hemoglobin Arab

03/01/2018 - "The study population comprised 35 homozygous Hb S (HBB: c.20A>T) patients, 29 compound heterozygous patients [16 Hb S/β0-thalassemia (β0-thal), four Hb S/β+-thal, seven Hb S/Hb C (HBB: c.19G>A) and two Hb S/Hb O-Arab (HBB: c.364G>A)] and 100 healthy subjects. "
12/01/1985 - "A study realized in a Tunisian family of 22 persons has revealed a double heterozygoty Hb O Arab/beta(0) thalassemia in a child of 16 years old. "
01/01/1989 - "[Hemoglobin O Arab in interaction with beta 0-thalassemia]."
08/01/1988 - "[Double heterozygous Hb O ARAB/beta+ thalassemia (in a Tunisian family)]."
01/01/1985 - "The interaction of hemoglobin O Arab with Hb S and beta+ thalassemia among Israeli Arabs."

01/01/2023 - "The study result is the first molecular confirmation of co-inherited Hb-O Arab/sickle cell disease clinical condition in Sudan. "
01/01/2023 - "The final study's main results revealed the presence of HB O-Arab genetic mutations among Sudanese Sickle cell disease patients, which estimated to be (5%) co-inherited mutations among our study population (Hb-O Arab; (HBB):c.364G>A (p.Glu122Lys)). "
01/01/2023 - "In this study, we screened the co-inheritance of hemoglobin O-Arab mutation among Sudanese sickle cell disease patients. "
01/01/2023 - "The frequency of Hb-O Arab gene mutations was determined among Sudanese sickle cell disease patients, and the results have shown a (5%) frequency of Hb-O Arab mutation. "
04/01/1992 - "The associations Hb S--Hb O Arab brings about a serious hemoglobinopathy which has clinical and hematological features like the sickle-cell disease (SSFA2)."

03/01/1986 - "Among them we observed 7 simple heterozygotes for Hb O Arab/Hb A, two double heterozygotes-compounds for Hb O/beta+-thalassemia and three compounds for Hb O/beta 0-thalassemia (the latter assumed). "
12/01/1985 - "[Double heterozygous Hb O Arab/beta-thalassemia in a Tunisian child]."
01/01/1982 - "[Double heterozygosity of Hb O ARAB/beta + thalassemia in an Algerian family]."
01/01/1978 - "[Hemoglobin O Arab--beta-thalassemia in a Bulgarian, a resident of Odessa]."
01/01/2007 - "Patients were divided into 4 groups: A (beta-thalassemia trait, n=62), B (iron-deficiency anemia [IDA], n=41), C (alpha-thalassemia trait, n=10) and D (hemoglobin O-Arab trait, n=28). "

04/01/1992 - "The associations Hb S--Hb O Arab brings about a serious hemoglobinopathy which has clinical and hematological features like the sickle-cell disease (SSFA2)."
04/01/1999 - "Hemoglobin S/O(Arab) (Hb S/O(Arab)) is a rare compound heterozygous hemoglobinopathy characterized by the presence of two variant beta-globin chains: beta6Glu --> Val (Hb S) and beta121Glu --> Lys (Hb O(Arab)). "
12/01/2006 - "We detected 52 incidences of apparent hemoglobinopathies in 32 recipients caused by blood transfusion, of which 46 were hemoglobin C, 4 were hemoglobin S, and 2 were hemoglobin O-Arab. "

01/01/2007 - "Patients were divided into 4 groups: A (beta-thalassemia trait, n=62), B (iron-deficiency anemia [IDA], n=41), C (alpha-thalassemia trait, n=10) and D (hemoglobin O-Arab trait, n=28). "
01/01/1977 - "A 22 year old American negro with mild anemia was found to be triply heterozygous for hemoglobin S, hemoglobin O Arab and alpha thalassemia. "