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Journal Abstract Search

255 related items for PubMed ID: 6445503

  • 1. Biochemistry of muscle membranes in Duchenne muscular dystrophy.
    Rowland LP.
    Muscle Nerve; 1980; 3(1):3-20. PubMed ID: 6445503
    [Abstract] [Full Text] [Related]

  • 2. Biochemical abnormalities of the sarcoplasmic reticulum in muscular dystrophy.
    Samaha FJ, Gergely J.
    N Engl J Med; 1969 Jan 23; 280(4):184-8. PubMed ID: 4235816
    [No Abstract] [Full Text] [Related]

  • 3. Echinogenic action of L-alpha-lysophosphatidylcholine in Duchenne muscular dystrophy: a study on carrier detection.
    Tangorra A, Curatola G, Milani-Comparetti M, Ferretti G.
    Am J Med Genet; 1989 Apr 23; 32(4):540-4. PubMed ID: 2774000
    [Abstract] [Full Text] [Related]

  • 4. [Membrane effects of insulin in x-chromosome recessive hereditary progressive muscular dystrophy (Duchenne form)].
    Blietz R, Kruchten J, Riedl K, Wagner J.
    Hoppe Seylers Z Physiol Chem; 1967 Dec 23; 348(12):1609-15. PubMed ID: 5586908
    [No Abstract] [Full Text] [Related]

  • 5. [Clinico-biochemical and genetic studies of myopathy].
    Davidenkova EF, Droznina TA, Markelov IM.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1966 Dec 23; 66(11):1623-8. PubMed ID: 6001049
    [No Abstract] [Full Text] [Related]

  • 6. Muscle and serum enzymes and isoenzymes in muscular dystrophies.
    Ibrahim GA, Zweber BA, Awad EA.
    Arch Phys Med Rehabil; 1981 Jun 23; 62(6):265-9. PubMed ID: 7235920
    [Abstract] [Full Text] [Related]

  • 7. [Human myopathy and animal muscular dystrophy].
    Schapira G, Dreyfus JC, Schapira F.
    Acta Zool Pathol Antverp; 1977 Aug 23; (68):93-110. PubMed ID: 335859
    [Abstract] [Full Text] [Related]

  • 8. [Serum enzyme activities in the families of patients with progressive muscular dystrophy].
    Tani J, Yano I, Masaki H, Fukuyama K, Saeki B.
    Iryo; 1967 Jul 23; 21(7):848-53. PubMed ID: 5582480
    [No Abstract] [Full Text] [Related]

  • 9. [Plasmatic enzyme studies in individuals with progressive muscular dystrophy in the course of various therapeutic trials].
    Mancini G, Lapi AS, Schwarzenberg TL, Canibus R, Natoli V.
    Arch Ital Pediatr Pueric; 1968 Jul 23; 26(1):36-46. PubMed ID: 5737311
    [No Abstract] [Full Text] [Related]

  • 10. [Progressive muscular dystrophy: CPK, LDH, ALD (aldolase)--EMG, ECG in patients and their families].
    Diotallevi P, Bargilli E, Danni M, Dellantonio R, Tocchini M, Milani-Comparetti M.
    Boll Soc Ital Biol Sper; 1988 Jun 23; 64(6):523-30. PubMed ID: 3190905
    [No Abstract] [Full Text] [Related]

  • 11. [Differentiation and dedifferentiation of muscular dystrophy].
    Ueda K, Ito T, Nakata T, Ohara T, Matsumoto K.
    Nihon Rinsho; 1968 Oct 23; 26(10):2423-42. PubMed ID: 5752013
    [No Abstract] [Full Text] [Related]

  • 12. Clinical and molecular studies in Duchenne muscular dystrophy.
    Emery AE.
    Prog Clin Biol Res; 1989 Oct 23; 306():15-28. PubMed ID: 2662210
    [Abstract] [Full Text] [Related]

  • 13. [Becker's benign muscular dystrophy. Observations on 1 family].
    Armocida G, Cottini R, Finavera L, Majeron MA.
    Minerva Med; 1978 May 19; 69(25):1745-8. PubMed ID: 662177
    [Abstract] [Full Text] [Related]

  • 14. [Muscle LDH isoenzymes in neuromuscular diseases and in carriers of recessive X-linked muscular dystrophy (duchenne)].
    Kowalewski S, Rotthauwe HW.
    Z Kinderheilkd; 1972 May 19; 113(1):55-70. PubMed ID: 5056500
    [No Abstract] [Full Text] [Related]

  • 15. [Clinico-statistical considerations on a group of 22 patients with progressive muscular dystrophy].
    Garofalo E, Marcer V.
    Fracastoro; 1966 May 19; 59(6):621-38. PubMed ID: 5998705
    [No Abstract] [Full Text] [Related]

  • 16. [Plasma level of hemopexin (Hpx) in families with progressive muscular dystrophy (PMD)].
    Diotallevi P, Balducci E, Canapa A, Danni M, Giamagli CA, Lucesoli S, Ravaglia P, Milani-Comparetti M.
    Boll Soc Ital Biol Sper; 1988 Jun 19; 64(6):531-8. PubMed ID: 3190906
    [No Abstract] [Full Text] [Related]

  • 17. Membrane abnormalities in Duchenne muscular dystrophy.
    Jones GE, Witkowski JA.
    J Neurol Sci; 1983 Feb 19; 58(2):159-74. PubMed ID: 6300338
    [No Abstract] [Full Text] [Related]

  • 18. Slowly progressive X-linked recessive muscular dystrophy (type 3b). Report of cases and review of the literature.
    Zellweger H, Hanson JW.
    Arch Intern Med; 1967 Nov 19; 120(5):525-35. PubMed ID: 6054585
    [No Abstract] [Full Text] [Related]

  • 19. [Autosomal recessive severe, proximal myopathy in children, common in Tunisia].
    Ben Hamida M, Attia N, Chabouni H, Fardeau M.
    Rev Neurol (Paris); 1983 Nov 19; 139(4):289-97. PubMed ID: 6612142
    [Abstract] [Full Text] [Related]

  • 20. [Effects of administration of phosphocreatine on the clinical, biochemical and electromyographic evolution of Duchenne's progressive muscular dystrophy].
    Radu H, Keresztes L, Stenzel K.
    Minerva Med; 1968 Dec 12; 59(99):5524-9. PubMed ID: 5718841
    [No Abstract] [Full Text] [Related]

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