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Journal Abstract Search

194 related items for PubMed ID: 5691597

  • 21. Iron in the Hallervorden-Spatz syndrome.
    Koeppen AH, Dickson AC.
    Pediatr Neurol; 2001 Aug; 25(2):148-55. PubMed ID: 11551745
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  • 23. Pathogenesis of pigment and spheroid formation in Hallervorden-Spatz syndrome and related disorders.
    Park BE, Netsky MG, Betsill WL.
    Neurology; 1975 Dec; 25(12):1172-8. PubMed ID: 1238961
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  • 26. [Infantile neuro-axonal dystrophy and Hallervorden-Spatz disease. Electro-clinical and anatomo-pathological and differential diagnostic aspects].
    Radermecker J, Martin JJ.
    Bull Acad R Med Belg; 1972 Jul; 12(7):459-502. PubMed ID: 4662801
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  • 29. Clinicopathological study of familial late infantile Hallervorden-Spatz disease: a particular form of neuroacanthocytosis.
    Malandrini A, Fabrizi GM, Bartalucci P, Salvadori C, Berti G, Sabò C, Guazzi GC.
    Childs Nerv Syst; 1996 Mar; 12(3):155-60. PubMed ID: 8697459
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  • 30. Hallervorden-Spatz syndrome restricted to the pallidal nuclei.
    Kessler C, Schwechheimer K, Reuther R, Born JA.
    J Neurol; 1984 Mar; 231(3):112-6. PubMed ID: 6481416
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  • 31. Adult onset Hallervorden-Spatz syndrome or Seitelberger's disease with late onset: variants of the same entity? A clinico-pathological study.
    Gaytan-Garcia S, Kaufmann JC, Young GB.
    Clin Neuropathol; 1990 Mar; 9(3):136-42. PubMed ID: 2364593
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  • 34. [Late Hallervorden-Spatz disease with important reticular and cerebellar participation].
    Evrard E, Hariga J, Martin JJ, Reznik M.
    Psychiatr Neurol Neurochir; 1968 Mar; 71(3):243-54. PubMed ID: 5687405
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  • 40. Late-onset Hallervorden-Spatz disease presenting as familial parkinsonism.
    Jankovic J, Kirkpatrick JB, Blomquist KA, Langlais PJ, Bird ED.
    Neurology; 1985 Feb; 35(2):227-34. PubMed ID: 3969211
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