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Journal Abstract Search

129 related items for PubMed ID: 4682070

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. [Muscular disease of X-linked autosomal recessive transmission with early muscular retractions and cardiac conduction disorders].
    Serratrice G, Pouget J, Pellissier JF, Gastaut JL, Cros D.
    Rev Neurol (Paris); 1982; 138(10):713-24. PubMed ID: 6891495
    [No Abstract] [Full Text] [Related]

  • 3. [A case of scapuloperoneal muscular atrophy with contracture of joints and cardiopathy (author's transl)].
    Kuriyama M, Ouchi M, Umezaki H, Sants T.
    Rinsho Shinkeigaku; 1977 Sep; 17(9):575-81. PubMed ID: 144575
    [No Abstract] [Full Text] [Related]

  • 4. Heart block and peroneal muscular atrophy. A family study.
    Littler WA.
    Q J Med; 1970 Jul; 39(155):431-40. PubMed ID: 5478510
    [No Abstract] [Full Text] [Related]

  • 5. Atrioventricular block and supraventricular arrhythmias with X-linked muscular dystrophy.
    ul Hassan Z, Fastabend CP, Mohanty PK, Isaacs ER.
    Circulation; 1979 Dec; 60(6):1365-9. PubMed ID: 498463
    [Abstract] [Full Text] [Related]

  • 6.
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  • 7. Scapuloperoneal syndrome with cardiomyopathy: report of a family with autosomal dominant inheritance and unusual features.
    Chakrabarti A, Pearce JM.
    J Neurol Neurosurg Psychiatry; 1981 Dec; 44(12):1146-52. PubMed ID: 7334411
    [Abstract] [Full Text] [Related]

  • 8. Familial heart block and sinus bradycardia. Classification and natural history.
    Sarachek NS, Leonard JL.
    Am J Cardiol; 1972 Apr; 29(4):451-8. PubMed ID: 5016825
    [No Abstract] [Full Text] [Related]

  • 9. Sensory signs and symptoms in scapuloperoneal atrophy: a report of a family.
    Sand T, Hestnes A.
    Eur Neurol; 1985 Apr; 24(6):405-13. PubMed ID: 4065160
    [Abstract] [Full Text] [Related]

  • 10.
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  • 11. Familial atrioventricular heart block; an autosomal dominant trait.
    Waxman MB, Catching JD, Felderhof CH, Downar E, Silver MD, Abbott MM.
    Circulation; 1975 Feb; 51(2):226-33. PubMed ID: 122919
    [Abstract] [Full Text] [Related]

  • 12.
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  • 13. Neurogenic scapuloperoneal syndrome in childhood.
    Mercelis R, Demeester J, Martin JJ.
    J Neurol Neurosurg Psychiatry; 1980 Oct; 43(10):888-96. PubMed ID: 7441268
    [Abstract] [Full Text] [Related]

  • 14. Progressive proximal spinal and bulbar muscular atrophy of late onset. A sex-linked recessive trait.
    Kennedy WR, Alter M, Sung JH.
    Neurology; 1968 Jul; 18(7):671-80. PubMed ID: 4233749
    [No Abstract] [Full Text] [Related]

  • 15.
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  • 16. Cardiac voltage-gated sodium channel mutations associated with left atrial dysfunction and stroke in children.
    Moreau A, Janin A, Millat G, Chevalier P.
    Europace; 2018 Oct 01; 20(10):1692-1698. PubMed ID: 29579189
    [Abstract] [Full Text] [Related]

  • 17. Altered HCN4 channel C-linker interaction is associated with familial tachycardia-bradycardia syndrome and atrial fibrillation.
    Duhme N, Schweizer PA, Thomas D, Becker R, Schröter J, Barends TR, Schlichting I, Draguhn A, Bruehl C, Katus HA, Koenen M.
    Eur Heart J; 2013 Sep 01; 34(35):2768-75. PubMed ID: 23178648
    [Abstract] [Full Text] [Related]

  • 18. [Relationships between genotype and phenotype in Charcot-Marie-Tooth disease].
    Câmpeanu E, Morariu M.
    Rev Roum Neurol; 1970 Sep 01; 7(1):47-56. PubMed ID: 5527990
    [No Abstract] [Full Text] [Related]

  • 19. The genetic heterogeneity of spinal muscular atrophy (SMA).
    Zellweger H.
    Birth Defects Orig Artic Ser; 1971 Feb 01; 7(2):82-9. PubMed ID: 5173130
    [Abstract] [Full Text] [Related]

  • 20. Peripheral neurofibromatosis and peroneal muscular atrophy.
    Bosch EP, Murphy MJ, Cancilla PA.
    Neurology; 1981 Nov 01; 31(11):1408-14. PubMed ID: 6796901
    [Abstract] [Full Text] [Related]

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