Results 111 to 120 of about 13,613 (255)

Sporadic Creutzfeldt-Jakob disease with unusual initial presentation as posterior reversible encephalopathy syndrome: a case report [PDF]

, 2016
Edgaras Diržius, Renata Balnytė, Vesta Steiblienė, Rymantė Gleiznienė, Inga Gudinavičienė, Andrius Radžiūnas, Kęstutis Petrikonis   +6 more
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The differential diagnosis of Huntington's disease-like syndromes: 'red flags' for the clinician [PDF]

, 2013
A growing number of progressive heredodegenerative conditions mimic the presentation of Huntington's disease (HD). Differentiating among these HD-like syndromes is necessary when a patient with a combination of movement disorders, cognitive decline ...
Bhatia, KP, Martino, D, Stamelou, M
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Intra- and interspecies interactions between prion proteins and effects of mutations and polymorphisms [PDF]

, 2003
Recently, crystallization of the prion protein in a dimeric form was reported. Here we show that native soluble homogenous FLAG-tagged prion proteins from hamster, man and cattle expressed in the baculovirus system are predominantly dimeric.
Bradley R., Campbell T.A., Clark W.W., Cutlip R.C., Edenhofer F., Goldfarb L.G., Krasemann S., Leucht C., Lopez L., Majtenyi C., Scott M.R., Weiss S.   +11 more
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Post-anoxic myoclonus

Southwest Respiratory and Critical Care Chronicles, 2014
Myoclonus is a movement disorder characterized by involuntary, sudden, brief muscle jerks caused by muscular contraction (positive myoclonus) or inhibition (negative myoclonus).1,2 Myoclonus is generally a medical sign and not a diagnosis.
Pavis Laengvejkal, Parunyou Julayanont, Drew Payne   +2 more
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Three cases of Creutzfeldt–Jakob disease presenting with a predominant dysexecutive syndrome

, 2022
Nick Corriveau‐Lecavalier, Wentao Li, Vijay K. Ramanan, Daniel A. Drubach, Gregory S. Day, David T. Jones   +5 more
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Sporadic cjd and retinitis punctata albescansa case report and literature review [PDF]

, 2014
Introduction Sporadic Creutzfeldt-Jakob disease (sCJD) is the most common form of CJD causing 85% of all cases. Various phenotypes of sCJD have been identified including Heidenhain variant which has early and predominant visual symptoms with most ...
Hanif Khan, Yusra, Khan, Quratulain
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Imaging and clinical characteristics of sporadic Creutzfeldt-Jakob disease

Chinese Journal of Contemporary Neurology and Neurosurgery, 2013
Five patients with sporadic Creutzfeldt-Jakob disease (sCJD) presented rapidly progressive dementia which were subacute onset from 1 to 4 months. Among these cases, periodic synchronous discharge (PSD) of electroencephalography (EEG) was seen in 2 ...
Yan GAO, Wei ZHANG, Juan FENG, Shun-chang HAN   +3 more
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Reversible Pseudo‐Creutzfeldt‐Jakob Syndrome Related to Cerebral Dural Arteriovenous Fistula [PDF]

, 2014
Kariné Chahbazian, Marie Théaudin, P. Lehmann, Marina Sachet, David Adams, Guillaume Saliou   +5 more
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Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease [PDF]

, 2017
Several molecular subtypes of sporadic Creutzfeldt-Jakob disease have been identified and electroencephalogram and cerebrospinal fluid biomarkers have been reported to support clinical diagnosis but with variable utility according to subtype.
Begue, C., Brandel, J. P., Breithaupt, M., Collie, D., Collins, S. J., Cras, P., Haik, S., Heinemann, U., Hewer, E., Jansen, Gerard H., Kallenberg, K., Ladogana, A., Meissner, B., Pimentel, J., Pocchiari, M., Roberts, H., Romero, C., Sanchez-Juan, P., Schuur, M., Smith, P., Stokin, G. B., Summers, D. M., Taratuto, A., van Duijn, C., Varges, D., Will, R. G., Zerr, I.   +26 more
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Case report: post COVID-19 encephalopathy and oral cenesthopathy

BMC Psychiatry
Post-COVID-19 encephalopathy is a neurological complication characterized by cognitive impairment, memory loss, and other neuropsychiatric symptoms in COVID-19 survivors.
Ju-I Wu, Shwu-Hua Lee, Pei-Jung Chen
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