Works matching IS 08853185 AND DT 2004 AND VI 19 AND IP 6
Results: 30
Partial lesion of thalamic ventral intermediate nucleus after chronic high-frequency stimulation.
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- Movement Disorders, 2004, v. 19, n. 6, p. 709, doi. 10.1002/mds.10709
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A novel movement disorder of the lower lip.
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- Movement Disorders, 2004, v. 19, n. 6, p. 663, doi. 10.1002/mds.10697
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Severe multivalvular heart disease: A new complication of the ergot derivative dopamine agonists.
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- Movement Disorders, 2004, v. 19, n. 6, p. 656, doi. 10.1002/mds.20201
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Cabergoline versus levodopa monotherapy.
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- Movement Disorders, 2004, v. 19, n. 6, p. 733, doi. 10.1002/mds.20032
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Clinicopathological investigation of vascular parkinsonism, including clinical criteria for diagnosis.
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- Movement Disorders, 2004, v. 19, n. 6, p. 630, doi. 10.1002/mds.20083
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Minocycline in Huntington's disease: A pilot study.
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- Movement Disorders, 2004, v. 19, n. 6, p. 692, doi. 10.1002/mds.20018
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Smoking and Parkinson's disease: Systematic review of prospective studies.
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- Movement Disorders, 2004, v. 19, n. 6, p. 614, doi. 10.1002/mds.20029
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Muscle relaxation is impaired in dystonia: A reaction time study.
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- Movement Disorders, 2004, v. 19, n. 6, p. 681, doi. 10.1002/mds.10711
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New concerns about old drugs: Valvular heart disease on ergot derivative dopamine agonists as an exemplary situation of pharmacovigilance.
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- Movement Disorders, 2004, v. 19, n. 6, p. 611, doi. 10.1002/mds.20202
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Cannabis-induced propriospinal myoclonus.
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- Movement Disorders, 2004, v. 19, n. 6, p. 708, doi. 10.1002/mds.10696
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Association study of dopamine D2, D3, D4 receptor and serotonin transporter gene polymorphisms with sleep attacks in Parkinson's disease.
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- Movement Disorders, 2004, v. 19, n. 6, p. 705, doi. 10.1002/mds.20134
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Re: Cabergoline versus levodopa monotherapy: A decision analysis.
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- Movement Disorders, 2004, v. 19, n. 6, p. 736, doi. 10.1002/mds.20031
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Neuropathology of primary restless leg syndrome: Absence of specific τ- and α-synuclein pathology.
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- Movement Disorders, 2004, v. 19, n. 6, p. 695, doi. 10.1002/mds.20042
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Reversible orofacial dyskinesia after ofloxacin treatment.
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- Movement Disorders, 2004, v. 19, n. 6, p. 731, doi. 10.1002/mds.20053
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Diagnosis and management of pergolide-induced fibrosis.
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- Movement Disorders, 2004, v. 19, n. 6, p. 699, doi. 10.1002/mds.20200
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Focal dystonia after removal of a parietal meningioma.
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- Movement Disorders, 2004, v. 19, n. 6, p. 714, doi. 10.1002/mds.20039
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Reply: Cabergoline versus levodopa therapy.
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- Movement Disorders, 2004, v. 19, n. 6, p. 734, doi. 10.1002/mds.20038
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A 100% increase of dopaminergic cells in the olfactory bulb may explain hyposmia in Parkinson's disease.
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- Movement Disorders, 2004, v. 19, n. 6, p. 687, doi. 10.1002/mds.10713
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Quality of life in Polish patients with long-lasting Parkinson's disease.
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- Movement Disorders, 2004, v. 19, n. 6, p. 667, doi. 10.1002/mds.10698
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Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease.
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- Movement Disorders, 2004, v. 19, n. 6, p. 649, doi. 10.1002/mds.20097
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Restless legs syndrome due to interferon-α.
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- Movement Disorders, 2004, v. 19, n. 6, p. 730, doi. 10.1002/mds.20049
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Parkinson's disease in Ireland: Clinical presentation and genetic heterogeneity in patients with parkin mutations.
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- Movement Disorders, 2004, v. 19, n. 6, p. 677, doi. 10.1002/mds.10703
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Deep brain stimulation in myoclonus-dystonia syndrome.
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- Movement Disorders, 2004, v. 19, n. 6, p. 724, doi. 10.1002/mds.20030
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Late-onset presentation of pyruvate dehydrogenase deficiency.
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- Movement Disorders, 2004, v. 19, n. 6, p. 727, doi. 10.1002/mds.20063
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Voluntary control and a wider clinical spectrum of essential palatal tremor.
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- Movement Disorders, 2004, v. 19, n. 6, p. 717, doi. 10.1002/mds.20034
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Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2).
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- Movement Disorders, 2004, v. 19, n. 6, p. 622, doi. 10.1002/mds.20074
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Status dissociatus after surgery for tegmental ponto-mesencephalic cavernoma: A state-dependent disorder of motor control during sleep.
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- Movement Disorders, 2004, v. 19, n. 6, p. 719, doi. 10.1002/mds.20027
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Severe resting clonus caused by thyrotoxicosis in a 16-year-old girl with hereditary spastic paraparesis: A case report.
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- Movement Disorders, 2004, v. 19, n. 6, p. 712, doi. 10.1002/mds.20015
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Clinical signs and symptoms in a large hereditary spastic paraparesis pedigree with a novel spastin mutation.
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- Movement Disorders, 2004, v. 19, n. 6, p. 641, doi. 10.1002/mds.20077
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Cerebellar metabolic symmetry in essential tremor studied with <sup>1</sup>H magnetic resonance spectroscopic imaging: Implications for disease pathology.
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- Movement Disorders, 2004, v. 19, n. 6, p. 672, doi. 10.1002/mds.20019
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