127 related articles for article (PubMed ID: 6005612)
1. An atypical hereditary spinocerebellar syndrome. A clinical and genetic study.
Giannelli A; Serra A; Bacciagaluppi M
Acta Neurol Scand; 1966; 41(4):387-412. PubMed ID: 6005612
[No Abstract] [Full Text] [Related]
2. Spino-pontine degeneration.
Boller F; Segarra JM
Eur Neurol; 1969; 2(6):356-73. PubMed ID: 5808476
[No Abstract] [Full Text] [Related]
3. [Familial atrophic form of spinocerebellar ataxia].
Gaj T; Grendus-Tota B
Neurol Neurochir Pol; 1973; 7(5):679-83. PubMed ID: 4763007
[No Abstract] [Full Text] [Related]
4. [Epidemiology and clinical polymorphism of hereditary ataxia].
Shutov AA; Dedik GK
Zh Nevropatol Psikhiatr Im S S Korsakova; 1978; 78(6):825-30. PubMed ID: 676607
[TBL] [Abstract][Full Text] [Related]
5. A new form of heredo-familial spinocerebellar degeneration with slow eye movements (nine families).
Wadia NH; Swami RK
Brain; 1971; 94(2):359-74. PubMed ID: 5571047
[No Abstract] [Full Text] [Related]
6. [Hereditary degenerative spinocerebellar diseases in Tunisia with manometric studies in bladder disorders (author's transl)].
Ben Hamida M; Madani S; Zmerli S; Chami I; Annabi A; Jamoussi M; Marzouki M; Rachdi M; Samoud S; Talbi M
Rev Neurol (Paris); 1980; 136(8-9):495-508. PubMed ID: 7221327
[TBL] [Abstract][Full Text] [Related]
7. [Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias].
Ben Hamida M; Attia-Romdhane N; Triki CH; Oueslati S; Hentati F
Rev Neurol (Paris); 1991; 147(12):798-808. PubMed ID: 1780608
[TBL] [Abstract][Full Text] [Related]
8. Comparative study of visual evoked potentials in spinocerebellar ataxias and multiple sclerosis.
Ghezzi A; Montanini R
Acta Neurol Scand; 1985 Mar; 71(3):252-6. PubMed ID: 3993330
[TBL] [Abstract][Full Text] [Related]
9. Computerized tomography of the head in the diagnosis of some forms of hereditary-familial ataxia.
Vereshchagin NV; Gurskaya NZ; Vavilov SB
Neurosci Behav Physiol; 1985; 15(1):22-7. PubMed ID: 4000467
[No Abstract] [Full Text] [Related]
10. Acute intermittent familial cerebellar ataxia.
Hill W; Sherman H
Arch Neurol; 1968 Apr; 18(4):350-7. PubMed ID: 5638538
[No Abstract] [Full Text] [Related]
11. Classification of the hereditary ataxias and paraplegias.
Harding AE
Lancet; 1983 May; 1(8334):1151-5. PubMed ID: 6133167
[No Abstract] [Full Text] [Related]
12. [Recessive hereditary ataxia with early onset. Clinical study of 27 cases].
Serlenga L; Trizio M; Pozio G; Oteri G; Caldarazzo M
Riv Neurol; 1987; 57(5):285-9. PubMed ID: 3445070
[TBL] [Abstract][Full Text] [Related]
13. The hereditary ataxias.
Wadia RS; Amin R
Neurol India; 1976 Mar; 24(1):24-40. PubMed ID: 1272503
[No Abstract] [Full Text] [Related]
14. Autosomal recessive cerebellar ataxias.
Palau F; Espinós C
Orphanet J Rare Dis; 2006 Nov; 1():47. PubMed ID: 17112370
[TBL] [Abstract][Full Text] [Related]
15. [Hereditary ataxia-problems in the classification, genetics and genetic counseling].
Bachmann H; Lössner J
Z Gesamte Inn Med; 1981 Jun; 36(11):387-93. PubMed ID: 7303765
[TBL] [Abstract][Full Text] [Related]
16. Prevalence and pattern of spinocerebellar degenerations in northeastern Libya.
Sridharan R; Radhakrishnan K; Ashok PP; Mousa ME
Brain; 1985 Dec; 108 ( Pt 4)():831-43. PubMed ID: 4075075
[TBL] [Abstract][Full Text] [Related]
17. Necrotizing encephalomyelopathy. Report of a case with relapsing polyneuropathy and hyperalaninemia and with manifestations resembling Friedreich's ataxia.
Dunn HG; Dolman CL
Neurology; 1969 Jun; 19(6):536-50. PubMed ID: 4306160
[No Abstract] [Full Text] [Related]
18. Genetic approaches to the nosology of nervous system defects.
Becker PE
Birth Defects Orig Artic Ser; 1971 Feb; 7(1):10-22. PubMed ID: 5173354
[TBL] [Abstract][Full Text] [Related]
19. [T inversion in Friedreich's ataxia].
Ruser HR; Ruser I
Z Kardiol; 1976 Sep; 65(9):795-9. PubMed ID: 969828
[TBL] [Abstract][Full Text] [Related]
20. [Spinocerebellar degeneration, optic atrophy, epilepsy, myoclonus and mitochondrial myopathy: a case report (author's transl)].
Roger J; Pellissier JF; Dravet C; Bureau-Paillas M; Arnoux M; Larrieu JL
Rev Neurol (Paris); 1982; 138(3):187-200. PubMed ID: 6810437
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
