Chorea and related disorders.

scientific article

Chorea and related disorders. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1136/PGMJ.2004.019356
P932PMC publication ID1743104
P698PubMed publication ID15356354
P5875ResearchGate publication ID8358395

P50authorRoongroj BhidayasiriQ37836973
P2093author name stringTruong DD
P2860cites workMutations in TITF-1 are associated with benign hereditary choreaQ24294966
Huntington disease: genetics and epidemiologyQ24675741
Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)Q28250990
Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brainQ29617982
Paroxysmal kinesigenic choreoathetosis: a report of 26 patientsQ33589494
HIV encephalitis presenting with severe generalized choreaQ49024362
Physical localisation of the chromosomal marker D13S31 places the Wilson disease locus at the junction of bands q14.3 and q21.1 of chromosome 13Q57828497
Delayed choreoathetosis following acute carbon monoxide poisoningQ70045990
Chorea in systemic lupus erythematosus and "lupus-like" disease: association with antiphospholipid antibodiesQ70346602
Abnormalities of the physiology of copper in Wilson's disease. 3. The excretion of copperQ70668973
Chorea in beh�et's syndromeQ72674184
Sydenham Chorea: magnetic resonance imaging reveals permanent basal ganglia injuryQ73089988
Hyperkinetic movement disorders during and after acute stroke: the Lausanne Stroke RegistryQ73170752
Hyperthyroidism presenting as recurrent short paroxysmal kinesigenic dyskinesiaQ74433576
Carbocyanine dyes. Novel markers for labelling neuronsQ95811093
Increased rate of suicide among patients with Huntington's diseaseQ33620527
Benign hereditary chorea--entity or syndrome?Q33884389
Acanthocytosis and neurological disorders.Q33941160
A polymorphic DNA marker genetically linked to Huntington's diseaseQ34255139
Chorea and its disordersQ34353562
Huntington's disease: a review of the literature on prevalence and treatment of neuropsychiatric phenomenaQ34484850
Neurologic outcome of choreoathetoid encephalopathy after cardiac surgeryQ34772427
Genetics of movement disorders and ataxia.Q35048944
Chorea disclosing deterioration of polycythaemia veraQ35509720
The epidemiology of Huntington's diseaseQ35882166
Are cognitive changes the first symptoms of Huntington's disease? A study of gene carriersQ36317837
Chorea in the antiphospholipid syndrome. Clinical, radiologic, and immunologic characteristics of 50 patients from our clinics and the recent literatureQ36866914
Differential diagnosis of choreiform tardive dyskinesiaQ37062768
Anti-basal ganglia antibodies in acute and persistent Sydenham's choreaQ40578126
Chorea gravidarumQ40582021
Sydenham's chorea. A model for childhood autoimmune neuropsychiatric disordersQ40692876
Psychopharmacologic treatment of pathologic aggressionQ41510588
Huntington Disease and the Related Disorder, Dentatorubral-Pallidoluysian Atrophy (DRPLA)Q41628677
Ocular motor abnormalities in Huntington's diseaseQ41678637
A double-blind trial of tetrabenazine, thiopropazate, and placebo in patients with choreaQ42230569
Hemichorea and hemiballism associated with contralateral hemiparesis and ipsilateral basal ganglia lesionsQ42472743
Paraneoplastic chorea associated with CRMP-5 neuronal antibody and lung carcinomaQ42523560
Tetrabenazine treatment for Huntington's disease-associated choreaQ44240628
Tetrabenazine in the treatment of severe pediatric chorea.Q44464250
Cause and course in a series of patients with sporadic choreaQ45289056
Clozapine in Huntington's choreaQ45290066
Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's diseaseQ45290871
Preferential loss of striato-external pallidal projection neurons in presymptomatic Huntington's diseaseQ45291252
Psychiatric, genetic, and positron emission tomographic evaluation of persons at risk for Huntington's diseaseQ45291899
Neuropathological classification of Huntington's diseaseQ45297167
Riluzole therapy in Huntington's disease (HD).Q45297539
The diagnosis of Huntington's diseaseQ45297907
Erythrocyte membrane abnormalities in patients with amyotrophic chorea with acanthocytosis. Part 1. Spin labeling studies and lipid analysesQ45299897
Huntington's disease: neurological assessment of potential gene carriers presenting for predictive DNA testingQ45300569
Hereditary nonprogressive chorea of early onsetQ45301157
Improvement of Huntington's disease with olanzapine and valproateQ45301330
Motor and cognitive improvements in patients with Huntington's disease after neural transplantationQ45301920
Hereditary benign chorea: clinical and genetic features of a distinct diseaseQ45303372
A randomized, placebo-controlled trial of coenzyme Q10 and remacemide in Huntington's diseaseQ45303631
Bilateral human fetal striatal transplantation in Huntington's disease.Q45305502
Restricted unilateral Sydenham's chorea: reversible contralateral striatal hypermetabolism demonstrated on single photon emission computed tomographic scanningQ48130950
Dentatorubral-pallidoluysian atrophy or Naito-Oyanagi diseaseQ48209189
The diversity of neurologic events in systemic lupus erythematosus. Prospective clinical and computed tomographic classification of 82 events in 71 patientsQ48369404
Chorea-acanthocytosis: neuropathology of brain and peripheral nerve.Q48609023
P433issue947
P407language of work or nameEnglishQ1860
P921main subjectHuntington's diseaseQ190564
P304page(s)527-534
P577publication date2004-09-01
P13046publication type of scholarly workreview articleQ7318358
P1433published inPostgraduate Medical JournalQ7234294
P1476titleChorea and related disorders
P478volume80

Reverse relations

cites work (P2860)
Q34560508A case of late-onset chorea
Q39785257A case of vascular hemichorea responding to topiramate
Q28504771Ablation of D1 dopamine receptor-expressing cells generates mice with seizures, dystonia, hyperactivity, and impaired oral behavior.
Q26765818Abnormal movements in critical care patients with brain injury: a diagnostic approach
Q41841066Acute and long‐term response of dopamine nigrostriatal synapses to a single, low‐dose episode of 3‐nitropropionic acid‐mediated chemical hypoxia
Q59460890Antipsychotikainduzierte tardive Syndrome
Q35520657Cachexia in malaria and heart failure: therapeutic considerations in clinical practice
Q35108608Chorea associated with high titers of antiphospholipid antibodies in the absence of antiphospholipid antibody syndrome
Q34772888Clinical and Neuroimaging Findings of Sydenham's Chorea
Q37945484Deep brain stimulation in the treatment of chorea
Q58597737Hemichorea associated with cavernous angioma and a small errhysis: A case report and literature review
Q26744786Movement Disorders Following Cerebrovascular Lesion in the Basal Ganglia Circuit
Q50147063Movement disorders in mitochondrial disease
Q33636308Oromandibular dyskinesia as the initial manifestation of late-onset huntington disease
Q53050899Phenotypic disruption to orofacial movement topography in conditional mutants with generalized CamKIIa/Cre D1Tox versus striatal-specific DARPP-32/Cre D1Tox ablation of D1 dopamine receptor-expressing cells.
Q38085546Post-stroke Movement Disorders: Clinical Manifestations and Pharmacological Management
Q45288618Pregnancy and active Huntington disease: a rare combination.
Q42931752Reversible Choreoathetosis After the Administration of Ceftriaxone Sodium in Patients With End-Stage Renal Disease
Q92671741Reversible chorea secondary to uremia in an older adult
Q43065095Schizophreniform symptoms in Chorea Minor--case report and literature review
Q48014197Successful Deep Brain Stimulation Surgery With Intraoperative Magnetic Resonance Imaging on a Difficult Neuroacanthocytosis Case
Q37777459Sydenham's Chorea: A Practical Overview of the Current Literature
Q26853651Sydenham's chorea in a family with Huntington's disease: case report and review of the literature
Q24289511Towards a unifying, systems biology understanding of large-scale cellular death and destruction caused by poorly liganded iron: Parkinson’s, Huntington’s, Alzheimer’s, prions, bactericides, chemical toxicology and others as examples
Q64289531Unilateral Hyperkinetic Choreiform Movements due to Calcification of the Putamen and Caudate from an Underlying Developmental Venous Anomaly
Q34829294Use of Antiepileptic Drugs for Hyperkinetic Movement Disorders
Q38009653What’s the role of topiramate in the management of patients with hyperkinetic movement disorders?

Search more.