BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

363 related articles for article (PubMed ID: 28550479)

  • 21. Myotonic dystrophy type 1 (DM1): a triplet repeat expansion disorder.
    Kumar A; Agarwal S; Agarwal D; Phadke SR
    Gene; 2013 Jun; 522(2):226-30. PubMed ID: 23570879
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Immortalized human myotonic dystrophy muscle cell lines to assess therapeutic compounds.
    Arandel L; Polay Espinoza M; Matloka M; Bazinet A; De Dea Diniz D; Naouar N; Rau F; Jollet A; Edom-Vovard F; Mamchaoui K; Tarnopolsky M; Puymirat J; Battail C; Boland A; Deleuze JF; Mouly V; Klein AF; Furling D
    Dis Model Mech; 2017 Apr; 10(4):487-497. PubMed ID: 28188264
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Myotonic dystrophy type 2 and related myotonic disorders.
    Meola G; Moxley RT
    J Neurol; 2004 Oct; 251(10):1173-82. PubMed ID: 15503094
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Utility and Results from a Patient-Reported Online Survey in Myotonic Dystrophies Types 1 and 2.
    Wenninger S; Stahl K; Montagnese F; Schoser B
    Eur Neurol; 2020; 83(5):523-533. PubMed ID: 33120389
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Analysis of MTMR1 expression and correlation with muscle pathological features in juvenile/adult onset myotonic dystrophy type 1 (DM1) and in myotonic dystrophy type 2 (DM2).
    Santoro M; Modoni A; Masciullo M; Gidaro T; Broccolini A; Ricci E; Tonali PA; Silvestri G
    Exp Mol Pathol; 2010 Oct; 89(2):158-68. PubMed ID: 20685272
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Assessing the influence of age and gender on the phenotype of myotonic dystrophy type 2.
    Montagnese F; Mondello S; Wenninger S; Kress W; Schoser B
    J Neurol; 2017 Dec; 264(12):2472-2480. PubMed ID: 29086017
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Myotonic Dystrophy Type 2: An Update on Clinical Aspects, Genetic and Pathomolecular Mechanism.
    Meola G; Cardani R
    J Neuromuscul Dis; 2015 Jul; 2(s2):S59-S71. PubMed ID: 27858759
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in Finland.
    Suominen T; Bachinski LL; Auvinen S; Hackman P; Baggerly KA; Angelini C; Peltonen L; Krahe R; Udd B
    Eur J Hum Genet; 2011 Jul; 19(7):776-82. PubMed ID: 21364698
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Dysautonomia as Onset Symptom of Myotonic Dystrophy Type 2.
    Rossi S; Romano A; Modoni A; Perna F; Rizzo V; Santoro M; Monforte M; Pieroni M; Luigetti M; Pomponi MG; Silvestri G
    Eur Neurol; 2018; 79(3-4):166-170. PubMed ID: 29533949
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Myotonic Muscular Dystrophies.
    Johnson NE
    Continuum (Minneap Minn); 2019 Dec; 25(6):1682-1695. PubMed ID: 31794466
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Peripheral nerve involvement in myotonic dystrophy type 2 - similar or different than in myotonic dystrophy type 1?
    Nojszewska M; Łusakowska A; Szmidt-Salkowska E; Gaweł M; Lipowska M; Sułek A; Krysa W; Rajkiewicz M; Seroka A; Kaczmarek K; Kamińska AM
    Neurol Neurochir Pol; 2015; 49(3):164-70. PubMed ID: 26048604
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Towards clinical outcome measures in myotonic dystrophy type 2: a systematic review.
    Rastelli E; Montagnese F; Massa R; Schoser B
    Curr Opin Neurol; 2018 Oct; 31(5):599-609. PubMed ID: 30048337
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The myotonic dystrophies: molecular, clinical, and therapeutic challenges.
    Udd B; Krahe R
    Lancet Neurol; 2012 Oct; 11(10):891-905. PubMed ID: 22995693
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Myotonic dystrophy].
    Nanba E
    Nihon Rinsho; 2005 Mar; 63(3):429-33. PubMed ID: 15773341
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Myotonic dystrophy type 2 found in two of sixty-three persons diagnosed as having fibromyalgia.
    Auvinen S; Suominen T; Hannonen P; Bachinski LL; Krahe R; Udd B
    Arthritis Rheum; 2008 Nov; 58(11):3627-31. PubMed ID: 18975316
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Cerebral involvement in myotonic dystrophies.
    Meola G; Sansone V
    Muscle Nerve; 2007 Sep; 36(3):294-306. PubMed ID: 17486579
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Phenotypic variability and molecular genetics in proximal myotonic myopathy.
    Papadimas GK; Kekou K; Papadopoulos C; Kararizou E; Kanavakis E; Manta P
    Muscle Nerve; 2015 May; 51(5):686-91. PubMed ID: 25186227
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Myotonic dystrophies.
    Huang CC; Kuo HC
    Chang Gung Med J; 2005 Aug; 28(8):517-26. PubMed ID: 16265841
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Progression of muscle histopathology but not of spliceopathy in myotonic dystrophy type 2.
    Cardani R; Giagnacovo M; Rossi G; Renna LV; Bugiardini E; Pizzamiglio C; Botta A; Meola G
    Neuromuscul Disord; 2014 Dec; 24(12):1042-53. PubMed ID: 25139674
    [TBL] [Abstract][Full Text] [Related]  

  • 40. New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2).
    Sallinen R; Vihola A; Bachinski LL; Huoponen K; Haapasalo H; Hackman P; Zhang S; Sirito M; Kalimo H; Meola G; Horelli-Kuitunen N; Wessman M; Krahe R; Udd B
    Neuromuscul Disord; 2004 Apr; 14(4):274-83. PubMed ID: 15019706
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 19.