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 *

197 related articles for article (PubMed ID: 12021957)

  • 61. [Myotonic dystrophy: DNA instability in monozygotic twins].
    Redondo L; Polo MA; Rodríguez F; Ramírez P; Aguilar J; Lucas M; Molano J
    Rev Neurol; 1999 Apr 1-15; 28(7):711-3. PubMed ID: 10363301
    [TBL] [Abstract][Full Text] [Related]  

  • 62. [Myotonic dystrophy type 2].
    Kimura T; Saito T
    Brain Nerve; 2011 Nov; 63(11):1151-60. PubMed ID: 22068467
    [TBL] [Abstract][Full Text] [Related]  

  • 63. A patient with proximal myotonic myopathy and parkinsonism.
    Chu K; Cho JW; Song EC; Jeon BS
    Can J Neurol Sci; 2002 May; 29(2):188-90. PubMed ID: 12035844
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Somatic instability of CTG repeats in the cerebellum of myotonic dystrophy type 1.
    Jinnai K; Mitani M; Futamura N; Kawamoto K; Funakawa I; Itoh K
    Muscle Nerve; 2013 Jul; 48(1):105-8. PubMed ID: 23629807
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Proof of genetic heterogeneity in the proximal myotonic myopathy syndrome (PROMM) and its relationship to myotonic dystrophy type 2 (DM2).
    Kress W; Mueller-Myhsok B; Ricker K; Schneider C; Koch MC; Toyka KV; Mueller CR; Grimm T
    Neuromuscul Disord; 2000 Oct; 10(7):478-80. PubMed ID: 10996776
    [TBL] [Abstract][Full Text] [Related]  

  • 66. A muscleblind knockout model for myotonic dystrophy.
    Kanadia RN; Johnstone KA; Mankodi A; Lungu C; Thornton CA; Esson D; Timmers AM; Hauswirth WW; Swanson MS
    Science; 2003 Dec; 302(5652):1978-80. PubMed ID: 14671308
    [TBL] [Abstract][Full Text] [Related]  

  • 67. [From gene to disease; altered RNA processing as a cause of myotonic dystrophy type 1].
    de Die-Smulders CE; Faber CG; Smeets HJ
    Ned Tijdschr Geneeskd; 2005 Sep; 149(37):2043-6. PubMed ID: 16184945
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Myopathies with finger flexor weakness: Not only inclusion-body myositis.
    Nicolau S; Liewluck T; Milone M
    Muscle Nerve; 2020 Oct; 62(4):445-454. PubMed ID: 32478919
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Muscle pathology in 57 patients with myotonic dystrophy type 2.
    Schoser BG; Schneider-Gold C; Kress W; Goebel HH; Reilich P; Koch MC; Pongratz DE; Toyka KV; Lochmüller H; Ricker K
    Muscle Nerve; 2004 Feb; 29(2):275-81. PubMed ID: 14755494
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Severity, type, and distribution of myotonic discharges are different in type 1 and type 2 myotonic dystrophy.
    Logigian EL; Ciafaloni E; Quinn LC; Dilek N; Pandya S; Moxley RT; Thornton CA
    Muscle Nerve; 2007 Apr; 35(4):479-85. PubMed ID: 17230537
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Skeletal muscle involvement in myotonic dystrophy type 2. A comparative muscle ultrasound study.
    Tieleman AA; Vinke A; van Alfen N; van Dijk JP; Pillen S; van Engelen BG
    Neuromuscul Disord; 2012 Jun; 22(6):492-9. PubMed ID: 22414627
    [TBL] [Abstract][Full Text] [Related]  

  • 72. The clinical and genetic correlates of MRI findings in myotonic dystrophy.
    Bachmann G; Damian MS; Koch M; Schilling G; Fach B; Stöppler S
    Neuroradiology; 1996 Oct; 38(7):629-35. PubMed ID: 8912317
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Myotonic dystrophy type 1 (DM1) presenting with laryngeal stridor and vocal fold paresis.
    Ahmadian JL; Heller SL; Nishida T; Altman KW
    Muscle Nerve; 2002 Apr; 25(4):616-8. PubMed ID: 11932983
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Congenital myotonic dystrophy: variability in muscle involvement and histopathological process.
    Kuo HC; Huang CC; Chu CC; Wai YY; Hsiao KM; Chu NS
    Acta Neurol Taiwan; 2006 Mar; 15(1):13-20. PubMed ID: 16599279
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Magnetization transfer measurements of cerebral white matter in patients with myotonic dystrophy.
    Naka H; Imon Y; Ohshita T; Honjo K; Kitamura T; Mimori Y; Nakamura S
    J Neurol Sci; 2002 Jan; 193(2):111-6. PubMed ID: 11790391
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Length-dependent toxicity of untranslated CUG repeats on Caenorhabditis elegans.
    Chen KY; Pan H; Lin MJ; Li YY; Wang LC; Wu YC; Hsiao KM
    Biochem Biophys Res Commun; 2007 Jan; 352(3):774-9. PubMed ID: 17150182
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Magnetic resonance imaging findings in adult-form myotonic dystrophy type 1.
    Jakkani R; Jyoti S; Ahmed M; Thomas MM
    Singapore Med J; 2012 Jul; 53(7):e150-2. PubMed ID: 22815033
    [TBL] [Abstract][Full Text] [Related]  

  • 78. [Current problems in myotonic dystrophy].
    Weglewski A; Juryńczyk J
    Neurol Neurochir Pol; 1998; 32(4):903-11. PubMed ID: 9864718
    [TBL] [Abstract][Full Text] [Related]  

  • 79. [Camptocornia presenting with a proximal myotonic myopathy].
    Rimbaux S; Pellieux S; Bergemer AM; Saïkali I; Gherardi R; Fouquet B
    Rev Neurol (Paris); 2003 Jul; 159(6-7 Pt 1):678-80. PubMed ID: 12910078
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Quantitative magnetic resonance imaging assessment of muscle composition in myotonic dystrophy mice.
    Bargiela A; Ten-Esteve A; Martí-Bonmatí L; Sevilla T; Perez Alonso M; Artero R
    Sci Rep; 2023 Jan; 13(1):503. PubMed ID: 36627397
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.