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PUBMED FOR HANDHELDS

Journal Abstract Search


104 related items for PubMed ID: 504864

  • 1. [Strümpell Lorrain's familial spasmodic paraplegia. An anatomical and clinical review and report on a new case (author's transl)].
    Buge A, Escourolle R, Rancurel G, Gray F, Pertuiset BF.
    Rev Neurol (Paris); 1979; 135(4):329-37. PubMed ID: 504864
    [Abstract] [Full Text] [Related]

  • 2. Familial spastic paraplegia-clinical and pathologic studies in a large kindred.
    Sack GH, Huether CA, Garg N.
    Johns Hopkins Med J; 1978 Oct; 143(4):117-21. PubMed ID: 703033
    [Abstract] [Full Text] [Related]

  • 3. [Strümpell-Lorrain's spastic paraplegia (primary lateral sclerosis, familial spastic paralysis, etc.)].
    González-Elipe J, Vilanova A, Rapado A, Fernández-Criado M, Perianes J.
    Rev Clin Esp; 1970 Nov 15; 119(3):233-40. PubMed ID: 5495928
    [No Abstract] [Full Text] [Related]

  • 4. [Optic neuropathy in Strumpell-Lorrain disease: presentation of a clinical case and literature review].
    Makhoul J, Cordonnier M, Van Nechel C.
    Bull Soc Belge Ophtalmol; 2002 Nov 15; (286):9-14. PubMed ID: 12564312
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  • 5. [Hereditary degenerative spinocerebellar diseases in Tunisia with manometric studies in bladder disorders (author's transl)].
    Ben Hamida M, Madani S, Zmerli S, Chami I, Annabi A, Jamoussi M, Marzouki M, Rachdi M, Samoud S, Talbi M.
    Rev Neurol (Paris); 1980 Nov 15; 136(8-9):495-508. PubMed ID: 7221327
    [Abstract] [Full Text] [Related]

  • 6. [Hereditary spastic paraplegia associated with peripheral neuropathy. Contribution of a family].
    García-Albea E, Peña P, Cabello A, Calandre L.
    Rev Clin Esp; 1979 Jan 31; 152(2):155-9. PubMed ID: 220681
    [No Abstract] [Full Text] [Related]

  • 7. Hereditary spastic paraplegia: a clinical and genetic study of cases in the north-east of England.
    Livingstone IR, Roberts DF.
    J Genet Hum; 1983 Dec 31; 31(4):295-305. PubMed ID: 6582228
    [Abstract] [Full Text] [Related]

  • 8. [Involvement of the peripheral motor neuron in hereditary spastic paraplegia (author's transl)].
    Malin JP.
    EEG EMG Z Elektroenzephalogr Elektromyogr Verwandte Geb; 1976 Sep 31; 7(3):140-5. PubMed ID: 829059
    [Abstract] [Full Text] [Related]

  • 9. [Autopsy cases of hereditary ataxia pathologically diagnosed as the Japanese type of Joseph disease--cliniconeuropathological findings].
    Kogure T, Oda T, Katoh Y.
    Seishin Shinkeigaku Zasshi; 1990 Sep 31; 92(3):161-83. PubMed ID: 2353076
    [Abstract] [Full Text] [Related]

  • 10. [Etiology and pathogenesis of familial spastic paraplegia (Strümpell-Lorrain disease)].
    Michałowicz R, Ignatowicz R, Kmieć T, Jóźwiak S.
    Pol Tyg Lek; 1984 Aug 06; 39(32):1083-6. PubMed ID: 6504736
    [No Abstract] [Full Text] [Related]

  • 11. Strümpell's familial spastic paraplegia: genetics and neuropathology.
    Behan WM, Maia M.
    J Neurol Neurosurg Psychiatry; 1974 Jan 06; 37(1):8-20. PubMed ID: 4813430
    [Abstract] [Full Text] [Related]

  • 12. [Hereditary spastic paraplegia. Case report and review with special reference to current neurophysiologic examination methods].
    Urnes O.
    Tidsskr Nor Laegeforen; 1983 May 30; 103(15):1249-51. PubMed ID: 6879555
    [No Abstract] [Full Text] [Related]

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  • 14. [Infantile neuro-axonal dystrophy: anatomo clinical study of one case (author's transl)].
    Onnis L, Nardelli E, Buonanno F, Galiazzo-Rizzuto S, Panizon F, Rizzuto N.
    Riv Patol Nerv Ment; 1975 May 30; 96(5):322-39. PubMed ID: 1235007
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  • 18. [Congenital autosomal-recessive familial spastic paraplegia].
    Badalian LO, Umakhanov RU, Temin PA, Arhipov BA, Bulaeva NV, Sakidebirov GM.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1991 May 30; 91(8):97-9. PubMed ID: 1661531
    [Abstract] [Full Text] [Related]

  • 19. The late form of pure familial spastic paraplegia.
    Vernea J, Symington GR.
    Clin Exp Neurol; 1977 May 30; 14():37-41. PubMed ID: 358187
    [No Abstract] [Full Text] [Related]

  • 20. [Adrenomyeloneuropathy. 4 cases developing with the features of familial spasmodic paraplegia].
    Rondot P, De Recondo J, Davous P, Dubas F, Khoubesserian P, Coignet A.
    Ann Med Interne (Paris); 1984 May 30; 135(7):542-7. PubMed ID: 6517427
    [Abstract] [Full Text] [Related]


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