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Logo of procrsmedFormerly medchtJournal of the Royal Society of MedicineProceedings of the Royal Society of Medicine
 
Proc R Soc Med. 1958 July; 51(7): 535–539.
PMCID: PMC1889648

A Form of Subacute Encephalopathy of Uncertain Ætiology

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Selected References

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  • DE AJURIAGUERRA J, HECAEN H, LAYANI F, SADOUN R. Dégénération cortico-strio-spinale; étude anatomo-clinique a propod de la maladie de Creutizfeldt-Jakob. Rev Neurol (Paris) 1953;89(2):81–100. [PubMed]
  • BORNSTEIN S, JERVIS GA. Presenile dementia of the Jakob type; corticostriospinal degeneration. AMA Arch Neurol Psychiatry. 1955 Dec;74(6):598–610. [PubMed]
  • JACOB H, PYRKOSCH W, STRUBE H. Die erbliche Form der Creutzfeldt-Jakobschen Krankheit (Familie Backer). Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr. 1950;184(7):653–674. [PubMed]
  • JONES DP, NEVIN S. Rapidly progressive cerebral degeneration (subacute vascular encephalopathy) with mental disorder, focal disturbances, and myoclonic epilepsy. J Neurol Neurosurg Psychiatry. 1954 May;17(2):148–159. [PMC free article] [PubMed]
  • MEYER A, LEIGH D, BAGG CE. A rare presenile dementia associated with cortical blindness (Heidenhain's syndrome). J Neurol Neurosurg Psychiatry. 1954 May;17(2):129–133. [PMC free article] [PubMed]
  • PALLIS CA, SPILLANE JD. A subacute progressive encephalopathy with mutism, hypokinesia, rigidity, and myoclonus. Q J Med. 1957 Jul;26(103):349–373. [PubMed]

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