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]