S. Perić

发表

Myopathic changes detected by quantitative electromyography in patients with MuSK and AChR positive myasthenia gravis

D. Lavrnić, V. Stojanović, I. Basta, 2016, Journal of Clinical Neuroscience.

Guillain‐Barré syndrome in the elderly

D. Lavrnić, I. Basta, I. Berisavac, 2016, Journal of the peripheral nervous system : JPNS.

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

V. Milošević, D. Lavrnić, G. Djordjević, 2014, Journal of the peripheral nervous system : JPNS.

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

D. Lavrnić, P. Stanarčević, M. Arsenijević, 2020, Irish Journal of Medical Science (1971 -).

Responsiveness of 2 Different Ability Outcome Measures in Guillain-Barré Syndrome

I. Bozovic, I. Basta, Aleksandar Stojanov, 2021, The neurologist.

N88S mutation in the BSCL2 gene in a Serbian family with distal hereditary motor neuropathy type V or Silver syndrome

V. Timmerman, V. Rakocevic-Stojanovic, J. Baets, 2010, Journal of the Neurological Sciences.

Cognitive assessment in patients with myotonic dystrophy type 2

G. Meola, V. Rakocevic-Stojanovic, Olivera Tamaš, 2022, Neuromuscular Disorders.

Guillain–Barré syndrome during pregnancy: A case series

A. Kačar, I. Berisavac, D. Jovanović, 2021, The journal of obstetrics and gynaecology research.

Body composition analysis in patients with myotonic dystrophy types 1 and 2

V. Rakocevic-Stojanovic, I. Bozovic, I. Basta, 2019, Neurological Sciences.

Myotonic Dystrophy Type 2 - Data from the Serbian Registry.

V. Rakocevic-Stojanovic, I. Bozovic, M. Božić, 2018, Journal of neuromuscular diseases.

Genotype–phenotype correlations in valosin-containing protein disease: a retrospective muticentre study

Sruthi S. Nair, K. Claeys, E. Malfatti, 2022, Journal of Neurology, Neurosurgery, and Psychiatry.

Autoimmune Diseases in Patients With Myotonic Dystrophy Type 2

G. Meola, V. Rakocevic-Stojanovic, Jelena Zlatar, 2022, Frontiers in neurology.

A longitudinal evaluation of fatigue in chronic inflammatory demyelinating polyneuropathy

Jeffrey A. Allen, I. Bozovic, M. Lutz, 2022, Brain and behavior.

Fatigue in chronic inflammatory demyelinating polyradiculoneuropathy

D. Cornblath, S. Perić, 2020, Muscle & nerve.

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

I. Bozovic, D. Lavrnić, I. Berisavac, 2020, Irish Journal of Medical Science (1971 -).

Incidence and mortality rates of Guillain‐Barré syndrome in Serbia

M. Stojanović, I. Bozovic, G. Djordjević, 2020, Journal of the peripheral nervous system : JPNS.

Amifampridine safety and efficacy in spinal muscular atrophy ambulatory patients: a randomized, placebo-controlled, crossover phase 2 trial

L. Maggi, G. Baranello, S. Iyadurai, 2022, Journal of Neurology.

Diabetes mellitus may affect short‐term outcome of Guillain‐Barré syndrome

V. Rakocevic-Stojanovic, I. Bozovic, D. Lavrnić, 2017, Journal of the peripheral nervous system : JPNS.

Phenotypic and Genetic Heterogeneity of Adult Patients with Hereditary Spastic Paraplegia from Serbia

A. Jordanova, D. Sokić, J. Drulovic, 2019, Journal of the Neurological Sciences.

Is there a difference between GBS triggered by COVID-19 and those of other origins?

I. Berisavac, D. Jovanović, Branka Mladenović, 2022, The Egyptian Journal of Neurology, Psychiatry and Neurosurgery.

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

D. Lavrnić, I. Basta, I. Berisavac, 2022, Neurological Sciences.

Association between the SMN2 gene copy number and clinical characteristics of patients with spinal muscular atrophy with homozygous deletion of exon 7 of the SMN1 gene.

G. Kekovic, S. Sekulic, Z. Stević, 2015, Vojnosanitetski pregled.

A novel recessive TTN founder variant is a common cause of distal myopathy in the Serbian population

D. MacArthur, M. Lek, Hanns Lochmüller, 2017, European Journal of Human Genetics.

Update of the pompe disease mutation database with 60 novel GAA sequence variants and additional studies on the functional effect of 34 previously reported variants

S. Marie, W. Robberecht, B. Engelen, 2012, Human mutation.

Downregulation of LKB1/AMPK Signaling in Blood Mononuclear Cells Is Associated with the Severity of Guillain–Barre Syndrome

M. Nikolić, V. Trajković, I. Bozovic, 2022, Cells.

Six‐month prospective study of quality of life in Guillain‐Barre syndrome

I. Bozovic, G. Djordjević, I. Basta, 2019, Acta neurologica Scandinavica.

Shorter CTG repeats length in an oligodendroglioma from a myotonic dystrophy type 1 patient

V. Rakocevic-Stojanovic, V. Dobričić, V. Ralić, 2015, Acta Neurologica Belgica.

Peripheral neuropathy in patients with myotonic dystrophy type 1

A. Kačar, D. Lavrnić, V. Stojanović, 2013, Neurological research.

Serbian Validation of the Individualized Neuromuscular Quality of Life Questionnaire (INQoL) in Adults With Myotonic Dystrophy Type 1

G. Meola, V. Rakocevic-Stojanovic, V. Sansone, 2011 .

Please cite this NEUROPATHIC PAIN IS AN INDEPENDENT PREDICTOR OF WORSE QUALITY OF LIFE IN PATIENTS WITH DIABETIC NEUROPATHY NEUROPATSKI BOL KAO NEZAVISAN PREDIKTOR LOŠIJEG KVALITETA ŽIVOTA KOD PACIJENATA SA DIJABETESNOM NEUROPATIJOM Authors

D. Lavrnić, I. Basta, A. Kovačević, 2020 .

VALIDATION OF THE BRIEF INTERNATIONAL COGNITIVE ASSESSMENT FOR MULTIPLE SCLEROSIS (BICAMS) IN A LARGE COHORT OF RELAPSING-REMITTING MS PATIENTS

R. Benedict, J. Drulovic, D. Aleksić, 2022, Acta clinica Croatica.

Proton magnetic resonance spectroscopy of the intrinsic tongue muscles in patients with myasthenia gravis with different autoantibodies

V. Rakocevic-Stojanovic, T. Stošić-Opinćal, D. Lavrnić, 2011, Journal of the Neurological Sciences.

Intravenous immunoglobulin therapy in two patients with myasthenia gravis and pemphigus vulgaris.

V. Rakocevic-Stojanovic, D. Lavrnić, I. Rakočević, 2009, Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.

Five‐year study of quality of life in myotonic dystrophy

V. Rakocevic-Stojanovic, D. Lavrnić, V. Dobričić, 2016, Acta neurologica Scandinavica.

Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness

Kristen M. Laricchia, D. MacArthur, M. Lek, 2020, Genetics in Medicine.

Clinical exome sequencing in Serbian patients with movement disorders: Single centre experience

V. Kostic, B. Peterlin, A. Maver, 2022, Genetika.

Titin antibodies in “seronegative” myasthenia gravis — A new role for an old antigen

N. Gilhus, K. Kleopa, R. Mantegazza, 2016, Journal of Neuroimmunology.

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

V. Arsenijević, E. Stefanova, D. Lavrnić, 2017, Journal of Neurology.

Corticosteroids in chronic inflammatory demyelinating polyneuropathy

I. Basta, L. Wieske, I. N. van Schaik, 2018, Journal of Neurology.

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

D. Lavrnić, I. Basta, I. Berisavac, 2022, Neurological Sciences.

Risk factors for potential drug–drug interactions in patients with myasthenia gravis

S. Janković, S. Peric, D. Aleksić, 2021, Neurological research.

A comprehensive analysis of the epidemiology and clinical characteristics of anti-LRP4 in myasthenia gravis.

K. Kleopa, T. Stojkovic, R. Mantegazza, 2014, Journal of autoimmunity.

Prospective measurement of quality of life in myotonic dystrophy type 1

C. Heatwole, A. Kačar, D. Lavrnić, 2017, Acta neurologica Scandinavica.

Cardiologic predictors of sudden death in patients with myotonic dystrophy type 1

S. Peric, D. Lavrnić, V. Stojanović, 2013, Journal of Clinical Neuroscience.

Significance of magnetic resonance imaging in differential diagnosis of nontraumatic brachial plexopathy.

D. Lavrnić, S. Lavrnić, D. Damjanovic, 2011, Vojnosanitetski pregled.

Phenotypic and genetic spectrum of patients with limb-girdle muscular dystrophy type 2A from Serbia

S. Peric, V. Rakocevic-Stojanovic, I. Bozovic, 2019, Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.

Heart involvement in patients with myotonic dystrophy type 2

Edita Z Cvitan, M. Kovačević, B. Bjelica, 2018, Acta Neurologica Belgica.

Anticipation as a Biological Phenomenon

S. Perić, 2015 .

Epidemiological Study of Adult-Onset Myasthenia Gravis in the Area of Belgrade (Serbia) in the Period 1979–2008

T. Pekmezović, V. Rakocevic-Stojanovic, I. Basta, 2013, Neuroepidemiology.

MuSK autoantibodies in myasthenia gravis detected by cell based assay — A multinational study

K. Kleopa, R. Mantegazza, T. Sharshar, 2015, Journal of Neuroimmunology.

Repeat Interruptions Modify Age at Onset in Myotonic Dystrophy Type 1 by Stabilizing DMPK Expansions in Somatic Cells

V. Rakocevic-Stojanovic, D. Savić-Pavićević, G. Brajušković, 2018, Front. Genet..

Chronic inflammatory demyelinating polyneuropathy associated with diabetes: a European multicentre comparative reappraisal

I. Bozovic, I. Basta, Aleksa Palibrk, 2020, Journal of Neurology, Neurosurgery, and Psychiatry.

One‐year follow‐up study of neuropathic pain in chronic inflammatory demyelinating polyradiculoneuropathy

A. Kačar, I. Bozovic, I. Basta, 2019, Journal of the peripheral nervous system : JPNS.

Neuromuscular disease‐specific questionnaire to assess quality of life in patients with chronic inflammatory demyelinating polyradiculoneuropathy

V. Rakocevic-Stojanovic, A. Kačar, I. Bozovic, 2018, Journal of the peripheral nervous system : JPNS.

Safety, efficacy, and tolerability of efgartigimod in patients with generalised myasthenia gravis (ADAPT): a multicentre, randomised, placebo-controlled, phase 3 trial

J. Statland, M. Pasnoor, J. Verschuuren, 2021, The Lancet Neurology.

Molecular and Clinical Implications of Variant Repeats in Myotonic Dystrophy Type 1

G. Meola, D. Savić-Pavićević, J. Pesovic, 2021, International journal of molecular sciences.

Recurrent Guillain-Barré Syndrome – Case Series

I. Bozovic, G. Djordjević, I. Basta, 2019, Neurology India.

Transcranial sonography in patients with Parkinson's disease with glucocerebrosidase mutations.

Christine Klein, Marina Svetel, Aleksandra Pavlović, 2013, Parkinsonism & related disorders.

Neuropathic pain in patients with Charcot-Marie-Tooth type 1A

A. Kačar, I. Bozovic, I. Basta, 2019, Neurological Sciences.

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

T. Pekmezović, V. Rakocevic-Stojanovic, D. Lavrnić, 2018, Muscle & nerve.

Disability and quality of life in Guillain-Barré syndrome – Longitudinal study

M. Stojanović, S. Peric, A. Kačar, 2020, Journal of Clinical Neuroscience.

The presence of dysautonomia in different subgroups of myasthenia gravis patients

D. Lavrnić, V. Stojanović, S. Popović, 2014, Journal of Neurology.

Leptin and the metabolic syndrome in patients with myotonic dystrophy type 1

S. Peric, S. Apostolski, I. Basta, 2010, Acta neurologica Scandinavica.

Dependent and paranoid personality patterns in myotonic dystrophy type 1

D. Lavrnić, I. Basta, I. Marjanović, 2014, Acta neurologica Scandinavica.

Elevated leukocyte count in cerebrospinal fluid of patients with chronic inflammatory demyelinating polyneuropathy

C. Verhamme, I. Basta, L. Wieske, 2018, Journal of the peripheral nervous system : JPNS.

Metabolic syndrome in patients with myotonic dystrophy type 1

S. Peric, V. Rakocevic-Stojanovic, V. Dobričić, 2015, Muscle & nerve.

Adult‐onset very‐long‐chain acyl‐CoA dehydrogenase deficiency (VLCADD)

M. Mroczek, H. Najmabadi, F. Fatehi, 2020, European journal of neurology.

Fatigue in myotonic dystrophy type 1: a seven-year prospective study

I. Bozovic, V. Stojanović, I. Basta, 2019, Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.

Biallelic ADPRHL2 mutations in complex neuropathy affect ADP ribosylation and DNA damage response

B. Ceulemans, I. Ahel, T. Deconinck, 2021, Life Science Alliance.

Biallelic ADPRHL2mutations in complex neuropathy affect ADP ribosylation and DNA damage response

B. Ceulemans, I. Ahel, T. Deconinck, 2021 .

Cerebrospinal fluid biomarkers of neurodegeneration in patients with juvenile and classic myotonic dystrophy type 1

V. Kostic, G. Mandić-Stojmenović, E. Stefanova, 2013, Journal of the Neurological Sciences.

Extending the clinical and mutational spectrum of TRIM32-related myopathies in a non-Hutterite population

D. MacArthur, M. Lek, T. Mongini, 2018, Journal of Neurology, Neurosurgery, and Psychiatry.

Identification of GAA variants through whole exome sequencing targeted to a cohort of 606 patients with unexplained limb-girdle muscle weakness

D. MacArthur, M. Lek, K. Claeys, 2017, Orphanet Journal of Rare Diseases.

Prognostic factors and survival of ALS patients from Belgrade, Serbia

V. Rakocevic-Stojanovic, D. Lavrnić, I. Basta, 2016, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Safety and efficacy of rozanolixizumab in patients with generalised myasthenia gravis (MycarinG): a randomised, double-blind, placebo-controlled, adaptive phase 3 study

Denny J. Padgett, Adam L. Comer, Yi-Chung Lee, 2023, The Lancet Neurology.

Efgartigimod improved health-related quality of life in generalized myasthenia gravis: results from a randomized, double-blind, placebo-controlled, phase 3 study (ADAPT)

J. Verschuuren, C. Qi, T. Vu, 2023, Journal of Neurology.

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

T. Pekmezović, D. Kisić-Tepavčević, S. Peric, 2012, Neurological Sciences.

Molecular genetic and clinical characterization of myotonic dystrophy type 1 patients carrying variant repeats within DMPK expansions

V. Rakocevic-Stojanovic, D. Savić-Pavićević, G. Brajušković, 2017, neurogenetics.

Quality of life in adult patients with limb–girdle muscular dystrophies

V. Rakocevic-Stojanovic, A. Kačar, I. Basta, 2017, Acta Neurologica Belgica.

Frontostriatal dysexecutive syndrome: a core cognitive feature of myotonic dystrophy type 2

G. Mandić-Stojmenović, E. Stefanova, V. Rakocevic-Stojanovic, 2014, Journal of Neurology.

Self-reported autonomic dysfunction in a recovery phase of Guillain-Barré syndrome

I. Bozovic, Aleksa Palibrk, M. Arsenijević, 2020, Clinical Neurology and Neurosurgery.

Three-Year Follow-Up Study in Patients with Guillain-Barré Syndrome

I. Bozovic, G. Djordjević, I. Basta, 2018, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

V. Rakocevic-Stojanovic, I. Basta, D. Lavrnić, 2010, Acta neurologica Belgica.

Heart involvement in patients with myotonic dystrophy type 2

Edita Z Cvitan, M. Kovačević, B. Bjelica, 2018, Acta Neurologica Belgica.

Non-routine cardiac tests still have no defined role in assessment of myotonic dystrophy type 2

S. Perić, 2019, Acta Neurologica Belgica.

Magnetic resonance imaging of leg muscles in patients with myotonic dystrophies

V. Rakocevic-Stojanovic, I. Bozovic, R. Maksimovic, 2017, Journal of Neurology.

Routine echocardiography in patients with myotonic dystrophy type 1

S. Peric, S. Raspopović, V. Stojanović, 2017, Journal of the Chinese Medical Association : JCMA.

Frequency and features of the central poststroke pain

D. Lavrnić, I. Basta, A. Kovačević, 2018, Journal of the Neurological Sciences.

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

S. Peric, I. Bozovic, D. Lavrnić, 2020, Vojnosanitetski pregled.

Variability of multisystemic features in myotonic dystrophy type 1 – lessons from Serbian registry

V. Rakocevic-Stojanovic, A. Kačar, V. Dobričić, 2015, Neurological research.

Metabolic impairments in patients with myotonic dystrophy type 2

S. Peric, V. Rakocevic-Stojanovic, M. Vujnić, 2018, Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.

Hypogonadism and erectile dysfunction in myotonic dystrophy type 1

D. Lavrnić, I. Basta, I. Marjanović, 2013, Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.

Influence of multisystemic affection on health-related quality of life in patients with myotonic dystrophy type 1

D. Lavrnić, V. Stojanović, I. Basta, 2013, Clinical Neurology and Neurosurgery.

Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease

G. Bassez, J. Puymirat, H. Lochmüller, 2018, Orphanet Journal of Rare Diseases.

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

M. Kostic, S. Peric, I. Bozovic, 2021, Journal of Neurology.

Cerebral involvement and related aspects in myotonic dystrophy type 2

G. Meola, S. Peric, V. Rakocevic-Stojanovic, 2021, Neuromuscular Disorders.

Multidimensional aspects of pain in myotonic dystrophies

V. Rakocevic-Stojanovic, D. Lavrnić, V. Dobričić, 2015, Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.

Yield of the PMP22 deletion analysis in patients with compression neuropathies

S. Peric, V. Rakocevic-Stojanovic, A. Kačar, 2020, Journal of Neurology.

Gait in amyotrophic lateral sclerosis: Is gait pattern differently affected in spinal and bulbar onset of the disease during dual task walking?

V. Kostic, I. Basta, M. Milićev, 2014, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Myotonic dystrophy type 1 in the COVID-19 era

G. Meola, V. Rakocevic-Stojanovic, I. Bozovic, 2023, Neurological Sciences.

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

I. Bozovic, D. Lavrnić, I. Basta, 2022, Acta Neurologica Belgica.

Clusters of cognitive impairment among different phenotypes of myotonic dystrophy type 1 and type 2

G. Meola, M. Mijajlovic, D. Savić-Pavićević, 2017, Neurological Sciences.

Quality of life in patients with MuSK positive myasthenia gravis

M. Stankovic, D. Lavrnić, I. Basta, 2018, Acta Neurologica Belgica.

Executive dysfunction and survival in patients with amyotrophic lateral sclerosis: Preliminary report from a Serbian centre for motor neuron disease

T. Pekmezović, T. Stojkovic, E. Stefanova, 2016, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Correlation of clinical and neurophysiological findings with health-related quality of life in patients with diabetic polyneuropathy.

T. Pekmezović, D. Lavrnić, I. Basta, 2014, Vojnosanitetski pregled.

Clinical score for early diagnosis of myotonic dystrophy type 2

G. Meola, V. Rakocevic-Stojanovic, I. Bozovic, 2022, Neurological Sciences.

Myotonic dystrophy type 1

S. Peric, V. Stojanović, I. Basta, 2015 .

Quality of life in patients with polyneuropathy associated with different types of monoclonal gammopathy of undetermined significance

I. Bozovic, I. Basta, Aleksa Palibrk, 2019, Acta Neurologica Belgica.

Brain sonography insight into the midbrain in myotonic dystrophy type 2

A. Pavlovic, V. Rakocevic-Stojanovic, D. Lavrnić, 2016, Muscle & nerve.

Comparison of temporal and stride characteristics in myotonic dystrophies type 1 and 2 during dual-task walking.

V. Kostic, V. Rakocevic-Stojanovic, V. Dobričić, 2016, Gait & posture.

The influence of the COVID-19 pandemic on patients with chronic inflammatory demyelinating polyradiculoneuropathy

S. Peric, I. Bozovic, G. Djordjević, 2021, Clinical Neurology and Neurosurgery.

Prospective analysis of disability and quality of life in patients with chronic inflammatory demyelinating polyradiculoneuropathy

D. Aleksić, I. Bozovic, Iva Bulatovic, 2021, Quality of Life Research.

Validation of the Serbian version of inflammatory Rasch‐built overall disability scale in patients with chronic inflammatory demyelinating polyradiculoneuropathy

I. Bozovic, I. Merkies, C. Faber, 2019, Journal of the peripheral nervous system : JPNS.

Employment status of patients with chronic inflammatory demyelinating polyradiculoneuropathy

A. Kačar, I. Bozovic, G. Djordjević, 2018, Journal of the peripheral nervous system : JPNS.

Quality of life predictors in patients with chronic inflammatory demyelinating polyradiculoneuropathy

I. Bozovic, G. Djordjević, I. Basta, 2017, Journal of Neurology.

Quality of life in hereditary neuropathy with liability to pressure palsies is as impaired as in Charcot–Marie–Tooth disease type 1A

I. Bozovic, Aleksa Palibrk, M. Branković, 2020, Acta Neurologica Belgica.

Quality of life in hereditary neuropathy with liability to pressure palsies is as impaired as in Charcot–Marie–Tooth disease type 1A

I. Bozovic, Aleksa Palibrk, M. Branković, 2020, Acta Neurologica Belgica.

Chronic Acquired Polyneuropathy Patient Reported Index (CAPPRI) in chronic inflammatory demyelinating polyradiculoneuropathy

I. Bozovic, T. Burns, I. Basta, 2019, Journal of the peripheral nervous system : JPNS.

Quality of life in patients with polyneuropathy associated with different types of monoclonal gammopathy of undetermined significance

I. Bozovic, I. Basta, Aleksa Palibrk, 2019, Acta Neurologica Belgica.

Quality of life in patients with multifocal motor neuropathy from Serbia

V. Rakocevic-Stojanovic, A. Kačar, I. Bozovic, 2019, Journal of the Neurological Sciences.

copy number as a modifying factor of survival in Serbian patients with sporadic amyotrophic lateral sclerosis

S. Peric, Z. Stević, D. Savić-Pavićević, 2018 .

C9orf72 genetic screening in amyotrophic lateral sclerosis patients from Serbia

E. Stefanova, V. Dobričić, I. Basta, 2023, Genetika.

Cognitive Impairment in Myotonic Dystrophy Type 1 Is Associated with White Matter Damage

M. Filippi, F. Agosta, M. Copetti, 2014, PloS one.

Redox imbalance in peripheral blood of type 1 myotonic dystrophy patients

Dragan Marinkovic, D. Blagojević, A. Nikolić-Kokić, 2016, Redox report : communications in free radical research.

Galactosylation of serum immunoglobulin G in myasthenia gravis with different autoantibodies

D. Lavrnić, I. Basta, M. Janković, 2023, Scandinavian journal of clinical and laboratory investigation.

Transcranial sonography in patients with myotonic dystrophy type 1

A. Pavlovic, D. Lavrnić, V. Dobričić, 2014, Muscle & nerve.

Extrathymic malignancies in a defined cohort of patients with myasthenia gravis

T. Pekmezović, V. Rakocevic-Stojanovic, D. Lavrnić, 2014, Journal of the Neurological Sciences.

Cardiac autonomic control in patients with myasthenia gravis and thymoma

V. Rakocevic-Stojanovic, S. Damjanovic, I. Basta, 2011, Journal of the Neurological Sciences.

Quality of life in adult patients with limb–girdle muscular dystrophies

V. Rakocevic-Stojanovic, A. Kačar, I. Basta, 2018, Acta Neurologica Belgica.

Update on Therapy for Myotonic Dystrophy Type 1

G. Meola, Z. Vukojević, S. Perić, 2023, Current Treatment Options in Neurology.

Association between metabolic syndrome and homocysteinemia in ischemic stroke

S. Peric, D. Račić, V. Djajić, 2013, Journal of the Neurological Sciences.

Hereditary myopathy with early respiratory failure: case report

I. Čekerevac, Miloš Ratinac, S. Perić, 2023, The Egyptian Journal of Neurology, Psychiatry and Neurosurgery.

Quality of life in patients with myotonic dystrophy type 2

D. Lavrnić, V. Stojanović, M. Vujnić, 2016, Journal of the Neurological Sciences.

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

A. Reuser, K. Fumic, S. Perić, 2013, Acta Neurologica Belgica.

Long-term Safety and Efficacy of Efgartigimod in Patients With Generalized Myasthenia Gravis: Interim Results of the ADAPT+ Study

M. Pasnoor, J. Verschuuren, R. Mantegazza, 2022, Neurology.

Cytokine Gene Polymorphisms in Patients with Chronic Inflammatory Demyelinating Polyneuropathy

V. Perovic, D. Popadic, I. Bozovic, 2023, Cells.

Chronic inflammatory demyelinating polyradiculoneuropathy: Diagnostic problems in clinical practice in Serbia

A. Kačar, I. Bozovic, I. Basta, 2023, Journal of the peripheral nervous system : JPNS.

Antecedent infections and vaccinations in chronic inflammatory demyelinating polyneuropathy: A European collaborative study

I. Bozovic, Aida Kalac, I. Basta, 2021, Muscle & nerve.

Quality of life in patients with MuSK positive myasthenia gravis

M. Stankovic, D. Lavrnić, I. Basta, 2018, Acta Neurologica Belgica.

Brain positron emission tomography in patients with myotonic dystrophy type 1 and type 2

V. Stojanović, I. Basta, Biljana Salak-Djokic, 2017, Journal of the Neurological Sciences.

Significant impact of behavioral and cognitive impairment on quality of life in patients with myotonic dystrophy type 1

E. Stefanova, V. Rakocevic-Stojanovic, V. Dobričić, 2014, Clinical Neurology and Neurosurgery.

Basophilic peripheral nerve inclusions in patient with L144F SOD1 amyotrophic lateral sclerosis

V. Rakocevic-Stojanovic, D. Aleksić, S. Milenković, 2021, Vojnosanitetski pregled.

Three-Year Follow-Up Study in Patients with Guillain-Barré Syndrome

I. Bozovic, G. Djordjević, I. Basta, 2018, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Psychometric longitudinal evaluation of the Chronic Acquired Polyneuropathy Patient‐Reported Index (CAPPRI) in patients with chronic inflammatory demyelinating polyneuropathy

I. Bozovic, T. Burns, I. Basta, 2020, Muscle & nerve.