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 *

166 related articles for article (PubMed ID: 20158653)

  • 1. Congenital myotonic dystrophy with cardiac conduction defect and eventration of the diaphragm.
    Kapoor V; Wright IM
    Pediatr Int; 2010 Feb; 52(1):e6-8. PubMed ID: 20158653
    [No Abstract]   [Full Text] [Related]  

  • 2. Getting a grip on the myotonic dystrophies.
    Thornton CA; Ashizawa T
    Neurology; 1999 Jan; 52(1):12-3. PubMed ID: 9921841
    [No Abstract]   [Full Text] [Related]  

  • 3. Preimplantation genetic diagnosis for myotonic dystrophy type 1 in the UK.
    Kakourou G; Dhanjal S; Mamas T; Gotts S; Doshi A; Fordham K; Serhal P; Ranieri DM; Delhanty JD; Harper JC; SenGupta SB
    Neuromuscul Disord; 2008 Feb; 18(2):131-6. PubMed ID: 18053720
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Triplet-primed PCR is more sensitive than southern blotting-long PCR for the diagnosis of myotonic dystrophy type1.
    Addis M; Serrenti M; Meloni C; Cau M; Melis MA
    Genet Test Mol Biomarkers; 2012 Dec; 16(12):1428-31. PubMed ID: 23030650
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A newborn girl with hypotonia and respiratory failure.
    Charrow J
    Pediatr Ann; 2007 Dec; 36(12):777, 781-2. PubMed ID: 18229518
    [No Abstract]   [Full Text] [Related]  

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

  • 7. Instability of the (CTG)n repeat in congenital myotonic dystrophy.
    Wong LJ; Ashizawa T
    Am J Hum Genet; 1997 Dec; 61(6):1445-8. PubMed ID: 9399912
    [No Abstract]   [Full Text] [Related]  

  • 8. Hypertrophic cardiomyopathy in congenital myotonic dystrophy.
    Igarashi H; Momoi MY; Yamagata T; Shiraishi H; Eguchi I
    Pediatr Neurol; 1998 Apr; 18(4):366-9. PubMed ID: 9588538
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Eight years' experience of direct molecular testing for myotonic dystrophy in Wales.
    Fokstuen S; Myring J; Meredith L; Ravine D; Harper PS
    J Med Genet; 2001 Dec; 38(12):E42. PubMed ID: 11748308
    [No Abstract]   [Full Text] [Related]  

  • 10. Molecular and clinical study of two myotonic dystrophy homozygotes.
    Akbas F; Serdaroglu P; Deymeer F; Aysal F; Erginel-Unaltuna N
    J Med Genet; 2001 Nov; 38(11):E40. PubMed ID: 11694554
    [No Abstract]   [Full Text] [Related]  

  • 11. [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]  

  • 12. Teaching video NeuroImages: shake Mom's hand to get the diagnosis.
    Ghosh PS; Indulkar S; Moodley M
    Neurology; 2011 Nov; 77(19):e114. PubMed ID: 22067971
    [No Abstract]   [Full Text] [Related]  

  • 13. Presymptomatic testing in myotonic dystrophy: genetic counselling approaches.
    Fokstuen S; Myring J; Evans C; Harper PS
    J Med Genet; 2001 Dec; 38(12):846-50. PubMed ID: 11768386
    [No Abstract]   [Full Text] [Related]  

  • 14. Trinucleotide repeat contraction: a pitfall in prenatal diagnosis of myotonic dystrophy.
    Amiel J; Raclin V; Jouannic JM; Morichon N; Hoffman-Radvanyi H; Dommergues M; Feingold J; Munnich A; Bonnefont JP
    J Med Genet; 2001 Dec; 38(12):850-2. PubMed ID: 11768387
    [No Abstract]   [Full Text] [Related]  

  • 15. Paternal transmission of congenital myotonic dystrophy.
    Bergoffen J; Kant J; Sladky J; McDonald-McGinn D; Zackai EH; Fischbeck KH
    J Med Genet; 1994 Jul; 31(7):518-20. PubMed ID: 7966187
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Transient complete atrioventricular block in a preterm neonate with congenital myotonic dystrophy: case report.
    Kim HN; Cho YK; Cho JH; Yang EM; Song ES; Choi YY
    J Korean Med Sci; 2014 Jun; 29(6):879-83. PubMed ID: 24932094
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetics correlates with lung function and nocturnal ventilation in myotonic dystrophy.
    Monteiro R; Bento J; Gonçalves MR; Pinto T; Winck JC
    Sleep Breath; 2013 Sep; 17(3):1087-92. PubMed ID: 23319325
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Presence of palmar xanthomas in myotonic dystrophy identifies different patterns of linkage disequilibrium between the apolipoprotein E and myotonic dystrophy protein kinase loci.
    Brisson D; Mathieu J; Vohl MC; Gaudet D
    Genet Med; 2005 Mar; 7(3):213-5. PubMed ID: 15775763
    [No Abstract]   [Full Text] [Related]  

  • 20. [Recommendations of good practices for the genetic diagnosis of myotonic dystrophy. Grupo AEGH/CIBERER].
    Garcia Planells J; Molano J; Borrego S;
    Med Clin (Barc); 2011 Mar; 136(7):303-8. PubMed ID: 20863536
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.