Differential Diagnosis of Chorea (Q37861587)

24 August 2017

1 reference

title

Differential diagnosis of chorea (English)

1 reference

24 August 2017

Differential Diagnosis of Chorea (English)

1 reference

DOI

https://api.crossref.org/works/10.1007/S11910-011-0202-2

29 November 2024

0 references

0 references

1

Ruth H. Walker

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:21465146

29 November 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=21465146

29 November 2024

publication date

1 August 2011

1 reference

24 August 2017

August 2011

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=21465146

full work available at URL

29 November 2024

http://link.springer.com/content/pdf/10.1007/s11910-011-0202-2.pdf

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

http://link.springer.com/article/10.1007/s11910-011-0202-2/fulltext.html

29 November 2024

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

http://link.springer.com/content/pdf/10.1007/s11910-011-0202-2

29 November 2024

1 reference

DOI

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Current Neurology and Neuroscience Reports

29 November 2024

published in

1 reference

24 August 2017

volume

11

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24 August 2017

issue

4

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24 August 2017

page(s)

385-395

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Autopsy-proven Huntington's disease with 29 trinucleotide repeats

24 August 2017

cites work

1 reference

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Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset

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Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease

21 January 2018

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A repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease-like 2.

21 January 2018

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Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes

21 January 2018

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21 January 2018

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Phenotypic features of Huntington's disease-like 2.

21 January 2018

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Huntington's disease--like 2 can present as chorea-acanthocytosis

21 January 2018

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Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond

21 January 2018

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Choreiform movements in spinocerebellar ataxia type 1.

21 January 2018

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Extrapyramidal signs are a common feature of spinocerebellar ataxia type 17.

21 January 2018

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Prevalence of dentatorubral-pallidoluysian atrophy in a large series of white patients with cerebellar ataxia

21 January 2018

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Dentatorubral pallidoluysian atrophy in South Wales.

21 January 2018

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The Haw River syndrome: dentatorubropallidoluysian atrophy (DRPLA) in an African-American family

21 January 2018

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https://api.crossref.org/works/10.1007/S11910-011-0202-2

Benign hereditary chorea: clinical, neuroimaging, and genetic findings

21 January 2018

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https://api.crossref.org/works/10.1007/S11910-011-0202-2

Mutations in TITF1 are not relevant to sporadic and familial chorea of unknown cause.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

A novel TITF-1 mutation causes benign hereditary chorea with response to levodopa

21 January 2018

1 reference

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Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

A novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: description of clinical features and implications for genotype-phenotype correlations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Identification of a locus on chromosome 14q for idiopathic basal ganglia calcification (Fahr disease).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr disease).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Autosomal dominant dystonia-plus with cerebral calcifications

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (Melas) associated with a Fahr disease and cerebellar calcifications

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

No evidence for cognitive dysfunction or depression in patients with mild restless legs syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Chorea-ballism associated with familial amyotrophic lateral sclerosis. A clinical, genetic, and neuropathological study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Association of chorea and motor neuron disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Behavioral variant of frontotemporal dementia mimicking Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Neurological manifestations in Wilson's disease: Report of 119 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Clinical spectrum of ataxia-telangiectasia in adulthood

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Clinical features and molecular bases of neuroacanthocytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Testing for acanthocytosis A prospective reader-blinded study in movement disorder patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

A conserved sorting-associated protein is mutant in chorea-acanthocytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Chorein detection for the diagnosis of chorea-acanthocytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Karak syndrome: a novel degenerative disorder of the basal ganglia and cerebellum

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Aceruloplasminemia, an iron metabolic disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

The neurological presentation of ceruloplasmin gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Atypical GLUT1 deficiency with prominent movement disorder responsive to ketogenic diet

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Adult nonketotic hyperglycinemia (NKH) crisis presenting as severe chorea and encephalopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Valproate-induced chorea and encephalopathy in atypical nonketotic hyperglycinemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Late-onset presentation of pyruvate dehydrogenase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Pyruvate dehydrogenase E3 binding protein (protein X) deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

McLeod neuroacanthocytosis: genotype and phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

McLeod myopathy revisited: more neurogenic and less benign

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Mosaic pattern of gliosis in the neostriatum of a north american man with craniocervical dystonia and parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Severe generalised dystonia associated with a mosaic pattern of striatal gliosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Remarkable improvement in adult Leigh syndrome with partial cytochrome c oxidase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

A missense mutation in the mitochondrial ND5 gene associated with a Leigh-MELAS overlap syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Adult-onset chorea and mitochondrial cytopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Leber hereditary optic neuropathy with chorea and dementia resembling Huntington disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Hemiballismus-hemichorea in older diabetic women: a clinical syndrome with MRI correlation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Persistent chorea triggered by hyperglycemic crisis in diabetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Serum vitamin B12 deficiency and hyperhomocystinemia: a reversible cause of acute chorea, cerebellar ataxia in an adult with cerebral ischemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Mimicry and autoantibody-mediated neuronal cell signaling in Sydenham chorea.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Chorea as a presenting feature of variant Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Reversible choreoathetosis as the early onset of HIV-encephalopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

HIV-induced chorea: evidence for basal ganglia dysregulation by SPECT.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Systemic lupus erythematosus (SLE) in childhood: analysis of clinical and immunological findings in 34 patients and comparison with SLE characteristics in adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Hemichorea with antiphospholipid antibodies in a patient with lupus nephritis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Primary Sjogren's syndrome presenting as a generalized chorea

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Choreic syndrome and coeliac disease: a hitherto unrecognised association

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Onco-neural antibodies and tumour type determine survival and neurological symptoms in paraneoplastic neurological syndromes with Hu or CV2/CRMP5 antibodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Slow evolution of cerebellar degeneration and chorea in a man with anti-Yo antibodies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Anti-NMDA-receptor encephalitis: a cause of psychiatric, seizure, and movement disorders in young adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Paraneoplastic anti-N-methyl-D-aspartate receptor encephalitis associated with ovarian teratoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Chorea in adults following pulmonary endarterectomy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Late-onset choreoathetotic syndrome following heart surgery

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

A case of late-onset chorea

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Acute methotrexate neurotoxicity with choreiform movements and focal neurological deficits: a case report

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Baclofen-induced chorea in complex regional pain syndrome-related dystonia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Methylphenidate-induced chorea: Case report and pharmacologic implications

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Co-occurrence of infantile epileptic seizures and childhood paroxysmal choreoathetosis in one family: clinical, EEG, and SPECT characterization of episodic events

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Myofibrillogenesis regulator 1 gene mutations cause paroxysmal dystonic choreoathetosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Long-term follow-up of Huntington disease treated by bilateral deep brain stimulation of the internal globus pallidus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Bilateral deep brain stimulation for treatment of medically refractory paroxysmal nonkinesigenic dyskinesia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Neural transplants in patients with Huntington's disease undergo disease-like neuronal degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Effect of fetal neural transplants in patients with Huntington's disease 6 years after surgery: a long-term follow-up study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Movement disorders associated with chronic GM2 gangliosidosis. Case report and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Spectrum of movement disorders in neuroferritinopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

Phenomenology of ?Lubag? or X-linked dystonia-parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-011-0202-2

The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia

21 January 2018

1 reference

12 December 2020

Schizophrenia in a patient with spinocerebellar ataxia 2: coincidence of two disorders or a neurodegenerative disease presenting with psychosis?

1 reference

12 December 2020

Chorea as the presenting feature of neurosyphilis

1 reference

12 December 2020

Intrathecal methotrexate-induced acute chorea

1 reference

12 December 2020

Autosomal dominant episodic ataxia: a heterogeneous syndrome

1 reference

12 December 2020

Reversible chorea and focal dystonia in vitamin B12 deficiency

1 reference

12 December 2020

Friedreich's ataxia with chorea and myoclonus caused by a compound heterozygosity for a novel deletion and the trinucleotide GAA expansion

1 reference

12 December 2020

Chorea-acanthocytosis genotype in the original critchley kentucky neuroacanthocytosis kindred

1 reference

12 December 2020

Chorea in the elderly with mutation positive polycythemia vera: a case report.

1 reference

12 December 2020

Malaysian siblings with friedreich ataxia and chorea: a novel deletion in the frataxin gene

1 reference

12 December 2020

Chorea induced by a luteinizing hormone-releasing hormone analog

1 reference

12 December 2020

Movement disorders in childhood organic acidurias. Clinical, neuroimaging, and biochemical correlations

1 reference

12 December 2020

TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea.

1 reference

12 December 2020

[Chorea-athetosis in the anti-Hu syndrome]

1 reference

12 December 2020

Case 1, 1995: psychosis, dementia, chorea, ataxia, and supranuclear gaze dysfunction

1 reference

12 December 2020

Chorea in new variant Creutzfeldt-Jacob disease

1 reference

12 December 2020

Chorea and rapidly progressive subcortical dementia in antiphospholipid syndrome.

1 reference

12 December 2020

Long-term follow-up of pallidal deep brain stimulation in two cases of Huntington's disease

1 reference

12 December 2020

Adult-onset chorea and dementia with propionic acidemia

1 reference

12 December 2020

Pyruvate dehydrogenase E3 binding protein (protein X) deficiency

1 reference

12 December 2020

Identifiers

DOI

1 reference

release_fjczfxetuffx5mzsklm5obrji4

24 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/fjczfxetuffx5mzsklm5obrji4

24 November 2022

mapped directly with Wikidata item

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