Search Results - "Ristić, Smiljana"
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Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis
Published in Scientific reports (16-06-2017)“…The genetic etiology and the contribution of rare genetic variation in multiple sclerosis (MS) has not yet been elucidated. Although familial forms of MS have…”
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Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis
Published in PloS one (11-01-2018)“…Prevalence of multiple sclerosis varies with geographic latitude. We hypothesized that this fact might be partially associated with the influence of latitude…”
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ACE I/D polymorphism and epidemiological findings for COVID-19: One year after the pandemic outbreak in Europe
Published in The Journal of infection (01-09-2021)Get full text
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The Role of Iron and Iron Overload in Chronic Liver Disease
Published in Medical science monitor (22-06-2016)“…The liver plays a major role in iron homeostasis; thus, in patients with chronic liver disease, iron regulation may be disturbed. Higher iron levels are…”
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Gantenerumab reduces amyloid-β plaques in patients with prodromal to moderate Alzheimer's disease: a PET substudy interim analysis
Published in Alzheimer's research & therapy (12-12-2019)“…We previously investigated low doses (105 or 225 mg) of gantenerumab, a fully human monoclonal antibody that binds and removes aggregated amyloid-β by Fc…”
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Pharmacogenomics of Multiple Sclerosis: A Systematic Review
Published in Frontiers in neurology (26-02-2019)“…Over the past two decades, various novel disease-modifying drugs for multiple sclerosis (MS) have been approved. However, there is high variability in the…”
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CCR5 Δ32 and CTLA-4 +49 A/G Gene Polymorphisms and Interferon-β Treatment Response in Croatian and Slovenian Multiple Sclerosis Patients
Published in International journal of molecular sciences (05-07-2024)“…The aim of the present study was to investigate the impact of CCR5 Δ32 and CTLA-4 polymorphisms on the response to IFN-β treatment in our cohort of MS patients…”
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Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genes
Published in Scientific reports (24-06-2019)“…The role of rare genetic variation and the innate immune system in the etiology of multiple sclerosis (MS) is being increasingly recognized. Recently, we…”
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Association between Insertion-Deletion Polymorphism of the Angiotensin-Converting Enzyme Gene and Treatment Response to Antipsychotic Medications: A Study of Antipsychotic-Naïve First-Episode Psychosis Patients and Nonadherent Chronic Psychosis Patients
Published in International journal of molecular sciences (12-10-2022)“…We investigated whether a functional insertion/deletion (I/D) polymorphism of angiotensin-converting enzyme (ACE) influenced antipsychotic treatment. At…”
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Secular change in body height and cephalic index of Croatian medical students (University of Rijeka)
Published in American journal of physical anthropology (01-01-2004)“…An investigation of body height and cephalic measurements was performed among five groups of first‐year medical students of the University of Rijeka School of…”
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Could the CCR5-Δ32 Mutation be Protective in SARS-CoV-2 Infection?
Published in Physiological research (30-12-2021)“…Increasing evidence points to host genetics as a factor in COVID-19 prevalence and outcome. CCR5 is a receptor for proinflammatory chemokines that are involved…”
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The Influence of Hemochromatosis Gene (HFE) Mutations on SARS-CoV-2 Susceptibility and COVID-19 Severity
Published in Balkan medical journal (08-05-2023)Get full text
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GiOPARK Project: The Genetic Study of Parkinson's Disease in the Croatian Population
Published in Genes (01-02-2024)“…Parkinson's disease is a neurological disorder that affects motor function, autonomic functions, and cognitive abilities. It is likely that both genetic and…”
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The impact of ACE gene I/D polymorphism on plasma glucose and lipid concentrations in schizophrenia patients
Published in Psychiatry research (30-05-2015)Get full text
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Potential protective role of a NOD2 polymorphism in the susceptibility to multiple sclerosis is not associated with interferon therapy
Published in Biomedical reports (01-12-2021)“…Pattern recognition receptors, such as specific nucleotide-binding oligomerization domain protein 2, and their polymorphisms may be involved in the…”
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The insertion/deletion polymorphism in the angiotensin-converting enzyme gene and nicotine dependence in schizophrenia patients
Published in Journal of Neural Transmission (01-04-2017)“…We investigated the relationship between the functional insertion/deletion (I/D) polymorphism in the angiotensin-converting enzyme (ACE) gene and the risk of…”
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Chronic iron overload induces gender-dependent changes in iron homeostasis, lipid peroxidation and clinical course of experimental autoimmune encephalomyelitis
Published in Neurotoxicology (Park Forest South) (01-12-2016)“…•Female and male DA rats were exposed to iron overload (IO) before immunization with BBH+CFA.•IO accelerated appearance of clinical signs of EAE in female…”
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