BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

216 related articles for article (PubMed ID: 24408567)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. Novel GNAL mutations in two German patients with sporadic dystonia.
    Ziegan J; Wittstock M; Westenberger A; Dobričić V; Wolters A; Benecke R; Klein C; Kamm C
    Mov Disord; 2014 Dec; 29(14):1833-4. PubMed ID: 25382112
    [No Abstract]   [Full Text] [Related]  

  • 6. 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]  

  • 7. TOR1A, THAP1, and GNAL mutational screening in Austrian patients with primary isolated dystonia.
    Zech M; Boesch S; Sycha T; Mueller J; Poewe W; Winkelmann J
    Mov Disord; 2015 Nov; 30(13):1853-4. PubMed ID: 26506956
    [No Abstract]   [Full Text] [Related]  

  • 8. Inherited isolated dystonia: clinical genetics and gene function.
    Dauer W
    Neurotherapeutics; 2014 Oct; 11(4):807-16. PubMed ID: 25155315
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controls.
    Zech M; Gross N; Jochim A; Castrop F; Kaffe M; Dresel C; Lichtner P; Peters A; Gieger C; Meitinger T; Haslinger B; Winkelmann J
    Mov Disord; 2014 Jan; 29(1):143-7. PubMed ID: 24151159
    [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. 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]  

  • 12. Novel THAP1 variants in Brazilian patients with idiopathic isolated dystonia.
    da Silva-Junior FP; dos Santos CO; Silva SM; Barbosa ER; Borges V; Ferraz HB; Limongi JC; Rocha MS; de Carvalho Aguiar P
    J Neurol Sci; 2014 Sep; 344(1-2):190-2. PubMed ID: 24976531
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Update on the Genetics of Dystonia.
    Lohmann K; Klein C
    Curr Neurol Neurosci Rep; 2017 Mar; 17(3):26. PubMed ID: 28283962
    [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. Mutations in GNAL: a novel cause of craniocervical dystonia.
    Kumar KR; Lohmann K; Masuho I; Miyamoto R; Ferbert A; Lohnau T; Kasten M; Hagenah J; Brüggemann N; Graf J; Münchau A; Kostic VS; Sue CM; Domingo AR; Rosales RL; Lee LV; Freimann K; Westenberger A; Mukai Y; Kawarai T; Kaji R; Klein C; Martemyanov KA; Schmidt A
    JAMA Neurol; 2014 Apr; 71(4):490-4. PubMed ID: 24535567
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutation screening of the DYT6/THAP1 gene in Serbian patients with primary dystonia.
    Dobričić VS; Kresojević ND; Svetel MV; Janković MZ; Petrović IN; Tomić AD; Novaković IV; Kostić VS
    J Neurol; 2013 Apr; 260(4):1037-42. PubMed ID: 23180184
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Inherited dystonias: clinical features and molecular pathways.
    Weisheit CE; Pappas SS; Dauer WT
    Handb Clin Neurol; 2018; 147():241-254. PubMed ID: 29325615
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Heterozygous Gnal Mice Are a Novel Animal Model with Which to Study Dystonia Pathophysiology.
    Pelosi A; Menardy F; Popa D; Girault JA; Hervé D
    J Neurosci; 2017 Jun; 37(26):6253-6267. PubMed ID: 28546310
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Deep Brain Stimulation in Isolated Dystonia With a GNAL Mutation.
    Sarva H; Trosch R; Kiss ZHT; Furtado S; Luciano MS; Glickman A; Raymond D; Ozelius LJ; Bressman SB; Saunders-Pullman R
    Mov Disord; 2019 Feb; 34(2):301-303. PubMed ID: 30536916
    [No Abstract]   [Full Text] [Related]  

  • 20. Genotype-phenotype correlations in THAP1 dystonia: molecular foundations and description of new cases.
    LeDoux MS; Xiao J; Rudzińska M; Bastian RW; Wszolek ZK; Van Gerpen JA; Puschmann A; Momčilović D; Vemula SR; Zhao Y
    Parkinsonism Relat Disord; 2012 Jun; 18(5):414-25. PubMed ID: 22377579
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.