D Primorac
Overview
Explore the profile of D Primorac including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
33
Citations
516
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Kuzmanic Samija R, Primorac D, Resic B, Pavlov V, Capkun V, Punda H, et al.
Braz J Med Biol Res
. 2014 Aug;
47(10):869-75.
PMID: 25140814
The aim of this study was to analyze the association of different clinical contributors of hypoxic-ischemic encephalopathy with NOS3 gene polymorphisms. A total of 110 children with hypoxic-ischemic encephalopathy and...
2.
Marjanovic D, Fornarino S, Montagna S, Primorac D, Hadziselimovic R, Vidovic S, et al.
Ann Hum Genet
. 2005 Nov;
69(Pt 6):757-63.
PMID: 16266413
The variation at 28 Y-chromosome biallelic markers was analysed in 256 males (90 Croats, 81 Serbs and 85 Bosniacs) from Bosnia-Herzegovina. An important shared feature between the three ethnic groups...
3.
Primorac D, Rowe D, Mottes M, Barisic I, Anticevic D, Mirandola S, et al.
Croat Med J
. 2001 Jul;
42(4):393-415.
PMID: 11471191
Osteogenesis imperfecta (OI), or brittle bone disease, is a heritable disorder characterized by increased bone fragility. Four different types of the disease are commonly distinguished, ranging from a mild condition...
4.
Culic S, Jakl R, Metlicic V, Resic B, culic V, KULJIS D, et al.
Arch Med Res
. 2001 Jul;
32(4):268-72.
PMID: 11440781
Background: Schönlein-Henoch syndrome (SHS) or anaphylactic purpura in childhood is the result of pathologic and immunologic responses to different antigens. These antigens could induce the formation of immune complexes responsible...
5.
Culic S, Jakobson A, culic V, Kuzmic I, Scukanec-Spoljar M, Primorac D
Pediatr Hematol Oncol
. 2001 Jun;
18(4):291-4.
PMID: 11400655
The treatment of patients who suffer from a disseminated form of Langerhans cell histiocytosis (LCH) is still controversial. So far, few larger randomized studies have been performed. The authors present...
6.
Gabriel M, Calloway C, Reynolds R, Andelinovic S, Primorac D
Croat Med J
. 2001 Jun;
42(3):328-35.
PMID: 11387647
Aim: To detect sequence variation in 105 Croatian individuals by the use of duplex polymerase chain reaction amplification of full-length hypervariable region I and II (HVI/HVII) products and subsequent hybridization...
7.
Alonso A, Andelinovic S, MARTIN P, Sutlovic D, Erceg I, Huffine E, et al.
Croat Med J
. 2001 Jun;
42(3):260-6.
PMID: 11387635
Aim: To evaluate the performance of three multiplex short tandem repeat (STR) systems (AmpflSTR Profiler, AmpflSTR Profiler Plus, and AmpflSTR COfiler), and a megaplex STR system (PowerPlex 16) on DNA...
8.
Juric I, Primorac D, ZAGAR Z, Biocic M, Pavic S, Furlan D, et al.
Pediatr Int
. 2001 Apr;
43(2):152-6.
PMID: 11285067
Background: Acute appendicitis is the most common condition requiring an emergency abdominal operation in childhood. In the present study, we analyzed the frequency of portal and systemic bacteremia in 42...
9.
Semino O, Passarino G, Oefner P, Lin A, Arbuzova S, Beckman L, et al.
Science
. 2000 Nov;
290(5494):1155-9.
PMID: 11073453
A genetic perspective of human history in Europe was derived from 22 binary markers of the nonrecombining Y chromosome (NRY). Ten lineages account for >95% of the 1007 European Y...
10.
JOHNSON C, Primorac D, McKinstry M, McNeil J, Rowe D, Lawrence J
J Cell Biol
. 2000 Aug;
150(3):417-32.
PMID: 10931857
This study illuminates the intra-nuclear fate of COL1A1 RNA in osteogenesis imperfecta (OI) Type I. Patient fibroblasts were shown to carry a heterozygous defect in splicing of intron 26, blocking...