Results 111 to 120 of about 5,425,074 (170)

A Case of sporadic Creutzfeldt-Jakob disease [PDF]

Revista da Sociedade Brasileira de Medicina Tropical, 2023
Fatma Şimşek, Recep Yevgi
doaj   +1 more source

Creutzfeldt-Jakob disease presenting as hyperparathyroidism and generalized tonic status epilepticus

, 2007
Creutzfeldt-Jakob disease is the most common disorder among the very rare human transmissible subacute spongiform encephalopathies. Sporadic, familial or iatrogenic forms of the disease can be seen. The common presentations of the disease include rapidly
KARATAS, HÜLYA, DERİCİOĞLU, NEŞE, SAYGI, SERAP, KURSUN, Oguzhan   +3 more
core   +1 more source

Sporadic Creutzfeldt–Jakob disease

, 2018
Sporadic Creutzfeldt-Jakob disease (CJD), the most common human prion disease, is generally regarded as a spontaneous neurodegenerative illness, arising either from a spontaneous PRNP somatic mutation or a stochastic PrP structural change. Alternatively,
Zerr, Inga, Inga Zerr, Piero Parchi, Parchi, Piero   +3 more
core   +1 more source

Chorea in Sporadic Creutzfeldt-Jakob Disease [PDF]

Journal of Movement Disorders, 2018
Ai Huey Tan, Tsun Haw Toh, Soon Chai Low, Si Lei Fong, Kah Kian Chong, Kee Wei Lee, Khean Jin Goh, Shen-Yang Lim   +7 more
doaj   +1 more source

Diffusion MR imaging in sporadic Creutzfeldt-Jakob disease

Çukurova Üniversitesi Tıp Fakültesi Dergisi, 2014
Creutzfeldt-Jakob disease (CJD) is a rare dementing disease and is thought to caused by a prion. It is characterized by rapidly progressive dementia, ataxia, myoclonus, akinetic mutism and eventual death.
Burcak Cakir Pekoz, Ozlem Alkan, Semih Giray, senay Demir, Naime Altinkaya   +4 more
doaj  

When Psychosis Masks Neurodegeneration: A Case of Sporadic Creutzfeldt-Jakob Disease. [PDF]

Cureus
Jayakumar G, Rahman E, Bakth RM, Moalin A, Yousif M.   +4 more
europepmc   +1 more source

A case report of sporadic Creutzfeldt-Jakob disease presenting with progressive opsoclonus-myoclonus-ataxia-Plus (OMAS-Plus) phenotype. [PDF]

Prion
Hulej R, Skáčik P, Žáková D, Koprušáková-Turčanová M, Grofik M, Kurča E.   +5 more
europepmc   +1 more source

Ten-year mortality from Creutzfeldt-Jakob disease in Cyprus

, 2008
715-719We report the mortality from sporadic Creutzfeldt-Jakob disease in Cyprus for a 10-year surveillance period [1995-2004]. In that time, 5 cases were identified out of a population of 749 000, giving an incidence of 0.7 cases per million population ...
Papacostas, S., Petsa, M., Kyriakides, T., Malikides, A.   +3 more
core  

From a Pinched Nerve to a Fatal Prognosis: Sporadic Creutzfeldt-Jakob Disease Masquerading as Cervical Myelopathy. [PDF]

Cureus
Bayati J.
europepmc   +1 more source

Probable Sporadic Creutzfeldt-Jakob Disease Presenting as Rapidly Progressive Dementia: A Case Report From Georgia. [PDF]

Cureus
Kvachadze N, Kotia G, Muradashvili M, Mrelashvili S, Basilaia N, Zambakhidze L.   +5 more
europepmc   +1 more source