BIOMAT Database Logo BIOMAT Database Logo

Analysis of high fetal hemoglobin production in sickle cell anemia patients from the Eastern Province of Saudi Arabia. 1987

B A Miller, and M Salameh, and M Ahmed, and N Olivieri, and T H Huisman, and S H Orkin, and D G Nathan
Division of Hematology/Oncology, Children's Hospital Medical Center, Boston, MA.

UI MeSH Term Description Entries
D003710 Demography Statistical interpretation and description of a population with reference to distribution, composition, or structure. Demographer,Demographic,Demographic and Health Survey,Population Distribution,Accounting, Demographic,Analyses, Demographic,Analyses, Multiregional,Analysis, Period,Brass Technic,Brass Technique,Demographers,Demographic Accounting,Demographic Analysis,Demographic Factor,Demographic Factors,Demographic Impact,Demographic Impacts,Demographic Survey,Demographic Surveys,Demographic and Health Surveys,Demographics,Demography, Historical,Demography, Prehistoric,Factor, Demographic,Factors, Demographic,Family Reconstitution,Historical Demography,Impact, Demographic,Impacts, Demographic,Multiregional Analysis,Period Analysis,Population Spatial Distribution,Prehistoric Demography,Reverse Survival Method,Stable Population Method,Survey, Demographic,Surveys, Demographic,Analyses, Period,Analysis, Demographic,Analysis, Multiregional,Demographic Analyses,Demographies, Historical,Demographies, Prehistoric,Distribution, Population,Distribution, Population Spatial,Distributions, Population,Distributions, Population Spatial,Family Reconstitutions,Historical Demographies,Method, Reverse Survival,Method, Stable Population,Methods, Reverse Survival,Methods, Stable Population,Multiregional Analyses,Period Analyses,Population Distributions,Population Methods, Stable,Population Spatial Distributions,Prehistoric Demographies,Reconstitution, Family,Reconstitutions, Family,Reverse Survival Methods,Spatial Distribution, Population,Spatial Distributions, Population,Stable Population Methods,Technic, Brass,Technique, Brass
D004262 DNA Restriction Enzymes Enzymes that are part of the restriction-modification systems. They catalyze the endonucleolytic cleavage of DNA sequences which lack the species-specific methylation pattern in the host cell's DNA. Cleavage yields random or specific double-stranded fragments with terminal 5'-phosphates. The function of restriction enzymes is to destroy any foreign DNA that invades the host cell. Most have been studied in bacterial systems, but a few have been found in eukaryotic organisms. They are also used as tools for the systematic dissection and mapping of chromosomes, in the determination of base sequences of DNAs, and have made it possible to splice and recombine genes from one organism into the genome of another. EC 3.21.1. Restriction Endonucleases,DNA Restriction Enzyme,Restriction Endonuclease,Endonuclease, Restriction,Endonucleases, Restriction,Enzymes, DNA Restriction,Restriction Enzyme, DNA,Restriction Enzymes, DNA
D004900 Erythroblasts Immature, nucleated ERYTHROCYTES occupying the stage of ERYTHROPOIESIS that follows formation of ERYTHROID PRECURSOR CELLS and precedes formation of RETICULOCYTES. The normal series is called normoblasts. Cells called MEGALOBLASTS are a pathologic series of erythroblasts. Erythrocytes, Nucleated,Normoblasts,Proerythroblasts,Pronormoblasts,Erythroblast,Erythrocyte, Nucleated,Normoblast,Nucleated Erythrocyte,Nucleated Erythrocytes,Proerythroblast,Pronormoblast
D005319 Fetal Hemoglobin The major component of hemoglobin in the fetus. This HEMOGLOBIN has two alpha and two gamma polypeptide subunits in comparison to normal adult hemoglobin, which has two alpha and two beta polypeptide subunits. Fetal hemoglobin concentrations can be elevated (usually above 0.5%) in children and adults affected by LEUKEMIA and several types of ANEMIA. Hemoglobin F,Hemoglobin, Fetal
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000755 Anemia, Sickle Cell A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin S. Hemoglobin S Disease,HbS Disease,Sickle Cell Anemia,Sickle Cell Disease,Sickle Cell Disorders,Sickling Disorder Due to Hemoglobin S,Anemias, Sickle Cell,Cell Disease, Sickle,Cell Diseases, Sickle,Cell Disorder, Sickle,Cell Disorders, Sickle,Disease, Hemoglobin S,Hemoglobin S Diseases,Sickle Cell Anemias,Sickle Cell Diseases,Sickle Cell Disorder
D012529 Saudi Arabia A country located in the Middle East, bordering the Persian Gulf and the Red Sea, north of Yemen. The capital is Riyadh. Kingdom of Saudi Arabia

Related Publications

B A Miller, and M Salameh, and M Ahmed, and N Olivieri, and T H Huisman, and S H Orkin, and D G Nathan
Depression among Sickle Cell Anemia Patients in the Eastern Province of Saudi Arabia.
January 2018, Saudi journal of medicine & medical sciences,
B A Miller, and M Salameh, and M Ahmed, and N Olivieri, and T H Huisman, and S H Orkin, and D G Nathan
Variability of sickle cell disease in the Eastern Province of Saudi Arabia.
June 1989, The Journal of pediatrics,
B A Miller, and M Salameh, and M Ahmed, and N Olivieri, and T H Huisman, and S H Orkin, and D G Nathan
Hydroxyurea in sickle cell disease patients from Eastern Saudi Arabia.
March 2002, Saudi medical journal,
B A Miller, and M Salameh, and M Ahmed, and N Olivieri, and T H Huisman, and S H Orkin, and D G Nathan
Vitamin D deficiency in sickle cell disease patients in the Eastern Province of Saudi Arabia.
January 2018, Annals of Saudi medicine,
B A Miller, and M Salameh, and M Ahmed, and N Olivieri, and T H Huisman, and S H Orkin, and D G Nathan
Splenic function in sickle cell disease in the Eastern Province of Saudi Arabia.
May 1984, The Journal of pediatrics,
B A Miller, and M Salameh, and M Ahmed, and N Olivieri, and T H Huisman, and S H Orkin, and D G Nathan
Homozygous sickle cell disease and priapism in the eastern province of Saudi Arabia.
January 1987, Acta haematologica,
B A Miller, and M Salameh, and M Ahmed, and N Olivieri, and T H Huisman, and S H Orkin, and D G Nathan
Sickle cell haemoglobinopathy and Salmonella osteomyelitis in the eastern province of Saudi Arabia.
March 1982, Tropical and geographical medicine,
B A Miller, and M Salameh, and M Ahmed, and N Olivieri, and T H Huisman, and S H Orkin, and D G Nathan
Neonatal screening for sickle cell disease in the Eastern Province of Saudi Arabia.
January 1984, Transactions of the Royal Society of Tropical Medicine and Hygiene,
B A Miller, and M Salameh, and M Ahmed, and N Olivieri, and T H Huisman, and S H Orkin, and D G Nathan
Fetal haemoglobin production and the sickle gene in the oases of Eastern Saudi Arabia.
November 1978, British journal of haematology,
B A Miller, and M Salameh, and M Ahmed, and N Olivieri, and T H Huisman, and S H Orkin, and D G Nathan
Serum immunoglobulin and complement levels in patients with sickle cell anaemia from eastern province of Saudi Arabia.
January 1988, Tropical and geographical medicine,
Copied contents to your clipboard!