Results 191 to 200 of about 13,613 (255)

A Unique Case of Genetic Creutzfeldt-Jakob Disease (E200K Mutation) with CSF-restricted Anti Myelin Oligodendrocyte Glycoprotein Antibody. [PDF]

Intern Med
Shimizu T, Horiuchi E, Matsukawa T, Yasuda T, Hashida H.   +4 more
europepmc   +1 more source

High Proportions of GAP43 Positivity in the Cerebrospinal Fluids of Patients with Sporadic and Certain Types of Genetic Creutzfeldt-Jakob Diseases by Western Blot Analysis. [PDF]

Int J Mol Sci
Jia XX, Hu C, Zeng JF, Xu B, Li JZ, A RH, Liang DL, Cao RD, Zhou W, Gao LP, Shi Q, Chen C, Dong XP.   +12 more
europepmc   +1 more source

M232R Familial Creutzfeldt-Jacob Disease Challenging to Diagnose Due to the Absence of Characteristic Laboratory Findings. [PDF]

Intern Med
Tanaka Y, Irie KI, Isogai M, Koga T, Mori S, Tateishi T.   +5 more
europepmc   +1 more source

Parkinsonism in Gerstmann-Sträussler-Scheinker disease: A case report. [PDF]

eNeurologicalSci
Poveda S, Montealegre-Claros JS, Lancheros LM, Cruz MA, Pacheco OB.   +4 more
europepmc   +1 more source

[Creutzfeldt-Jakob syndrome. A new variant in Great Britain].

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 1996
openaire   +1 more source

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Lithium-Induced Creutzfeldt-Jakob Syndrome

Clinical Neuropharmacology, 1996
a 67-year-old man with bipolar disorder developed a Creutzfeldt-Jakob like syndrome during lithium carbonate treatment. Lithium serum level was within the therapeutic range. Complete clinical-electroencephalographic recovery was achieved after lithium therapy was discontinued.
B, Casanova, M, de Entrambasaguas, C, Perla, E, Gómez-Siurana, A, Benetó, J A, Burguera   +5 more
openaire   +2 more sources

Balint syndrome due to Creutzfeldt–Jakob disease

Neurology, 2004
Since Balint originally described a patient with striking disturbances in vision and movement,1 this syndrome has been reported to result from stroke, metastatic lesions, demyelinating disorders, carbon monoxide poisoning, corticobasal ganglionic degeneration, Alzheimer disease, and HIV infection.2 We report a patient with Balint syndrome resulting ...
B M, Ances, J M, Ellenbogen, S T, Herman, D, Jacobs, D S, Liebeskind, A, Chatterjee, S L, Galetta   +6 more
openaire   +2 more sources

Creutzfeldt-Jakob syndrome presenting as epilepsia partialis continua

Journal of Clinical Neuroscience, 2001
Creutzfeldt-Jakob disease (CJD) is an uncommon rapidly progressive neurological disorder which can have protean clinical presentations. We report an autopsy-proven case of CJD presenting initially as epilepsia partialis continua but then developing the typical clinical features of CJD over several weeks.
J, Parry, P, Tuch, W, Knezevic, V, Fabian   +3 more
openaire   +2 more sources

Creutzfeldt-Jakob–Like Syndrome due to Hypercalcemic Encephalopathy

Clinical EEG and Neuroscience, 2014
Hypercalcemia can cause a subacute syndrome of progressive dementia and marked changes in the electroencephalogram (EEG). We report a case of iatrogenic hypercalcemia with a close correlation between the clinical course and the EEG changes. A 73-year-old woman presented with a subacute syndrome of progressive dementia and bursts of 1.5 to 2 Hz ...
Johannes, Rösche, Catharina, Sieveking, Christina, Kampf, Reiner, Benecke   +3 more
openaire   +2 more sources