Search Results - "Novakovic, I."

Five-year study of quality of life in myotonic dystrophy by Peric, S., Vujnic, M., Dobricic, V., Marjanovic, A., Basta, I., Novakovic, I., Lavrnic, D., Rakocevic-Stojanovic, V.

“…Background – Myotonic dystrophy type 1 (DM1) is the most common muscular dystrophy in adults. There is a complete lack of studies that assessed quality of life…”
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Identification of mutations in the PARK2 gene in Serbian patients with Parkinson's disease by Jankovic, M.Z., Dobricic, V., Kresojevic, N., Markovic, V., Petrovic, I., Svetel, M., Pekmezovic, T., Novakovic, I., Kostic, V.

“…Mutations in the PARK2 (PRKN) gene are the most common cause of autosomal-recessive (AR) juvenile parkinsonism and young-onset Parkinson's disease (YOPD). >100…”
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Are Leber’s mitochondial DNA mutations associated with aquaporin-4 autoimmunity? by Dujmovic, I, Jancic, J, Dobricic, V, Jankovic, M, Novakovic, I, Comabella, M, Drulovic, J

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A genome-wide survey and functional brain imaging study identify CTNNBL1 as a memory-related gene by Papassotiropoulos, A, Stefanova, E, Vogler, C, Gschwind, L, Ackermann, S, Spalek, K, Rasch, B, Heck, A, Aerni, A, Hanser, E, Demougin, P, Huynh, K-D, Luechinger, R, Klarhöfer, M, Novakovic, I, Kostic, V, Boesiger, P, Scheffler, K, de Quervain, D J-F

“…Unbiased genome-wide screens combined with imaging data on brain function may identify novel molecular pathways related to human cognition. Here we performed a…”
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P.1.a.036 Subclinical psychotic experiences in healthy adults: relationship between genetic variants of FKBP5 gene, neuroticism and childhood trauma by Mihaljevic, M, Pekmezovic, T, Andric, S, Mirjanic, T, Novakovic, I, Maric, N

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Polymorphism of Kibra gene in patients with terminal renal insufficiency: PS237 by Paovica, N, Bajovic, D, Novakovic, I

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Intellectual Ability in the Duchenne Muscular Dystrophy and Dystrophin Gene Mutation Location by Rasic, Milic V., Vojinovic, D., Pesovic, J., Mijalkovic, G., Lukic, V., Mladenovic, J., Kosac, A., Novakovic, I., Maksimovic, N., Romac, S., Todorovic, S., Pavicevic, Savic D.

“…Duchenne muscular dystrophy (DMD) is the most common form of muscular dystrophy during childhood. Mutations in dystrophin (DMD) gene are also recognized as a…”
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Genotype-phenotype correlation in Friedreich's ataxia by Kovacevic, G, Todorovic, S, Novakovic, I, Pavicevic Savic, D, Rasic, V. Milic, Svetel, M, Dobricic, V

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Increased total homocysteine level is associated with clinical status and severity of white matter changes in symptomatic patients with subcortical small vessel disease by Pavlovic, A.M, Pekmezovic, T, Obrenovic, R, Novakovic, I, Tomic, G, Mijajlovic, M, Sternic, N

“…Abstract Objective Elevated plasma total homocysteine (tHcy) is an independent risk factor for ischemic stroke and has been linked to cerebral small vessel…”
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P.2.b.018 Effect of accumulation of 5-HTTLPR, BDNF Vall66Met and COMT Val158Met polymorphisms on brain morphology in patients with major depressive disorder by Kostic, M, Canu, E, Munjiza, A, Agosta, F, Novakovic, I, Dobricic, V, Jerkovic, V, Jerkovic, M, Pekmezovic, T, Lecic Tosevski, D, Filippi, M

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4.Electromyography test as diagnostic procedure in recessive cerebellar ataxias by Milic Rasic, V, Todorovic, S, Brankovic, V, Novakovic, I, Baets, J, Vermeer, S

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Association of dihydrofolate reductase (DHFR) -317AA genotype with poor response to methotrexate in patients with rheumatoid arthritis by MILIC, V, JEKIC, B, RADUNOVIC, G, PEJNOVIC, N, KRAJINOVIC, M, LUKOVIC, L, BUNJEVACKI, V, MILASIN, J, NOVAKOVIC, I, DAMNJANOVIC, T, POPOVIC, B, MAKSIMOVIC, N, DAMJANOV, N

“…Identifying genetic predictors of methotrexate (MTX) treatment response in patients with rheumatoid arthritis (RA) may have great importance for optimising…”
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A genome-wide survey of human short-term memory by Papassotiropoulos, A, Henke, K, Stefanova, E, Aerni, A, Müller, A, Demougin, P, Vogler, C, Sigmund, J C, Gschwind, L, Huynh, K-D, Coluccia, D, Mondadori, C R, Hänggi, J, Buchmann, A, Kostic, V, Novakovic, I, van den Bussche, H, Kaduszkiewicz, H, Weyerer, S, Bickel, H, Riedel-Heller, S, Pentzek, M, Wiese, B, Dichgans, M, Wagner, M, Jessen, F, Maier, W, de Quervain, D J-F

“…Recent advances in the development of high-throughput genotyping platforms allow for the unbiased identification of genes and genomic sequences related to…”
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Transcranial sonography in dopa‐responsive dystonia by Svetel, M., Tomić, A., Mijajlović, M., Dobričić, V., Novaković, I., Pekmezović, T., Brajković, L., Kostić, V. S.

“…Background and purpose Mutations in the GCH1 gene, encoding GTP cyclohydrolase 1, the enzyme critically important for dopamine production in nigrostriatal…”
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A novel Notch3 Gly89Cys mutation in a Serbian CADASIL family by Pavlovic, Aleksandra M., Dobricic, V., Semnic, R., Lackovic, V., Novakovic, I., Bajcetic, M., Sternic, N.

“…Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most common heritable cause of stroke and vascular…”
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Occurrence of bisphenol A and microplastics in landfill leachate: lessons from South East Europe by Narevski, Aleksandra C., Novaković, Mladenka I., Petrović, Maja Z., Mihajlović, Ivana J., Maoduš, Nikola B., Vujić, Goran V.

“…In order to confirm the landfills as potential sources of microplastics and bisphenol A (BPA), the investigation of microplastics occurrence and concentration…”
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Plasma homocysteine levels and cognitive status in patients with ischemic cerebrovascular disease by Sternic, N, Pavlovic, A, Pekmezovic, T, Zidverc-Trajkovic, J, Jovanovic, Z, Mijajlovic, M, Radojicic, A, Tomic, G, Novakovic, I, Obrenovic, R, Kostic, V.S

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Fuzzy role of hyperhomocysteinemia in hemodialysis patients’ mortality by Simic-Ogrizovic, S., Stosovic, M., Novakovic, I., Pejanovic, S., Jemcov, T., Radovic, M., Djukanovic, L.

“…Recent studies give contradictory data regarding the role of hyperhomocysteinemia (hyperHcy) in cardiovascular (CV) morbidity and mortality in hemodialysis…”
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Molecular analysis of Y chromosome microdeletions in idiopathic cases of male infertility in Serbia by Ristanovic, M., Bunjevacki, V., Tulic, C., Novakovic, I., Nikolic, A.

“…The aim of this study was to detect frequency of microdeletions of Y chromosome in idiopathic cases of male infertility in Serbian population. Patients were…”
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Association of the brain-derived neurotrophic factor Val66Met polymorphism with body mass index, fasting glucose levels and lipid status in adolescents by Vidović, V, Maksimović, N, Novaković, I, Damnjanović, T, Jekić, B, Vidović, S, Majkić Singh, N, Stamenković-Radak, M, Nikolić, D, Marisavljević, D

“…Brain-derived neurotrophic factor (BDNF) has an important role in energy balance. It suppresses food intake, reduces hepatic glucose production and converts…”
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