Results 201 to 210 of about 13,613 (255)

Sjögren syndrome presenting with encephalopathy mimicking Creutzfeldt–Jakob disease

Journal of the Neurological Sciences, 2013
A 61-year-old man developed subacute progressive dementia, general fatigue, a tonic-clonic seizure, and a decreased level of consciousness. He had a past history of chronic hepatitis type C and was diagnosed as having hepatic encephalopathy due to hyperammonemia.
Koushun, Matsuo, Makoto, Saburi, Hiroki, Ishikawa, Kou, Tei, Youhei, Hosokawa, Chihiro, Fujii, Toshiki, Mizuno, Masanori, Nakagawa   +7 more
openaire   +2 more sources

Presentation of Creutzfeldt–Jakob disease as acute corticobasal degeneration syndrome

Movement Disorders, 2004
AbstractWe provide a brief report with videotape documentation of a possible case of Creutzfeldt–Jakob disease.
Galit, Kleiner-Fisman, Catherine, Bergeron, Anthony E, Lang   +2 more
openaire   +2 more sources

MRI Detection of the Cerebellar Syndrome in Creutzfeldt–Jakob Disease

The Cerebellum, 2009
Creutzfeldt-Jakob Disease (CJD) is characterized by bilateral basal ganglia hyperintensities on T2W and diffusion-weighted imaging (DWI) magnetic resonance imaging (MRI) scans, consistent with its extrapyramidal neurological manifestations. MRI is diagnostically uninformative about the cerebellar symptoms, equally prominent in CJD.
Oren S, Cohen, Chen, Hoffmann, Hedok, Lee, Joab, Chapman, Robert K, Fulbright, Isak, Prohovnik   +5 more
openaire   +2 more sources

Creutzfeldt-Jakob disease presenting as Wernicke-Korsakoff syndrome

Journal of the Neurological Sciences, 1992
A 47-year-old man began to suffer from progressive truncal ataxia and mental alterations typical of Wernicke-Korsakoff syndrome. He showed confusional state, hallucinations, delirium of jealousy and a serious impairment of recent memory. The symptomatology lasted 13 months, but only in the last weeks was it complicated by myoclonias.
openaire   +2 more sources

Zur Klinik und Elektroencephalographie des Creutzfeldt-Jakob-Syndroms

Archiv f�r Psychiatrie und Nervenkrankheiten Vereinigt mit Zeitschrift f�r die Gesamte Neurologie und Psychiatrie, 1967
Die klinische Symptomatik und der Verlauf eines sporadischen Falles von Creutzfeldt-Jakob-Syndrom werden beschrieben und die Untersuchungsergebnisse diskutiert. Insbesondere wird auf charakteristische Veranderungen des Elektroencephalogramms mit periodischem Auftreten bilateral synchroner Steilwellen und langsamer Wellen hingewiesen, die auch bei ...
M. Bergener, L. Gerhard
openaire   +1 more source

Drug‐induced creutzfeldt‐jakob like syndrome: A review

Human Psychopharmacology: Clinical and Experimental, 1992
AbstractCreutzfeldt‐Jakob disease is an untreatable degenerative disorder which presents problems in diagnosis. The clinical picture is said to be characterised by dementia, myoclonus and periodic triphasic discharge on the electroencephalogram. The high profile given to this disorder recently will lead inevitably to more diagnoses being made.
openaire   +1 more source

Characterising the uncommon corticobasal syndrome presentation of sporadic Creutzfeldt-Jakob disease

Parkinsonism & Related Disorders, 2013
Corticobasal syndrome (CBS), which encompasses cortical sensory loss, alien limb, bradykinesia, rigidity, limb apraxia and dystonia, is the classic presentation of corticobasal degeneration (CBD). It may occur in other neurodegenerative disorders including sporadic Creutzfeldt-Jakob disease (sCJD).
Lee, W, Simpson, M, Ling, H, Mclean, C, Collins, S, Williams, DR   +5 more
openaire   +3 more sources

MV2 subtype of sporadic Creutzfeldt‐Jakob disease presenting as corticobasal syndrome

Movement Disorders, 2007
Clinicopathologic correlative studies have shown that the corticobasal syndrome (CBS) is associated with various pathologies, including PSP, AD or sporadic Creutzfeldt-Jakob disease (sCJD), in addition to corticobasal degeneration (CBD. sCJD is generally distinguished from CBD by the much shorter duration of illness and the finding of either a 14-3-3 ...
Anna Magherini, Roberta Pentore, Giuliana Galassi, Carlo M. Stucchi, CAPELLARI, SABINA, PARCHI, PIERO   +5 more
openaire   +1 more source

Balint's syndrome revealing Creutzfeldt-Jakob disease

Revue Neurologique, 2022
M, Escalere, C, Joly, J, Palisson, C, Budowski, M, Mongin, B, Degos   +5 more
openaire   +2 more sources

Transmission of Creutzfeldt–Jakob disease with scrapie-like syndromes to mice

Nature, 1978
THE transmission of Creutzfeldt–Jakob disease of man, one of the subacute spongiform virus encephalopathies1, to guinea pigs2,3 and to hamsters4 has been reported from this laboratory; Brownell et al. have also claimed transmission of Creutzfeldt–Jakob disease to mice5,6.
E E, Manuelidis, E J, Gorgacz, L, Manuelidis   +2 more
openaire   +2 more sources