نتایج جستجو برای: extrapyramidal symptoms

تعداد نتایج: 280630  

Journal: :L'Encephale 1979
E Diepart M J Cottereau P Deniker

Neuroleptics can induce not only early but also tardive extrapyramidal side effects. The former were described as early as in the beginning of the therapeutic era; the latter, known as tardive dyskinesia, are essentially made of bucco-linguomasticatory dyskinesia, sometimes accompanied by other extrapyramidal symptoms, among others choreo-athetoid movements of the limbs. This complication was m...

Journal: :Molecular genetics and metabolism 2012
Adeline Vanderver Davide Tonduti Sarah Auerbach Johanna L Schmidt Sumit Parikh Gordon C Gowans Kelly E Jackson Pamela L Brock Marc Patterson Michelle Nehrebecky Rena Godfrey Wadih M Zein William Gahl Camilo Toro

OBJECTIVE To report the detection of secondary neurotransmitter abnormalities in a group of SPG11 patients and describe treatment with l-dopa/carbidopa and sapropterin. DESIGN Case reports. SETTING National Institutes of Health in the Undiagnosed Disease Program; Children's National Medical Center in the Myelin Disorders Bioregistry Program. PATIENTS Four SPG11 patients with a clinical pi...

Journal: :Toxicological sciences : an official journal of the Society of Toxicology 2003
Rosane Maria Salvi Diogo R Lara Eduardo S Ghisolfi Luis V Portela Renato D Dias Diogo O Souza

Long-term exposure to low levels of organophosphate pesticides (OP) may produce neuropsychiatric symptoms. We performed clinical, neuropsychiatric, and laboratory evaluations of 37 workers involved in family agriculture of tobacco from southern Brazil who had been exposed to OP for 3 months, and in 25 of these workers, after 3 months without exposure to OP. Plasma acetylcholinesterase activity ...

باغبانیان, سید محمد, خوش نما, ابراهیم, زروانی, اشرف, عابدینی, محمود,

Hallervorden Spatz Disease is a rare neurodegenerative disorder with the prevalence of one to three per million. The onset of symptoms is usually in late childhood and early adolescence. However, some cases of the disease were reported in adulthood which could be familial or sporadic. The familial cases are autosomal-recessive resulting from mutation in the pantothenate kinase 2 gene located on...

Journal: :Journal of neurology, neurosurgery, and psychiatry 1985
R O McKeran P Bradbury D Taylor G Stern

A case of type 1 (adult) Gaucher's disease with a late onset tapeto-retinal degeneration and an initially dopamine responsive extrapyramidal syndrome is described. The literature reporting neurological involvement in type 1 Gaucher's disease is reviewed, and it is concluded that the absence of symptoms and signs of nervous system involvement cannot be used as the sole basis for the classificati...

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