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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

84 related items for PubMed ID: 564079

  • 1. [Myotonic dystrophy: genetic aspects; cytochemical findings].
    LO Curto F, Nappi G, Poloni M, Castello A.
    Riv Neurol; 1977; 47(6):664-7. PubMed ID: 564079
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. Myotonic dystrophy in infancy and childhood.
    Hanson PA.
    Pediatr Ann; 1984 Feb; 13(2):123-4, 126. PubMed ID: 6709403
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Five years experience of predictive testing for myotonic dystrophy using linked DNA markers.
    Reardon W, Floyd JL, Myring J, Lazarou LP, Meredith AL, Harper PS.
    Am J Med Genet; 1992 Aug 01; 43(6):1006-11. PubMed ID: 1415325
    [Abstract] [Full Text] [Related]

  • 7. First-trimester prediction in fetus at risk for myotonic dystrophy.
    Lunt PW, Meredith AL, Harper PS.
    Lancet; 1986 Aug 09; 2(8502):350-1. PubMed ID: 2874363
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. [Myotonic dystrophy].
    Nesterov LN, Sushcheva GP, Viatkina SIa, Nesterova IM.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1983 Aug 09; 83(11):1636-41. PubMed ID: 6232784
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Prenatal diagnosis for the unstable CTG repeat sequence in myotonic dystrophy: a retrospective study in a French family.
    Lucotte G, Berriche S, David F, Mariotti M, Turpin JC.
    Genet Couns; 1994 Aug 09; 5(2):171-4. PubMed ID: 7917127
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Myotonic dystrophy with no trinucleotide repeat expansion.
    Thornton CA, Griggs RC, Moxley RT.
    Ann Neurol; 1994 Mar 09; 35(3):269-72. PubMed ID: 8122879
    [Abstract] [Full Text] [Related]

  • 16. [An unstable mutation as cause of myotonic dystrophy].
    Brunner HG, Höweler CJ, Smeets HJ, Wieringa B.
    Ned Tijdschr Geneeskd; 1993 Nov 27; 137(48):2468-72. PubMed ID: 8272119
    [No Abstract] [Full Text] [Related]

  • 17. Electrocardiographic findings in myotonic dystrophy.
    Olofsson BO, Forsberg H, Andersson S, Bjerle P, Henriksson A, Wedin I.
    Arctic Med Res; 1988 Nov 27; 47 Suppl 1():420-2. PubMed ID: 3272655
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. [Myotonic dystrophy of Steinert].
    Junien C.
    J Genet Hum; 1989 Jan 27; 37(1):51-4. PubMed ID: 2565953
    [Abstract] [Full Text] [Related]

  • 20. [Electrocardiographic aspects of hereditary degenerative diseases of the nervous system].
    Franken RA, Sanvito WL, Tilbery CP, Chryssovergis G, Campana JO.
    AMB Rev Assoc Med Bras; 1975 Jun 27; 21(6):181-4. PubMed ID: 1080861
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 5.