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1.
PAFMJ-Pakistan Armed Forces Medical Journal. 1992; 42 (1): 47-51
in English | IMEMR | ID: emr-25913
2.
PAFMJ-Pakistan Armed Forces Medical Journal. 1988; 41 (1-2): 23-30
in English | IMEMR | ID: emr-11469

Subject(s)
Neoplasms/etiology
3.
PAFMJ-Pakistan Armed Forces Medical Journal. 1987; 40 (1): 18-22
in English | IMEMR | ID: emr-9532
4.
PAFMJ-Pakistan Armed Forces Medical Journal. 1987; 40 (3-4): 15-23
in English | IMEMR | ID: emr-9544

Subject(s)
Endocrinology
5.
RMJ-Rawal Medical Journal. 1987; 16 (1-4): 19-26
in English | IMEMR | ID: emr-9753
6.
PAFMJ-Pakistan Armed Forces Medical Journal. 1985; 37 (1): 26-9
in English | IMEMR | ID: emr-6294

Subject(s)
Ferritins , Cells
7.
Pakistan Journal of Biochemistry. 1985; 18 (1-2): 49-52
in English | IMEMR | ID: emr-6370

ABSTRACT

Seasonal variations in the composition of plasma iron-binding protein of Varanus bengalensis is reported with the help of gel filtration and cellulose acetate membrane electro-phoresis followed by autoradiography. Two types of plasma transferrins were recorded in winter whereas only one was present in early summer


Subject(s)
Reptiles , Seasons
8.
RMJ-Rawal Medical Journal. 1984; 13 (3-4): 1-9
in English | IMEMR | ID: emr-5125

ABSTRACT

A prospective study of 300 adult subjects of either sex was conducted to evaluate the existence of hereditary persistence of foetal haemoglobin [HPFH] in our population. The majority of the subjects [98%] were found to have H[b]F values less than 2% with a mean SD of 0.73 +/- 0.54% and showed H[b]A2 levels as 2.67 +/- 0.66%. Only six subjects [2%] had moderate elevation of H[b]F [2% and above] and they all showed associated increase of H[b]A2 levels above the normal. Increased H[b]A2 levels in conjuction with elevation of H[b]F indicated the presence of heterozygous beta thalassaemia trait among this group. The incidence of thalassaemia trait in the 300 subjects studied was found to be 1.6%. The distribution of H[b]F in the erythrocytes was found to be heterocellular. Moderate rise of H[b]F in the individuals with uneven distribution, ruled out the existence of pancellular form of HPFH while the associated elevation of H[b]A2 was not consistent with heterocellular form of HPFH. Thus the existence of gene for HPFH among these subjects could not be proved


Subject(s)
Thalassemia/congenital , Thalassemia/epidemiology , Follow-Up Studies
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