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PUBMED FOR HANDHELDS

Journal Abstract Search


151 related items for PubMed ID: 4195731

  • 21. [Metabolic myopathies].
    Lössner J, Kühn HJ.
    Psychiatr Neurol Med Psychol (Leipz); 1984 Sep; 36(9):513-26. PubMed ID: 6595679
    [Abstract] [Full Text] [Related]

  • 22. [The ultrastructure of the liver in various thesaurismoses].
    van Hoof F, Hers HG.
    Rev Int Hepatol; 1967 Sep; 17(8):815-26. PubMed ID: 4234430
    [No Abstract] [Full Text] [Related]

  • 23. Some rare congenital and metabolic myopathies.
    Walton JN.
    Birth Defects Orig Artic Ser; 1971 Feb; 7(2):2-14. PubMed ID: 5293616
    [Abstract] [Full Text] [Related]

  • 24. Acid maltase deficiency of adult life.
    Engel AG.
    Trans Am Neurol Assoc; 1969 Feb; 94():250-2. PubMed ID: 4244774
    [No Abstract] [Full Text] [Related]

  • 25. [On 2 uncommon cases of cardio-muscular glycogenosis (with enzyme study)].
    Berio A, Marchi AG, Bertolotti E, Nordio S.
    Minerva Pediatr; 1967 Apr 07; 19(14):688-92. PubMed ID: 5247206
    [No Abstract] [Full Text] [Related]

  • 26. [Method for the differentiation of glycogenoses].
    Schaub J.
    Monatsschr Kinderheilkd (1902); 1970 Jun 07; 118(6):427-9. PubMed ID: 4331992
    [No Abstract] [Full Text] [Related]

  • 27. [CONTRIBUTION TO THE MECHANISM OF GLOBULIN REACTIONS IN THE CEREBROSPINAL FLUID AND THEIR RELATION TO INDIVIDUAL PROTEIN FRACTIONS].
    VYMAZAL J.
    Cesk Neurol; 1963 Nov 07; 26():388-93. PubMed ID: 14112995
    [No Abstract] [Full Text] [Related]

  • 28. Ultrastructure of skeletal muscle in muscular dystrophy, the carrier state and other human myopathies.
    Papadimitriou JM, Kakulas BA.
    Proc Aust Assoc Neurol; 1968 Nov 07; 5(1):87-94. PubMed ID: 5250033
    [No Abstract] [Full Text] [Related]

  • 29. [Glycogenosis type III with peripheral nerve disorder and muscular hypertrophy in an adult].
    Hokezu Y, Nagamatsu K, Nakagawa M, Osame M, Ohnishi A.
    Rinsho Shinkeigaku; 1983 Jun 07; 23(6):473-9. PubMed ID: 6317246
    [No Abstract] [Full Text] [Related]

  • 30. [2 causes of muscle ache and reddish-brown urine following exertion].
    Jennekens FG, Scholte HR, Koster JF, Bouvy JJ.
    Ned Tijdschr Geneeskd; 1979 Sep 08; 123(36):1562-8. PubMed ID: 289908
    [No Abstract] [Full Text] [Related]

  • 31. [Glycogen disease in children].
    Bodkaĭlo LV, Kobrusev VV, Merems BS, Morozova GS.
    Sov Zdravookhr Kirg; 1971 Sep 08; 5():39-43. PubMed ID: 5292970
    [No Abstract] [Full Text] [Related]

  • 32. Electrophysiological abnormalities in metabolic myopathies and neuropathies.
    Buchthal F.
    Acta Neurol Scand; 1970 Sep 08; 46(S43):129-76. PubMed ID: 4318671
    [No Abstract] [Full Text] [Related]

  • 33. AGAR-GEL MICRO-ELECTROPHORESIS OF PROTEINS IN THE CEREBROSPINAL FLUID NORMAL AND PATHOLOGICAL FINDINGS.
    CLAUSEN J, MATZKE J, GERHARDT W.
    Acta Neurol Scand Suppl; 1964 Sep 08; 40():SUPPL 10:49-56. PubMed ID: 14194813
    [No Abstract] [Full Text] [Related]

  • 34. Peripheral neuropathy. Changing concepts, differential diagnosis and classification.
    Dyck PJ.
    Med Clin North Am; 1968 Jul 08; 52(4):895-908. PubMed ID: 4192680
    [No Abstract] [Full Text] [Related]

  • 35. Generalized glycogenosis type II (Pompe's disease).
    Nihill MR, Wilson DS, Hugh-Jones K.
    Arch Dis Child; 1970 Feb 08; 45(239):122-9. PubMed ID: 4245388
    [Abstract] [Full Text] [Related]

  • 36. [Metabolic myopathies in childhood. A review in summarized form].
    Schaub J.
    Monatsschr Kinderheilkd; 1984 Aug 08; 132(8):566-73. PubMed ID: 6090889
    [Abstract] [Full Text] [Related]

  • 37. [Peripheral neuropathy as a presentation of metabolic disorders in childhood].
    Desguerre I, Barnerias C, Valayannopoulos V.
    Rev Neurol (Paris); 2007 Dec 08; 163(12):1256-9. PubMed ID: 18355478
    [No Abstract] [Full Text] [Related]

  • 38. Role of amniocentesis in the intrauterine detection of genetic disorders.
    Nadler HL, Gerbie AB.
    N Engl J Med; 1970 Mar 12; 282(11):596-9. PubMed ID: 4244215
    [No Abstract] [Full Text] [Related]

  • 39. [Peripheral nerve involvement in congenital metabolic disorders (author's transl)].
    Nonaka I.
    No To Shinkei; 1979 May 12; 31(5):445-54. PubMed ID: 90516
    [No Abstract] [Full Text] [Related]

  • 40. [Progressive neuronal degeneration and childhood cirrhosis].
    Kumada S, Okaniwa M.
    Ryoikibetsu Shokogun Shirizu; 1995 May 12; (8):442-5. PubMed ID: 8581675
    [No Abstract] [Full Text] [Related]


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