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

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About: Milder variant of sickle-cell disease in Arabs in Kuwait associated with unusually high level of foetal haemoglobin Goto Sponge NotDistinct Permalink

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scientific article published on 01 November 1970

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в листопаді 1970 (uk) im November 1970 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 01 November 1970 (en) artículu científicu espublizáu en payares de 1970 (ast)
publication date	wds:Q71597915-2EEA40F2-A307-42CB-8CEB-1A0FEE2E4689
publication date	1970-11-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q71597915-CC29CAF0-36AE-4B90-8576-D4D2664F60CC
language of work or name	English
cites work	wds:Q71597915-4DF73B2E-D36D-4827-90EC-BD468BF8B121
cites work	Sickle cell anemia, a molecular disease
author name string	wds:Q71597915-2D12ECC3-28ED-47AC-AC7A-8C19406EB63A
author name string	S A Ali
rdfs:label	Milder variant of sickle-cell disease in Arabs in Kuwait associated with unusually high level of foetal haemoglobin (en) Milder variant of sickle-cell disease in Arabs in Kuwait associated with unusually high level of foetal haemoglobin (nl)
skos:prefLabel	Milder variant of sickle-cell disease in Arabs in Kuwait associated with unusually high level of foetal haemoglobin (en) Milder variant of sickle-cell disease in Arabs in Kuwait associated with unusually high level of foetal haemoglobin (nl)
name	Milder variant of sickle-cell disease in Arabs in Kuwait associated with unusually high level of foetal haemoglobin (en) Milder variant of sickle-cell disease in Arabs in Kuwait associated with unusually high level of foetal haemoglobin (nl)
title	wds:Q71597915-A80B734E-AECE-4028-811D-DAB93A11B0E3
title	Milder variant of sickle-cell disease in Arabs in Kuwait associated with unusually high level of foetal haemoglobin (en)
page(s)	wds:Q71597915-BCE05DE2-C4C2-466F-A08D-A14178F39CE9
page(s)	613-619
instance of	wds:Q71597915-5A81BE3B-7EA1-4648-89C6-C4ECCA5E7087
instance of	scholarly article
main subject	wds:Q71597915-BCB4BAC0-C543-4E1F-A452-4B608D62149D
main subject	sickle-cell disease
PubMed ID	wds:Q71597915-6E0D54BF-6F7F-4EC0-A33E-71963CD9FD90
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/5481506
PubMed ID	5481506
published in	wds:Q71597915-0769F893-DC59-4935-9798-5013E2D808D7
published in	British Journal of Haematology
issue	wds:Q71597915-9001FE99-72E5-49A1-86C6-3E1AC9D24F08
volume	wds:Q71597915-A3496A6F-FE30-444F-90D9-6CD7CB5AB2D3
issue	5
volume	19
DOI	wds:Q71597915-3AAFA72D-A8D4-4082-B4CE-EDE54D2CE5D3
DOI	http://dx.doi.org/10.1111/J.1365-2141.1970.TB01645.X
DOI	10.1111/J.1365-2141.1970.TB01645.X
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q71597915
is cites work of	Sickle cell disease in Africa: burden and research priorities Neither DNA hypomethylation nor changes in the kinetics of erythroid differentiation explain 5-azacytidine's ability to induce human fetal hemoglobin Geographical survey of beta S-globin gene haplotypes: evidence for an independent Asian origin of the sickle-cell mutation. Sickle cell anemia as a syndrome: A review of diagnostic features Benign sickle-cell anaemia Binding of HMG-I(Y) elicits structural changes in a silencer of the human beta-globin gene Cholelithiasis in sickle cell anemia in a caucasian population Mild sickle-cell anaemia in Iran associated with high levels of fetal haemoglobin Sickle cell disease in Middle East Arab countries Comparison of renal function markers in Kuwaiti patients with sickle cell disease Sickle cell syndromes. II. The sickle cell anemia-alpha-thalassemia syndrome Sequence of the -530 region of the beta-globin gene of sickle cell anemia patients with the Arabian haplotype Sickle Cell Disease in Africa and the Arabian Peninsula: Current Management and Challenges Lack of influence of fetal hemoglobin levels or erythrocyte indices on the severity of sickle cell anemia Normal and Abnormal Human Hemoglobins Benign sickle cell disease in Saudi Arabia: survival estimate and population dynamics Heterogeneity of sickle-cell anemia based on a profile of hematological variables Evaluation of haematological findings in 50 Bahraini patients with sickle cell disease and in some of their parents On the nature of sickle-cell disease in the Arabian Peninsula Chemical heterogeneity of fetal hemoglobin in subjects with sickle cell anemia, homozygous hb-c disease, sc-disease, and various combinations of hemoglobin variants Hydroxyurea promotes the reduction of spontaneous BFU-e to normal levels in SS and S/beta thalassemic patients Clinico-Haematological Profile of Hereditary Haemolytic Anaemias in a Tertiary Health Care Hospital in South India Amelioration of clinical severity through raised fetal hemoglobin in sickle cell anaemia Five-year follow-up of Jamaican adults with sickle cell anaemia Hematological and Clinical Features of Sickle Cell Diseases: a Review Stability over time of hematological variables in 197 children with sickle cell anemia Hb F levels, longevity of homozygotes and clinical course of sickle cell anemia in Brazil Recent developments in foetal haemoglobin research Ocular manifestations of sickle cell anaemia in Arab children Pregnancy in sickle-cell anemia in a Caucasian group Natural Remedies for the Treatment of Beta-Thalassemia and Sickle Cell Anemia-Current Status and Perspectives in Fetal Hemoglobin Reactivation. Increased fetal hemoglobin production in a child with congenital hyperinsulinism
is cites work of	wds:Q33587548-E75AF86A-423A-4379-80A6-BC53E2E3DF78 wds:Q36384665-DE12AB32-1347-429B-8B22-C6CAA0227AD3 wds:Q38329569-6134FE77-2E8C-4D08-BD8E-A4FA9CBA9487 wds:Q57321346-3B85B87F-3884-42B4-A130-028DF92F6001 wds:Q24615860-426108BE-FB2A-4C13-9064-3772311832CB wds:Q39956507-251DF506-4D4D-4D9D-9F3C-A9DE2BF70E7C wds:Q41176950-2E468EBF-EFD3-485A-AC28-C3CB8841D42E wds:Q66931599-5D26FD99-3C40-42E1-852C-B290A6A079D2 wds:Q72744716-969D1C76-D38D-4F88-974F-7660B8E74C44 wds:Q41550380-39071E48-4BF1-4685-9483-7D7D220E20BA wds:Q43573425-D768C9D5-2E8C-41FD-8AD2-33E2958A4A00 wds:Q67538173-CDA3E463-3E3D-40D7-AB5E-6A5313AA5302 wds:Q72697060-90A7F3A0-8F60-4005-BE48-C10615BF07AC wds:Q72494110-52F4C3A0-8590-4953-8AA3-CCC485364C0E wds:Q34056437-2F65755E-2E31-4403-A134-73AB97E73987 wds:Q35769975-65DD74A3-C111-437D-AB14-1C19642EE983 wds:Q46818940-F105F534-B74A-4723-B531-F77912B1F65A wds:Q40591317-E6873A70-08B9-4979-9593-BFB3D017220E wds:Q46331998-7C48247C-3EC5-4303-BA6A-FCF5697E10FA wds:Q67296649-B61AFE59-58FC-4AF1-9E73-460BC2024FDA wds:Q33672093-93240765-9523-4018-827D-15599E929257 wds:Q37021584-9FF743A1-36E5-4369-92E5-A195C7A0B816 wds:Q38879274-54C19775-6829-4259-8633-443DEE8F7EF0 wds:Q66993298-11CEEC03-381A-4BB4-83AE-56C42C26F466 wds:Q70388558-E6A45A6C-92A2-470C-A20D-00CB1411407B wds:Q93730107-D2C994E1-51D0-404E-A27E-6E245A459512 wds:Q36715984-176D39BA-A3BD-4948-B6A7-82DB3B1922A6

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