Search Results - "Rakocevic Stojanovic, V."
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Adult‐onset very‐long‐chain acyl‐CoA dehydrogenase deficiency (VLCADD)
Published in European journal of neurology (01-11-2020)“…Background and purpose Very‐long‐chain acyl‐CoA dehydrogenase deficiency (VLCADD) is a hereditary disorder of mitochondrial long‐chain fatty acid oxidation…”
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Electrophysiological findings in patients with low density lipoprotein receptor related protein 4 positive myasthenia gravis
Published in European journal of neurology (01-11-2016)“…Background and purpose The aim was to determine the electrophysiological profile of our cohort of low density lipoprotein receptor related protein 4 (LRP4)…”
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Prospective measurement of quality of life in myotonic dystrophy type 1
Published in Acta neurologica Scandinavica (01-12-2017)“…Introduction Generic patient reported outcome measures have had varied success in tracking QoL in myotonic dystrophy type 1 (DM1). Aim To analyze changes of…”
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Five-year study of quality of life in myotonic dystrophy
Published in Acta neurologica Scandinavica (01-11-2016)“…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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High frequency of DQB105 and absolute absence of DRB113 in muscle-specific tyrosine kinase positive myasthenia gravis
Published in European journal of neurology (01-01-2015)“…Background and purpose Myasthenia gravis (MG) is an autoimmune disease but certain genetic factors predispose its development. Since susceptibility to…”
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Cerebrospinal fluid biomarkers of neurodegeneration in patients with juvenile and classic myotonic dystrophy type 1
Published in European journal of neurology (01-02-2014)“…Background and purpose The aim of the present study was to analyze cerebrospinal fluid (CSF) levels of total tau (T‐tau), phosphorylated tau (P‐tau) and the…”
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Dependent and paranoid personality patterns in myotonic dystrophy type 1
Published in Acta neurologica Scandinavica (01-04-2014)“…Objectives To analyze frequency and type of personality pattern in patients with myotonic dystrophy type 1 (DM1), to correlate these findings with clinical…”
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Rupture of the middle cerebral artery aneurysm as a presenting symptom of late-onset Pompe disease in an adult with a novel GAA gene mutation
Published in Acta neurologica Belgica (01-06-2014)“…Pompe disease is an autosomal recessive disorder caused by deficient activity of acid alpha-glucosidase [1]. Infantile Pompe disease presents in the first…”
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Epidemiology of Charcot-Marie-Tooth disease in the population of Belgrade, Serbia
Published in Neuroepidemiology (01-01-2011)“…The aim of this study was to determine prevalence and 15-year survival in Charcot-Marie-Tooth disease (CMT). The study covers the period from 1 January 1988 to…”
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10
Leptin and the metabolic syndrome in patients with myotonic dystrophy type 1
Published in Acta neurologica Scandinavica (01-02-2010)“…Rakocevic Stojanovic V, Peric S, Lavrnic D, Popovic S, Ille T, Stevic Z, Basta I, Apostolski S. Leptin and the metabolic syndrome in patients with myotonic…”
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Survival and mortality of myotonic dystrophy type 1 (Steinert's disease) in the population of Belgrade
Published in European journal of neurology (01-05-2006)“…The purpose of this investigation was to determine survival and mortality in patients with myotonic dystrophy type 1 (DM1) in the Belgrade population within…”
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Cyclosporine in the treatment of myasthenia gravis
Published in Acta neurologica Scandinavica (01-04-2005)“…Cyclosporine A (CsA) treatment was evaluated in 52 patients with severe generalized myasthenia gravis (MG) whose illness was not controlled by…”
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Prospective analysis of gait characteristics in chronic inflammatory demyelinating polyradiculoneuropathy
Published in Journal of clinical neuroscience (01-10-2020)“…•Most gait parameters show significant differences when compared between CIDP and HC.•Findings in CIDP were shorter SL, prolonged CT and DST and increased CV…”
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Significant impact of behavioral and cognitive impairment on quality of life in patients with myotonic dystrophy type 1
Published in Clinical neurology and neurosurgery (01-11-2014)“…Highlights • Patients with juvenile form of DM1 had lower quality of life than adult onset DM1 patients. • Significant predictors of quality of life in…”
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Influence of multisystemic affection on health-related quality of life in patients with myotonic dystrophy type 1
Published in Clinical neurology and neurosurgery (01-03-2013)“…Abstract Aim To assess health-related quality of life (HRQoL) in patients with DM1, to identify muscular, multisystemic, central and social factors that may…”
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Extrathymic malignancies in a defined cohort of patients with myasthenia gravis
Published in Journal of the neurological sciences (15-11-2014)“…Abstract Introduction Myasthenia gravis (MG) may be associated with extrathymic malignancies, especially in patients with thymoma. Aim To determine the…”
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Brain sonography insight into the midbrain and basal ganglia in myotonic dystrophy type 2
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Epidemiological study of adult-onset myasthenia gravis in the area of Belgrade (Serbia) in the period 1979-2008
Published in Neuroepidemiology (01-03-2013)“…The aim of this study was to analyze the prevalence and incidence of adult-onset myasthenia gravis (MG) in the Belgrade population from 1979 to 2008. Data on…”
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Cardiac autonomic control in patients with myasthenia gravis and thymoma
Published in Journal of the neurological sciences (15-08-2011)“…Abstract Objective To evaluate cardiac autonomic control in patients with myasthenia gravis (MG) and thymoma. Materials and methods The study was performed on…”
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Neuroanatomical patterns of central nervous system involvement in myotonic dystrophy type 1 and clinical correlates
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