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Journal Abstract Search

163 related items for PubMed ID: 5104423

  • 41. [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]

  • 42. [Progressive supranuclear palsy with familial occurrence of spinocerebellar degeneration].
    Yamamura Y, Kito S, Itoga E, Kajiwara H.
    Rinsho Shinkeigaku; 1982 Jul; 22(7):586-93. PubMed ID: 7172528
    [No Abstract] [Full Text] [Related]

  • 43. Visual evoked potentials in two forms of hereditary spastic paraplegia.
    Happel LT, Rothschild H, Garcia C.
    Electroencephalogr Clin Neurophysiol; 1980 Feb; 48(2):233-6. PubMed ID: 6153340
    [Abstract] [Full Text] [Related]

  • 44. [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]

  • 45. [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 Nov 15; 22(3):235-8. PubMed ID: 303794
    [No Abstract] [Full Text] [Related]

  • 46. Manifesting heterozygosity in sex-linked spastic paraplegia?
    Young ID, Pye IF, Moore JR.
    J Neurol Neurosurg Psychiatry; 1984 Mar 15; 47(3):311-3. PubMed ID: 6707681
    [Abstract] [Full Text] [Related]

  • 47. The autosomal dominant form of "pure" familial spastic paraplegia: clinical findings and linkage analysis of a large pedigree.
    Boustany RM, Fleischnick E, Alper CA, Marazita ML, Spence MA, Martin JB, Kolodny EH.
    Neurology; 1987 Jun 15; 37(6):910-5. PubMed ID: 3587641
    [Abstract] [Full Text] [Related]

  • 48. [Familial spastic paraplegia. Genetic-scientific discussion apropos of an affected family].
    Gonçalves A.
    Arq Neuropsiquiatr; 1980 Jun 15; 38(2):144-9. PubMed ID: 7436797
    [Abstract] [Full Text] [Related]

  • 49. Spasticity and its amelioration.
    Nathan PW.
    Mod Trends Neurol; 1970 Jun 15; 5(0):41-59. PubMed ID: 5528134
    [No Abstract] [Full Text] [Related]

  • 50. [Strumpell-Lorrain disease: single nosologic entity?].
    Bettinazzi G, Amato L, Arcara A, Scoppa F.
    Acta Neurol (Napoli); 1986 Jun 15; 8(3):259-62. PubMed ID: 3739774
    [No Abstract] [Full Text] [Related]

  • 51. Clinical and neurophysiological correlations of spasticity.
    Milanov I.
    Funct Neurol; 1999 Jun 15; 14(4):193-201. PubMed ID: 10713892
    [Abstract] [Full Text] [Related]

  • 52. Spinal somatosensory evoked potentials in hereditary spastic paraplegia.
    Thomas PK, Jefferys JG, Smith IS, Loulakakis D.
    J Neurol Neurosurg Psychiatry; 1981 Mar 15; 44(3):243-6. PubMed ID: 7229648
    [Abstract] [Full Text] [Related]

  • 53. Familial occurrence of HTLV-I--associated myelopathy.
    Mori M, Ban N, Kinoshita K.
    Ann Neurol; 1988 Jan 15; 23(1):100. PubMed ID: 2894196
    [No Abstract] [Full Text] [Related]

  • 54. [Three siblings of familial spastic paraplegia with sensory disturbance and cataracts (author's transl)].
    Kayanuma K, Adachi N, Nakajima M, Yanagisawa N, Tsukagoshi H.
    Rinsho Shinkeigaku; 1979 Jun 15; 19(6):388-93. PubMed ID: 477140
    [No Abstract] [Full Text] [Related]

  • 55. Familial spastic paraparesis, optic atrophy, and dementia. Clinical observations of affected kindred.
    Rothner AD, Yahr F, Yahr MD.
    N Y State J Med; 1976 May 15; 76(5):756-8. PubMed ID: 1063327
    [No Abstract] [Full Text] [Related]

  • 56. Hereditary spastic paraplegia.
    Choi IS, Cho HK, Kim KW.
    Yonsei Med J; 1983 May 15; 24(1):83-6. PubMed ID: 6659558
    [No Abstract] [Full Text] [Related]

  • 57. The Troyer syndrome. A recessive form of spastic paraplegia with distal muscle wasting.
    Cross HE, McKusick VA.
    Arch Neurol; 1967 May 15; 16(5):473-85. PubMed ID: 6022528
    [No Abstract] [Full Text] [Related]

  • 58. Confirmation of locus heterogeneity in the pure form of familial spastic paraplegia.
    Speer MC, Kingston HM, Boustany RM, Gaskell PC, Robinson LC, Lennon F, Wolpert CM, Yamaoka LH, Kahler SG, Hogan EL.
    Am J Med Genet; 1995 Aug 14; 60(4):307-11. PubMed ID: 7485266
    [Abstract] [Full Text] [Related]

  • 59. Strümpell's familial spastic paraplegia: genetics and neuropathology.
    Behan WM, Maia M.
    J Neurol Neurosurg Psychiatry; 1974 Jan 14; 37(1):8-20. PubMed ID: 4813430
    [Abstract] [Full Text] [Related]

  • 60. Interest of peripheral anesthetic blocks as a diagnosis and prognosis tool in patients with spastic equinus foot: a clinical and electrophysiological study of the effects of block of nerve branches to the triceps surae muscle.
    Buffenoir K, Decq P, Lefaucheur JP.
    Clin Neurophysiol; 2005 Jul 14; 116(7):1596-600. PubMed ID: 15905125
    [Abstract] [Full Text] [Related]

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