Striatal dopaminergic functioning in patients with sporadic and hereditary spastic paraplegias with parkinsonism (Q37329628)

19 August 2017

Striatal dopaminergic functioning in patients with sporadic and hereditary spastic paraplegias with parkinsonism (English)

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19 August 2017

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6

Beom S Jeon

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19 August 2017

Ji Seon Kim

1

1 reference

19 August 2017

Jong Min Kim

2

1 reference

19 August 2017

Yu Kyeong Kim

3

1 reference

19 August 2017

Sang Eun Kim

4

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19 August 2017

Ji Young Yun

5

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19 August 2017

language of work or name

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31 October 2013

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Journal of Korean Medical Science

19 August 2017

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19 August 2017

28

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19 August 2017

11

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19 August 2017

1661-1666

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Genetics of motor neuron disorders: new insights into pathogenic mechanisms

19 August 2017

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835511

Normal dopaminergic nigrostriatal innervation in SPG3A hereditary spastic paraplegia

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835511

Spastin and microtubules: Functions in health and disease.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835511

A case of Machado-Joseph disease presenting with spastic paraparesis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835511

Classification of the hereditary ataxias and paraplegias

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835511

Serial dopamine transporter imaging of nigrostriatal function in patients with idiopathic rapid-eye-movement sleep behaviour disorder: a prospective study

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835511

Spinocerebellar ataxia type 17 mutation as a causative and susceptibility gene in parkinsonism

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835511

Widespread thalamic and cerebellar degeneration in a patient with a complicated hereditary spastic paraplegia (HSP).

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835511

SPG11 spastic paraplegia. A new cause of juvenile parkinsonism

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835511

Loss of spastic paraplegia gene atlastin induces age-dependent death of dopaminergic neurons in Drosophila

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835511

Autopsy case of hereditary spastic paraplegia with thin corpus callosum showing severe gliosis in the cerebral white matter.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835511

Combination of 'idiopathic' REM sleep behaviour disorder and olfactory dysfunction as possible indicator for alpha-synucleinopathy demonstrated by dopamine transporter FP-CIT-SPECT.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835511

Levodopa-responsive parkinsonism in hereditary spastic paraplegia with thin corpus callosum.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835511

The hereditary spastic paraplegia gene, spastin, regulates microtubule stability to modulate synaptic structure and function.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835511

The cellular and molecular pathology of the motor system in hereditary spastic paraparesis due to mutation of the spastin gene

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835511

The clinical benefit of imaging striatal dopamine transporters with [123I]FP-CIT SPET in differentiating patients with presynaptic parkinsonism from those with other forms of parkinsonism

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835511

Decreased striatal dopaminergic innervation in REM sleep behavior disorder

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835511

Reduced striatal dopamine transporters in idiopathic rapid eye movement sleep behaviour disorder. Comparison with Parkinson's disease and controls

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835511

Machado-Joseph disease versus hereditary spastic paraplegia: case report

2 September 2018

1 reference

12 December 2020

Machado-Joseph disease: A proposal of spastic paraplegic subtype

1 reference

12 December 2020

Hereditary spastic paraplegia; report of a family with associated extrapyramidal signs

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12 December 2020

Hereditary spastic paraplegia associated with dopa-responsive parkinsonism

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12 December 2020

Hereditary spastic paraplegia or spinocerebellar ataxia? Not always as easy as it seems

1 reference

12 December 2020

Six cases of SCA3/MJD patients that mimic hereditary spastic paraplegia in clinic

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12 December 2020

Novel mutations in SPG11 cause hereditary spastic paraplegia associated with early-onset levodopa-responsive Parkinsonism

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12 December 2020

10.3346/JKMS.2013.28.11.1661

Identifiers

DOI

1 reference

19 August 2017

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19 August 2017

PubMed publication ID

24265532

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