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Journal Abstract Search

121 related items for PubMed ID: 3981172

  • 1. Cerebellar degeneration in dominantly inherited spastic paraplegia.
    Scholtz CL, Swash M.
    J Neurol Neurosurg Psychiatry; 1985 Feb; 48(2):145-9. PubMed ID: 3981172
    [Abstract] [Full Text] [Related]

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

  • 3. Strumpell's pure familial spastic paraplegia: case study and review of the literature.
    Holmes GL, Shaywitz BA.
    J Neurol Neurosurg Psychiatry; 1977 Oct; 40(10):1003-8. PubMed ID: 591968
    [Abstract] [Full Text] [Related]

  • 4. A study of posterior column function in familial spastic paraplegia.
    Dimitrijevic MR, Lenman JA, Prevec T, Wheatly K.
    J Neurol Neurosurg Psychiatry; 1982 Jan; 45(1):46-9. PubMed ID: 7062069
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 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 branchial myoclonus with spastic paraparesis and cerebellar ataxia: a new autosomal dominant disorder.
    de Yebenes JG, Vazquez A, Rabano J, de Seijas EV, Urra DG, Obregon MC, Barquero MS, Arribas MA, Moreno JL, Alenda JR.
    Neurology; 1988 Apr 31; 38(4):569-72. PubMed ID: 3352913
    [Abstract] [Full Text] [Related]

  • 8. Recessively inherited spastic paraplegia associated with ataxia, congenital cataracts, thin corpus callosum and axonal neuropathy.
    Yamashita I, Sasaki H, Yabe I, Kikuchi S, Chin S, Fukazawa T, Okumura H, Tashiro K.
    Acta Neurol Scand; 2000 Jul 31; 102(1):65-9. PubMed ID: 10893066
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. Strümpell's familial spastic paraplegia: an electrophysiological demonstration of selective central distal axonopathy.
    Uncini A, Treviso M, Basciani M, Gambi D.
    Electroencephalogr Clin Neurophysiol; 1987 Feb 31; 66(2):132-6. PubMed ID: 2431877
    [Abstract] [Full Text] [Related]

  • 11. Hereditary cerebellar atrophy (Holmes type) with optic atrophy: a clinico-pathological study of four generations in a family.
    Budka H, Seemann D, Danielczyk W.
    Arch Psychiatr Nervenkr (1970); 1979 Apr 12; 226(4):311-8. PubMed ID: 454144
    [Abstract] [Full Text] [Related]

  • 12. A novel GBA2 gene missense mutation in spastic ataxia.
    Votsi C, Zamba-Papanicolaou E, Middleton LT, Pantzaris M, Christodoulou K.
    Ann Hum Genet; 2014 Jan 12; 78(1):13-22. PubMed ID: 24252062
    [Abstract] [Full Text] [Related]

  • 13. Joseph's disease: clinical and pathological studies in a Japanese family.
    Yuasa T, Ohama E, Harayama H, Yamada M, Kawase Y, Wakabayashi M, Atsumi T, Miyatake T.
    Ann Neurol; 1986 Feb 12; 19(2):152-7. PubMed ID: 3963757
    [Abstract] [Full Text] [Related]

  • 14. [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 Feb 12; 135(4):329-37. PubMed ID: 504864
    [Abstract] [Full Text] [Related]

  • 15. A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34.
    Thiffault I, Rioux MF, Tetreault M, Jarry J, Loiselle L, Poirier J, Gros-Louis F, Mathieu J, Vanasse M, Rouleau GA, Bouchard JP, Lesage J, Brais B.
    Brain; 2006 Sep 12; 129(Pt 9):2332-40. PubMed ID: 16672289
    [Abstract] [Full Text] [Related]

  • 16. [Strumpell's disease in childhood].
    Popov'ian MD, Dubinskaia EE, Allaverdova RA.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1982 Sep 12; 82(10):29-32. PubMed ID: 7180276
    [No Abstract] [Full Text] [Related]

  • 17. Dominantly inherited early-onset non-progressive cerebellar ataxia syndrome.
    Imamura S, Tachi N, Oya K.
    Brain Dev; 1993 Sep 12; 15(5):372-6. PubMed ID: 8279653
    [Abstract] [Full Text] [Related]

  • 18. Increased Diagnostic Yield of Spastic Paraplegia with or Without Cerebellar Ataxia Through Whole-Genome Sequencing.
    Kim A, Kumar KR, Davis RL, Mallawaarachchi AC, Gayevskiy V, Minoche AE, Walls Z, Kim HJ, Jang M, Cowley MJ, Choi JH, Shin C, Sue CM, Jeon B.
    Cerebellum; 2019 Aug 12; 18(4):781-790. PubMed ID: 31104286
    [Abstract] [Full Text] [Related]

  • 19. Hereditary ataxias. Occurrence and clinical features.
    Werdelin L.
    Acta Neurol Scand Suppl; 1986 Aug 12; 106():1-124. PubMed ID: 3460301
    [No Abstract] [Full Text] [Related]

  • 20. Autosomal recessive spino-olivo-cerebellar degeneration without ataxia.
    Staal A, Stefanko SZ, Jennekens FG, Vries-Bos LH, van Gijn J.
    J Neurol Neurosurg Psychiatry; 1983 Jul 12; 46(7):648-52. PubMed ID: 6886703
    [Abstract] [Full Text] [Related]

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