Literature DB >> 13567726

A form of subacute encephalopathy of uncertain aetiology.

S NEVIN, W H McMENEMEY.   

Abstract

Entities:  

Keywords:  BRAIN/diseases

Mesh：

Year:  1958        PMID： 13567726      PMCID： PMC1889648     

Source DB:  PubMed          Journal:  Proc R Soc Med        ISSN： 0035-9157


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  6 in total

1.  A subacute progressive encephalopathy with mutism, hypokinesia, rigidity, and myoclonus.

Authors:  C A PALLIS; J D SPILLANE
Journal:  Q J Med       Date:  1957-07

2.  Presenile dementia of the Jakob type; corticostriospinal degeneration.

Authors:  S BORNSTEIN; G A JERVIS
Journal:  AMA Arch Neurol Psychiatry       Date:  1955-12

3.  [Cortico-strio-spinal degeneration; anatomoclinical studies of Creutzfeldt-Jakob disease].

Authors:  J DE AJURIAGUERRA; H HECAEN; F LAYANI; R SADOUN
Journal:  Rev Neurol (Paris)       Date:  1953       Impact factor: 2.607

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

Authors:  A MEYER; D LEIGH; C E BAGG
Journal:  J Neurol Neurosurg Psychiatry       Date:  1954-05       Impact factor: 10.154

5.  Rapidly progressive cerebral degeneration (subacute vascular encephalopathy) with mental disorder, focal disturbances, and myoclonic epilepsy.

Authors:  D P JONES; S NEVIN
Journal:  J Neurol Neurosurg Psychiatry       Date:  1954-05       Impact factor: 10.154

6.  [The hereditary form of Creutzfeldt-Jakob disease (the Backer family)].

Authors:  H JACOB; W PYRKOSCH; H STRUBE
Journal:  Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr       Date:  1950
  6 in total
  1 in total

1.  Creutzfeld-Jakob disease: clinical, EEG and neuropathological findings in a cluster of eleven patients.

Authors:  A Lechi; F Tedeschi; D Mancia; V Pietrini; F Tagliavini; M G Terzano; G Trabattoni
Journal:  Ital J Neurol Sci       Date:  1983-04
  1 in total

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