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Journal Abstract Search

162 related items for PubMed ID: 7103414

  • 1.
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  • 2. 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; 9(3):136-42. PubMed ID: 2364593
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  • 3. An autopsy case of late infantile and juvenile neuroaxonal dystrophy with diffuse Lewy bodies and neurofibrillary tangles.
    Hayashi S, Akasaki Y, Morimura Y, Takauchi S, Sato M, Miyoshi K.
    Clin Neuropathol; 1992; 11(1):1-5. PubMed ID: 1372197
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  • 4. Infantile neuroaxonal dystrophy--immunohistochemical and ultrastructural studies on the central and peripheral nervous systems in infantile neuroaxonal dystrophy.
    Itoh K, Negishi H, Obayashi C, Hayashi Y, Hanioka K, Imai Y, Itoh H.
    Kobe J Med Sci; 1993 Aug; 39(4):133-46. PubMed ID: 8289437
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  • 8. [Generalized infantile neuroaxonal dystrophies with pigmentation and lipophanerosis of the pallidum in concordant twins (author's transl)].
    Peiffer J, Brunner N, Landolt RF, Müller G, Schlote W.
    Neuropadiatrie; 1976 Aug; 7(3):327-50. PubMed ID: 183173
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  • 9. [An intermediate, generalized form of neuroaxonal dystrophy--light- and electron microscopic findings].
    Lehmann J, Goebel HH.
    Acta Histochem Suppl; 1992 Aug; 42():311-8. PubMed ID: 1584981
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  • 11. Neuropathological spectrum of synucleinopathies.
    Jellinger KA.
    Mov Disord; 2003 Sep; 18 Suppl 6():S2-12. PubMed ID: 14502650
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  • 12. Neuroaxonal dystrophy combined with diffuse Lewy body disease in a young adult.
    Sugiyama H, Hainfellner JA, Schmid-Siegel B, Budka H.
    Clin Neuropathol; 1993 Sep; 12(3):147-52. PubMed ID: 8391956
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  • 13. Infantile neuroaxonal dystrophy: what's most important for the diagnosis?
    Carrilho I, Santos M, Guimarães A, Teixeira J, Chorão R, Martins M, Dias C, Gregory A, Westaway S, Nguyen T, Hayflick S, Barbot C.
    Eur J Paediatr Neurol; 2008 Nov; 12(6):491-500. PubMed ID: 18359254
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  • 14. Neuroaxonal dystrophy in a Jack Russell terrier pup resembling human infantile neuroaxonal dystrophy.
    Sacre BJ, Cummings JF, De Lahunta A.
    Cornell Vet; 1993 Apr; 83(2):133-42. PubMed ID: 8467699
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  • 15. [1st juvenile case of complex neurolipidosis and neuroaxonal dystrophy involving the central nervous system].
    Bovet J.
    Schweiz Arch Neurol Neurochir Psychiatr; 1984 Apr; 134(2):305-32. PubMed ID: 6087445
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  • 16. [Some problems on the clinical phenotype of Machado-Joseph disease in relation between their ages at onset].
    Iwabuchi K, Kogure T, Oda T, Kato Y, Ohtani K, Endo K, Kosaka K, Amano N, Yagishita S.
    No To Shinkei; 1993 Mar; 45(3):246-54. PubMed ID: 8323819
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  • 17. Rectal biopsy findings in infantile neuroaxonal dystrophy.
    Goebel HH, Kohlschütter A, Schulte FJ.
    Neuropediatrics; 1980 Nov; 11(4):388-92. PubMed ID: 7207709
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  • 18. Feline hereditary neuroaxonal dystrophy.
    Woodard JC, Collins GH, Hessler JR.
    Am J Pathol; 1974 Mar; 74(3):551-66. PubMed ID: 4814900
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  • 19. Infantile neuroaxonal dystrophy and giant axonal neuropathy--overlap diseases of neuronal cytoskeletal elements in childhood?
    Mahadevan A, Santosh V, Gayatri N, Ratnavalli E, NandaGopal R, Vasanth A, Roy AK, Shankar SK.
    Clin Neuropathol; 2000 Mar; 19(5):221-9. PubMed ID: 11048747
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  • 20. Late infantile neuroaxonal dystrophy. An unusual case with predominantly myoclonic-epileptic symptomatology.
    Barontini F, Papini M.
    Riv Patol Nerv Ment; 1981 Mar; 101(4):171-84. PubMed ID: 6789439
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