Hb F Synthesis in Sickle Cell Anaemia: a Comparison of Saudi Arab Cases with those of African Origin (Q46222871)

20 December 2017

title

Hb F Synthesis in Sickle Cell Anaemia: a Comparison of Saudi Arab Cases with those of African Origin (English)

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1980.TB07163.X

17 August 2023

0 references

Graham Roger Serjeant

3

object named as

G. R. Serjeant

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17 August 2023

author name string

W. G. Wood

1

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17 August 2023

M. E. Pembrey

2

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17 August 2023

R. P. Perrine

4

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17 August 2023

D. J. Weatherall

5

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17 August 2023

language of work or name

English

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publication date

1 July 1980

1 reference

20 December 2017

full work available at URL

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1365-2141.1980.tb07163.x

1 reference

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http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1980.tb07163.x/fullpdf

17 August 2023

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https://api.crossref.org/works/10.1111/J.1365-2141.1980.TB07163.X

British Journal of Haematology

17 August 2023

published in

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20 December 2017

volume

45

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20 December 2017

issue

3

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20 December 2017

page(s)

431-445

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20 December 2017

Irreversibly sickled erythrocytes: a consequence of the heterogeneous distribution of hemoglobin types in sickle-cell anemia

cites work

1 reference

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Hemoglobin Interaction: Modification of Solid Phase Composition in the Sickling Phenomenon

21 January 2018

1 reference

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Participation of haemoglobins A, F, A2 and C in polymerisation of haemoglobin S

21 January 2018

1 reference

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alpha-Globin gene organisation in blacks precludes the severe form of alpha-thalassaemia

21 January 2018

1 reference

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Negro alpha-thalassaemia is caused by deletion of a single alpha-globin gene

21 January 2018

1 reference

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Cellular regulation of hemoglobin switching: evidence for inverse relationship between fetal hemoglobin synthesis and degree of maturity of human erythroid cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.1980.TB07163.X

Reliable routine estimation of small amounts of foetal haemoglobin by alkali denaturation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.1980.TB07163.X

Natural history of sickle cell anemia in Saudi Arabs. A study of 270 subjects

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.1980.TB07163.X

On the levels of hemoglobins F and A2 in sickle-cell anemia and some related disorders

21 January 2018

1 reference

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Estimation of Small Percentages of Fœtal Hæmoglobin

21 January 2018

1 reference

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Annals of Internal Medicine

21 January 2018

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Bickers J.N.

1974

1 reference

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Globin synthesis in normal human bone marrow

17 August 2023

6

1 reference

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Abnormal human haemoglobins. Separation and characterization of the alpha and beta chains by chromatography, and the determination of two new variants, hb Chesapeak and hb J (Bangkok)

17 August 2023

8

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1980.TB07163.X

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

17 August 2023

10

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1980.TB07163.X

Production of erythrocytes that contain fetal hemoglobin in anemia. Transient in vivo changes

17 August 2023

11

1 reference

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Studies on the heterogeneity of hemoglobin. XIV. Chromatography of normal and abnormal human hemoglobin types on CM-Sephadex

17 August 2023

12

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1980.TB07163.X

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

17 August 2023

14

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1980.TB07163.X

Erythropoiesis in Sickle Cell Anaemia during Acute Infection and Crisis

17 August 2023

15

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1980.TB07163.X

Amelioration of sickle cell disease by persistent fetal hemoglobin

17 August 2023

17

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1980.TB07163.X

Semiquantitative computerized image analysis of fetal hemoglobin distribution patterns in sickle cell anemia and its variants

17 August 2023

20

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1980.TB07163.X

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

17 August 2023

21

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1980.TB07163.X

Fluctuation of fetal hemoglobin in sickle-cell anemia

17 August 2023

22

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https://api.crossref.org/works/10.1111/J.1365-2141.1980.TB07163.X

Haemoglobin Bart's in Saudi Arabia

17 August 2023

25

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1980.TB07163.X

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

17 August 2023

26

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1980.TB07163.X

Benign sickle-cell anaemia

17 August 2023

27

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1980.TB07163.X

Heterocellular hereditary persistence of fetal haemoglobin and homozygous sickle-cell disease

17 August 2023

31

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1980.TB07163.X

The pattern of disordered haemoglobin synthesis in homozygous and heterozygous beta-thalassaemia

17 August 2023

36

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1980.TB07163.X

Heterocellular hereditary persistence of fetal haemoglobin (heterocellular HPFH) and its interaction with beta thalassaemia

17 August 2023

37

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1980.TB07163.X

17 August 2023

Identifiers

1 reference

20 December 2017

1 reference

20 December 2017