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Naslov Neuromuscular disorders and bone mineral density (Meeting Abstract)
Autori Kosac Ana P  Milic-Rasic Vedrana M  Susic Gordana Z  Vojinovic Dina  Todorovic Slobodanka 
Info EUROPEAN JOURNAL OF NEUROLOGY, (2012), vol. 19 br. , Suppl. 1, str. 785-785
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Epidemiology of Charcot-Marie-Tooth Disease in the Population of Belgrade, Serbia (Article)
Autori Mladenovic Jelena M  Milic-Rasic Vedrana M  Keckarevic-Markovic Milica  Romac Stanka P  Todorovic Slobodanka  Rakocevic-Stojanovic Vidosava M  Kisic-Tepavcevic Darija B  Hofman A  Pekmezovic Tatjana D 
Info NEUROEPIDEMIOLOGY, (2011), vol. 36 br. 3, str. 177-182
Projekat Ministry of Science and Technology, Republic of Serbia [175087]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Targeted Next-Generation Sequencing of a 12.5 Mb Homozygous Region Reveals ANO10 Mutations in Patients with Autosomal-Recessive Cerebellar Ataxia (Article)
Autori Vermeer Sascha  ...  Todorovic Slobodanka  Milic-Rasic Vedrana M  ...  (broj koautora 30) 
Info AMERICAN JOURNAL OF HUMAN GENETICS, (2010), vol. 87 br. 6, str. 813-819
Projekat Netherlands Organization of Health Research and Development [ZonMW RM000085, 917-66-36, 911-08-025]; European Community [FP7/2007-2013, 223143]; Verum Foundation ; French National Agency for Research ; Agence Nationale pour la Recherche-Maladies Neurologi
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Epilepsy in the population of neuromuscular patients (Meeting Abstract)
Autori Todorovic Slobodanka  Milic-Rasic Vedrana M  Jovic Nebojsa J  Romac Stanka P 
Info EPILEPSIA, (2009), vol. 50 br. , Suppl. Suppl. 4, str. 214-215
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Eosinophilic myositis as presenting symptom in gamma-sarcoglycanopathy (Article)
Autori Baumeister Sarah K  Todorovic Slobodanka  Milic-Rasic Vedrana M  Dekomien Gabriele  Lochmueller Hanns  Walter Maggie C 
Info NEUROMUSCULAR DISORDERS, (2009), vol. 19 br. 2, str. 167-171
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov A novel 9-bp duplication in the connexin 32 gene causing X-linked Charcot-Marie-Tooth disease (Meeting Abstract)
Autori Keckarevic-Markovic Milica  Milic-Rasic Vedrana M  Kecmanovic Miljana  Keckarevic Dusan P  Todorovic Slobodanka  Romac Stanka P 
Info JOURNAL OF NEUROLOGY, (2008), vol. 255 br. , Suppl. Suppl. 2, str. 76-77
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Hereditary motor and sensory neuropathy type Lom in Serbian Romany family (Meeting Abstract)
Autori Keckarevic-Markovic Milica  Milic-Rasic Vedrana M  Dobricic Valerija S  Kecmanovic Miljana  Dimitrijevic Rajko N  Saric M  Savic-Pavicevic Dusanka Lj  Keckarevic Dusan P  Todorovic Slobodanka  Romac Stanka P 
Info JOURNAL OF NEUROLOGY, (2007), vol. 254 br. , Suppl. Suppl. 3, str. 109-109
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Epidemiology of myotonic dystrophy type 1 (Steinert disease) in Belgrade (Serbia) (Article)
Autori Mladenovic Jelena M  Pekmezovic Tatjana D  Todorovic Slobodanka  Rakocevic-Stojanovic Vidosava M  Savic Dusanka Lj  Romac Stanka P  Apostolski Slobodan A 
Info CLINICAL NEUROLOGY AND NEUROSURGERY, (2006), vol. 108 br. 8, str. 757-760
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Clinical case report atypical myopathy in a young girl with 91 CTG repeats in DM1 locus and a positive DM1 family history (Article)
Autori Savic Dusanka Lj  Keckarevic Dusan P  Brankovic-Sreckovic Vesna  Apostolski Slobodan A  Todorovic Slobodanka  Romac Stanka P 
Info INTERNATIONAL JOURNAL OF NEUROSCIENCE, (2006), vol. 116 br. 12 , Suppl. , str. 1509 -1518
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Novel mutations in the CHRNB1 gene in three patients affected by a congenital myasthenic syndrome (Meeting Abstract)
Autori Mueller Juliane S  Hoellen Friederike  Schara Ulrike  Johannsen J  Bentele K  Rakocevic-Stojanovic Vidosava M  Milic-Rasic Vedrana M  Todorovic Slobodanka  Abicht Angela  Lochmueller Hanns 
Info NEUROMUSCULAR DISORDERS, (2006), vol. 16 br. 9-10, str. 661-661
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
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