(Q44422105)

2 December 2017

title

Glucose-6-phosphate dehydrogenase deficiency in India. (English)

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glucose-6-phosphate dehydrogenase deficiency

2 December 2017

main subject

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Dipika Mohanty

1

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2 December 2017

Malay B Mukherjee

series ordinal

2

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2 December 2017

Roshan B Colah

series ordinal

3

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2 December 2017

publication date

1 June 2004

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Indian Journal of Pediatrics

2 December 2017

published in

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2 December 2017

volume

71

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2 December 2017

issue

6

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2 December 2017

page(s)

525-529

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https://scigraph.springernature.com/pub.10.1007/bf02724295

2 December 2017

exact match

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cites work

G6PD: population genetics and clinical manifestations

1 reference

https://api.crossref.org/works/10.1007%2FBF02724295

Acute renal failure due to intravascular hemolysis in the North Indian patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02724295

Ascorbic-acid-induced haemolysis in G-6-PD deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02724295

Oxidant injury of caucasian glucose-6-phosphate dehydrogenase—deficient red blood cells by phagocytosing leukocytes during infection

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02724295

The molecular biology of G6PD variants and other red cell enzyme defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02724295

Molecular cloning and nucleotide sequence of cDNA for human glucose-6-phosphate dehydrogenase variant A(-).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02724295

Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02724295

G6PD Canton a common deficient variant in South East Asia caused by a 459 Arg----Leu mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02724295

Molecular characterization of G6PD Insuli--a novel 989 CGC --> CAC (330 Arg --> His) mutation in the Indian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02724295

G6PD gene mutations in India producing drug-induced haemolytic anaemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02724295

A single mutation is responsible for the high prevalence of G6PD deficiency in the Vataliya Prajapatis--an endogamous caste group from Western India

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02724295

Three major G6PD-deficient polymorphic variants identified among the Mauritian population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02724295

Malaria in African children with deficient erythrocyte glucose-6-phosphate dehydrogenase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02724295

Adaptation of Plasmodium falciparum to glucose 6-phosphate dehydrogenase-deficient host red cells by production of parasite-encoded enzyme

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02724295

The adaptation of Plasmodium falciparum to oxidative stress in G6PD deficient human erythrocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02724295

G6PD deficiency and malaria in India

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02724295

A Rapid Screening Dye Test for the Detection of Glucose-6-Phosphate Dehydrogenase Deficiency in Red Cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02724295

Glucose-6-phosphate dehydrogenase deficiency in India and its clinical significance

21 January 2018

1 reference

12 December 2020

G6PD Kalyan and G6PD Kerala; two deficient variants in India caused by the same 317 Glu-->Lys mutation

1 reference

12 December 2020

Intravascular haemolysis and renal insufficiency in children with glucose-6-phosphate dehydrogenase deficiency, following antimalarial therapy

1 reference

12 December 2020

1 reference

12 December 2020

Glucose-6-phosphate dehydrogenase deficiency & neonatal hyperbilirubinaemia.

1 reference

12 December 2020

G6PD Nara: a new class 1 glucose-6-phosphate dehydrogenase variant with an eight amino acid deletion

1 reference

12 December 2020

ROLE OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN ACUTE HEMOLYTIC CRISIS AND NEONATAL JAUNDICE

1 reference

12 December 2020

Human glucose-6-phosphate dehydrogenase variants

1 reference

12 December 2020

The genetics of glucose-6-phosphate dehydrogenase deficiency.

1 reference

12 December 2020

Glucose-6-phosphate dehydrogenase isoenzyme pattern and evaluation of screening methods for G-6-PD deficiency in neonatal hyperbilirubinemia

1 reference

12 December 2020

Glucose-6-phosphate dehydrogenase deficiency--a genetic disorder of red cell metabolism

1 reference

12 December 2020

G-6-PD deficiency in newborns

1 reference

12 December 2020

Molecular study of eight Japanese cases of glucose-6-phosphate dehydrogenase deficiency by nonradioisotopic single-strand conformation polymorphism analysis

1 reference

12 December 2020

Glucose-6-phosphate dehydrogenase deficiency as a cause of drug-induced hemolysis with renal shut down and kernicterus

1 reference

12 December 2020

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

1 reference

12 December 2020

A new glucose-6-phosphate dehydrogenase variant, G6PD Orissa (44 Ala-->Gly), is the major polymorphic variant in tribal populations in India.

1 reference

12 December 2020

Incidence of glucose-6-phosphate dehydrogenase deficiency in jaundiced punjabi neonates

1 reference

12 December 2020

Glucose-6-phosphate dehydrogenase deficiency. WHO Working Group

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF02724295

1 reference

2 December 2017

1 reference