These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

96 related articles for article (PubMed ID: 1224113)

  • 1. [Heredo-degenerative disease with predominant extra-pyramidal symptoms].
    Pépin B; Haguenau M; Job C
    Rev Neurol (Paris); 1975 Apr; 131(4):294-7. PubMed ID: 1224113
    [No Abstract]   [Full Text] [Related]  

  • 2. [Hereditary degenerative spinocerebellar syndrome with extrapyramidal symptoms].
    Consoloni E; Rossi R; Ioppoli C; Cartei MA; Fonte F
    Riv Neurol; 1980; 50(4):221-30. PubMed ID: 7466218
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [2 families in the Himeji area with spinocerebellar degeneration with primary symptoms of divergence paralysis].
    Itoga E; Kito S; Yamamoto M; Uchida Y
    Rinsho Shinkeigaku; 1975 Apr; 15(4):212-7. PubMed ID: 1170060
    [No Abstract]   [Full Text] [Related]  

  • 4. Spinocerebellar degeneration with divergence paralysis as the earliest sign.
    Itoga E
    Hiroshima J Med Sci; 1980 Dec; 29(4):155-61. PubMed ID: 7204104
    [No Abstract]   [Full Text] [Related]  

  • 5. [Association of multiple basal cell carcinomas of the face and spinocerebellar degeneration. Study of 4 familial cases including an anatomo-clinical description].
    Pasquier B; Couderc P; Tommasi M; Groslambert R; Pasquier D
    Sem Hop; 1975 Dec; 51(49):3009-17. PubMed ID: 174221
    [TBL] [Abstract][Full Text] [Related]  

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

  • 7. [Familial form of cutaneous epitheliomatosis with complex neurological characteristics similar to hereditary spinocerebellar degeneration. Apropos of 4 cases including one case with anatomo-clinical description].
    Chateau R; Tommasi M; Groslambert R; Perret J; Pasquier B
    Rev Neurol (Paris); 1975 Jun; 131(6):387-406. PubMed ID: 1209055
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Nigro-spino-dentatal degeneration with nuclear ophthalmoplegia. A unique and partially treatable clinico-pathological entity.
    Woods BT; Schaumburg HH
    J Neurol Sci; 1972 Oct; 17(2):149-66. PubMed ID: 5053922
    [No Abstract]   [Full Text] [Related]  

  • 9. [A heredo-familial spinocerebellar degeneration with slow eye movements--a study of five cases (author's transl)].
    Kanehisa Y; Suda M; Yagi K; Beppu H; Uono M
    Rinsho Shinkeigaku; 1979 Apr; 19(4):209-16. PubMed ID: 445925
    [No Abstract]   [Full Text] [Related]  

  • 10. Heredo - familial spinocerebellar degeneration with slow eye movements--another variety of olivopontocerebellar degeneration.
    Wadia NH
    Neurol India; 1977 Sep; 25(3):147-60. PubMed ID: 613260
    [No Abstract]   [Full Text] [Related]  

  • 11. Familial spinocerebellar degeneration, hemolytic anemia, and glutathione deficiency.
    Richards F; Cooper MR; Pearce LA; Cowan RJ; Spurr CL
    Arch Intern Med; 1974 Sep; 134(3):534-7. PubMed ID: 4852017
    [No Abstract]   [Full Text] [Related]  

  • 12. [Cerebello-pyramidal syndrome of regressive evolution associated with Gougerot-Sjögren disease].
    Viala JJ; Masson R
    Rev Otoneuroophtalmol; 1970 Mar; 42(2):58-66. PubMed ID: 5454518
    [No Abstract]   [Full Text] [Related]  

  • 13. [Peripheral nerve involvement in spino-cerebellar degenerations. 1. Clinical characteristics].
    Sugimura K; Matsuoka Y; Iida M; Sobue I
    Rinsho Shinkeigaku; 1984 Jun; 24(6):593-8. PubMed ID: 6094071
    [No Abstract]   [Full Text] [Related]  

  • 14. 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]  

  • 15. [Combined spinal and spino-cerebellar sclerosis associated with pituitary dysfunction].
    Mantovani M; Nuzzo G
    Riv Sper Freniatr Med Leg Alien Ment; 1969 Feb; 93(1):152-60. PubMed ID: 5402875
    [No Abstract]   [Full Text] [Related]  

  • 16. [Progressive nuclear ophthalmoplegia and hereditary spinal cerebellar degeneration. Study of 1 anatomo-clinical case].
    Brion S; De Recondo J
    Rev Neurol (Paris); 1967 May; 116(5):383-400. PubMed ID: 6052813
    [No Abstract]   [Full Text] [Related]  

  • 17. [Clinical observations on 2 cases of hereditary areflexic dystasia].
    Fabiani F
    Riv Neurobiol; 1965; 11(2):219-27. PubMed ID: 5837065
    [No Abstract]   [Full Text] [Related]  

  • 18. [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]  

  • 19. [Progressive supranuclear palsy with familial occurrence of spinocerebellar degeneration].
    Yamamura Y; Kito S; Itoga E; Kajiwara H
    Rinsho Shinkeigaku; 1982 Jul; 22(7):586-93. PubMed ID: 7172528
    [No Abstract]   [Full Text] [Related]  

  • 20. [Transmission of a neurologic degeneration in a family for 4 generations manifested under variable semiologic aspects (pure pyramidal, pure cerebello-pyramidal involvement or involvement with abolition of reflexes and severe sensory disorders].
    Mettey R; Hoppeler A; Gil R
    J Genet Hum; 1981 Sep; 29(3):227-34. PubMed ID: 7334346
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.