(Q37329628)

19 August 2017

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

1 reference

19 August 2017

1 reference

1 reference

1 reference

6

Beom S Jeon

1 reference

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

1 reference

19 August 2017

Ji Young Yun

5

1 reference

19 August 2017

language of work or name

1 reference

31 October 2013

1 reference

Journal of Korean Medical Science

19 August 2017

1 reference

19 August 2017

28

1 reference

19 August 2017

11

1 reference

19 August 2017

1661-1666

1 reference

Genetics of motor neuron disorders: new insights into pathogenic mechanisms

19 August 2017

1 reference

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

1 reference

12 December 2020

Hereditary spastic paraplegia associated with dopa-responsive parkinsonism

1 reference

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

1 reference

12 December 2020

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

1 reference

12 December 2020

10.3346/JKMS.2013.28.11.1661

Identifiers

DOI

1 reference

19 August 2017

1 reference

19 August 2017

PubMed publication ID

24265532

1 reference