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PUBMED FOR HANDHELDS

Journal Abstract Search


190 related items for PubMed ID: 4681150

  • 1. [Study on the relationship of spino-cerebellar hereditary degeneration and progressive muscular atrophy].
    Ramelli E, Mapelli G.
    Riv Neurobiol; 1972; 18(2):101-34. PubMed ID: 4681150
    [No Abstract] [Full Text] [Related]

  • 2. [Genetic aspects of some spino-cerebellar degenerations].
    Badiu G.
    Stud Cercet Neurol; 1969; 14(5):311-24. PubMed ID: 4906012
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  • 4. Hereditary spino-cerebellar degeneration and Ramsay-Hunt disease.
    Penneau D, Bigorgne JC, Fressinaud-Masdefeix L.
    Cah Med; 1974 Feb; 15(2):93-6. PubMed ID: 4848865
    [No Abstract] [Full Text] [Related]

  • 5. [Family with progressive myelopathic muscular atrophy with proximal distribution and onset in adulthood].
    Mapelli G.
    Riv Patol Nerv Ment; 1983 Feb; 104(4):159-70. PubMed ID: 6681331
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  • 6. [2 autopsy cases of the spinocerebellar degeneration with cerebral atrophy].
    Kato Y, Takayama K, Tsujiyama Y, Kaga T, Satowa H.
    No To Shinkei; 1970 Oct; 22(10):1201-8. PubMed ID: 5536190
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  • 7. Electroretinographic changes in a case of spino-cerebellar degeneration (SCD).
    Stanescu B, Evrard P, Michiels J, Lyon G.
    Metab Pediatr Ophthalmol; 1980 Oct; 4(4):221-3. PubMed ID: 7206914
    [No Abstract] [Full Text] [Related]

  • 8. [Pseudomyopathic progressive spinal amyotrophy of adults].
    Cazzato G.
    Acta Neurol (Napoli); 1969 Oct; 24(3):341-70. PubMed ID: 5401556
    [No Abstract] [Full Text] [Related]

  • 9. [Sporadic proximal spinal amyotrophy (Kugelberg-Welander) with a late onset. Its place in the framework degenerations].
    de Barsy T, Hariga J, Claes C.
    Encephale; 1966 Oct; 55(6):541-57. PubMed ID: 5982328
    [No Abstract] [Full Text] [Related]

  • 10. [Progressive spinal amyotrophy. Nosographic problems].
    Lanzi G, Besana D, Rosano Burgio F, Lorini R.
    Riv Neurol; 1977 Oct; 47(1):58-82. PubMed ID: 323954
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  • 17. A family with Kugelberg-Welander sydrome. Hereditary proximal spinal muscul atrophy--some additional features.
    Almog C, Tal E.
    Confin Neurol; 1968 Oct; 30(5):313-24. PubMed ID: 5729137
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  • 20. [XO-XY-sex-chromosomes-mosaicism in a child with progressive spinal muscular atrophy (author's transl)].
    Kunze J, Tolksdorf M.
    Z Kinderheilkd; 1973 Nov 19; 115(4):283-94. PubMed ID: 4778568
    [No Abstract] [Full Text] [Related]


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