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Journal Abstract Search

171 related items for PubMed ID: 7180276

  • 21. [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
    [Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23. 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]

  • 24. [Juvenile autosomal-recessive spastic paraplegia].
    Badalian LO, Iadgarov IS, Arkhipov BA, Temin PA, Bulaeva NV.
    Pediatriia; 1989 Jan; (2):90-2. PubMed ID: 2726376
    [No Abstract] [Full Text] [Related]

  • 25. Two distinct types of autosomal dominant spastic paraplegia.
    Thurmon TF, Walker BA.
    Birth Defects Orig Artic Ser; 1971 Feb; 7(1):216-8. PubMed ID: 5173364
    [No Abstract] [Full Text] [Related]

  • 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
    [No Abstract] [Full Text] [Related]

  • 27. [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 Jan 31; 22(3):235-8. PubMed ID: 303794
    [No Abstract] [Full Text] [Related]

  • 28.
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  • 29. [Two siblings with spastic paraplegia, optic atrophy and peripheral neuropathy].
    Joshita Y, Atsumi T, Miyatake T.
    Rinsho Shinkeigaku; 1982 Oct 31; 22(10):901-8. PubMed ID: 6303658
    [No Abstract] [Full Text] [Related]

  • 30. Cerebellar degeneration in dominantly inherited spastic paraplegia.
    Scholtz CL, Swash M.
    J Neurol Neurosurg Psychiatry; 1985 Feb 31; 48(2):145-9. PubMed ID: 3981172
    [Abstract] [Full Text] [Related]

  • 31. 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]

  • 32. Hereditary "pure" spastic paraplegia: a clinical and genetic study of 22 families.
    Harding AE.
    J Neurol Neurosurg Psychiatry; 1981 Oct 31; 44(10):871-83. PubMed ID: 7310405
    [Abstract] [Full Text] [Related]

  • 33. [Familial spastic diplegia (study of a Mexican family)].
    Gamboa I, Hernández Peniche J.
    Rev Invest Clin; 1973 Oct 31; 25(1):47-50. PubMed ID: 4805167
    [No Abstract] [Full Text] [Related]

  • 34. X-linked hereditary spastic paraplegia.
    Raggio JF, Thurmon TF, Anderson EE.
    J La State Med Soc; 1973 Jan 31; 125(1):4-5. PubMed ID: 4684346
    [No Abstract] [Full Text] [Related]

  • 35. Hereditary spastic paraplegia (a review of two families with eight case reports).
    Rath RN, Das RK, Panda RK, Santhalia RR.
    J Assoc Physicians India; 1978 Jun 31; 26(6):535-40. PubMed ID: 721758
    [No Abstract] [Full Text] [Related]

  • 36. Slowly progressive autosomal dominant spastic paraplegia with late onset, variable expression and reduced penetrance: a basis for diagnosis and counseling.
    Burdick AB, Owens LA, Peterson CR.
    Clin Genet; 1981 Jan 31; 19(1):1-7. PubMed ID: 7460376
    [Abstract] [Full Text] [Related]

  • 37. [Strumpell-Lorrain disease: single nosologic entity?].
    Bettinazzi G, Amato L, Arcara A, Scoppa F.
    Acta Neurol (Napoli); 1986 Jun 31; 8(3):259-62. PubMed ID: 3739774
    [No Abstract] [Full Text] [Related]

  • 38. Linkage studies of X-linked recessive spastic paraplegia using DNA probes.
    Kenwrick S, Ionasescu V, Ionasescu G, Searby C, King A, Dubowitz M, Davies KE.
    Hum Genet; 1986 Jul 31; 73(3):264-6. PubMed ID: 3460961
    [Abstract] [Full Text] [Related]

  • 39. [Familial spastic paraplegia occurring in siblings].
    Ogawa A, Shiohira A.
    Nihon Shonika Gakkai Zasshi; 1965 Oct 31; 69(10):884-8. PubMed ID: 5894648
    [No Abstract] [Full Text] [Related]

  • 40. Jancar syndrome: mental retardation, spasticity, and distal transverse limbs defects.
    Zlotogora J, Glick B.
    Am J Med Genet; 1993 Aug 01; 47(1):89-90. PubMed ID: 8368260
    [Abstract] [Full Text] [Related]

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