Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Andrija, Kaštelan"'
Autor:
Marija Kaštelan, Larisa Prpić Massari, Ines Brajac, Sandra Peternel, Esma Čečuk Jeličić, Zorana Grubić, Andrija Kaštelan
Publikováno v:
Medicina Fluminensis : Medicina Fluminensis
Volume 51
Issue 2
Volume 51
Issue 2
Cilj: Istražiti učestalost haplotipskih sveza HLA-DRB1-DQA1-DQB1 te produženog haplotipa Cw*0602-B57-DRB1*07-DQA1*0201 DQB1*0201 u pacijenata s pozitivnom i negativnom obiteljskom anamnezom psorijaze. Ispitanici i metode: Istraživanje povezanosti
Autor:
R. Zunec, J. Ille, I. Kuvacic, Maria I. New, Vesna Plavšić, Miroslav Dumić, L. Brkljacic, Andrija Kaštelan, Robert C. Wilson
Publikováno v:
American Journal of Medical Genetics. 72:302-306
We report on the prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase in 20 at-risk pregnancies (16 salt-wasting and 4 simple virilizing families). We have diagnosed 3 affected fetuses (2 males and 1 female), 3 healthy homozygot
Publikováno v:
Ocular Immunology and Inflammation. 4:193-201
Patients with endogenous uveitis represent 6.5+ of patients in University Hospital Split, which serves most of South Croatia. Within a four-year period 208 patients were treated for endogenous uveitis. Results of clinical-laboratory examinations and
Autor:
Zorana Grubić, Katarina Štingl, Andrija Kaštelan, Natalija Martinez, Biserka Palfi, Vesna Brkljačić-Kerhin
Publikováno v:
International Congress Series. 1261:535-537
During the 3-year period, 111 cases of paternity disputes were processed in our laboratory. The analysis was performed on nine STR (TH01, VWA31, FES/FPS, F13A01, SE33, D1S1656, D12S391, D18S535, and D22S683) loci and one VNTR (D1S80) locus. Out of 11
Publikováno v:
Tissue Antigens. 46:293-298
HLA-class II polymorphisms have been studied in a population of 141 unrelated healthy Croatians using PCR amplification, followed by non- radioactive oligonucleotide hybridization. Thirty one DRB1, 8 DQA1, 13 DQB1 and 16 DPB1 alleles were found in th
Publikováno v:
Clinical and Experimental Dermatology. 28:200-202
In this study, we have analysed the distribution of HLA class II alleles and the extended haplotype HLA-Cw-B-DRB1-DQA1-DQB1 in Croatian patients with type I and type II psoriasis by hybridization with specific oligonucleotide probes. Type I psoriasis
Publikováno v:
International Congress Series. 1239:171-173
We have analysed polymorphism at 4 STR loci in our population.All tested loci showed high level of informativness and heterozygosity.
Publikováno v:
Forensic Science International. 127:147-149
Population study was carried out on the sample of 167 unrelated donors from the wider area of the Croatia's capital, Zagreb, using the short tandem reapet (STR) loci: TH01, VWFA31, FES/FPS, F13A01, D1S1656, D12S391, D18S535 and D22S683.
Publikováno v:
European Journal of Immunogenetics. 26:385-387
We investigated DR52 haplotype polymorphism in a population of 78 Croatian families with at least one parent and one offspring positive for a DR52-associated allele, using the PCR-SSOP method. The haplotypes DRB1*0301-DQA1*0501-DQB1*0201, DRB1*11-DQA
Autor:
Vesna Plavšić, Ljerka Brkljačić, Maria I. New, Phyllis W. Speiser, Andrija Kaštelan, Elizabeth Wood, Christopher Crawford, Ana Radica, Miro Dumić, Slobodan Radmanović, Miloš Baničeviác
Publikováno v:
Acta Endocrinologica. 122:703-710
Nonclassic steroid 21-hydroxylase deficiency is an attenuated adrenal enzyme defect that is commonly the basis of hyperandrogenic syndromes. Inherited as an autosomal recessive trait, it is known to occur with high frequency in the general population