First report of co-morbidity of pantothenate kinase-associated neurodegeneration and three types of chronic hemolytic anemias. (Q36374574)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26740874%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

title

First report of co-morbidity of pantothenate kinase-associated neurodegeneration and three types of chronic hemolytic anemias (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26740874%20AND%20SRC:MED&resulttype=core&format=json

pantothenate kinase-associated neurodegeneration

4 March 2020

main subject

0 references

1 reference

1 reference

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4 March 2020

Iman M Talaat

1 reference

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4 March 2020

Ebtessam H K El Melegy

1 reference

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4 March 2020

Hamed A Alghamdi

1 reference

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4 March 2020

Mohammed F Aljabri

1 reference

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4 March 2020

Enas A A Abdallah

1 reference

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4 March 2020

Mohammed Sarar

1 reference

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4 March 2020

Mohamed A Alshahrani

1 reference

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4 March 2020

language of work or name

1 reference

10 November 2015

1 reference

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Annals of medicine and surgery (2012)

4 March 2020

published in

1 reference

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4 March 2020

volume

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4 March 2020

page(s)

11-13

1 reference

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Childhood disorders of neurodegeneration with brain iron accumulation (NBIA).

4 March 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4680082

Clinical and genetic delineation of neurodegeneration with brain iron accumulation

30 September 2017

1 reference

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Iron in chronic brain disorders: imaging and neurotherapeutic implications

30 September 2017

1 reference

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

30 September 2017

1 reference

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Frequency of glucose 6 phosphate dehydrogenase deficiency and related hemolytic anemia in Riyadh, Saudi Arabia.

30 September 2017

1 reference

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Rare causes of hereditary iron overload

30 September 2017

1 reference

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

30 September 2017

1 reference

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Marked regional variations in the prevalence of sickle cell disease and β-thalassemia in Saudi Arabia: findings from the premarital screening and genetic counseling program

30 September 2017

1 reference

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Hallervorden-Spatz disease.

21 September 2018

1 reference

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Neurological complications of sickle cell anemia in Nigerian Africans--a case-control study.

21 September 2018

1 reference

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Thalassemia syndromes in Saudi Arabia. Meta-analysis of local studies

21 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26740874

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.AMSU.2015.10.015

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26740874%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

1 reference

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4 March 2020

PubMed publication ID

26740874

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26740874%20AND%20SRC:MED&resulttype=core&format=json