Hematological and Clinical Features of Sickle Cell Diseases: a Review (Q40098666)

17 September 2017

1 reference

title

Hematological and clinical features of sickle cell diseases: a review (English)

1 reference

17 September 2017

Hematological and Clinical Features of Sickle Cell Diseases: a Review (English)

1 reference

https://api.crossref.org/works/10.3109/03630268008996214

17 August 2023

author name string

D. R. Harkness

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6158496

17 August 2023

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=6158496

17 August 2023

publication date

1 January 1980

1 reference

full work available at URL

17 September 2017

http://www.tandfonline.com/doi/pdf/10.3109/03630268008996214

1 reference

https://api.crossref.org/works/10.3109/03630268008996214

17 August 2023

1 reference

17 September 2017

volume

4

1 reference

17 September 2017

issue

3-4

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17 September 2017

page(s)

313-334

1 reference

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

17 September 2017

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The Clinical Features of Sickle-Cell/β Thalassaemia in Jamaica

21 January 2018

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21 January 2018

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

21 January 2018

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Relatively benign sickle-cell anaemia in 60 patients aged over 30 in the West Indies

21 January 2018

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Mild sickle cell disease. Clinical and laboratory studies

21 January 2018

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

21 January 2018

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

21 January 2018

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Conformational requirements for the polymerization of hemoglobin S: Studies of mixed liganded hybrids

21 January 2018

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

21 January 2018

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Sickle cell anemia as a syndrome: A review of diagnostic features

21 January 2018

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

21 January 2018

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Alpha-thalassemia in Negro infants

21 January 2018

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Trimodality in the percentages of beta chain variants in heterozygotes: the effect of the number of active Hbalpha structural loci

21 January 2018

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

21 January 2018

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Hemoglobin Bart's levels in umbilical cord blood: failure as a method for distinguishing mild from severe alpha-thalassemia trait in the Chinese

21 January 2018

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Possible relationship between the level of Hb Bart's (gamma4) and the relative amount of Hb S or Hb C in black heterozygous newborn

21 January 2018

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Hemoglobin synthesis studies of a family with ?-thalassemia trait and sickle cell trait

21 January 2018

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Unbalanced globin chain synthesis in reticulocytes of sickle cell trait individuals with low concentrations of hemoglobin S

21 January 2018

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Modification of Hemoglobin H Disease by Sickle Trait

21 January 2018

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Hemoglobin O Arab in Four Negro Families and Its Interaction with Hemoglobin S and Hemoglobin C

21 January 2018

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A third case of hemoglobin Memphis-sickle cell disease. Whole blood viscosity used as a screening test

21 January 2018

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Alpha Thalassaemia in Adults with Sickle-Cell Trait

21 January 2018

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Interaction of heterocellular hereditary persistence of foetal haemoglobin with β thalassaemia and sickle cell anaemia

21 January 2018

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Gene deletion as the cause of α thalassaemia: Genetic lesion in homozygous α thalassaemia (hydrops fetalis)

21 January 2018

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Deletion of alpha-globin genes in haemoglobin-H disease demonstrates multiple alpha-globin structural loci

21 January 2018

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The development of haemoglobin A2 in normal negro infants and in sickle cell disease

21 January 2018

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A comparison of erythrocyte characteristics in sickle cell syndromes in Jamaica

17 August 2023

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

17 August 2023

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Determinants of Haemoglobin Level in Sickle Cell-Haemoglobin C Disease

17 August 2023

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Ocular findings in homozygous sickle cell anemia in Jamaica

17 August 2023

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Ocular findings in hemoglobin SC disease in Jamaica

17 August 2023

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Homozygous sickle cell disease in Jamaica

17 August 2023

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Haemoglobin SC disease in Jamaica

17 August 2023

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Milder variant of sickle-cell disease in Arabs in Kuwait associated with unusually high level of foetal haemoglobin

17 August 2023

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Benign sickle-cell anaemia

17 August 2023

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Mild sickle-cell anaemia in Iran associated with high levels of fetal haemoglobin

17 August 2023

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Sickle cell anemia and trait in southern India: further studies

17 August 2023

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17 August 2023

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Benign sickle cell disease in Saudi Arabia: survival estimate and population dynamics

17 August 2023

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

17 August 2023

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Abnormal haemoglobins in the neonatal period and their relationship to thalassaemia

17 August 2023

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The severe form of alpha thalassaemia is caused by a haemoglobin gene deletion

17 August 2023

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Differences in Affinity of Variant β Chains for a Chains: A Possible Explanation for the Variation in the Percentages of β Chain Variants in Heterozygotes

17 August 2023

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Competition of normal beta chains and sickle haemoglobin beta chains for alpha chains as a post-translational control mechanism

17 August 2023

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

17 August 2023

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Benign Obstetric History in Women with Sickle-cell Anaemia Associated with -Thalassaemia

17 August 2023

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

17 August 2023

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

17 August 2023

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Sickle cellhemoglobin D disease

17 August 2023

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Haemoglobin D Punjab in a Cuban family and its interaction with haemoglobin S

17 August 2023

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Hemoglobin S-G (S-D) syndrome

17 August 2023

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Sickle-cell haemoglobin O disease in a Sudanese family

17 August 2023

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17 August 2023

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Characterization of α23GluNH2 in Hemoglobin Memphis. Hemoglobin Memphis/S, a New Variant of Molecular Disease*

17 August 2023

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17 August 2023

Identifiers

1 reference

17 September 2017

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