PubMed Health⌕ Search

Biomedical subjects

B Dinić

Publications and source records attributed to B Dinić.

13 recordsLinked to original sources

[Paleoserological study of human bone remains from archaeological locations in Serbia].

Paleoserological investigations make possible "biological reconstruction" of old populations and comparison of their characteristics with corresponding characteristics of contemporary population on the same area. The work presents results of the investigation of ABO system blood group distribution from the following archaeological locations: Vlasac (5000 B. C., Mesolithic), Gamzigrad (near Zajecar, III-IV era A. D., Roman period), Vinca (near Grocka, IX era A. D.) and Ras (near N. Pazar, IX-XI era A. D.). At the same time the work presents distribution of ABO blood groups among present population on the same area.

ABO Blood-Group System↗

[A new case of D/D blood].

A second case of the -D-/-D- blood in this country is described. A woman, belonging to this rare blood group is from the same region, from which is the first our case published 15 years ago.

Adult↗

[Congenital deficiency of humoral and cellular immunity].

The study involves 10 children with primary immunologic deficiency of the humoral and cellular immunity diagnosed on the basis of the clinical symptoms of the disease and immunologic investigation. In 7 children, out of whome three were infants, suffering of recurrent respiratory tract infections, examinations revealed either absence or deficiency of the IgA in the serum and saliva. 2 children presented a classical picture of the Wiskott-Aldrich's syndrome followed by eczema, recurrent infections and trombocytopenia. Having studied the immunologic status in these two children in vitro and in vivo, the authors established deficiency in the humoral and cellular immunity. In an infant aged three months, with diagnosed histiocytosis X after histologic examination of the skin, the authors had examined the function of the T and B cells after which it was concluded that it was a case of rare form of the combined primary immunodeficiency.

Child↗

[ABO blood-group system in the fossil remains at the mesolithic cemetary in Vlasac (6,300-5,400 B.C.)].

By the several generally accepted methods, the authors tested the ABO blood group system of human fossil remains of the mezolit cementery of Vlasac (lower flow of the River Danube). The results of these examinations showed a biological similarity of the population in all of the three cementery layers and a difference in blood groups in these people and the present inhabitants of that region. These examinations are of great interest for the study of the structure of the prehistorical population and its migrations.

ABO Blood-Group System↗

[Blood groups in chromosome disorders].

The authors investigated blood groups of two cases of polisomia, and 6 cases of chromosomal aberations. While the polisomia demonstrated no abnormalities of the blood groups, three cases of the chromosomal aberation show an alteration on the chromosome 2 and atypical inheritance of the MNSs groups, confirming autosomal location of these blood groups.

Blood Group Antigens↗

[Blood groups of human fossil remains].

The results of the blood grouping of the fossil human bones, from different mesolyte necropoles, are presented. These results, giving the informations concerning biological individualities of the ancestors of our country, will be of great importance for anthropology and ethnology of this region.

Adolescent↗

[Probable position of MN gene locus on the human karyotype].

Kariotype of the propositus and his father revealed a balanced reciprocal translocation between long arm of a chromosome No. 2, and the long arm of a No 19-20, so that their complements were 46, XY, t(2q-; 19--20q+). There is no connection with congenital malformations of the propositus, but his and kariotype of his father, as well as blood group pedigree of all members of his family, suggests, likewise to assertion of German and coworkers, that locus for the MN gene is on the long arm of the chromosome No 2.

Child↗