(Q34764846)

4 August 2017

title

Characterization of G6PD genotypes and phenotypes on the northwestern Thailand-Myanmar border (English)

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4 August 2017

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5

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4 August 2017

Germana Bancone

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Cindy Chu

object named as

Cindy S Chu

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Nicholas John White

7

object named as

Nicholas J White

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4 August 2017

8

François H Nosten

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4 August 2017

4

Nongnud Chowwiwat

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Raweewan Somsakchaicharoen

4 August 2017

3

object named as

Raweewan Somsakchaicharoen

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4 August 2017

author name string

Prakaykaew Charunwatthana

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4 August 2017

language of work or name

English

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publication date

23 December 2014

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4 August 2017

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4 August 2017

volume

9

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4 August 2017

issue

12

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4 August 2017

page(s)

e116063

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Creative Commons Attribution 4.0 International

4 August 2017

copyright license

start time

23 December 2014

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

A population survey of the glucose-6-phosphate dehydrogenase (G6PD) 563C>T (Mediterranean) mutation in Afghanistan

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4275285

Spatial distribution of G6PD deficiency variants across malaria-endemic regions

7 July 2018

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Malaria burden and artemisinin resistance in the mobile and migrant population on the Thai-Myanmar border, 1999-2011: an observational study

7 July 2018

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G6PD deficiency prevalence and estimates of affected populations in malaria endemic countries: a geostatistical model-based map

7 July 2018

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Prevalence and distribution of glucose-6-phosphate dehydrogenase (G6PD) variants in Thai and Burmese populations in malaria endemic areas of Thailand

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4275285

Performance of the CareStart™ G6PD deficiency screening test, a point-of-care diagnostic for primaquine therapy screening

7 July 2018

1 reference

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Glucose-6-phosphate dehydrogenase (G6PD) mutations and haemoglobinuria syndrome in the Vietnamese population

7 July 2018

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Effective and cheap removal of leukocytes and platelets from Plasmodium vivax infected blood

7 July 2018

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Allelic heterogeneity of G6PD deficiency in West Africa and severe malaria susceptibility

7 July 2018

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Glucose-6-phosphate dehydrogenase deficiency

7 July 2018

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Mutations and haplotype diversity in 70 Portuguese G6PD-deficient individuals: an overview on the origin and evolution of mutated alleles

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4275285

Glucose-6-phosphate dehydrogenase mutations in Mon and Burmese of southern Myanmar.

7 July 2018

1 reference

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Seven different glucose-6-phosphate dehydrogenase variants including a new variant distributed in Lam Dong Province in southern Vietnam

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4275285

Distribution of glucose-6-phosphate dehydrogenase mutations in Southeast Asia

7 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4275285

A glucose-6-phosphate dehydrogenase (G6PD) splice site consensus sequence mutation associated with G6PD enzyme deficiency

7 July 2018

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Human enzyme polymorphism in the Canary Islands. VII. G6PD Seattle in Canarians and North African Berbers

7 July 2018

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Glucose-6-phosphate dehydrogenase deficiency in Italy. A study of the distribution and severity of the enzymatic defect

7 July 2018

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G6PD mahidol, a common deficient variant in South East Asia is caused by a (163)glycine----serine mutation.

7 July 2018

1 reference

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The NT 1311 polymorphism of G6PD: G6PD Mediterranean mutation may have originated independently in Europe and Asia.

7 July 2018

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International Committee for Standardization in Haematology: recommended methods for red-cell enzyme analysis.

7 July 2018

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Glucose-6-phosphate dehydrogenase (G6PD) mutations in Cambodia: G6PD Viangchan (871G>A) is the most common variant in the Cambodian population

7 July 2018

1 reference

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Glucose-6-phosphate dehydrogenase (G6PD) mutations in Thailand: G6PD Viangchan (871G>A) is the most common deficiency variant in the Thai population

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0116063

Molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) variants in the south of Thailand and identification of a novel variant (G6PD Songklanagarind).

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0116063

Glucose-6-phosphate dehydrogenase (G6PD) mutations in Myanmar: G6PD Mahidol (487G>A) is the most common variant in the Myanmar population

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0116063

Purification and detailed study of two clinically different human glucose 6-phosphate dehydrogenase variants, G6PD(Plymouth) and G6PD(Mahidol): Evidence for defective protein folding as the basis of disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0116063

Quantitative neonatal glucose-6-phosphate dehydrogenase screening: distribution, reference values, and classification by phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0116063

G6PD deficiency assessment in Freetown, Sierra Leone, reveals further insight into the molecular heterogeneity of G6PD A-.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0116063

Evaluating assay precision.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4275285

The role of the G6PD AEth376G/968C allele in glucose-6-phosphate dehydrogenase deficiency in the seerer population of Senegal.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4275285

Molecular characterisation of the glucose-6-phosphate dehydrogenase (G6PD) Ferrara II variant

26 October 2018

1 reference

12 December 2020

Molecular Heterogeneity of the Glucose-6-Phosphate Dehydrogenase Deficiency in the Hellenic Population

1 reference

12 December 2020

Incidence and complete molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Guangxi Zhuang autonomous region of southern China: description of four novel mutations

1 reference

12 December 2020

Special modifications of the fluorescent screening method for glucose-6-phosphate dehydrogenase deficiency

1 reference

12 December 2020

Neonatal jaundice and molecular mutations in glucose-6-phosphate dehydrogenase deficient newborn infants

1 reference

12 December 2020

G-6-PD Mahidol. The most common glucose-6-phosphate dehydrogenase variant in Thailand

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0116063

Identifiers

DOI

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4 August 2017

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4 August 2017

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