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Sporadic Creutzfeldt Jakob disease: Case series in Peru. [PDF]

Colomb Med (Cali)
Espinoza S, Canales D, Calderón C, Diaz D, Barreto-Acevedo E.   +4 more
europepmc   +1 more source

Sporadic Creutzfeldt-Jakob disease: Brain MRI lesion features from 2 cases reports. [PDF]

Radiol Case Rep
Au HD, Lan NT, Binh NT, Linh LT, Hien MM, Duc NM.   +5 more
europepmc   +1 more source

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Sporadic Creutzfeldt-Jakob disease

The American Journal of Emergency Medicine, 2022
Being considered among the most fatal neurological conditions, Creutzfeldt-Jakob disease is a transmissible spongiform encephalopathy characterized by its unknown etiology and rapidly progressive neurodegenerative symptoms that often lead to a mean survival of 6 to 12 months.
Parnia, Salehi, Mark, Clark, Jeffer, Pinzon, Abhijit, Patil   +3 more
openaire   +2 more sources

Sporadic Creutzfeldt Jakob disease

Neurology India, 2016
A. Pauranik
openaire   +3 more sources

Sporadic Creutzfeldt–Jakob Disease—A Review

International Journal of Neuroscience, 2009
The objective is to study a patient with sporadic Creutzfeldt-Jakob disease (CJD). The patient, a 70-year-old woman with a history spanning over 1 month, with acute onset, progressive abnormal behavior, and cognitive decline with generalized asymmetrical myoclonic jerking, startle phenomenon, and cortical blindness, was referred to the hospital.
Stuti, Sharma, Madhurima, Mukherjee, Vivekananda, Kedage, Manjunatha S, Muttigi, Anjali, Rao, Suryanarayana, Rao   +5 more
openaire   +2 more sources

MRI of sporadic Creutzfeldt–Jakob disease

Journal of Medical Imaging and Radiation Oncology, 2008
SummaryThe key MRI findings in five cases of sporadic Creutzfeldt–Jakob disease (CJD) are illustrated with four ‘definite’ and one ‘probable’ according to World Health Organization criteria. Close attention to fluid‐attenuation inversion recovery and diffusion‐weighted imaging sequences are important for diagnosis, noting especially restricted ...
A, Kong, T, Kleinig, A, Van der Vliet, P, Bergin, C, Coscia, S, Ring, R, Brooder   +6 more
openaire   +2 more sources

MM2-type sporadic Creutzfeldt-Jakob disease: new diagnostic criteria for MM2-cortical type

Journal of Neurology Neurosurgery & Psychiatry, 2020
Objective To clinically diagnose MM2-cortical (MM2C) and MM2-thalamic (MM2T)-type sporadic Creutzfeldt-Jakob disease (sCJD) at early stage with high sensitivity and specificity.
T. Hamaguchi, N. Sanjo, Ryusuke Ae, Yosikazu Nakamura, K. Sakai, M. Takao, S. Murayama, Y. Iwasaki, K. Satoh, H. Murai, M. Harada, T. Tsukamoto, H. Mizusawa, M. Yamada   +13 more
semanticscholar   +1 more source

Sporadic Creutzfeldt Jakob disease in two adolescents

Journal of Neurology, Neurosurgery & Psychiatry, 2008
Sporadic Creutzfeldt-Jakob disease (CJD) is a condition predominantly affecting older age groups, with cases aged less than 45 years rare and an age at onset or death of less than 20 years exceptional.Data from the systematic study of sporadic CJD in the UK are available from 1970 onwards.
K, Murray, D L, Ritchie, M, Bruce, C A, Young, M, Doran, J W, Ironside, R G, Will   +6 more
openaire   +2 more sources