Results 81 to 90 of about 21,599 (190)
Creutzfeldt‐Jakob‐Like Presentation in Anti‐AMPAR Encephalitis
Annals of Neurology, Volume 99, Issue 6, Page 1466-1467, June 2026.
Kate Durbano +3 more
wiley +1 more source
Sporadic Creutzfeldt-Jakob disease prion infection of human cerebral organoids
Acta Neuropathologica Communications, 2019 For the transmissible, neurogenerative family of prion diseases, few human models of infection exist and none represent structured neuronal tissue. Human cerebral organoids are self-organizing, three-dimensional brain tissues that can be grown from ...
Bradley R. Groveman +6 more
doaj +1 more source
[Alien hand syndrome in Creutzfeldt-Jakob disease].
Neurologia (Barcelona, Spain), 2001 Alien hand syndrome is defined by uncontrolable actions of the arm and hand that seem to have a purpose. It is usually associated with acute focal lesions after a stroke or surgery of the corpus callosum. It has been described in chronic dementiating diseases such as cortico-basal degeneration, Alzheimer's disease, orthochromatic leukodystrophy and ...
E, Colomer Rubio +6 more
openaire +1 more source
Neurobiology of Disease, 2014 Prion diseases are progressive disorders that affect the central nervous system leading to memory loss, personality changes, ataxia and neurodegeneration.
A. Murali, R.A. Maue, P.J. Dolph
doaj +1 more source
Infectio, 2007 Se presenta el caso de una paciente de 65 años de edad con alucinaciones auditivas y visuales, rigidez en el hemicuerpo izquierdo que progresó al hemicuerpo derecho, con demostración por electroencefalograma de ondas trifásicas abundantes lentas ...
VILLAMIL WILMER +6 more
doaj
Rapidly Progressive Corticobasal Degeneration Syndrome
Case Reports in Neurology, 2011 Introduction: Corticobasal syndrome (CBS) has a heterogeneous clinical presentation with no specific pathologic substratum. Its accurate diagnosis is a challenge for neurologists; in order to establish CBS definitively, postmortem confirmation is ...
Ana Herrero Valverde +4 more
doaj +1 more source
Chinese Journal of Contemporary Neurology and NeurosurgeryObjective To report the clinical diagnosis and treatment of a case of sporadic Creutzfeldt-Jakob disease (sCJD), Heidenhain variant, presenting initially with Balint syndrome following severe acute respiratory syndrome coronavirus (SARS-CoV-2) infection,
YE Wen-lu +4 more
doaj +1 more source
Creutzfeldt–Jakob disease with unusual presentation of peripheral neuropathy and ophthalmoplegia
Avicenna Journal of Medicine, 2018 Creutzfeldt–Jakob disease (CJD) is a well-described disease. It is characterized by rapidly progressive dementia, myoclonus, ataxia, pyramidal, and extrapyramidal signs.
Mais Arwani +3 more
doaj +1 more source
Creutzfeldt–Jakob disease-like syndrome induced by gabapentin toxicity
Ageing Research, 2010 Patients with Creutzfeldt–Jakob disease (CJD) may exhibit characteristic abnormalities on the electroencephalogram (EEG). However, these abnormalities have been associated with a number of cases of drug toxicity. We report a case of CJD-like syndrome associated with gabapentin. A 78-year-old man was hospitalized for recurrent falls.
Vicky Chau +3 more
openaire +2 more sources
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 +3 more
doaj