نتایج جستجو برای: extrapyramidal signs

تعداد نتایج: 102669  

2001
Olivier Beauchet Pascal Giraux Fabien Schneider Roland Peyron Fabrice Barral Bernard Laurent

Corticobasal degeneration is a neurodegenerative disease characterized, by cortical dysfunction and extrapyramidal signs. The most consistent symptom is a unilateral limb apraxia, which consists of an isolated disorder of gestural production involving primarily the upper limb. The objective of this study is to investigate the functional abnormalities that may underlie motor dysfunction, and tho...

Journal: :Arquivos de neuro-psiquiatria 2011
Melina Moré Bertotti Marcelo Neves Linhares Rafael Ferreira Daniel Sousa Santos Athos Tiradentes Athayde Antonio Cesar Melo Mussi Jorge W Moritz Thiago Siminiano Jung Humberto Kluge Schroeder Igor Kunze Rodrigues

Leukoencephalopathy with intracranial calcifications and cysts (LCC) is a rare and recently described entity characterized radiologically by white matter abnormalities, calcifications, cysts and enhancing nodules. LCC is a disorder of unknown etiology and its neurological manifestations include cognitive decline, seizure, obstructive hydrocephalus, progressive cerebellar, besides extrapyramidal...

2014
Manuel Morrens Lise Docx Sebastian Walther

MOTOR SYMPTOMS OF SCHIZOPHRENIA Schizophrenia is typically conceived as an illness characterized by positive, negative, and cognitive symptoms. However, most schizophrenia patients also display a wide range of symptoms characterized by aberrant motor functioning. Symptoms of schizophrenia that fit this description are catatonic features, the motoric neurological soft signs (NSS), extrapyramidal...

Journal: :Journal of psychiatry & mental disorders 2021

Trihexyphenidyl or Artane® /Parkinane® is an anti-cholinergic drug belonging to the antimuscarinic class. It used in treatment of Parkinson’s disease and widely psychiatry for management extrapyramidal side effects neuroleptics. Its overdose leads a central peripheral anticholinergic syndrome. We report here case seven-year-old Senegalese boy who developed signs intoxication due accidental inge...

Journal: :AJNR. American journal of neuroradiology 2009
E De Grandis M Di Rocco A Pessagno E Veneselli A Rossi

SUMMARY Late infantile GM1 gangliosidosis is a rare lysosomal disorder characterized by mental deterioration and progressive spastic, cerebellar, and extrapyramidal signs, without facial dysmorphisms and organomegaly. Neuroimaging findings have been reported in only a few cases. Here we report on predominant globus pallidus MR signal-intensity abnormalities in 2 patients with the late infantile...

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