Olivopontocerebellar atrophy with slow eye movements and peripheral neuropathy - Wadia type

Journal of Association of Physicians of India

Volumn 45, Issue 10, 1997, Pages 812-813

  Biswas, A ^b   Porwal, S ^b   Singh, S ^b   Prasad, A ^b   Anand, K S ^a  

^a INSTITUTE OF HUMAN BEHAVIOUR AND ALLIED SCIENCES   (India)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0008646447     PISSN: 00045772     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (5)

1. Kini PM, Venugopal NS. Hereditary cerebellar ataxia. Report of a family. J Assoc Phys India 1967; 15 : 369-71.
2. Wadia NH. Autosomal dominant cerebellar ataxia with slow saccades and peripheral neuropathy - a variety of olivopontocerebellar degeneration (Wadia type) In : Vinken PJ, Bruyn GW, Dejong JMBV, eds. Handbook of clinical Neurology, rev ser. Amsterdam: Elsevier. 1991; 16 (60) : 1-14.
3. Durr A, Smadja D, Cancel G, et al. Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies): clinical and neuropathological analysis of 53 patients from three unrelated SCA 2 families. Brain 1995; 118 : 1573-81.
4. Wadia NH. Hereditary cerebellar ataxia with slow eye movements (Indian Variety). Genetic linkage study (abstract). Abstracts of the international workshop on molecular genetics of Friedreich's and dominant ataxias. World Federation of Neurology. Research group on hereditary ataxia, 1993 June 20-22; Capri, Naples, Italy: Jean Gilder Congressi SNR. 1993; 59 : 59.
5. Gispert S, Twells R, Orozco G, et al. Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA 2) to chromosome 12 q 23-24.1. Nat Genet 1993; 4 : 295-9.