Acquired von Willebrand syndrome and post-operative drainage: a comparison of patients with aortic stenosis versus coronary artery disease
ConclusionThis study has shown that there is a correlation between von Willebrand factor antigen, von Willebrand factor activity and total drainage to the level of statistical significance in aortic stenosis patients and in the overall study population. (Source: General Thoracic and Cardiovascular Surgery)
Source: General Thoracic and Cardiovascular Surgery - January 27, 2024 Category: Cardiovascular & Thoracic Surgery Source Type: research
Viruses, Vol. 16, Pages 180: Seroepidemiology of Human Parvovirus B19 Infection among the Population of Vojvodina, Serbia, over a 16-Year Period (2008 & ndash;2023)
This study aimed to estimate the serological status and dynamic changes in the prevalence of Parvovirus B19 (PVB19) antibodies within the general population residing in the northern part of the Republic of Serbia (Province of Vojvodina) during a 16-year period. Serum samples were analyzed for Human PVB19-specific IgM and IgG antibodies using enzyme-linked immunosorbent assay (ELISA). Throughout the study period, the overall seroprevalence was 49.51%. Approximately 10% of patients exhibited a serologic profile positive for PVB19 IgM antibodies. Notably, seroprevalence varied significantly, ranging from 9.12% in the pediatri...
Source: Viruses - January 25, 2024 Category: Virology Authors: Vladimir Vukovi ć Aleksandra Pati ć Mioljub Risti ć Gordana Kova čević Ivana Hrnjakovi ć Cvjetković Vladimir Petrovi ć Tags: Article Source Type: research
Cancers, Vol. 16, Pages 485: Association of HOTAIR, MIR155HG, TERC, miR-155, -196a2, and -146a Genes Polymorphisms with Papillary Thyroid Cancer Susceptibility and Prognosis
Gordana Supic
Polymorphisms in long non-coding RNA and microRNA genes may play a significant role in the susceptibility and progression of papillary thyroid carcinoma (PTC). The current study investigates the polymorphisms HOTAIR rs920778, MIR155HG rs1893650, TERC rs10936599, miR-155 rs767649, miR-196a2 rs11614913 and miR-146a rs2910164 in 102 PTC patients and 106 age- and sex-matched controls of the Caucasian Serbian population, using real-time PCR. We observed differences in genotype distributions of the HOTAIR rs920778 (p = 0.016) and MIR155HG rs1893650 (p = 0.0002) polymorphisms between PTC patients and controls....
Source: Cancers - January 23, 2024 Category: Cancer & Oncology Authors: Jelena Karajovic Bozidar Kovacevic Bojana Uzelac Debora Stefik Bojana Jovanovic Petar Ristic Snezana Cerovic Gordana Supic Tags: Article Source Type: research
Erratum: Predicting the survival probability of functional neuroendocrine tumors treated with peptide receptor radionuclide therapy: Serbian experience
(Source: Frontiers in Endocrinology)
Source: Frontiers in Endocrinology - January 22, 2024 Category: Endocrinology Source Type: research
Prevalence of metabolic syndrome and its association with rapid weight loss among former elite combat sports athletes in Serbia
In terms of the potential influence of rapid weight loss (RWL) on the metabolic health of former combat sports athletes (CSA), the scientific literature is quite scarce. Therefore, the objective of the present... (Source: BMC Public Health)
Source: BMC Public Health - January 22, 2024 Category: Consumer Health News Authors: Nemanja Maksimovic, Ognjen Cvjeticanin, Carlo Rossi, Marko Manojlovic, Roberto Roklicer, Antonino Bianco, Attilio Carraro, Damir Sekulic, Aleksandra Milovancev, Tatjana Trivic and Patrik Drid Tags: Research Source Type: research
Clinical performance of a glass-hybrid system in comparison with a resin composite in two-surface class II restorations: a 5-year randomised multi-centre study
ConclusionsIn terms of success and survival rates, both the glass-hybrid restorative system and the nano-hybrid resin composite have been shown to perform satisfactorily.Clinical relevanceThe results of this study indicate that EQUIA Forte can be one of the therapeutic options for moderate to large two-surface class II restorations of posterior teeth. (Source: Clinical Oral Investigations)
Source: Clinical Oral Investigations - January 20, 2024 Category: Dentistry Source Type: research
Speech-language pathologists' professional stress level and factors affecting it in the Republic of Serbia
CONCLUSION: Since it is noted that SLPs are experiencing mild to moderate levels of professional stress, it is important to emphasize the need for adaptation of existing work terms as well as to provide additional support to speech therapists in order to improve their mental health.PMID:38217561 | DOI:10.3233/WOR-230036 (Source: Work)
Source: Work - January 13, 2024 Category: Occupational Health Authors: Ivana Milanovi ć Nina Stanojevi ć Sa ška Fatić Ma ša Marisavljević Silvana Puni šić Vladimir Janji ć Mi ško Subotić Slavica Maksimovi ć Source Type: research
The first case of combined oxidative phosphorylation deficiency-1 due to a GFM1 mutation in the Serbian population: a case report and literature review
CONCLUSIONS: To the best of our knowledge, 28 cases of COXPD1 disease caused by mutations in the GFM1 gene have been described in the literature. COXPD1 should be considered due to symptoms and signs which begin during intrauterine life or at birth. Signs of impaired energy metabolism should indicate that the disease is in the group of metabolic encephalopathies.PMID:38204316 | DOI:10.24953/turkjped.2022.1082 (Source: The Turkish Journal of Pediatrics)
Source: The Turkish Journal of Pediatrics - January 11, 2024 Category: Pediatrics Authors: Dejan Aleksic Marina Gazdic Jankovic Stefan Todorovic Marija Kovacevic Milan Borkovic Source Type: research
The first case of combined oxidative phosphorylation deficiency-1 due to a GFM1 mutation in the Serbian population: a case report and literature review
CONCLUSIONS: To the best of our knowledge, 28 cases of COXPD1 disease caused by mutations in the GFM1 gene have been described in the literature. COXPD1 should be considered due to symptoms and signs which begin during intrauterine life or at birth. Signs of impaired energy metabolism should indicate that the disease is in the group of metabolic encephalopathies.PMID:38204316 | DOI:10.24953/turkjped.2022.1082 (Source: The Turkish Journal of Pediatrics)
Source: The Turkish Journal of Pediatrics - January 11, 2024 Category: Pediatrics Authors: Dejan Aleksic Marina Gazdic Jankovic Stefan Todorovic Marija Kovacevic Milan Borkovic Source Type: research
The first case of combined oxidative phosphorylation deficiency-1 due to a GFM1 mutation in the Serbian population: a case report and literature review
CONCLUSIONS: To the best of our knowledge, 28 cases of COXPD1 disease caused by mutations in the GFM1 gene have been described in the literature. COXPD1 should be considered due to symptoms and signs which begin during intrauterine life or at birth. Signs of impaired energy metabolism should indicate that the disease is in the group of metabolic encephalopathies.PMID:38204316 | DOI:10.24953/turkjped.2022.1082 (Source: The Turkish Journal of Pediatrics)
Source: The Turkish Journal of Pediatrics - January 11, 2024 Category: Pediatrics Authors: Dejan Aleksic Marina Gazdic Jankovic Stefan Todorovic Marija Kovacevic Milan Borkovic Source Type: research
The first case of combined oxidative phosphorylation deficiency-1 due to a GFM1 mutation in the Serbian population: a case report and literature review
CONCLUSIONS: To the best of our knowledge, 28 cases of COXPD1 disease caused by mutations in the GFM1 gene have been described in the literature. COXPD1 should be considered due to symptoms and signs which begin during intrauterine life or at birth. Signs of impaired energy metabolism should indicate that the disease is in the group of metabolic encephalopathies.PMID:38204316 | DOI:10.24953/turkjped.2022.1082 (Source: The Turkish Journal of Pediatrics)
Source: The Turkish Journal of Pediatrics - January 11, 2024 Category: Pediatrics Authors: Dejan Aleksic Marina Gazdic Jankovic Stefan Todorovic Marija Kovacevic Milan Borkovic Source Type: research
The first case of combined oxidative phosphorylation deficiency-1 due to a GFM1 mutation in the Serbian population: a case report and literature review
CONCLUSIONS: To the best of our knowledge, 28 cases of COXPD1 disease caused by mutations in the GFM1 gene have been described in the literature. COXPD1 should be considered due to symptoms and signs which begin during intrauterine life or at birth. Signs of impaired energy metabolism should indicate that the disease is in the group of metabolic encephalopathies.PMID:38204316 | DOI:10.24953/turkjped.2022.1082 (Source: The Turkish Journal of Pediatrics)
Source: The Turkish Journal of Pediatrics - January 11, 2024 Category: Pediatrics Authors: Dejan Aleksic Marina Gazdic Jankovic Stefan Todorovic Marija Kovacevic Milan Borkovic Source Type: research
The first case of combined oxidative phosphorylation deficiency-1 due to a GFM1 mutation in the Serbian population: a case report and literature review
CONCLUSIONS: To the best of our knowledge, 28 cases of COXPD1 disease caused by mutations in the GFM1 gene have been described in the literature. COXPD1 should be considered due to symptoms and signs which begin during intrauterine life or at birth. Signs of impaired energy metabolism should indicate that the disease is in the group of metabolic encephalopathies.PMID:38204316 | DOI:10.24953/turkjped.2022.1082 (Source: The Turkish Journal of Pediatrics)
Source: The Turkish Journal of Pediatrics - January 11, 2024 Category: Pediatrics Authors: Dejan Aleksic Marina Gazdic Jankovic Stefan Todorovic Marija Kovacevic Milan Borkovic Source Type: research
The first case of combined oxidative phosphorylation deficiency-1 due to a GFM1 mutation in the Serbian population: a case report and literature review
CONCLUSIONS: To the best of our knowledge, 28 cases of COXPD1 disease caused by mutations in the GFM1 gene have been described in the literature. COXPD1 should be considered due to symptoms and signs which begin during intrauterine life or at birth. Signs of impaired energy metabolism should indicate that the disease is in the group of metabolic encephalopathies.PMID:38204316 | DOI:10.24953/turkjped.2022.1082 (Source: The Turkish Journal of Pediatrics)
Source: The Turkish Journal of Pediatrics - January 11, 2024 Category: Pediatrics Authors: Dejan Aleksic Marina Gazdic Jankovic Stefan Todorovic Marija Kovacevic Milan Borkovic Source Type: research
The first case of combined oxidative phosphorylation deficiency-1 due to a GFM1 mutation in the Serbian population: a case report and literature review
CONCLUSIONS: To the best of our knowledge, 28 cases of COXPD1 disease caused by mutations in the GFM1 gene have been described in the literature. COXPD1 should be considered due to symptoms and signs which begin during intrauterine life or at birth. Signs of impaired energy metabolism should indicate that the disease is in the group of metabolic encephalopathies.PMID:38204316 | DOI:10.24953/turkjped.2022.1082 (Source: The Turkish Journal of Pediatrics)
Source: The Turkish Journal of Pediatrics - January 11, 2024 Category: Pediatrics Authors: Dejan Aleksic Marina Gazdic Jankovic Stefan Todorovic Marija Kovacevic Milan Borkovic Source Type: research
