[Type Heidenhain of the subacute spongious encephalopathy (SSE) Creutzfeldt-Jakob (author's transl)].

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作者信息

Hopf H C, Althaus H H, Sabuncu S

出版信息

Z Neurol. 1974 Feb 27;206(2):149-56.

PMID:4133864

Abstract

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本文引用的文献

CLINICAL OBSERVATIONS ON SEVEN PATHOLOGICALLY PROVED CASES OF CREUTZFELDT-JAKOB DISEASE.

Trans Am Neurol Assoc. 1963;88:30-2.

The clinical picture in Creutzfeldt-Jakob disease.

Trans Am Neurol Assoc. 1960;85:147-50.

[Subacute degenerative presenile polioencephalopathy with akinetic stupor and decorticate rigidity with myoclonus ("myoclonic" variety of the Jakob-Creutzfeld disease)].

Riv Sper Freniatr Med Leg Alien Ment. 1959 Dec 31;83(4)Suppl:1485-623.

A rare presenile dementia associated with cortical blindness (Heidenhain's syndrome).

J Neurol Neurosurg Psychiatry. 1954 May;17(2):129-33. doi: 10.1136/jnnp.17.2.129.

[The subacute encephalopathy Creutzfeldt-Jakob, an abiotrophic degeneration during the presenium].

Dtsch Z Nervenheilkd. 1968 Jun 5;193(4):351-69.

[Subacute spongiform encephalopathy (Jakob-Cretzfeldt syndrome). Clinico-pathological evaluation of 9 cases].

Arch Psychiatr Nervenkr (1970). 1971;214(3):207-27. doi: 10.1007/BF00342625.

[Subacute presenile spongiforme encephalopathy with occipital predilection and cortical blindness (Heidenhain-syndrome)].

Arch Psychiatr Nervenkr (1970). 1970;213(4):345-69. doi: 10.1007/BF00341552.

The clinical characteristics of transmissible Creutzfeldt-Jakob disease.

Brain. 1973;96(1):1-20. doi: 10.1093/brain/96.1.1.

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