BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

318 related articles for article (PubMed ID: 22332444)

  • 1. Clinical, electrophysiologic and pathologic findings in 10 patients with myotonic dystrophy 2.
    Dabby R; Sadeh M; Herman O; Leibou L; Kremer E; Mordechai S; Watemberg N; Frand J
    Isr Med Assoc J; 2011 Dec; 13(12):745-7. PubMed ID: 22332444
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24.
    Le Ber I; Martinez M; Campion D; Laquerrière A; Bétard C; Bassez G; Girard C; Saugier-Veber P; Raux G; Sergeant N; Magnier P; Maisonobe T; Eymard B; Duyckaerts C; Delacourte A; Frebourg T; Hannequin D
    Brain; 2004 Sep; 127(Pt 9):1979-92. PubMed ID: 15215218
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Myotonic dystrophy type 2 with focal asymmetric muscle weakness and no electrical myotonia.
    Milone M; Batish SD; Daube JR
    Muscle Nerve; 2009 Mar; 39(3):383-5. PubMed ID: 19208413
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. The expanding clinical and genetic spectrum of the myotonic dystrophies.
    Ricker K
    Acta Neurol Belg; 2000 Sep; 100(3):151-5. PubMed ID: 11098287
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Myotonia congenita and myotonic dystrophy in the same family: coexistence of a CLCN1 mutation and expansion in the CNBP (ZNF9) gene.
    Sun C; Van Ghelue M; Tranebjærg L; Thyssen F; Nilssen Ø; Torbergsen T
    Clin Genet; 2011 Dec; 80(6):574-80. PubMed ID: 21204798
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Proximal myotonic myopathy: clinical, electrophysiological and pathological findings in a family.
    Kohler A; Burkhard P; Hefft S; Bottani A; Pizzolato GP; Magistris MR
    Eur Neurol; 2000; 43(1):50-3. PubMed ID: 10601809
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Proximal myotonial myopathy (PROMM): clinical and histology study].
    Bassez G; Attarian S; Laforêt P; Azulay JP; Rouche A; Ferrer X; Urtizberea JA; Pellissier JF; Duboc D; Fardeau M; Pouget J; Eymard B
    Rev Neurol (Paris); 2001 Feb; 157(2):209-18. PubMed ID: 11283467
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Unusual clinical, laboratory, and muscle histopathological findings in a family with myotonic dystrophy type 2.
    Toth C; Dunham C; Suchowersky O; Parboosingh J; Brownell K
    Muscle Nerve; 2007 Feb; 35(2):259-64. PubMed ID: 17068784
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Proximal myotonic myopathy. Analysis of 3 Swedish cases.
    Schuitevoerder K; Ansved T; Solders G; Borg K
    Acta Neurol Scand; 1997 Oct; 96(4):266-70. PubMed ID: 9325482
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Cardiac, respiratory and sleep disorders in patients with myotonic dystrophy].
    Banach M; Rakowicz M; Antczak J; Rola R; Witkowski G; Waliniowska E
    Przegl Lek; 2009; 66(12):1065-8. PubMed ID: 20514907
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Proximal myotonic myopathy: clinical, neuropathologic, and molecular genetic features.
    Eisenschenk S; Triggs WJ; Pearl GS; Rojiani AM
    Ann Clin Lab Sci; 2001 Apr; 31(2):140-6. PubMed ID: 11337902
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Absent, unrecognized, and minimal myotonic discharges in myotonic dystrophy type 2.
    Young NP; Daube JR; Sorenson EJ; Milone M
    Muscle Nerve; 2010 Jun; 41(6):758-62. PubMed ID: 20513102
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Muscle pathology in myotonic dystrophy: light and electron microscopic investigation in eighteen patients.
    Nadaj-Pakleza A; Lusakowska A; Sułek-Piątkowska A; Krysa W; Rajkiewicz M; Kwieciński H; Kamińska A
    Folia Morphol (Warsz); 2011 May; 70(2):121-9. PubMed ID: 21630234
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Homozygosity for CCTG mutation in myotonic dystrophy type 2.
    Schoser BG; Kress W; Walter MC; Halliger-Keller B; Lochmüller H; Ricker K
    Brain; 2004 Aug; 127(Pt 8):1868-77. PubMed ID: 15231584
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hyper-CK-emia as the sole manifestation of myotonic dystrophy type 2.
    Merlini L; Sabatelli P; Columbaro M; Bonifazi E; Pisani V; Massa R; Novelli G
    Muscle Nerve; 2005 Jun; 31(6):764-7. PubMed ID: 15704146
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Myotonic dystrophy type 2.
    Finsterer J
    Eur J Neurol; 2002 Sep; 9(5):441-7. PubMed ID: 12220374
    [TBL] [Abstract][Full Text] [Related]  

  • 19. An unusual case with myotonia.
    Da YW; Wang M; Li Y; Lu Y; Jia JP
    Kaohsiung J Med Sci; 2013 Mar; 29(3):172-5. PubMed ID: 23465422
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Myotonic dystrophy Curschmann-Steinert].
    Papageorgiou E; Bock SW; Schiefer U
    Klin Monbl Augenheilkd; 2007 Jan; 224(1):70-5. PubMed ID: 17260325
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.