These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

79 related items for PubMed ID: 303794

  • 1. [Classical Strumpell-Lorrain disease in a father and congenital diplegia in his son].
    Christodorescu D.
    Rev Med Interna Neurol Psihiatr Neurochir Dermatovenerol Neurol Psihiatr Neurochir; 1977; 22(3):235-8. PubMed ID: 303794
    [No Abstract] [Full Text] [Related]

  • 2. [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]

  • 3. [Strumpell-Lorrain disease: single nosologic entity?].
    Bettinazzi G, Amato L, Arcara A, Scoppa F.
    Acta Neurol (Napoli); 1986 Jun 06; 8(3):259-62. PubMed ID: 3739774
    [No Abstract] [Full Text] [Related]

  • 4. Peroneal somatosensory evoked potentials in the "pure" form of hereditary spastic paraplegia.
    Görke W, Grimm T.
    Neuropediatrics; 1986 Aug 06; 17(3):162-4. PubMed ID: 3762873
    [Abstract] [Full Text] [Related]

  • 5. [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 Aug 06; (286):9-14. PubMed ID: 12564312
    [Abstract] [Full Text] [Related]

  • 6. [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]

  • 7. [Familial spastic paraplegia in 3 families].
    Fujiwara H, Akabori O, Akashi K, Moriya S.
    Seikei Geka; 1971 Nov 15; 22(6):471-6. PubMed ID: 5104423
    [No Abstract] [Full Text] [Related]

  • 8. [Strumpell's disease in childhood].
    Popov'ian MD, Dubinskaia EE, Allaverdova RA.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1982 Nov 15; 82(10):29-32. PubMed ID: 7180276
    [No Abstract] [Full Text] [Related]

  • 9. Troyer syndrome: a recessively inherited form of spastic paraplegia with distal muscle wasting.
    Cross HE.
    Birth Defects Orig Artic Ser; 1971 Feb 15; 7(1):211-3. PubMed ID: 5173362
    [No Abstract] [Full Text] [Related]

  • 10. Familial spastic paraplegia.
    Rischbieth RH.
    Proc Aust Assoc Neurol; 1973 Feb 15; 10(0):31-3. PubMed ID: 4792159
    [No Abstract] [Full Text] [Related]

  • 11. [Complicated spastic paraplegia with sex-linked inheritance (report of a family)].
    Galassi G, Penne A, Colombo A, Forabosco A.
    Acta Neurol (Napoli); 1977 Feb 15; 32(6):746-56. PubMed ID: 605830
    [No Abstract] [Full Text] [Related]

  • 12. X-linked hereditary spastic paraplegia.
    Raggio JF, Thurmon TF, Anderson EE.
    J La State Med Soc; 1973 Jan 15; 125(1):4-5. PubMed ID: 4684346
    [No Abstract] [Full Text] [Related]

  • 13. [Hereditary familial spastic paraparesis (Strumpell-Lorraine disease)].
    Wróblewski T, Smoliński J.
    Pediatr Pol; 1978 Feb 15; 53(2):211-3. PubMed ID: 634661
    [No Abstract] [Full Text] [Related]

  • 14. Familial spastic paraplegia-clinical and pathologic studies in a large kindred.
    Sack GH, Huether CA, Garg N.
    Johns Hopkins Med J; 1978 Oct 15; 143(4):117-21. PubMed ID: 703033
    [Abstract] [Full Text] [Related]

  • 15. [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]

  • 16. [Various neurophysiologic mechanisms of compensating for movement disorders in pyramidal system lesions (electromyographic analysis)].
    Novikova VP.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1982 May 30; 82(7):50-4. PubMed ID: 7124224
    [No Abstract] [Full Text] [Related]

  • 17. [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 May 30; 135(4):329-37. PubMed ID: 504864
    [Abstract] [Full Text] [Related]

  • 18. Hereditary spastic paraplegia.
    Charkabarti AK, Lloyd GH, Johnson SC.
    J Indian Med Assoc; 1977 Oct 01; 69(7):141-6. PubMed ID: 611148
    [No Abstract] [Full Text] [Related]

  • 19. [Clinical manifestations and mode of inheritance of hereditary spastic paraplegia in 20 families].
    Gao HW.
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1985 Feb 01; 18(1):24-6. PubMed ID: 3987454
    [No Abstract] [Full Text] [Related]

  • 20. [Atypical forms of familial amyotrophic lateral sclerosis].
    Serratrice G.
    Rev Neurol (Paris); 1985 Feb 01; 141(4):322-4. PubMed ID: 4012149
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 4.