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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

108 related items for PubMed ID: 7217977

  • 21.
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  • 22. [Involvement of the peripheral motor neuron in hereditary spastic paraplegia (author's transl)].
    Malin JP.
    EEG EMG Z Elektroenzephalogr Elektromyogr Verwandte Geb; 1976 Sep; 7(3):140-5. PubMed ID: 829059
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  • 26. [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
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  • 27. A founder mutation p.H701P identified as a major cause of SPG7 in Norway.
    Rydning SL, Wedding IM, Koht J, Chawla M, Øye AM, Sheng Y, Vigeland MD, Selmer KK, Tallaksen CM.
    Eur J Neurol; 2016 Apr 31; 23(4):763-71. PubMed ID: 26756429
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  • 30. [Familial spastic paraplegia. A case report].
    Luo DR, Hu CH.
    Hua Xi Yi Ke Da Xue Xue Bao; 1987 Mar 31; 18(1):93-5. PubMed ID: 3623530
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  • 31. The Troyer syndrome. A recessive form of spastic paraplegia with distal muscle wasting.
    Cross HE, McKusick VA.
    Arch Neurol; 1967 May 31; 16(5):473-85. PubMed ID: 6022528
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  • 35. [Familial spastic paraplegia associated with large stature and chromosomal abnormalities].
    Tanaka M, Uchiyama T, Komatsu M, Morimatsu M, Hirai S.
    Rinsho Shinkeigaku; 1982 Oct 31; 22(10):940-6. PubMed ID: 7182095
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  • 38. [Hereditary spastic paraplegia associated with peroneal muscular atrophy].
    Laso FJ, Cacho J, Díez Jarilla JL, González Macías J.
    Med Clin (Barc); 1982 Apr 16; 78(8):329-31. PubMed ID: 7087602
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