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 *

164 related articles for article (PubMed ID: 9391889)

  • 41. Different patterns of obstetric complications in myotonic dystrophy in relation to the disease status of the fetus.
    Rudnik-Schöneborn S; Nicholson GA; Morgan G; Röhrig D; Zerres K
    Am J Med Genet; 1998 Dec; 80(4):314-21. PubMed ID: 9856556
    [TBL] [Abstract][Full Text] [Related]  

  • 42. [Direct genotype analysis in congenital myotonic dystrophy with an unusual family anamnesis].
    Bindl L; Rummel W; Walter S; Haverkamp F; Kowalewski S; Lentze MJ; Koch M
    Klin Padiatr; 1993; 205(5):367-9. PubMed ID: 8411905
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Instability of normal (CTG)n alleles in the DM kinase gene.
    Dow DJ; Rubinsztein DC; Yates JR; Barton DE; Ferguson-Smith MA
    J Med Genet; 1997 Oct; 34(10):871-3. PubMed ID: 9350827
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Correlation between distribution of muscle weakness, electrophysiological findings and CTG expansion in myotonic dystrophy.
    Khoshbakht R; Soltanzadeh A; Zamani B; Abdi S; Gharagozli K; Kahrizi K; Khoshbakht R; Nafissi S
    J Clin Neurosci; 2014 Jul; 21(7):1123-6. PubMed ID: 24417793
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Intergenerational contraction of the CTG repeats in 2 families with myotonic dystrophy type 1.
    Puymirat J; Giguère Y; Mathieu J; Bouchard JP
    Neurology; 2009 Dec; 73(24):2126-7. PubMed ID: 20018643
    [No Abstract]   [Full Text] [Related]  

  • 46. [Effects of CTG repeat expansion on quantitative muscle histopathology in myotonic dystrophy].
    Utsugisawa K; Yamagata M; Nagane Y; Tohgi H
    Nihon Rinsho; 1997 Dec; 55(12):3214-8. PubMed ID: 9436439
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Decrease in the size of the myotonic dystrophy CTG repeat during transmission from parent to child: implications for genetic counselling and genetic anticipation.
    Hunter AG; Jacob P; O'Hoy K; MacDonald I; Mettler G; Tsilfidis C; Korneluk RG
    Am J Med Genet; 1993 Feb; 45(3):401-7. PubMed ID: 8434633
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Contribution of molecular analyses to the estimation of the risk of congenital myotonic dystrophy.
    Cobo AM; Poza JJ; Martorell L; López de Munain A; Emparanza JI; Baiget M
    J Med Genet; 1995 Feb; 32(2):105-8. PubMed ID: 7760317
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [Localization of DM-PK in normal and myotonic dystrophy muscles].
    Tachi N; Ohya K
    Nihon Rinsho; 1997 Dec; 55(12):3210-3. PubMed ID: 9436438
    [TBL] [Abstract][Full Text] [Related]  

  • 50. CTG repeat length in muscle from patients affected with myotonic dystrophy (DM).
    Zatz M; Passos-Bueno MR; Cerqueira A; Vainzof M
    J Med Genet; 1996 Feb; 33(2):173. PubMed ID: 8929960
    [No Abstract]   [Full Text] [Related]  

  • 51. [Molecular genetics diagnosis of Steinert's myotonic dystrophy].
    Spiegel R; Einschenk I; Schinzel A; Shelbourne P; Johnson K; Boltshauser E; Schmid W
    Schweiz Med Wochenschr; 1992 Oct; 122(42):1553-8. PubMed ID: 1411415
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Machado-Joseph disease/SCA3 and myotonic dystrophy type 1 in a single patient.
    Miura S; Ohyagi Y; Miike T; Noda K; Motomura K; Ayabe M; Aizawa H; Taniwaki T
    Clin Neurol Neurosurg; 2009 Dec; 111(10):791-4. PubMed ID: 19713033
    [TBL] [Abstract][Full Text] [Related]  

  • 53. 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]  

  • 54. Clinical expression of myotonic dystrophy: the predictive role of DNA diagnosis.
    Can B; Schaefer FV; Malik S; Floyd M; Say B
    J Okla State Med Assoc; 1998; 91(1):7-10. PubMed ID: 9503753
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Mitochondrial DNA does not appear to influence the congenital onset type of myotonic dystrophy.
    Poulton J; Harley HG; Dasmahapatra J; Brown GK; Potter CG; Sykes B
    J Med Genet; 1995 Sep; 32(9):732-5. PubMed ID: 8544195
    [TBL] [Abstract][Full Text] [Related]  

  • 56. [Steinert's disease and pregnancy. A case report and recent literature].
    Delest A; Elhage A; Cosson M; Leclercq G; Gremillet C; Pasquier F; Manouvrier-Hanu S; Decocq J; Delahousse G
    J Gynecol Obstet Biol Reprod (Paris); 1995; 24(2):177-80. PubMed ID: 7782590
    [TBL] [Abstract][Full Text] [Related]  

  • 57. [Molecular pathways to myotonic dystrophy].
    Ishiura S
    Nihon Rinsho; 2005 Mar; 63(3):515-21. PubMed ID: 15773354
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Epidemiological and genetic studies of myotonic dystrophy type 1 in Taiwan.
    Hsiao KM; Chen SS; Li SY; Chiang SY; Lin HM; Pan H; Huang CC; Kuo HC; Jou SB; Su CC; Ro LS; Liu CS; Lo MC; Chen CM; Lin CC
    Neuroepidemiology; 2003; 22(5):283-9. PubMed ID: 12902623
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Direct molecular analysis of myotonic dystrophy in the German population: important considerations in genetic counselling.
    Meiner A; Wolf C; Carey N; Okitsu A; Johnson K; Shelbourne P; Kunath B; Sauermann W; Thiele H; Kupferling P
    J Med Genet; 1995 Aug; 32(8):645-9. PubMed ID: 7473660
    [TBL] [Abstract][Full Text] [Related]  

  • 60. An expanded CTG trinucleotide repeat causes trans RNA interference: a new hypothesis for the pathogenesis of myotonic dystrophy.
    Sasagawa N; Takahashi N; Suzuki K; Ishiura S
    Biochem Biophys Res Commun; 1999 Oct; 264(1):76-80. PubMed ID: 10527844
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.