease.
    Yan YP, Zhang B, Shen T, Si XL, Guo ZY, Tian J, Xu CY, Zhang BR.
    Neurobiol Aging; 2018 Aug 30; 68():159.e3-159.e6. PubMed ID: 29724574
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  • 18. GCH1 mutations in hereditary spastic paraplegia.
    Varghaei P, Yoon G, Estiar MA, Veyron S, Leveille E, Dupré N, Trempe JF, Rouleau GA, Gan-Or Z.
    Clin Genet; 2021 Jul 30; 100(1):51-58. PubMed ID: 33713342
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