It has been observed that all of the erythrocytes of individuals with sickle-cell trait undergo sickling and that a greater reduction in partial pressure of oxygen is required to produce complete sickling in sickle-cell trait erythrocytes than in those of sickle-cell anemics (1). These observations indicate that each sicklemia erythrocyte contains both normal hemoglobin and sickle-cell anemia hemoglobin. In a pooled sample of blood from five sicklemic individuals the ratio of t,he abnormal to the normal hemoglobin was found to be 39:61 (7). In the light of this knowledge it was considered pertinent to ascertain the extent of the variation of the ratio of sickle-cell anemia hemoglobin (SCA hemoglobin) to normal hemoglobin in sicklemic in...
Sickle-cell anemia is a hereditary disease produced by hemoglobin S inits homozygous form, (HBsHbs)....
Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud Universit...
Only five Hb S heterozygotes with an associated Hb H Disease i.e. the ASH condition or AS: --/-α hav...
It has been observed that all of the erythrocytes of individuals with sickle-cell trait undergo sick...
The erythrocytes of certain human individuals undergo a reversible change in shape known as sickling...
Previous work from these Laboratories has established the existence of an abnormal hemoglobin in sic...
S ICKLE cell anemia is a congenital chronic hemolytic type of anemia char-acterized hematologically ...
In view of the well recognized differences be-tween sickle and normal hemoglobin (1, 2), it was thou...
IF ONE takes a drop of blood from each member of an unselected series of negroes, seals the drops un...
The deoxygenation of blood from patients with sickle cell anemia leads to transformation of the red ...
cell trait is generally presumed to be constant throughout life,1’2 but varia-tions in this proporti...
S ICKLE CELL-THALASSEMIA DISEASE is known to be a severe or moderately severe type of congenital hem...
Sickle cell anemia is one of the first diseases to be understood at the molecular level. The amino a...
Sickle cell anemia is a recessive genetic disease caused by the presence in the red blood cell, of a...
In homozygous 8-thalassemia the erythrocyte population is largely nonhomogeneous; no other condition...
Sickle-cell anemia is a hereditary disease produced by hemoglobin S inits homozygous form, (HBsHbs)....
Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud Universit...
Only five Hb S heterozygotes with an associated Hb H Disease i.e. the ASH condition or AS: --/-α hav...
It has been observed that all of the erythrocytes of individuals with sickle-cell trait undergo sick...
The erythrocytes of certain human individuals undergo a reversible change in shape known as sickling...
Previous work from these Laboratories has established the existence of an abnormal hemoglobin in sic...
S ICKLE cell anemia is a congenital chronic hemolytic type of anemia char-acterized hematologically ...
In view of the well recognized differences be-tween sickle and normal hemoglobin (1, 2), it was thou...
IF ONE takes a drop of blood from each member of an unselected series of negroes, seals the drops un...
The deoxygenation of blood from patients with sickle cell anemia leads to transformation of the red ...
cell trait is generally presumed to be constant throughout life,1’2 but varia-tions in this proporti...
S ICKLE CELL-THALASSEMIA DISEASE is known to be a severe or moderately severe type of congenital hem...
Sickle cell anemia is one of the first diseases to be understood at the molecular level. The amino a...
Sickle cell anemia is a recessive genetic disease caused by the presence in the red blood cell, of a...
In homozygous 8-thalassemia the erythrocyte population is largely nonhomogeneous; no other condition...
Sickle-cell anemia is a hereditary disease produced by hemoglobin S inits homozygous form, (HBsHbs)....
Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud Universit...
Only five Hb S heterozygotes with an associated Hb H Disease i.e. the ASH condition or AS: --/-α hav...