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Mutations in SACS cause atypical and late-onset forms of ARSACS

Neurology, 2010-09, Vol.75 (13), p.1181-1188

2010

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

Journal of the neurological sciences, 2010-09, Vol.296 (1), p.107-109

2010

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Intellectual Ability in the Duchenne Muscular Dystrophy and Dystrophin Gene Mutation Location

Balkan journal of medical genetics, 2014-12, Vol.17 (2), p.25-35

2014

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Serum leptin levels in children and adolescents with spinal muscular atrophy types 2 and 3

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2022-10, Vol.29 (7), p.480-483

2022

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Epidemiology of Charcot-Marie-Tooth Disease in the Population of Belgrade, Serbia

Neuroepidemiology, 2011-01, Vol.36 (3), p.177-182

2011

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31.Familial autoimmune myasthenia gravis

Clinical neurophysiology, 2012-07, Vol.123 (7), p.e84-e84

2012

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Electroneuromyography study in subclinical hyper-CK-emia

Clinical neurophysiology, 2008-03, Vol.119 (3), p.e67-e67

Milic-Rasic, V

2008

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4.Electromyography test as diagnostic procedure in recessive cerebellar ataxias

Clinical neurophysiology, 2012-07, Vol.123 (7), p.e78-e78

2012

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19. Multimodal evoked potentials in hereditary motor and sensory neuropathy type 1

Clinical neurophysiology, 2010-04, Vol.121 (4), p.e9-e9

2010

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4. Neurophysiologic and clinical characteristic of neuromyotonia in new hereditary neuromuscular disorder

Clinical neurophysiology, 2013-07, Vol.124 (7), p.e10-e10

2013

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MFN2 mutation distribution and genotype/phenotype correlation in Charcot–Marie–Tooth type 2

Brain (London, England : 1878), 2006-08, Vol.129 (8), p.2093-2102

2006

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Treatment of congenital myasthenic syndromes

European journal of paediatric neurology, 2008, Vol.12, p.S23-S23

2008

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Malignant Peripheral Nerve Sheath Tumor of the Oculomotor Nerve

Acta radiologica (1987), 2006-07, Vol.47 (6), p.595-598

2006

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156P Phosphorylated neurofilament heavy chain in cerebrospinal fluid and plasma in clinically silent and childhood-onset SMA individuals from Serbia

Neuromuscular disorders : NMD, 2024-10, Vol.43, p.104441, Article 104441.591

2024

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9. Electroneuromyography in children with neuromuscular disorders, once and now

Clinical neurophysiology, 2010-04, Vol.121 (4), p.e7-e7

Rasic, V. Milic

2010

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P193 – 1897 Single-center register of early onset ataxias (EOA)

European journal of paediatric neurology, 2013-09, Vol.17, p.S106-S106

2013

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P25.7 Rehabilitation possibility depends on electromyography and genotype in hereditary neuropathy

Clinical neurophysiology, 2011, Vol.122, p.S173-S174

2011

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Guillain Barre syndrome with facial, ocular and bulbar signs

Clinical neurophysiology, 2007-04, Vol.118 (4), p.e126-e126

Rasic, V. Milic

2007

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PP12.16 – 2973: Congenital cerebellar ataxias – Clinical, radiological and genetic considerations

European journal of paediatric neurology, 2015-05, Vol.19, p.S81-S82

2015

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INITIAL CLINICAL AND MRI FINDINGS IN SUBACUTE SCLEROSING PANENCEPHALITIS (SSPE)

Neuropediatrics, 2006, Vol.37 (S 1)

2006

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Genotype-phenotype correlation in Friedreich's ataxia

European journal of paediatric neurology, 2017-06, Vol.21, p.e205-e206

2017

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O4 – 2020 Electroneuromyography parameters in hereditary and congenital ataxia

European journal of paediatric neurology, 2013-09, Vol.17, p.S2-S2

2013

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P5.18 Electromyography findings in family with cerebellar ataxia and new genotype

Clinical neurophysiology, 2011, Vol.122, p.S81-S82

2011

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5. Molecular genetics of myotonic disorders in Serbian patients

Clinical neurophysiology, 2013-07, Vol.124 (7), p.e10-e10

2013

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21. Polyneuropathic clinical picture and neurophysiological myoptaic finding – Case report

Clinical neurophysiology, 2009-03, Vol.120 (3), p.e132-e132

2009

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Mutations in SACS cause atypical and late-onset forms of ARSACS

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

Intellectual Ability in the Duchenne Muscular Dystrophy and Dystrophin Gene Mutation Location

Serum leptin levels in children and adolescents with spinal muscular atrophy types 2 and 3

Epidemiology of Charcot-Marie-Tooth Disease in the Population of Belgrade, Serbia

31.Familial autoimmune myasthenia gravis

Electroneuromyography study in subclinical hyper-CK-emia

4.Electromyography test as diagnostic procedure in recessive cerebellar ataxias

19. Multimodal evoked potentials in hereditary motor and sensory neuropathy type 1

4. Neurophysiologic and clinical characteristic of neuromyotonia in new hereditary neuromuscular disorder

MFN2 mutation distribution and genotype/phenotype correlation in Charcot–Marie–Tooth type 2

Treatment of congenital myasthenic syndromes

Malignant Peripheral Nerve Sheath Tumor of the Oculomotor Nerve

156P Phosphorylated neurofilament heavy chain in cerebrospinal fluid and plasma in clinically silent and childhood-onset SMA individuals from Serbia

9. Electroneuromyography in children with neuromuscular disorders, once and now

P193 – 1897 Single-center register of early onset ataxias (EOA)

P25.7 Rehabilitation possibility depends on electromyography and genotype in hereditary neuropathy

Guillain Barre syndrome with facial, ocular and bulbar signs

PP12.16 – 2973: Congenital cerebellar ataxias – Clinical, radiological and genetic considerations

INITIAL CLINICAL AND MRI FINDINGS IN SUBACUTE SCLEROSING PANENCEPHALITIS (SSPE)

Genotype-phenotype correlation in Friedreich's ataxia

O4 – 2020 Electroneuromyography parameters in hereditary and congenital ataxia

P5.18 Electromyography findings in family with cerebellar ataxia and new genotype

5. Molecular genetics of myotonic disorders in Serbian patients

21. Polyneuropathic clinical picture and neurophysiological myoptaic finding – Case report

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