BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

418 related articles for article (PubMed ID: 17027035)

  • 21. Expression profiling in peripheral blood reveals signature for penetrance in DYT1 dystonia.
    Walter M; Bonin M; Pullman RS; Valente EM; Loi M; Gambarin M; Raymond D; Tinazzi M; Kamm C; Glöckle N; Poths S; Gasser T; Bressman SB; Klein C; Ozelius LJ; Riess O; Grundmann K
    Neurobiol Dis; 2010 May; 38(2):192-200. PubMed ID: 20053375
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Three brothers with a very-late-onset writer's cramp.
    Bhidayasiri R; Jen JC; Baloh RW
    Mov Disord; 2005 Oct; 20(10):1375-7. PubMed ID: 15954129
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Clinical and genetic characterization of a large Dutch family with primary focal dystonia.
    Contarino MF; Berger-Plantinga E; Foncke EM; Ritz K; Mellema J; Baas F; Speelman JD; Tijssen MA
    Mov Disord; 2008 Oct; 23(14):1998-2003. PubMed ID: 18823044
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Wide expressivity variation and high but no gender-related penetrance in two dopa-responsive dystonia families with a novel GCH-I mutation.
    Uncini A; De Angelis MV; Di Fulvio P; Ragno M; Annesi G; Filla A; Stuppia L; Gambi D
    Mov Disord; 2004 Oct; 19(10):1139-45. PubMed ID: 15390021
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Phenotype of the DYT1 mutation in the TOR1A gene in a Polish population of patients with dystonia. A preliminary report.
    Gajos A; Piaskowski S; Sławek J; Ochudło S; Opala G; Łobińska A; Honczarenko K; Budrewicz S; Koszewicz M; Pełszyńska B; Liberski PP; Bogucki A
    Neurol Neurochir Pol; 2007; 41(6):487-94. PubMed ID: 18224570
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Autosomal dominant dystonia-plus with cerebral calcifications.
    Wszolek ZK; Baba Y; Mackenzie IR; Uitti RJ; Strongosky AJ; Broderick DF; Baker MC; Melquist S; Hutton ML; Tsuboi Y; Allanson JE; Carr J; Kumar A; Calne SM; Miklossy J; McGeer PL; Calne DB; Stoessl AJ
    Neurology; 2006 Aug; 67(4):620-5. PubMed ID: 16924015
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Phenotypic expression of the DYT1 mutation: a family with writer's cramp of juvenile onset.
    Gasser T; Windgassen K; Bereznai B; Kabus C; Ludolph AC
    Ann Neurol; 1998 Jul; 44(1):126-8. PubMed ID: 9667600
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Clinical characteristics of carriers of a GAG deletion in the DYT1 gene amongst Polish patients with primary dystonia.
    Szczaluba K; Jurek M; Milewski M; Friedman A; Kadziolka B; Szolna A; Bal J; Mazurczak T
    Eur J Neurol; 2007 Jun; 14(6):659-62. PubMed ID: 17539945
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Writer's cramp in an Australian pedigree with DYT1 dystonia.
    van den Bos M; Marotta R; Goldup S; Chataway T; Firgaira F; Thyagarajan D
    J Clin Neurosci; 2004 Jun; 11(5):537-9. PubMed ID: 15177405
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Clinical features, DYT1 mutation screening and genotype-phenotype correlation in patients with dystonia from Iran.
    Akbari MT; Zand Z; Shahidi GA; Hamid M
    Med Princ Pract; 2012; 21(5):462-6. PubMed ID: 22487959
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Clinical and genetic evaluation in a French population presenting with primary focal dystonia.
    Dhaenens CM; Krystkowiak P; Douay X; Charpentier P; Bele S; Destée A; Sablonnière B
    Mov Disord; 2005 Jul; 20(7):822-5. PubMed ID: 15726581
    [TBL] [Abstract][Full Text] [Related]  

  • 32. DYT1 mutation in a cohort of Taiwanese primary dystonias.
    Lin YW; Chang HC; Chou YH; Chen RS; Hsu WC; Wu WS; Weng YH; Lu CS
    Parkinsonism Relat Disord; 2006 Jan; 12(1):15-9. PubMed ID: 16198613
    [TBL] [Abstract][Full Text] [Related]  

  • 33. DYT13, a novel primary torsion dystonia locus, maps to chromosome 1p36.13--36.32 in an Italian family with cranial-cervical or upper limb onset.
    Valente EM; Bentivoglio AR; Cassetta E; Dixon PH; Davis MB; Ferraris A; Ialongo T; Frontali M; Wood NW; Albanese A
    Ann Neurol; 2001 Mar; 49(3):362-6. PubMed ID: 11261511
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Functional brain networks in DYT1 dystonia.
    Eidelberg D; Moeller JR; Antonini A; Kazumata K; Nakamura T; Dhawan V; Spetsieris P; deLeon D; Bressman SB; Fahn S
    Ann Neurol; 1998 Sep; 44(3):303-12. PubMed ID: 9749595
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Linkage studies in alcohol-responsive myoclonic dystonia.
    Gasser T; Bereznai B; Müller B; Pruszak-Seel R; Damrich R; Deuschl G; Oertel WH
    Mov Disord; 1996 Jul; 11(4):363-70. PubMed ID: 8813214
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Phenotypic variability of DYT1-PTD: does the clinical spectrum include psychogenic dystonia?
    Bentivoglio AR; Loi M; Valente EM; Ialongo T; Tonali P; Albanese A
    Mov Disord; 2002 Sep; 17(5):1058-63. PubMed ID: 12360559
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Dystonia in Ashkenazi Jews: clinical characterization of a founder mutation.
    Bressman SB; de Leon D; Kramer PL; Ozelius LJ; Brin MF; Greene PE; Fahn S; Breakefield XO; Risch NJ
    Ann Neurol; 1994 Nov; 36(5):771-7. PubMed ID: 7979224
    [TBL] [Abstract][Full Text] [Related]  

  • 38. DYT1 mutation in Korean primary dystonia patients.
    Im JH; Ahn TB; Kim KB; Ko SB; Jeon BS
    Parkinsonism Relat Disord; 2004 Oct; 10(7):421-3. PubMed ID: 15465399
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Haplotype analysis at the DYT1 locus in Ashkenazi Jewish patients with occupational hand dystonia.
    Gasser T; Bove CM; Ozelius LJ; Hallett M; Charness ME; Hochberg FH; Breakefield XO
    Mov Disord; 1996 Mar; 11(2):163-6. PubMed ID: 8684386
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Clinical characterization and evaluation of DYT1 gene in Indian primary dystonia patients.
    Naiya T; Biswas A; Neogi R; Datta S; Misra AK; Das SK; Ray K; Ray J
    Acta Neurol Scand; 2006 Sep; 114(3):210-5. PubMed ID: 16911351
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 21.