Creutzfeldt-Jakob disease in Oman: report of two cases

Author:

Scrimgeour Euan M,Chand Pratap R,Kenny Kimbra,Brown Paul

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference5 articles.

1. Creutzfeldt-Jakob disease; the dilemma of the uncertain diagnosis;Al-Tahan;Saudi Med J,1991

2. Brown P. (1994) Transmissible human spongiform encephalopathy (infectious cerebral amyloidosis): Creutzfeldt-Jakob disease, Gerstmann-Straussler-Scheinker syndrome, and kuru. In: Calne DB (ed), Neurodegenerative diseases. W.B. Saunders, Philadelphia, pp. 839–876.

3. Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease;Brown;Ann Neurol,1994

4. Abnormal proteins in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease;Harrington;N Engl J Med,1986

5. Cerebrospinal fluid concentration of neuron-specific enolase in diagnosis of Creutzfeldt-Jakob disease;Zerr;Lancet,1995

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2. A systemic analysis of Creutzfeldt Jakob disease cases in Asia;Prion;2024-02-07

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4. Some recollections about kuru in a patient at Rabaul in 1978, and subsequent experiences with prion diseases;Philosophical Transactions of the Royal Society B: Biological Sciences;2008-11-27

5. Infectious and tropical diseases in Oman: a review.;The American Journal of Tropical Medicine and Hygiene;1999-12-01

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