Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Olivera, Stojiljkovic"'
Autor:
Stojan Peric, Ilija Gunjic, Neda Delic, Olivera Stojiljkovic Tamas, Biljana Salak-Djokic, Jovan Pesovic, Ivana Petrovic Djordjevic, Vukan Ivanovic, Dusanka Savic-Pavicevic, Giovanni Meola, Vidosava Rakocevic-Stojanovic
Publikováno v:
Neuromuscular Disorders. 32:743-748
Myotonic dystrophy type 2 (DM2) is an autosomal dominant multisystemic disorder. Previous studies conducted on small cohorts of DM2 patients indicated presence of a cognitive dysfunction. We aimed to assess cognitive functions in a larger cohort of S
Autor:
Aleksa Palibrk, Stojan Peric, Olivera Stojiljkovic-Tamas, Ivana Basta, Aleksandar Stojanov, Ivana Berisavac, Ivo Bozovic, Mirjana Arsenijevic
Publikováno v:
The Neurologist. 26:244-247
Background The most frequently used ability outcome measure in Guillain-Barre syndrome (GBS) is the GBS disability scale (GDS). Recently developed inflammatory Rasch-built overall disability (I-RODS) scale has been suggested to be used in inflammator
Akademický článek
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Autor:
Ivana Berisavac, Mirjana Arsenijevic, Ivo Bozovic, Olivera Stojiljkovic-Tamas, Stojan Peric, Balsa Vujovic, Aleksa Palibrk, Sonja Lukic-Rajic
Publikováno v:
Clinical neurology and neurosurgery. 201
Autonomic dysfunction occurs in approximately two-thirds of Guillain-Barré syndrome (GBS) patients in the acute phase of the disease. Although improving over time, subclinical autonomic involvement may be present for 3-8 years after the GBS episode.
Autor:
Aleksandar Stojanov, Dejana R. Jovanović, Gordana Djordjevic, Ivana Basta, Mirjana Arsenijevic, Vesna Martic, Miroslav Stojanovic, Milutin Petrovic, Stojan Peric, Olivera Stojiljkovic-Tamas, Ivana Berisavac, Ivo Bozovic, Zita Jovin, Sonja Lukic-Rajic
Publikováno v:
Journal of the peripheral nervous system : JPNSREFERENCES. 25(4)
Guillain-Barre syndrome (GBS) is an acute auto-immune polyradiculoneuropathy. A huge variety of GBS incidence and mortality rates has been noted across the world. The objective of the present multi-centric study was to assess the incidence and mortal
Autor:
Zorica Stevic, Stojan Peric, Vesna Martic, Ivana Basta, Marija Grunauer, Sonja Rajic, Ivana Berisavac, Mina Cobeljic, Olivera Stojiljkovic Tamas, Ivo Bozovic, Dejana R. Jovanović, Aleksandra Dominovic Kovacevic, Milica Babic, Bogdan Bjelica, Aleksandar Stojanov, Gordana Djordjevic, Milutin Petrovic, Vanja Djuric, Balsa Vujovic, Nenad Komatina
Publikováno v:
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 45:269-274
A majority of patients with Guillain-Barre syndrome (GBS) have tendency of a good recovery. Our aim was to evaluate the outcome of the disease 1 and 3 years after GBS symptom onset. METHODS During 2014, GBS was diagnosed in 82 patients in seven terti
Akademický článek
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Autor:
Dragana Lavrnic, Zorica Stevic, Ivana Basta, Vidosava Rakocevic-Stojanovic, Olivera Stojiljkovic, Stojan Peric, Ljiljana Beslac-Bumbasirevic, Bogdan Bjelica, Ivana Berisavac, Ivo Bozovic
Publikováno v:
Journal of the Peripheral Nervous System. 22:127-130
We sought to determine influence of diabetes mellitus on Guillain-Barre syndrome (GBS) course and short-term prognosis. Among the 257 GBS patients included in this retrospective study, diabetes mellitus was present in 17%. The degree of disability at
Autor:
Dragana Lavrnic, Ivana Basta, Milan Cvijanovic, Ljiljana Beslac-Bumbasirevic, Olivera Stojiljkovic Tamas, Aleksandra Dominovic-Kovacevic, Ivana Berisavac, Sonja Rajic, Stojan Peric, Milica Babic
Publikováno v:
Journal of the Peripheral Nervous System. 21:105-110
The aim of the study was to analyze specific features of Guillain-Barre syndrome (GBS) in old people. The study included 403 GBS patients (62% young [ 80 years]). Diagnosis of GBS was made according to the National Institute of Neurological Disorders
Autor:
Marija Zarkov, Aleksandra Stojadinovic, Slobodan Sekulic, Iva Barjaktarovic, Olivera Stojiljkovic, Stojan Peric, Goran Kekovic, Biljana Draskovic, Zorica Stevic
Publikováno v:
Vojnosanitetski Pregled, Vol 72, Iss 10, Pp 859-863 (2015)
Vojnosanitetski Pregled
Vojnosanitetski Pregled
Background/Aim. Spinal muscular atrophy (SMA) is an autosomal recessive disease characterized by degeneration of alpha motor neurons in the spinal cord and the medulla oblongata, causing progressive muscle weakness and atrophy. The aim of this study