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2.
HolmesG. M., Familial and Hereditary Ataxia, In Albutt and Rolleston's System of Medicine, 7: 770, 1910.
3.
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4.
RoussyG., and LevyG., Sept cas d'une maladie familiale particuliere. Rev. Neurol., (i), 427, 1926. A propos de la dystasie areflexique hereditaire, Ibid (ii), 763, 1934.
5.
FraserD., Defect of the cerebellum occurring in a brother and a sister, Glasgow Med. J., 13: 199, 1880.
6.
NonneM., Ueber eine eigentumliche familiare Erkrankungsform des Centralnervensystems, Arch. Psychiat. u. Nervenkr., 22: 283, 1891.
7.
BrownSanger, On hereditary ataxy with a series of 21 cases, Brain, 15: 250, 1892.
8.
MariePierre, Sur l'heredo-ataxie cerebelleuse, La semaine med., 13: 444, 1893.
9.
MenzelP., Beitrage zur Kenntnis der herditaren Ataxie und Kleinhirnatrophic, Arch. Psychiat. u Nervenkr., 22: 160, 1891.
10.
AkelaitisA. J., Hereditary form of primary parenchymatous atrophy of cerebellar cortex associated with mental deterioration, Amer. J. Psychiat., 94: 1115, 1938.
11.
BellJ. M., and CarmichaelE. A., On hereditary ataxia and spastic paraplegia, Ibid., Vol. IV, Part 3, 1939.
12.
HuntJ. R., Dyssynergia cerebellaris myoclonica, Ibid., 44: 490, 1939.
13.
LiversedgeL. A., and EmeryV., Electroencepholographic changes in cerebellar degenerative lesions, J. Neurol. Neurosurg. and Psychiat., 24: 326, 1961.
