Milić Rašić, V.: search on Z-Library

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1

Common features of the cerebral perforating arteries and their clinical significance

Djulejić, Vuk, Marinković, Slobodan, Milić, Vedrana, Georgievski, Biljana, Rašić, Melanija, Aksić, Milan, Puškaš, Laslo

Journal:

Acta Neurochirurgica

Year:

2015

Language:

english

File:

PDF, 2.22 MB

english, 2015

2

Proteomic analysis in giant axonal neuropathy: New insights into disease mechanisms

Silke Mussche, Boel De Paepe, Joél Smet, Katrien Devreese, Willy Lissens, Vedrana Milic Rasic, Matthew Murnane, Bart Devreese, Rudy Van Coster

Journal:

Year:

2012

Language:

english

File:

PDF, 1.30 MB

english, 2012

3

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

Rasic, Milic V., Vojinovic, D., Pesovic, J., Mijalkovic, G., Lukic, V., Mladenovic, J., Kosac, A., Novakovic, I., Maksimovic, N., Romac, S., Todorovic, S., Pavicevic, Savic D.

Journal:

Balkan Journal of Medical Genetics

Year:

2014

Language:

english

File:

PDF, 380 KB

english, 2014

4

Common features of the cerebral perforating arteries and their clinical significance

Djulejić, Vuk, Marinković, Slobodan, Milić, Vedrana, Georgievski, Biljana, Rašić, Melanija, Aksić, Milan, Puškaš, Laslo

Journal:

Acta Neurochirurgica

Year:

2015

Language:

english

File:

PDF, 182 KB

english, 2015

5

[IEEE 6th International Conference on Telecommunications in Modern Satellite, Cable and Broadcasting Service, 2003. TELSIKS 2003. - Serbia, Montenegro, Nis (Oct. 1-3, 2003)] 6th International Conference on Telecommunications in Modern Satellite, Cable and Broadcasting Service, 2003. TELSIKS 2003. - Telemedicine as a new multimedia services: concepts and advances

Samcovic, A., Bojkovic, Z., Milic-Rasic, V.

Year:

2003

Language:

english

File:

PDF, 318 KB

english, 2003

6

P18.4 Analysis of the Giant Axonal Neuropathy fibroblasts proteome

S. Mussche, B. De Paepe, J. Smet, W. Lissens, V. Milić-Rašić, M. Murnane, B. Devreese, R. van Coster

Journal:

European Journal of Paediatric Neurology

Year:

2011

Language:

english

File:

PDF, 36 KB

english, 2011

7

Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeats

Gagic, Milica, Markovic, Milica Keckarevic, Kecmanovic, Miljana, Keckarevic, Dusan, Mladenovic, Jelena, Dackovic, Jelena, Milic-Rasic, Vedrana, Romac, Stanka

Journal:

Clinical Chemistry and Laboratory Medicine

Year:

2015

Language:

english

File:

PDF, 1.38 MB

english, 2015

8

Electromyoneurographic findings in patient with congenital muscular dystrophy

Kovačević, G., Rašić, V. Milić, Zamurović, D., Ostojić, S.

Journal:

Clinical Neurophysiology

Year:

2015

Language:

english

File:

PDF, 40 KB

english, 2015

9

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

Journal:

Clinical Neurophysiology

Year:

2010

Language:

english

File:

PDF, 38 KB

english, 2010

10

Genotype-phenotype correlation in Friedreich's ataxia

Kovacevic, G., Todorovic, S., Novakovic, I., Pavicevic Savic, D., Rasic, V. Milic, Svetel, M., Dobricic, V.

Journal:

European Journal of Paediatric Neurology

Year:

2017

Language:

english

File:

PDF, 60 KB

english, 2017

11

P222 Is headache an important symptom in children with arterial ischemic stroke?

V. Brankovic-Sreckovic, V. Milic Rasic, S. Todorovic

Journal:

European Journal of Paediatric Neurology

Year:

2009

Language:

english

File:

PDF, 37 KB

english, 2009

12

Genotype–phenotype analysis in patients with giant axonal neuropathy (GAN)

Olga Koop, Anja Schirmacher, Eva Nelis, Vincent Timmerman, Peter De Jonghe, Bernd Ringelstein, Vedrana Milic Rasic, Philippe Evrard, Jutta Gärtner, Kristl G. Claeys, Silke Appenzeller, Bernd Rautenstr

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 200 KB

english, 2007

13

P163 Electroneuromyography findings in patients with hereditary motor and sensory neuropathy type II

Jelena Nikodinović, Vedrana Milić-Rašić, Slobodanka Todorović, Slobodan Apostolski, Vidosava Rakočević-Stojanović, Jelena Mladenović, Jelena Dačković

Journal:

Clinical Neurophysiology

Year:

2008

Language:

english

File:

PDF, 62 KB

english, 2008

14

O4 – 2020 Electroneuromyography parameters in hereditary and congenital ataxia

Rasic, V Milic, Brankovic, V, Mladenovic, J, Kosac, A, Todorovic, S

Journal:

European Journal of Paediatric Neurology

Year:

2013

Language:

english

File:

PDF, 70 KB

english, 2013

15

11. Neurophysiological findings in patients with new mutation in GJB1 as a cause of X-linked Charcot–Marie–Tooth disease

J. Mladenovic, M. Keckarevic, V. Milic Rasic, J. Nikodinovic, S. Pržulj Toković, S. Todorovic

Journal:

Clinical Neurophysiology

Year:

2010

Language:

english

File:

PDF, 38 KB

english, 2010

16

Childhood Cerebral X-Linked Adrenoleukodystrophy More Than 5 Years After Hematopoietic Cell Transplantation: The First Case From Serbia and Southeastern Europe

Potic, A., Rovelli, A. M., Uziel, G., Kozic, D., Mladenovic, J., Milic-Rasic, V.

Journal:

Journal of Child Neurology

Year:

2010

Language:

english

File:

PDF, 394 KB

english, 2010

17

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

Milic Rasic, V., Nikodinovic, J., Mladenovic, J., De Jonghe, P., Jordanova, A., Baets, J., Zimon, M., Keckarevic Markovic, M., Savic Pavicevic, D., Todorovic, S.

Journal:

Clinical Neurophysiology

Year:

2013

Language:

english

File:

PDF, 40 KB

english, 2013

18

INTRADURAL PUNCTURE OF THE SPINAL CORD.

Milic Rasic, V., Nikodinovic, J., Mladenovic, J., De Jonghe, P., Jordanova, A., Baets, J., Zimon, M., Keckarevic Markovic, M., Savic Pavicevic, D., Todorovic, S.

Journal:

Year:

1896

Language:

english

File:

PDF, 185 KB

english, 1896

19

Further developments with antisense treatment for myasthenia gravis

Sussman, Jon, Argov, Zohar, Wirguin, Yitzhak, Apolski, Slobodan, Milic-Rasic, Vedrana, Soreq, Hermona

Journal:

Annals of the New York Academy of Sciences

Year:

2012

Language:

english

File:

PDF, 464 KB

english, 2012

20

5. Molecular genetics of myotonic disorders in Serbian patients

Savić Pavićević, D., Milić Rašić, V., Mladenović, J., Rakočević Stojanović, V., Brajušković, G., Jordanova, A., De Jonghe, P., Todorović, S., Romac, S.

Journal:

Clinical Neurophysiology

Year:

2013

Language:

english

File:

PDF, 40 KB

english, 2013

21

Joint effect of the SMN2 and SERF1A genes on childhood-onset types of spinal muscular atrophy in Serbian patients

Brkušanin, Miloš, Kosać, Ana, Jovanović, Vladimir, Pešović, Jovan, Brajušković, Goran, Dimitrijević, Nikola, Todorović, Slobodanka, Romac, Stanka, Milić Rašić, Vedrana, Savić-Pavićević, Dušanka

Journal:

Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 579 KB

english, 2015

22

Multiple sclerosis: Onset before age 10 years

Dusan N. Vranjesevic, Aleksandra Djukic, Vedrana M. Milic-Rasic, Nebojsa S. Jovic, Vesna M. Brankovic

Journal:

Pediatric Neurology

Year:

1994

Language:

english

File:

PDF, 123 KB

english, 1994

23

18. Non-dystrophinopathy muscular dystrophies at childhood age

B. Vukadinović-Pajović, V. Milić-Rašić, S. Todorović

Journal:

Clinical Neurophysiology

Year:

2009

Language:

english

File:

PDF, 40 KB

english, 2009

24

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

Brankovic, V., Zekavica, A., Popara, J., Rasic, V. Milic

Journal:

European Journal of Paediatric Neurology

Year:

2015

Language:

english

File:

PDF, 114 KB

english, 2015

25

2FC2.5 Serbian serie of congenital myasthenic syndromes (CMS): Correlation between phenotype and genotype

S. Miloš Todorovic, V. Milić-Rašić, H. Lochmüller

Journal:

European Journal of Paediatric Neurology

Year:

2011

Language:

english

File:

PDF, 36 KB

english, 2011

26

P106 Hereditary neuropathy in Gypsy population

V. Milic Rasic, S. Todorovic, M. Keckarevic Markovic, J. Mladenovic, V. Brankovic

Journal:

European Journal of Paediatric Neurology

Year:

2009

Language:

english

File:

PDF, 42 KB

english, 2009

27

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

J. Jancic, V. Milic-Rasic, J. Mladenovic

Journal:

Clinical Neurophysiology

Year:

2010

Language:

english

File:

PDF, 37 KB

english, 2010

28

Truncating and Missense Mutations in IGHMBP2 Cause Charcot-Marie Tooth Disease Type 2

Cottenie, Ellen, Kochanski, Andrzej, Jordanova, Albena, Bansagi, Boglarka, Zimon, Magdalena, Horga, Alejandro, Jaunmuktane, Zane, Saveri, Paola, Rasic, Vedrana Milic, Baets, Jonathan, Bartsakoulia, Ma

Journal:

The American Journal of Human Genetics

Year:

2014

Language:

english

File:

PDF, 2.94 MB

english, 2014

29

Treatment of congenital myasthenic syndromes

V. Milic Rasic, S. Todorovic, J. Mueller, H. Lochmueller

Journal:

European Journal of Paediatric Neurology

Year:

2008

Language:

english

File:

PDF, 46 KB

english, 2008

30

Electroneuromyography study in subclinical hyper-CK-emia

Journal:

Clinical Neurophysiology

Year:

2008

Language:

english

File:

PDF, 54 KB

english, 2008

31

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

J. Mladenovic, V. Milic Rasic, V. Rakocevic Stojanovc, S. Przulj Tokovic

Journal:

Clinical Neurophysiology

Year:

2009

Language:

english

File:

PDF, 36 KB

english, 2009

32

GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia

Dobričić, Valerija, Tomić, Aleksandra, Branković, Vesna, Kresojević, Nikola, Janković, Milena, Westenberger, Ana, Rašić, Vedrana Milić, Klein, Christine, Novaković, Ivana, Svetel, Marina, Kostić, Vlad

Journal:

Parkinsonism & Related Disorders

Year:

2017

Language:

english

File:

PDF, 207 KB

english, 2017

33

NMP08 Asymptomatic Charcot Marie Tooth

V. Milic Rasic, S. Todorovic, E. Nelis, M. Keckarevic, L. Kalaydjieva, V. Brankovic

Journal:

European Journal of Paediatric Neurology

Year:

2007

Language:

english

File:

PDF, 44 KB

english, 2007

34

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

Brankovic-Sreckovic, V, Milic Rasic, V, Popara, J, Zekavica, A, Todorovic, S

Journal:

European Journal of Paediatric Neurology

Year:

2013

Language:

english

File:

PDF, 66 KB

english, 2013

35

Arterial Ischemic Stroke in a Child with -Thalassemia Trait and Methylentetrahydrofolate Reductase Mutation

Brankovic-Sreckovic, V., Milic Rasic, V., Djordjevic, V., Kuzmanovic, M., Pavlovic, S.

Journal:

Journal of Child Neurology

Year:

2007

Language:

english

File:

PDF, 422 KB

english, 2007

36

PO32-FR-24 Heterozygous missense mutation in the BSCL2 gene in a Serbian family with distal hereditary motor neuropathy or silver syndrome

Rakocevic Stojanovic, V., Rasic, V. Milic, Van Broeckhoven, C., De Jonghe, P., Nelis, E., Nikolic, A., Tasic, Z., Marjanovic, I., Lavrnic, D.

Journal:

Journal of the Neurological Sciences

Year:

2009

Language:

english

File:

PDF, 46 KB

english, 2009

37

The Recurrence Risk of Ischemic Stroke in Childhood

Brankovic-Sreckovic, Vesna, Milic-Rasic, Vedrana, Jovic, Nebojsa, Milic, Natasa, Todorovic, Slobodanka

Journal:

Medical Principles and Practice

Year:

2004

Language:

english

File:

PDF, 141 KB

english, 2004

38

Multiple sclerosis in successive generations: Study of 5 families

Dusan N. Vranjesevic, Nebojsa S. Jovic, Aleksandra Djukic, Vedrana M. Milic-Rasic

Journal:

Pediatric Neurology

Year:

1994

Language:

english

File:

PDF, 127 KB

english, 1994

39

Malignant Peripheral Nerve Sheath Tumor of the Oculomotor Nerve

Kozic, D., Nagulic, M., Ostojic, J., Samardzic, M., Milic-Rasic, V., Skender Gazibara, M., Nuri Sener, R.

Journal:

Acta Radiologica

Year:

2006

Language:

english

File:

PDF, 261 KB

english, 2006

40

P16.3 Neuromyotonia as a main sign of a possible new type of hereditary axonal neuropathy

V. Milić-Rašić, S. Todorovic, J. Nikodinovic, J. Mladenovic, P. DeJonghe, A. Jordanova, J. Baets, M. Zimo, M. Keckarevic, V. Brankovic

Journal:

European Journal of Paediatric Neurology

Year:

2011

Language:

english

File:

PDF, 38 KB

english, 2011

41

P19.9 Rare forms of acquired demylinating CNS disorder -report of three cases

V. Brankovic-Sreckovic, A. Kosac, V. Milić-Rašić, S. Todorovic

Journal:

European Journal of Paediatric Neurology

Year:

2011

Language:

english

File:

PDF, 35 KB

english, 2011

42

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

D. Matanovic, V. Milic Rasic

Journal:

Clinical Neurophysiology

Year:

2011

Language:

english

File:

PDF, 48 KB

english, 2011

43

Neurophysiological parameters in patients with hereditary motor and sensory neuropathy type II

J. Nikodinović, V. Milić-Rašić, S. Todorović, S. Apostolski, V. Rakočević-Stojanović, J. Mladenović, J. Dačković

Journal:

Clinical Neurophysiology

Year:

2007

Language:

english

File:

PDF, 44 KB

english, 2007

44

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

V. Rakočević-Stojanović, V. Milić-Rašić, S. Perić, J. Baets, V. Timmerman, I. Dierick, S. Pavlović, P. De Jonghe

Journal:

Journal of the Neurological Sciences

Year:

2010

Language:

english

File:

PDF, 202 KB

english, 2010

45

ANO10mutations cause ataxia and coenzyme Q10deficiency

Balreira, Andrea, Boczonadi, Veronika, Barca, Emanuele, Pyle, Angela, Bansagi, Boglarka, Appleton, Marie, Graham, Claire, Hargreaves, Iain P., Rasic, Vedrana Milic, Lochmüller, Hanns, Griffin, Helen,

Journal:

Journal of Neurology

Year:

2014

Language:

english

File:

PDF, 657 KB

english, 2014

46

Elevated level of creatinine phosphokinase in the blood of patients with peripheral polyneuropathies

Mladenović, J., Glumac, J. Nikodinović, Kosać, A., Marković, M. Keckarević, Baets, J., Rašić, V. Milić

Journal:

Clinical Neurophysiology

Year:

2015

Language:

english

File:

PDF, 57 KB

english, 2015

47

Phenotype of PLP1 -related disorder caused by novel mutation: A case report

Kresojević, Nikola, Petrović, Igor, Dobričić, Valerija, Tomić, Aleksandra, Branković, Vesna, Milić Rašić, Vedrana, Svetel, Marina, Kostić, Vladimir

Journal:

Movement Disorders Clinical Practice

Year:

2018

Language:

english

File:

PDF, 1.91 MB

english, 2018

48

4.Electromyography test as diagnostic procedure in recessive cerebellar ataxias

V. Milic Rasic, S. Todorovic, V. Brankovic, I. Novakovic, J. Baets, S. Vermeer

Journal:

Clinical Neurophysiology

Year:

2012

Language:

english

File:

PDF, 35 KB

english, 2012

49

31.Familial autoimmune myasthenia gravis

D. Vojinovic, V. Milic Rasic

Journal:

Clinical Neurophysiology

Year:

2012

Language:

english

File:

PDF, 38 KB

english, 2012

50

P155 The value of neurophysiologic study in patients with hereditary neuropathies

V. Milic Rasic, S. Todorovic, E. Nelis, M. Keckarevic, J. Mladenovic, J. Nikodinovic

Journal:

Clinical Neurophysiology

Year:

2008

Language:

english

File:

PDF, 60 KB

english, 2008

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