The Interaction of Alpha-Thalassemia and Homozygous Sickle-Cell Disease (Q72666088)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6176865%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

title

The interaction of alpha-thalassemia and homozygous sickle-cell disease (English)

1 reference

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28 October 2019

The Interaction of Alpha-Thalassemia and Homozygous Sickle-Cell Disease (English)

1 reference

https://api.crossref.org/works/10.1056/NEJM198206173062402

21 August 2023

1 reference

1 reference

6

R. J. Hayes

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21 August 2023

Graham Roger Serjeant

11

object named as

G. R. Serjeant

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10

B. E. Serjeant

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21 August 2023

author name string

D. R. Higgs

1

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B. E. Aldridge

2

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21 August 2023

J. Lamb

3

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J. B. Clegg

4

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D. J. Weatherall

5

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Y. Grandison

7

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Y. Lowrie

8

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K. P. Mason

9

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language of work or name

English

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publication date

1 June 1982

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28 October 2019

17 June 1982

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=6176865

full work available at URL

21 August 2023

http://www.nejm.org/doi/pdf/10.1056/NEJM198206173062402

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The New England Journal of Medicine

21 August 2023

published in

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28 October 2019

volume

306

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28 October 2019

issue

24

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28 October 2019

page(s)

1441-1446

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A New Sickling Disorder Resulting from Interaction of the Genes for Haemoglobin S and α-Thalassaemia

28 October 2019

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Sickle cell syndromes. II. The sickle cell anemia-alpha-thalassemia syndrome

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The association of sickle cell anemia with heterozygous and homozygous alpha-thalassemia-2: in vitro HB chain synthesis

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Lack of influence of fetal hemoglobin levels or erythrocyte indices on the severity of sickle cell anemia

21 August 2023

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Alpha-Thalassemia-2 and the Variability of Hematological Values in Children with Sickle Cell Anemia

21 August 2023

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Concurrent sickle-cell anemia and alpha-thalassemia: effect on severity of anemia

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The genetics and molecular basis of alpha thalassaemia in association with Hb S in Jamaican Negroes

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The Irreversibly Sickled Cell; a Determinant of Haemolysis in Sickle Cell Anaemia

21 August 2023

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Factors affecting the rate of coupling of bilirubin and conjugated bilirubin in the van de Bergh reaction

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Comparison of haematological features of the beta0 and beta+ thalassaemia traits in Jamaican Negroes

21 August 2023

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Estimation of Small Percentages of Fœtal Hæmoglobin

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Clinical longitudinal standards for height, weight, height velocity, weight velocity, and stages of puberty

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The genetic basis of Hb Q-H disease

21 August 2023

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Erythrocyte Hb-S concentration. An important factor in the low oxygen affinity of blood in sickle cell anemia

21 August 2023

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The Concentration Dependence of the Oxygen Affinity of Haemoglobin S

21 August 2023

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Individual Variation in the Production and Survival of F Cells in Sickle-Cell Disease

21 August 2023

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Fetal haemoglobin production and the sickle gene in the oases of Eastern Saudi Arabia

21 August 2023

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Comparison of Sickle Cell-β° Thalassaemia with Homozygous Sickle Cell Disease

21 August 2023

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Haematological factors associated with proliferative retinopathy in homozygous sickle cell disease

21 August 2023

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Haematological factors associated with avascular necrosis of the femoral head in homozygous sickle cell disease

21 August 2023

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21 August 2023

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6176865%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

1 reference