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Long-term outcome in patients with myasthenia gravis: one decade longitudinal study

Journal of neurology, 2022-04, Vol.269 (4), p.2039-2045

2022

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Guillain-Barré syndrome in the elderly

Journal of the peripheral nervous system, 2016-06, Vol.21 (2), p.105-110

2016

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Clinical and epidemiological features of Guillain-Barré syndrome in the Western Balkans

Journal of the peripheral nervous system, 2014-12, Vol.19 (4), p.317-321

2014

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Childhood-Onset Myasthenia Gravis With Thymoma

Pediatric neurology, 2012-05, Vol.46 (5), p.329-331

2012

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The coexistence of myasthenia gravis and myotonic dystrophy type 2 in a single patient

Journal of Clinical Neurology, 2013, 9(2), , pp.130-132

2013

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Survival and mortality of adult‐onset myasthenia gravis in the population of Belgrade, Serbia

Muscle & nerve, 2018-11, Vol.58 (5), p.708-712

2018

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Assessment of health-related quality of life in patients with myasthenia gravis in Belgrade (Serbia)

Neurological sciences, 2012-12, Vol.33 (6), p.1375-1381

2012

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Galactosylation of serum immunoglobulin G in myasthenia gravis with different autoantibodies

Scandinavian journal of clinical and laboratory investigation, 2023-09, Vol.ahead-of-print (ahead-of-print), p.1-8

2023

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Amifampridine phosphate (Firdapse®) is effective and safe in a phase 3 clinical trial in LEMS

Muscle & nerve, 2016-05, Vol.53 (5), p.717-725

2016

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Myopathy, muscle atrophy and tongue lipid composition in MuSK myasthenia gravis

Acta neurologica Belgica, 2015-09, Vol.115 (3), p.361-365

2015

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Comparison of the clinical and cognitive features of genetically positive ALS patients from the largest tertiary center in Serbia

Journal of neurology, 2017-06, Vol.264 (6), p.1091-1098

2017

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Rate of progression of Guillain-Barré syndrome is not associated with the short-term outcome of the disease

Irish journal of medical science, 2021-02, Vol.190 (1), p.357-361

2021

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Assessment of the neuropathic component in a chronic low back pain syndrome

Vojnosanitetski pregled, 2022, Vol.79 (1), p.25-30

2022

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COVID-19 infection and vaccination against SARS-CoV-2 in myasthenia gravis

Acta neurologica Belgica, 2023-04, Vol.123 (2), p.529-536

2023

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Association between Cytotoxic T-Lymphocyte-Associated Antigen 4 (CTLA-4) Locus and Early-Onset Anti-acetylcholine Receptor-Positive Myasthenia Gravis in Serbian Patients

Molecular neurobiology, 2024-04

2024

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Myasthenia gravis treated in the neurology intensive care unit: a 14-year single-centre experience

Neurological sciences, 2022-12, Vol.43 (12), p.6909-6918

2022

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Neuropathic pain as independent predictor of worse quality of life in patients with diabetic neuropathy

Vojnosanitetski pregled, 2021, Vol.78 (9), p.981-986

2021

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The presence of dysautonomia in different subgroups of myasthenia gravis patients

Journal of neurology, 2014-11, Vol.261 (11), p.2119-2127

2014

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Unraveling ALS due to SOD1 mutation through the combination of brain and cervical cord MRI

Neurology, 2018-02, Vol.90 (8)

2018

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Frequency and features of the central poststroke pain

Journal of the neurological sciences, 2018-08, Vol.391, p.100-103

2018

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Quality of life in patients with multifocal motor neuropathy from Serbia

Journal of the neurological sciences, 2019-04, Vol.399, p.151-154

2019

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A misdiagnosed myasthenia gravis with anti-muscle-specific tyrosine kinase antibodies with possible childhood onset

Vojnosanitetski pregled, 2015-07, Vol.72 (7), p.639-641

2015

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Longitudinal study of neuropathic pain in patients with Guillain-Barré syndrome

Irish journal of medical science, 2021-08, Vol.190 (3), p.1137-1142

2021

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Unraveling disease burden in familial ALS due to SOD1 mutation through the combination of brain and cervical cord MRI (P5.074)

Neurology, 2017-04, Vol.88 (16_supplement)

2017

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Quality of life in patients with MuSK positive myasthenia gravis

Acta neurologica Belgica, 2018-09, Vol.118 (3), p.423-427

2018

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Long-term outcome in patients with myasthenia gravis: one decade longitudinal study

Guillain-Barré syndrome in the elderly

Clinical and epidemiological features of Guillain-Barré syndrome in the Western Balkans

Childhood-Onset Myasthenia Gravis With Thymoma

The coexistence of myasthenia gravis and myotonic dystrophy type 2 in a single patient

Survival and mortality of adult‐onset myasthenia gravis in the population of Belgrade, Serbia

Assessment of health-related quality of life in patients with myasthenia gravis in Belgrade (Serbia)

Galactosylation of serum immunoglobulin G in myasthenia gravis with different autoantibodies

Amifampridine phosphate (Firdapse®) is effective and safe in a phase 3 clinical trial in LEMS

Myopathy, muscle atrophy and tongue lipid composition in MuSK myasthenia gravis

Comparison of the clinical and cognitive features of genetically positive ALS patients from the largest tertiary center in Serbia

Rate of progression of Guillain-Barré syndrome is not associated with the short-term outcome of the disease

Assessment of the neuropathic component in a chronic low back pain syndrome

COVID-19 infection and vaccination against SARS-CoV-2 in myasthenia gravis

Association between Cytotoxic T-Lymphocyte-Associated Antigen 4 (CTLA-4) Locus and Early-Onset Anti-acetylcholine Receptor-Positive Myasthenia Gravis in Serbian Patients

Myasthenia gravis treated in the neurology intensive care unit: a 14-year single-centre experience

Neuropathic pain as independent predictor of worse quality of life in patients with diabetic neuropathy

The presence of dysautonomia in different subgroups of myasthenia gravis patients

Unraveling ALS due to SOD1 mutation through the combination of brain and cervical cord MRI

Frequency and features of the central poststroke pain

Quality of life in patients with multifocal motor neuropathy from Serbia

A misdiagnosed myasthenia gravis with anti-muscle-specific tyrosine kinase antibodies with possible childhood onset

Longitudinal study of neuropathic pain in patients with Guillain-Barré syndrome

Unraveling disease burden in familial ALS due to SOD1 mutation through the combination of brain and cervical cord MRI (P5.074)

Quality of life in patients with MuSK positive myasthenia gravis

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