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 *

243 related articles for article (PubMed ID: 23449625)

  • 1. Role of Gα(olf) in familial and sporadic adult-onset primary dystonia.
    Vemula SR; Puschmann A; Xiao J; Zhao Y; Rudzińska M; Frei KP; Truong DD; Wszolek ZK; LeDoux MS
    Hum Mol Genet; 2013 Jun; 22(12):2510-9. PubMed ID: 23449625
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Heterogeneity in primary dystonia: lessons from THAP1, GNAL, and TOR1A in Amish-Mennonites.
    Saunders-Pullman R; Fuchs T; San Luciano M; Raymond D; Brashear A; Ortega R; Deik A; Ozelius LJ; Bressman SB
    Mov Disord; 2014 May; 29(6):812-8. PubMed ID: 24500857
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Screening of mutations in GNAL in sporadic dystonia patients.
    Dufke C; Sturm M; Schroeder C; Moll S; Ott T; Riess O; Bauer P; Grundmann K
    Mov Disord; 2014 Aug; 29(9):1193-6. PubMed ID: 24408567
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Gnal haploinsufficiency causes genomic instability and increased sensitivity to haloperidol.
    Khan MM; Xiao J; Hollingsworth TJ; Patel D; Selley DE; Ring TL; LeDoux MS
    Exp Neurol; 2019 Aug; 318():61-70. PubMed ID: 31034808
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Blepharospasm in a multiplex African-American pedigree.
    Xiao J; Thompson MM; Vemula SR; LeDoux MS
    J Neurol Sci; 2016 Mar; 362():299-303. PubMed ID: 26944167
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations in GNAL cause primary torsion dystonia.
    Fuchs T; Saunders-Pullman R; Masuho I; Luciano MS; Raymond D; Factor S; Lang AE; Liang TW; Trosch RM; White S; Ainehsazan E; Hervé D; Sharma N; Ehrlich ME; Martemyanov KA; Bressman SB; Ozelius LJ
    Nat Genet; 2013 Jan; 45(1):88-92. PubMed ID: 23222958
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel THAP1 sequence variants in primary dystonia.
    Xiao J; Zhao Y; Bastian RW; Perlmutter JS; Racette BA; Tabbal SD; Karimi M; Paniello RC; Wszolek ZK; Uitti RJ; Van Gerpen JA; Simon DK; Tarsy D; Hedera P; Truong DD; Frei KP; Dev Batish S; Blitzer A; Pfeiffer RF; Gong S; LeDoux MS
    Neurology; 2010 Jan; 74(3):229-38. PubMed ID: 20083799
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutation screening of GNAL gene in patients with primary dystonia from Northeast China.
    Miao J; Wan XH; Sun Y; Feng JC; Cheng FB
    Parkinsonism Relat Disord; 2013 Oct; 19(10):910-2. PubMed ID: 23759320
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Screening of GNAL variants in Brazilian patients with isolated dystonia reveals a novel mutation with partial loss of function.
    Dos Santos CO; Masuho I; da Silva-Júnior FP; Barbosa ER; Silva SM; Borges V; Ferraz HB; Rocha MS; Limongi JC; Martemyanov KA; de Carvalho Aguiar P
    J Neurol; 2016 Apr; 263(4):665-8. PubMed ID: 26810727
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel GNAL mutation with intra-familial clinical heterogeneity: Expanding the phenotype.
    Carecchio M; Panteghini C; Reale C; Barzaghi C; Monti V; Romito L; Sasanelli F; Garavaglia B
    Parkinsonism Relat Disord; 2016 Feb; 23():66-71. PubMed ID: 26725140
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutations in CIZ1 cause adult onset primary cervical dystonia.
    Xiao J; Uitti RJ; Zhao Y; Vemula SR; Perlmutter JS; Wszolek ZK; Maraganore DM; Auburger G; Leube B; Lehnhoff K; LeDoux MS
    Ann Neurol; 2012 Apr; 71(4):458-69. PubMed ID: 22447717
    [TBL] [Abstract][Full Text] [Related]  

  • 12. De novo mutation in the GNAL gene causing seemingly sporadic dystonia in a Serbian patient.
    Dobričić V; Kresojević N; Westenberger A; Svetel M; Tomić A; Ralić V; Petrović I; Lukić MJ; Lohmann K; Novaković I; Klein C; Kostić VS
    Mov Disord; 2014 Aug; 29(9):1190-3. PubMed ID: 24729450
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Gα(olf) mutation allows parsing the role of cAMP-dependent and extracellular signal-regulated kinase-dependent signaling in L-3,4-dihydroxyphenylalanine-induced dyskinesia.
    Alcacer C; Santini E; Valjent E; Gaven F; Girault JA; Hervé D
    J Neurosci; 2012 Apr; 32(17):5900-10. PubMed ID: 22539851
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A new mutation in the GNAL gene in familial dystonia presenting with mental symptoms.
    Fan S; Cao Q; Peng B; Yin B; Xiao T; Sun L; Dong H
    Neurol Sci; 2022 Jul; 43(7):4547-4549. PubMed ID: 35396637
    [TBL] [Abstract][Full Text] [Related]  

  • 15.
    Millett M; Heuberger A; Castosa EM; Comite A; Wagner P; Hall D; Gallardo I; Chambers NE; Wagner L; Moehle MS
    bioRxiv; 2024 Apr; ():. PubMed ID: 38617339
    [TBL] [Abstract][Full Text] [Related]  

  • 16. An African-American family with dystonia.
    Puschmann A; Xiao J; Bastian RW; Searcy JA; LeDoux MS; Wszolek ZK
    Parkinsonism Relat Disord; 2011 Aug; 17(7):547-50. PubMed ID: 21601506
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutational spectrum of GNAL, THAP1 and TOR1A genes in isolated dystonia: study in a population from Spain and systematic literature review.
    Gómez-Garre P; Jesús S; Periñán MT; Adarmes A; Alonso-Canovas A; Blanco-Ollero A; Buiza-Rueda D; Carrillo F; Catalán-Alonso MJ; Del Val J; Escamilla-Sevilla F; Espinosa-Rosso R; Fernández-Moreno MC; García-Moreno JM; García-Ruiz PJ; Giacometti-Silveira S; Gutiérrez-García J; López-Valdés E; Macías-García D; Martínez-Castrillo JC; Martínez-Torres I; Medialdea-Natera MP; Mínguez-Castellanos A; Moya MÁ; Ochoa-Sepulveda JJ; Ojea T; Rodríguez N; Sillero-Sánchez M; Tejera-Parrado C; Mir P
    Eur J Neurol; 2021 Apr; 28(4):1188-1197. PubMed ID: 33175450
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genotype-Phenotype Relations for Isolated Dystonia Genes: MDSGene Systematic Review.
    Lange LM; Junker J; Loens S; Baumann H; Olschewski L; Schaake S; Madoev H; Petkovic S; Kuhnke N; Kasten M; Westenberger A; Domingo A; Marras C; König IR; Camargos S; Ozelius LJ; Klein C; Lohmann K
    Mov Disord; 2021 May; 36(5):1086-1103. PubMed ID: 33502045
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Recessive mutations in the α3 (VI) collagen gene COL6A3 cause early-onset isolated dystonia.
    Zech M; Lam DD; Francescatto L; Schormair B; Salminen AV; Jochim A; Wieland T; Lichtner P; Peters A; Gieger C; Lochmüller H; Strom TM; Haslinger B; Katsanis N; Winkelmann J
    Am J Hum Genet; 2015 Jun; 96(6):883-93. PubMed ID: 26004199
    [TBL] [Abstract][Full Text] [Related]  

  • 20. GNAL mutation in isolated laryngeal dystonia.
    Putzel GG; Fuchs T; Battistella G; Rubien-Thomas E; Frucht SJ; Blitzer A; Ozelius LJ; Simonyan K
    Mov Disord; 2016 May; 31(5):750-5. PubMed ID: 27093447
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.