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Journal Abstract Search
142 related items for PubMed ID: 220681
41. [Ultrastructural study of amyloid neuropathy with special reference to changes of the peripheral nerves in asymptomatic siblings]. Takahashi K, Nakamura H, Ishitobi K, Harada Y. Rinsho Shinkeigaku; 1974 Mar; 14(3):266-74. PubMed ID: 4371501 [No Abstract] [Full Text] [Related]
42. Disordered pigmentation, spastic paraparesis and peripheral neuropathy in three siblings: a new neurocutaneous syndrome. Abdallat A, Davis SM, Farrage J, McDonald WI. J Neurol Neurosurg Psychiatry; 1980 Nov; 43(11):962-6. PubMed ID: 7441281 [Abstract] [Full Text] [Related]
43. [Familial recurring polytopic neuropathy. A case report]. Eckert P, Meyer-Wahl L. Nervenarzt; 1982 Oct; 53(10):598-602. PubMed ID: 6292756 [No Abstract] [Full Text] [Related]
44. [Strumpell's disease in childhood]. Popov'ian MD, Dubinskaia EE, Allaverdova RA. Zh Nevropatol Psikhiatr Im S S Korsakova; 1982 Oct; 82(10):29-32. PubMed ID: 7180276 [No Abstract] [Full Text] [Related]
45. Hereditary spastic paraplegia. Choi IS, Cho HK, Kim KW. Yonsei Med J; 1983 Oct; 24(1):83-6. PubMed ID: 6659558 [No Abstract] [Full Text] [Related]
46. [Familial spastic paraplegia. A case report]. Luo DR, Hu CH. Hua Xi Yi Ke Da Xue Xue Bao; 1987 Mar; 18(1):93-5. PubMed ID: 3623530 [No Abstract] [Full Text] [Related]
47. [Familial spastic paraplegia occurring in siblings]. Ogawa A, Shiohira A. Nihon Shonika Gakkai Zasshi; 1965 Oct; 69(10):884-8. PubMed ID: 5894648 [No Abstract] [Full Text] [Related]
48. Recessively inherited 'pure' spastic paraplegia: case study. de Coo IF, Gabreëls FJ, Renier WO, Colon EJ, ter Haar BG. Clin Neurol Neurosurg; 1982 Oct; 84(4):247-53. PubMed ID: 6301736 [Abstract] [Full Text] [Related]
49. [Familial spastic paraplegia. Genetic-scientific discussion apropos of an affected family]. Gonçalves A. Arq Neuropsiquiatr; 1980 Jun; 38(2):144-9. PubMed ID: 7436797 [Abstract] [Full Text] [Related]
50. Adrenomyeloneuropathy: report of a family and electron microscopical findings in peripheral nerve. Tanaka K, Koyama A, Koike R, Ohno T, Atsumi T, Miyatake T. J Neurol; 1985 Jun; 232(2):73-8. PubMed ID: 4020396 [Abstract] [Full Text] [Related]
51. 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]
53. [HLA antigens in certain hereditary diseases of the central nervous system]. Fedrunova VS, Nazarova EK, Pevnitskiĭ LA, Ivanova-Smolenskaia IA, Alieva LM. Zh Nevropatol Psikhiatr Im S S Korsakova; 1979 Dec; 79(11):1500-3. PubMed ID: 160174 [No Abstract] [Full Text] [Related]
57. The R495W mutation in SPG3A causes spastic paraplegia associated with axonal neuropathy. Scarano V, Mancini P, Criscuolo C, De Michele G, Rinaldi C, Tucci T, Tessa A, Santorelli FM, Perretti A, Santoro L, Filla A. J Neurol; 2005 Aug; 252(8):901-3. PubMed ID: 15742100 [Abstract] [Full Text] [Related]
58. 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; 66(2):132-6. PubMed ID: 2431877 [Abstract] [Full Text] [Related]