BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

194 related articles for article (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
    [No Abstract]   [Full Text] [Related]  

  • 3. [Epilepsy and hereditary spino-cerebellar degeneration].
    Gayral L; Gayral J
    J Genet Hum; 1969 May; 17(1):127-36. PubMed ID: 4980118
    [No Abstract]   [Full Text] [Related]  

  • 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; 104(4):159-70. PubMed ID: 6681331
    [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. Electroretinographic changes in a case of spino-cerebellar degeneration (SCD).
    Stanescu B; Evrard P; Michiels J; Lyon G
    Metab Pediatr Ophthalmol; 1980; 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; 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; 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; 47(1):58-82. PubMed ID: 323954
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Cumulative familial incidence of Kugelberg-Welander disease].
    Nemes A; Károly E; Csenkér E; Pintér S
    Orv Hetil; 1986 Nov; 127(45):2735-9. PubMed ID: 3796971
    [No Abstract]   [Full Text] [Related]  

  • 12. Late-onset X-linked recessive spinal and bulbar muscular atrophy.
    Ringel SP; Lava NS; Treihaft MM; Lubs ML; Lubs HA
    Muscle Nerve; 1978; 1(4):297-307. PubMed ID: 571530
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Spinal muscular atrophy.
    McLeod JG; Williams IM
    Minn Med; 1971 Jun; 54(6):457-61. PubMed ID: 5559368
    [No Abstract]   [Full Text] [Related]  

  • 14. Amyotrophy in multisystem genetic diseases.
    Rosenberg RN
    Adv Neurol; 1982; 36():149-58. PubMed ID: 6217729
    [No Abstract]   [Full Text] [Related]  

  • 15. [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]  

  • 16. 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]  

  • 17. A family with Kugelberg-Welander sydrome. Hereditary proximal spinal muscul atrophy--some additional features.
    Almog C; Tal E
    Confin Neurol; 1968; 30(5):313-24. PubMed ID: 5729137
    [No Abstract]   [Full Text] [Related]  

  • 18. [A case of Wohlfart-Kugelberg-Welander disease or hereditary familial spinal juvenile muscular atrophy].
    Manara F; Gasco P; Milani L
    Minerva Med; 1977 Feb; 68(6):417-24. PubMed ID: 840437
    [No Abstract]   [Full Text] [Related]  

  • 19. [Familial occurrence of Kugelberg-Welander pseudomyopathic spinal muscular atrophy].
    Zeiler K; Mamoli B; Heiss WD
    Nervenarzt; 1976 Jul; 47(7):444-8. PubMed ID: 958547
    [No Abstract]   [Full Text] [Related]  

  • 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; 115(4):283-94. PubMed ID: 4778568
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.