(Q48507793)

English

Pantothenate kinase 2 mutation with classic pantothenate-kinase-associated neurodegeneration without 'eye-of-the-tiger' sign on MRI in a pair of siblings

scientific article published on 7 June 2006

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16758184

Pantothenate kinase 2 mutation with classic pantothenate-kinase-associated neurodegeneration without 'eye-of-the-tiger' sign on MRI in a pair of siblings (English)

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16758184

pantothenate kinase-associated neurodegeneration

0 references

1 reference

based on heuristic

inferred from title

neurodegeneration

1 reference

based on heuristic

inferred from title

author name string

Zarazuela Zolkipli

1

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16758184

Hisham Dahmoush

2

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16758184

Dawn E Saunders

3

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16758184

W K Kling Chong

4

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16758184

Robert Surtees

5

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16758184

publication date

7 June 2006

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16758184

Pediatric Radiology

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16758184

36

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16758184

8

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16758184

884-886

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16758184

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

1 reference

https://api.crossref.org/works/10.1007%2FS00247-006-0205-3

21 January 2018

Hallervorden-Spatz disease: MR and pathologic findings.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16758184

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16758184

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16758184

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hallervorden-Spatz syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16758184

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16758184

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p12.3-p13

1 reference

https://pubmed.ncbi.nlm.nih.gov/16758184

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The nosology of Hallervorden-spatz disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16758184

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16758184

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16758184

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00247-006-0205-3

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16758184

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/16758184

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