Zobrazeno 1 - 8
of 8
pro vyhledávání: '"V S, Kostic"'
Publikováno v:
Behavioural Neurology, Vol 11, Iss 2, Pp 105-108 (1998)
A 19-year-old man developed the Kleine-Levin syndrome three weeks after the head trauma and subsequent neurosurgical evacuation of right-sided, fronto-temporal epidural hematoma. The expression of periodic episodes was observed for hypersomnolence an
Externí odkaz:
https://doaj.org/article/9cdeb25e3cd740dc8d1680d85d95b421
Publikováno v:
Acta Radiologica. 47:624-627
Long-term follow-up abdominal imaging studies have not been reported previously in patients with the hepatic form of Wilson's disease (WD). This paper reports the case of a 35-year-old woman with symptoms dating back several months and with multiple,
Autor:
I, Topisirovic, N, Dragasevic, D, Savic, A, Ristic, M, Keckarevic, D, Keckarevic, B, Culjkovic, I, Petrovic, S, Romac, V S, Kostic
Publikováno v:
Clinical genetics. 62(4)
Spinocerebellar ataxia type 8 (SCA8) is a slowly progressive ataxia causally associated with untranslated CTG repeat expansion on chromosome 13q21. However, the role of the CTG repeat in SCA8 pathology is not yet well understood. Therefore, we studie
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 15(6)
This study tested the role of basal ganglia in visuomotor skill learning. Thirty-nine patients early in the course of Parkinson's disease (PD) and 30 patients after operation for an aneurysm of the anterior communicating artery (ACoA) were compared w
Publikováno v:
Clinical neuropharmacology. 21(2)
In this open study, the therapeutic effect of moclobemide, a reversible selective monoamine oxidase A inhibitor, was tested in 20 patients with Parkinson's disease who developed levodopa-induced motor response complications. Moclobemide as adjunct th
Publikováno v:
Acta Neurologica Belgica. 112:323-323
Publikováno v:
Journal of Neurology. 236:111-114
The activity of glutamate dehydrogenase, the enzyme of glutamate degradation, was measured in platelets of 27 healthy controls and 85 patients with different degenerative cerebellar and/or basal ganglia disorders. A group of 7 patients was selected w
Publikováno v:
Stroke. 15(2)
We examined a patient who had signs of a cerebral hemisphere lesion: right hemiparesis, facial weakness, right hemianopsy, acustico-mnestic dysphasia, "empty speech," acalculia, visuo-spatial agnosia and constructional apraxia, but without changes in