Unusual Late-onset Type of Hallervorden-Spatz Disease. Clinico-pathological Study of a Case Presenting As Parkinsonism
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References
1.
Klawans Jr H, Ringel S
. Observations on the efficacy of L-dopa in progressive supranuclear palsy. Eur Neurol. 1971; 5(2):115-29.
DOI: 10.1159/000114065.
View
2.
Jellinger K, TARNOWSKA-DZIDUSZKO E
. [CNS lesions in olivo-ponto-cerebellar atrophies]. Z Neurol. 1971; 199(3):192-214.
View
3.
ROZDILSKY B, Cumings J, HUSTON A
. Hallervorden-Spatz disease. Late infantile and adult types, report of two cases. Acta Neuropathol. 1968; 10(1):1-16.
DOI: 10.1007/BF00690505.
View
4.
Yanagisawa N, Shiraki H, Minakawa M, Narabayashi H
. Clinico-pathological and histochemical studies of Hallervorden-Spatz disease with torsion dystonia with special reference to diagnostic criteria of the disease from the clinico-pathological viewpoint. Prog Brain Res. 1966; 21:373-425.
DOI: 10.1016/s0079-6123(08)64238-7.
View
5.
Neumayer E
. [Parkinson's disease concurring with other diseases of the central nervous system]. Z Neurol. 1971; 199(4):306-18.
View