Clinical and genetic delineation of neurodegeneration with brain iron accumulation (Q28315639)

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scientific article (publication date: February 2009)

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English	Clinical and genetic delineation of neurodegeneration with brain iron accumulation	scientific article (publication date: February 2009)

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title

Clinical and genetic delineation of neurodegeneration with brain iron accumulation (English)

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main subject

brain

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neurodegeneration with brain iron accumulation

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iron

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neurodegeneration

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based on heuristic

inferred from title

author name string

A Gregory

series ordinal

1

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B J Polster

series ordinal

2

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S J Hayflick

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3

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language of work or name

English

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publication date

February 2009

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published in

Journal of Medical Genetics

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volume

46

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issue

2

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page(s)

73-80

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cites work

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Mitochondrial localization of human PANK2 and hypotheses of secondary iron accumulation in pantothenate kinase-associated neurodegeneration

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Iron in the Hallervorden-Spatz syndrome

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Widespread expression of alpha-synuclein and tau immunoreactivity in Hallervorden-Spatz syndrome with protracted clinical course

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Neurodegeneration with brain iron accumulation, type 1 is characterized by alpha-, beta-, and gamma-synuclein neuropathology

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Hallervorden-Spatz Syndrome and Brain Iron Metabolism

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Acanthocytosis, retinitis pigmentosa, pallidal degeneration. Report of two cases without serum lipid abnormalities

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

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A study of iron metabolism in neuropsychiatric patients. Hallervorden-Spatz disease.

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2 June 2018

[Infantile neuro-axonal dystrophy and Hallervorden-Spatz disease. Electro-clinical and anatomo-pathological and differential diagnostic aspects]

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2 June 2018

Diagnostic difficulties in infantile neuroaxonal dystrophy. A clinicopathological study of eight cases

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2 June 2018

MR imaging of a group I case of Hallervorden-Spatz disease.

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2 June 2018

Hallervorden-Spatz disease in a psychiatric setting.

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2 June 2018

Follow-up MR studies in Hallervorden-Spatz disease

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2 June 2018

Racial hygiene, active euthanasia, and Julius Hallervorden

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Genotypic and phenotypic spectrum of PANK2 mutations in patients with neurodegeneration with brain iron accumulation

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27 November 2018

The eye-of-the-tiger sign is not a reliable disease marker for Hallervorden-Spatz syndrome

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27 November 2018

Pallidal stimulation improves pantothenate kinase-associated neurodegeneration

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27 November 2018

Cranial MRI changes may precede symptoms in Hallervorden-Spatz syndrome

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27 November 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

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27 November 2018

Infantile neuroaxonal dystrophy: neuroradiological studies in 11 patients.

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27 November 2018

Infantile neuroaxonal dystrophy: clinical spectrum and diagnostic criteria

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27 November 2018

Lewy body in neurodegeneration with brain iron accumulation type 1 is immunoreactive for alpha-synuclein

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27 November 2018

The use of magnetic resonance imaging in diagnosing infantile neuroaxonal dystrophy

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27 November 2018

Neuroaxonal dystrophy combined with diffuse Lewy body disease in a young adult.

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27 November 2018

Hallervordern Spatz disease and acanthocytes

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12 December 2020

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Alpha-synuclein immunoreactivity is present in axonal swellings in neuroaxonal dystrophy and acute traumatic brain injury

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12 December 2020

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Infantile neuroaxonal dystrophy. Early form with preferential cerebellar involvement

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18981035

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12 December 2020

based on heuristic

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Hallervorden-Spatz syndrome

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18981035

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pigmentary Degeneration of the Retina in the Hallervorden-Spatz Syndrome

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18981035

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile neuroaxonal dystrophy

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18981035

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early cerebellar degeneration in twins with infantile neuroaxonal dystrophy

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18981035

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12 December 2020

based on heuristic

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MRI in infantile neuroaxonal dystrophy

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18981035

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12 December 2020

based on heuristic

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MRI as an aid for diagnosis of infantile neuroaxonal dystrophy

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18981035

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transsynaptic degeneration of lateral geniculate bodies in blind children: in vivo MR demonstration

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18981035

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cellular responses to excess phospholipid

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18981035

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12 December 2020

based on heuristic

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Metabolism of glycerolipids. 2. The enzymatic acylation of lysolecithin

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18981035

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12 December 2020

based on heuristic

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Identifiers

DOI

10.1136/JMG.2008.061929

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1499962

OpenCitations bibliographic resource ID

1499962

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1499962

PMC publication ID

2675558

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1499962

PubMed publication ID

18981035

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1499962

ResearchGate publication ID

23448408

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