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 *

118 related articles for article (PubMed ID: 9649014)

  • 1. Abnormal liver test results in myotonic dystrophy.
    Achiron A; Barak Y; Magal N; Shohat M; Cohen M; Barar R; Gadoth N
    J Clin Gastroenterol; 1998 Jun; 26(4):292-5. PubMed ID: 9649014
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspring.
    Redman JB; Fenwick RG; Fu YH; Pizzuti A; Caskey CT
    JAMA; 1993 Apr; 269(15):1960-5. PubMed ID: 8464127
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Abnormal liver function tests in a patient with myotonic dystrophy type 1.
    Kalafateli M; Triantos C; Tsamandas A; Kounadis G; Labropoulou-Karatza C
    Ann Hepatol; 2012; 11(1):130-3. PubMed ID: 22166572
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [DNA diagnosis in myotonic dystrophy].
    Tachi N
    Hokkaido Igaku Zasshi; 1996 Jan; 71(1):3-8. PubMed ID: 8727368
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular and clinical characteristics of myotonic dystrophy type 1 in koreans.
    Kim SY; Kim JY; Kim GP; Sung JJ; Lim KS; Lee KW; Chae JH; Hong YH; Seong MW; Park SS
    Korean J Lab Med; 2008 Dec; 28(6):483-92. PubMed ID: 19127114
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular analysis of the CTG trinucleotide repeat in South African myotonic dystrophy families--implications for diagnosis and counselling.
    Goldman A; Ramsay M; Jenkins T
    S Afr Med J; 1995 Nov; 85(11):1161-4. PubMed ID: 8597005
    [TBL] [Abstract][Full Text] [Related]  

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

  • 8. Cardiac involvement in a large kindred with myotonic dystrophy. Quantitative assessment and relation to size of CTG repeat expansion.
    Tokgozoglu LS; Ashizawa T; Pacifico A; Armstrong RM; Epstein HF; Zoghbi WA
    JAMA; 1995 Sep; 274(10):813-9. PubMed ID: 7650805
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Myotonic dystrophy with no trinucleotide repeat expansion.
    Thornton CA; Griggs RC; Moxley RT
    Ann Neurol; 1994 Mar; 35(3):269-72. PubMed ID: 8122879
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The myotonic dystrophies.
    Thornton C
    Semin Neurol; 1999; 19(1):25-33. PubMed ID: 10711986
    [TBL] [Abstract][Full Text] [Related]  

  • 11. CTG repeat size and histologic findings of skeletal muscle from patients with congenital myotonic dystrophy.
    Tachi N; Kozuka N; Ohya K; Chiba S; Kikuchi K
    J Child Neurol; 1996 Nov; 11(6):430-2. PubMed ID: 9120218
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Clinical, familial and hereditary analysis of myotonic dystrophy].
    Wu Z; Yang J; Cao J; Hu Z; Zhan Y; Li J; Li Y; Wang Y; Zhang C
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2011 Jun; 36(6):520-4. PubMed ID: 21743143
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Proton spectroscopy in myotonic dystrophy: correlations with CTG repeats.
    Chang L; Ernst T; Osborn D; Seltzer W; Leonido-Yee M; Poland RE
    Arch Neurol; 1998 Mar; 55(3):305-11. PubMed ID: 9520004
    [TBL] [Abstract][Full Text] [Related]  

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

  • 15. Cardiovascular autonomic control in myotonic dystrophy type 1: a correlative study with clinical and genetic data.
    Di Leo R; Rodolico C; De Gregorio C; Recupero A; Coglitore S; Annesi G; Toscano A; Messina C; Vita G
    Neuromuscul Disord; 2004 Feb; 14(2):136-41. PubMed ID: 14733960
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Detection of the CTG repeat expansion in congenital myotonic dystrophy.
    Ohya K; Tachi N; Sato T; Kon S; Kikuchi K; Chiba S
    Jpn J Hum Genet; 1997 Mar; 42(1):169-80. PubMed ID: 9183996
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Proximal myotonic myopathy. Clinical features of a multisystem disorder similar to myotonic dystrophy.
    Ricker K; Koch MC; Lehmann-Horn F; Pongratz D; Speich N; Reiners K; Schneider C; Moxley RT
    Arch Neurol; 1995 Jan; 52(1):25-31. PubMed ID: 7826272
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A molecular protocol for diagnosing myotonic dystrophy.
    Guida M; Marger RS; Papp AC; Snyder PJ; Sedra MS; Kissel JT; Mendell JR; Prior TW
    Clin Chem; 1995 Jan; 41(1):69-72. PubMed ID: 7813083
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Investigation of molecular diagnosis in Chinese patients with myotonic dystrophy type 1.
    Li M; Wang Z; Cui F; Yang F; Chen Z; Ling L; Pu C; Huang X
    Chin Med J (Engl); 2014; 127(6):1084-8. PubMed ID: 24622439
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Delineation of CTG repeats and clinical features in a Taiwanese myotonic dystrophy family.
    Jou SB; Lin HM; Pan H; Chiu YL; Li SY; Lee CC; Hsiao KM
    Proc Natl Sci Counc Repub China B; 2001 Jan; 25(1):40-4. PubMed ID: 11254171
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.