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Literature DB >> 14338125

AN ATAXIC FORM OF SUBACUTE PRESENILE POLIOENCEPHALOPATHY (CREUTZFELDT-JAKOB DISEASE).

B BROWNELL, D R OPPENHEIMER.

Abstract

Entities: Disease

Keywords: ATAXIA; BRAIN DISEASES; CENTRAL NERVOUS SYSTEM DISEASES; CEREBRAL CORTEX; GANGLIA, BASAL; PATHOLOGY; THALAMUS

Mesh：

Year: 1965 PMID： 14338125 PMCID： PMC495916 DOI： 10.1136/jnnp.28.4.350

Source DB: PubMed Journal: J Neurol Neurosurg Psychiatry ISSN： 0022-3050 Impact factor: 10.154

× No keyword cloud information.

7 in total

1. CREUTZFELDT-JAKOB'S DISEASE. CLINICOPATHOLOGIC REPORT OF 15 CASES AND REVIEW OF THE LITERATURE (WITH SPECIAL REFERENCE TO A RELATED DISORDER DESIGNATED AS SUBACUTE SPONGIFORM ENCEPHALOPATHY).

Authors: H SIEDLER; N MALAMUD
Journal: J Neuropathol Exp Neurol Date: 1963-07 Impact factor: 3.685

2. Cerebellar edema. A metabolic and cellstatistical analysis.

Authors: R L FRIEDE
Journal: Arch Neurol Date: 1963-01

3. [Clinical aspects & neuropathology of subacute presenile spongiform atrophy with dyskinetic terminal stage].

Authors: H JACOB; W EICKE; H ORTHNER
Journal: Dtsch Z Nervenheilkd Date: 1958

4. Subacute spongiform encephalopathy--a subacute form of encephalopathy attributable to vascular dysfunction (spongiform cerebral atrophy).

Authors: S NEVIN; W H McMENEMEY; S BEHRMAN; D P JONES
Journal: Brain Date: 1960-12 Impact factor: 13.501

5. A case of Jakob-Creutzfeldt disease. I. Clinicopathological analysis.

Authors: R KATZMAN; E H KAGAN; H M ZIMMERMAN
Journal: J Neuropathol Exp Neurol Date: 1961-01 Impact factor: 3.685

6. A case of Jakob-Creutzfeldt diseases. 2. Analysis of some constituents of the brain of a patient with Jakob-Creutzfeldt disease.

Authors: S R KOREY; R KATZMAN; J ORLOFF
Journal: J Neuropathol Exp Neurol Date: 1961-01 Impact factor: 3.685

7. The electroencephalogram in diffuse encephalopathies; significance of periodic synchronous discharges.

Authors: S LESSE; P F HOEFER; J H AUSTIN
Journal: AMA Arch Neurol Psychiatry Date: 1958-04

7 in total

30 in total

1. Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease.

Authors: Piero Parchi; Maura Cescatti; Silvio Notari; Walter J Schulz-Schaeffer; Sabina Capellari; Armin Giese; Wen-Quan Zou; Hans Kretzschmar; Bernardino Ghetti; Paul Brown
Journal: Brain Date: 2010-09-07 Impact factor: 13.501

8. [The clinical syndrome of presenile idiopathic encephalopathy ("Jakob-Creutzfeldt-syndrome") or spongiform encephalopathy (author's transl)].

Authors: R Meyendorf; C Förster
Journal: Arch Psychiatr Nervenkr (1970) Date: 1973-11-27

9. Subacute spongiform encephalopathy and its relation to Jakob-Creutzfeldt disease: report on six cases.

Authors: Y Goldhammer; J J Bubis; I Sarova-Pinhas; J Braham
Journal: J Neurol Neurosurg Psychiatry Date: 1972-02 Impact factor: 10.154

10. Gerstmann-Sträussler's disease, atypical multiple sclerosis and carcinomas in a family of sheepbreeders.

Authors: J Peiffer
Journal: Acta Neuropathol Date: 1982 Impact factor: 17.088

AN ATAXIC FORM OF SUBACUTE PRESENILE POLIOENCEPHALOPATHY (CREUTZFELDT-JAKOB DISEASE).

1. CREUTZFELDT-JAKOB'S DISEASE. CLINICOPATHOLOGIC REPORT OF 15 CASES AND REVIEW OF THE LITERATURE (WITH SPECIAL REFERENCE TO A RELATED DISORDER DESIGNATED AS SUBACUTE SPONGIFORM ENCEPHALOPATHY).

2. Cerebellar edema. A metabolic and cellstatistical analysis.

3. [Clinical aspects & neuropathology of subacute presenile spongiform atrophy with dyskinetic terminal stage].

4. Subacute spongiform encephalopathy--a subacute form of encephalopathy attributable to vascular dysfunction (spongiform cerebral atrophy).

5. A case of Jakob-Creutzfeldt disease. I. Clinicopathological analysis.

6. A case of Jakob-Creutzfeldt diseases. 2. Analysis of some constituents of the brain of a patient with Jakob-Creutzfeldt disease.

7. The electroencephalogram in diffuse encephalopathies; significance of periodic synchronous discharges.

1. Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease.

2. On some aspects of cerebral degeneration in later life.

3. Parkinsonism-physiology and pharmacology.

4. Further observation of Japanese Creutzfeldt-Jacob disease with widespread amyloid plaques.

5. Sporadic Creutzfeldt-Jakob disease with cerebellar ataxia at onset in the UK.

6. Familial clustering of the ataxic form of Creutzfeldt-Jakob disease with Hirano bodies.

7. Acute ascending polyradiculoneuritis in a case of Creutzfeldt-Jakob disease.

8. [The clinical syndrome of presenile idiopathic encephalopathy ("Jakob-Creutzfeldt-syndrome") or spongiform encephalopathy (author's transl)].

9. Subacute spongiform encephalopathy and its relation to Jakob-Creutzfeldt disease: report on six cases.

10. Gerstmann-Sträussler's disease, atypical multiple sclerosis and carcinomas in a family of sheepbreeders.