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PUBMED FOR HANDHELDS

Journal Abstract Search


176 related items for PubMed ID: 4112646

  • 21. Neuroaxonal dystrophy. A case of non pigmented type and protracted course.
    Thibault J.
    Acta Neuropathol; 1972; 21(3):232-8. PubMed ID: 5056009
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  • 24. [Pathogenesis of Hallervorden-Spatz disease-its neuropathology from viewpoint of systemic degenerative disorder and precocious senility].
    Shiraki H.
    Shinkei Kenkyu No Shimpo; 1968 Aug; 12(2):389-413. PubMed ID: 5752596
    [No Abstract] [Full Text] [Related]

  • 25. Seitelberger's infantile neuroaxonal dystrophy. A case report.
    Rizzuto N, Vio M, Ghersini L, Panizzon F.
    Eur Neurol; 1973 Aug; 9(6):321-32. PubMed ID: 4712541
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  • 26. Unusual late-onset type of hallervorden-Spatz disease. Clinico-pathological study of a case presenting as parkinsonism.
    Jellinger K, Neumayer E.
    Z Neurol; 1972 Aug; 203(2):105-18. PubMed ID: 4119022
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  • 27. Hallervorden spatz disease associated with lewy type inclusions.
    Bornstein B, Sandbank U, Fried Y.
    Confin Neurol; 1966 Aug; 27(5):397-405. PubMed ID: 5959225
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  • 30. Amyotrophic lateral sclerosis-dementia complex, neuroaxonal dystrophy, and Hallervorden-Spatz disease.
    Bots GT, Staal A.
    Neurology; 1973 Jan; 23(1):35-9. PubMed ID: 4734498
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  • 34. [A further contribution to the knowledge of the Hallervorden-Spatz disease].
    Gallyas F, Környey S.
    Arch Psychiatr Nervenkr (1970); 1968 Jan; 212(1):33-45. PubMed ID: 5733780
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  • 35. Neuroaxonal dystrophy in subacute dementia. Case report.
    Torack RM, Hughes CP.
    Acta Neuropathol; 1972 Jan; 22(3):264-8. PubMed ID: 4637008
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  • 37. [CONTRIBUTION TO LATE INFANTILE HALLERVORDEN-SPATZ DISEASE].
    SEITELBERGER F, GOOTZ E, GROSS H.
    Acta Neuropathol; 1963 Sep 02; 3():16-28. PubMed ID: 14197653
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  • 40. "Hallervorden-Spatz syndrome--infantile neuroaxonal dystrophy" complex. Case report.
    Bresolin AU, Pascuzzi L, Melaragno Filho R, Fontana MH, Pecora R, Souza Dias JC.
    Arq Neuropsiquiatr; 1988 Mar 02; 46(1):69-72. PubMed ID: 3408385
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