Abnormal haemoglobins: detection &amp; characterization. (Q37956961)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22089618%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

review article

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title

Abnormal haemoglobins: detection & characterization (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22089618%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

3 references

22 April 2019

27 November 2019

14 December 2019

3 references

22 April 2019

27 November 2019

14 December 2019

1 reference

27 November 2019

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14 December 2019

Henri Wajcman

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22089618%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Kamran Moradkhani

series ordinal

2

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16 January 2020

language of work or name

English

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publication date

1 October 2011

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22 April 2019

27 November 2019

14 December 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22089618%20AND%20SRC:MED&resulttype=core&format=json

Indian Journal of Medical Research

16 January 2020

published in

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22 April 2019

27 November 2019

14 December 2019

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16 January 2020

volume

134

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16 January 2020

page(s)

538-546

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Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported

16 January 2020

copyright license

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22 April 2019

27 November 2019

on focus list of Wikimedia project

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copyright status

copyrighted

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ScienceSource

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cites work

Molecular basis and hematological features of hemoglobin variants in Southern Thailand

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

A brief review on newborn screening methods for hemoglobinopathies and preliminary results selecting beta thalassemia carriers at birth by quantitative estimation of the HbA fraction

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

The significance of the hemoglobin A(2) value in screening for hemoglobinopathies

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

Globin chain analysis: an important tool in phenotype study of hemoglobin disorders

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

Genetic modifiers in hemoglobinopathies

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

Unstable and thalassemic alpha chain hemoglobin variants: a cause of Hb H disease and thalassemia intermedia

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

6 September 2017

Hemoglobin e syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

An overview of current microarray-based human globin gene mutation detection methods

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

Sickle cell anemia, a molecular disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

Screening and genetic diagnosis of haemoglobin disorders

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

Inherited haemoglobin disorders: an increasing global health problem

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

Abnormal hemoglobins: laboratory methods

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

Evidence for the multicentric origin of the sickle cell hemoglobin gene in Africa

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

Hemoglobin S Antilles: a variant with lower solubility than hemoglobin S and producing sickle cell disease in heterozygotes

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

Global epidemiology of hemoglobin disorders

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

Haemoglobin Constant Spring--a chain termination mutant?

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

Hb S-San Martin: a new sickling hemoglobin with two amino acid substitutions [β6(A3)Glu→Val;β105(G7)Leu→Pro] in an Argentinean family

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

Evaluation of an automated capillary electrophoresis system in the screening for hemoglobinopathies.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

Evaluating five dedicated automatic devices for haemoglobinopathy diagnostics in multi-ethnic populations

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

Frequency of alpha-globin gene triplications and their interaction with beta-thalassemia mutations.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

Effectiveness of red cell osmotic fragility test with varying degrees of saline concentration in detecting beta-thalassaemia trait.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

Evaluation of a new Sebia kit for analysis of hemoglobin fractions and variants on the Capillarys system.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

Evaluation of the Bio-Rad VARIANT II HbA2/HbA1C Dual Program for measurement of hemoglobin concentrations and detection of variants.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

DNA diagnosis of hemoglobin mutations.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

Electrophoretic methods for study of hemoglobins

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

Determination of Hb F levels: the routine methods.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

Sickle cell disease among tribes of Andhra Pradesh and Orissa, India

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3237254

NESTROFF as a screening test for detection of Beta-thalassemia trait

5 November 2018

1 reference

12 December 2020

Hemoglobin mobility in citrate agar electrophoresis - its relationship to anion binding

1 reference

12 December 2020

HPLC retention time as a diagnostic tool for hemoglobin variants and hemoglobinopathies: a study of 60000 samples in a clinical diagnostic laboratory

1 reference

12 December 2020

Rapid identification of HBB gene mutations by high-resolution melting analysis

1 reference

12 December 2020

Red blood cell indices, cation content, and membrane cation transports

1 reference

12 December 2020

Newborn screening for hemoglobinopathies using capillary electrophoresis technology: Testing the Capillarys Neonat Fast Hb device

1 reference

12 December 2020

DETERMINATION OF DENSITY DISTRIBUTION OF RED CELL POPULATION

1 reference

12 December 2020

Use of combined mass spectrometry methods for the characterization of a new variant of human hemoglobin: The double mutant hemoglobin villeparisis β77(EF1) His → Tyr, β 80 (EF4) Asn → Ser

1 reference

12 December 2020

Idiopathic Heinz body anaemia: Hb-Bristol (beta67 (E11) Val to Asp)

1 reference

12 December 2020

HbS-oman heterozygote: a new dominant sickle syndrome

1 reference

12 December 2020

Strategy linking several analytical methods of neonatal screening for sickle cell disease

1 reference

12 December 2020

Interaction of Human Hemoglobin and Its Variants with Agar

1 reference

12 December 2020

New results of hemoglobin variant structure determinations by fast atom bombardment mass spectrometry

1 reference

12 December 2020

Genotype-phenotype relationship of the δ-thalassemia and Hb A(2) variants: observation of 52 genotypes

1 reference

12 December 2020

Implementing neonatal screening for haemoglobinopathies in the Netherlands

1 reference

12 December 2020

Cation-exchange HPLC evaluated for presumptive identification of hemoglobin variants

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22089618%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

1 reference