Ataxic type of Creutzfeldt-Jakob disease with disproportionate enlargement of the fourth ventricle: a serial CT study.

Author:

Berciano J,Pascual J,Polo J M,Combarros O,Figols J,Diez C

Publisher

BMJ

Subject

Psychiatry and Mental health,Clinical Neurology,Surgery

Reference10 articles.

1. CT findings in spinocerebellar degeneration;Ramos, A.; Quintana, F.; Diez, C.; Leno, C.; Berciano, J.;AJNR Am J Neuroradiol,1987

2. CT appearance of panencephalopathic and ataxic type of Creutzfeldt-Jakob disease;Berciano, J.; Diez, C.; Polo, J.M.; Pascual, J.; Figols, J.;J ComputAssist Tomogr,1991

3. Serial positron emission tomography with fluodeoxyglucose F 18 in Creutzfeldt-Jakob disease;Oganda, T.; Inugami, A.; Fujita, H.;AJNR Am J Neuroradiol,1995

4. Minamata disease (organic mercury poisoning): neuroradiologic and electrophysiologic studies;Tokuomi, H.; Uchino, M.; Imamura, S.; Yamanaga, H.; Nakanishi, R.; Ideta, T.;Neurology,1982

5. Paraneoplastic cerebellar degeneration: a clinical comparison of patients with and without Purkinje cell cytoplasmic antibodies;Mammack, J.E.; Kimmel, D.W.; O'Neill, B.P.; Lennon, V.A.

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