(Q36316794)

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Neuro-ophthalmologic and electroretinographic findings in pantothenate kinase-associated neurodegeneration (formerly Hallervorden-Spatz syndrome)

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scholarly article

1 reference

Europe PubMed Central

13 August 2017

Neuro-ophthalmologic and electroretinographic findings in pantothenate kinase-associated neurodegeneration (formerly Hallervorden-Spatz syndrome) (English)

1 reference

Europe PubMed Central

13 August 2017

pantothenate kinase-associated neurodegeneration

0 references

author name string

Robert A Egan

1

1 reference

Europe PubMed Central

13 August 2017

Richard G Weleber

2

1 reference

Europe PubMed Central

13 August 2017

Penelope Hogarth

3

1 reference

Europe PubMed Central

13 August 2017

Allison Gregory

4

1 reference

Europe PubMed Central

13 August 2017

Jason Coryell

5

1 reference

Europe PubMed Central

13 August 2017

Shawn K Westaway

6

1 reference

Europe PubMed Central

13 August 2017

Jane Gitschier

7

1 reference

Europe PubMed Central

13 August 2017

Soma Das

8

1 reference

Europe PubMed Central

13 August 2017

Susan J Hayflick

9

1 reference

Europe PubMed Central

13 August 2017

language of work or name

0 references

publication date

1 August 2005

1 reference

Europe PubMed Central

13 August 2017

American Journal of Ophthalmology

1 reference

Europe PubMed Central

13 August 2017

140

1 reference

Europe PubMed Central

13 August 2017

2

1 reference

Europe PubMed Central

13 August 2017

267-274

1 reference

Europe PubMed Central

13 August 2017

Clinical heterogeneity of neurodegeneration with brain iron accumulation (Hallervorden-Spatz syndrome) and pantothenate kinase-associated neurodegeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169522

30 September 2017

Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169522

30 September 2017

Iron in the Hallervorden-Spatz syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169522

30 September 2017

A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169522

30 September 2017

Hallervorden-Spatz Syndrome and Brain Iron Metabolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169522

30 September 2017

Ocular clinicopathologic correlation of Hallervorden-Spatz syndrome with acanthocytosis and pigmentary retinopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169522

29 June 2018

Clinicopathologic correlation and pathogenesis of ocular and central nervous system manifestations in Hallervorden-Spatz syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169522

29 June 2018

Pantothenate kinase-associated neurodegeneration: MR imaging, proton MR spectroscopy, and diffusion MR imaging findings.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169522

22 September 2018

How broad is the phenotype of Hallervorden-Spatz disease?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169522

22 September 2018

Early clinical and imaging (high-field MRI) diagnosis of Hallervorden-Spatz disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169522

22 September 2018

The frequency of posterior subcapsular cataract in the hereditary retinal degenerations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169522

22 September 2018

Alpha-synuclein accumulation in a case of neurodegeneration with brain iron accumulation type 1 (NBIA-1, formerly Hallervorden-Spatz syndrome) with widespread cortical and brainstem-type Lewy bodies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169522

21 October 2018

Standard for clinical electroretinography (1994 update)

1 reference

https://pubmed.ncbi.nlm.nih.gov/16023068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Optic atrophy as the first symptom in Hallervorden-Spatz syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16023068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The dystrophic retina in multisystem disorders: the electroretinogram in neuronal ceroid lipofuscinoses

1 reference

https://pubmed.ncbi.nlm.nih.gov/16023068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Posterior subcapsular cataract in Degos disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16023068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hallervorden-Spatz disease with bilateral involvement of globus pallidus and substantia nigra: MR demonstration

1 reference

https://pubmed.ncbi.nlm.nih.gov/16023068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[A case of Hallervorden-Spatz syndrome with marked atrophy of the brainstem and cerebellum]

1 reference

https://pubmed.ncbi.nlm.nih.gov/16023068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Telangiectasia and Optic Atrophy in Cone-Rod Degenerations

1 reference

https://pubmed.ncbi.nlm.nih.gov/16023068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The effect of age on human cone and rod ganzfeld electroretinograms

1 reference

https://pubmed.ncbi.nlm.nih.gov/16023068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk Factors for Genetic Typing and Detection in Retinitis Pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/16023068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hallervorden-Spatz syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16023068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.AJO.2005.03.024

1 reference

Europe PubMed Central

13 August 2017

1 reference

Europe PubMed Central

13 August 2017

1 reference

Europe PubMed Central

13 August 2017

ResearchGate publication ID

0 references

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