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Journal Abstract Search

136 related items for PubMed ID: 5076139

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  • 22. Neuroaxonal leukoencephalopathy with axonal spheroids.
    Yamashita M, Yamamoto T.
    Eur Neurol; 2002; 48(1):20-5. PubMed ID: 12138305
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  • 30. Characteristic clinical findings in some neurogenic myopathies and in some myogenic myopathies causing muscular weakness, hypotonia and atrophy in infancy and early childhood.
    Gamstorp I.
    Birth Defects Orig Artic Ser; 1971 Feb; 7(2):72-81. PubMed ID: 5173129
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  • 32. [Lipid storage myopathy--a contribution to the problem of the differential diagnosis of muscle dystrophy (Duchenne)].
    Schmidt A, Hässler A.
    Zentralbl Allg Pathol; 1983 Feb; 127(3-4):229-36. PubMed ID: 6880434
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  • 34. Infantile neuroaxonal dystrophy. An electron microscopic study of a case clinically resembling neuronal ceroid-lipofuscinosis.
    Butzer JF, Schochet SS, Bell WE.
    Acta Neuropathol; 1975 Feb; 31(1):35-43. PubMed ID: 1121924
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  • 35. Spastic paraplegia with neurogenic amyotrophy manifesting ballooned axons in sural nerve.
    Shimono M, Ohta M, Kuroiwa Y.
    Acta Neuropathol; 1977 Jul 15; 39(1):9-12. PubMed ID: 899737
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  • 36. Hallervorden-Spatz disease and infantile neuroaxonal dystrophy. Clinical characteristics and nosological considerations.
    Gilman S, Barrett RE.
    J Neurol Sci; 1973 Jun 15; 19(2):189-205. PubMed ID: 4712933
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