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Naslov Schizophrenia and Apolipoprotein E Gene Polymorphism in Serbian Population (Article)
Autori Kecmanovic Miljana  Dobricic Valerija S  Dimitrijevic Rajna D  Keckarevic Dusan P  Savic-Pavicevic Dusanka Lj  Keckarevic-Markovic Milica  Ivkovic Maja  Romac Stanka P 
Info INTERNATIONAL JOURNAL OF NEUROSCIENCE, (2010), vol. 120 br. 7, str. 502-506
Projekat Serbian Ministry of Sciences [143013]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Polymorphisms of the Prion Protein Gene (PRNP) in a Serbian Population (Article)
Autori Dimitrijevic Rajna D  Cadez Ivana  Keckarevic-Markovic Milica  Keckarevic Dusan P  Kecmanovic Miljana  Dobricic Valerija S  Savic-Pavicevic Dusanka Lj  Brajuskovic Goran N  Romac Stanka P 
Info INTERNATIONAL JOURNAL OF NEUROSCIENCE, (2010), vol. 120 br. 7, str. 496-501
Projekat Serbian Ministry of Science and Environmental Protection [143013]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Mutational analysis of GJB1, MPZ, PMP22, EGR2, and LITAF/SIMPLE in Serbian Charcot-Marie-Tooth patients (Article)
Autori Keckarevic-Markovic Milica  Milic-Rasic Vedrana M  Mladenovic Jelena M  Dackovic Jelena  Kecmanovic Miljana  Keckarevic Dusan P  Savic-Pavicevic Dusanka Lj  Romac Stanka P 
Info JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, (2009), vol. 14 br. 2, str. 125-136
Projekat Serbian Ministry of Sciences [143013]; The Institute of Neurology, Institute of Neurology and Psychiatry for Children and Youth ; Institute for a Mother and a Child, Belgrade, Serbia
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Congenital cataracts facial dysmorphism neuropathy in Serbian Romani patients (Meeting Abstract)
Autori Keckarevic-Markovic Milica  Milic-Rasic Vedrana M  Kecmanovic Miljana  Keckarevic Dusan P  Romac Stanka P 
Info JOURNAL OF NEUROLOGY, (2009), vol. 256 br. , Suppl. Suppl. 2, str. S182-S182
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Coexistence of Unverricht-Lundborg disease and congenital deafness: Molecular resolution of a complex comorbidity (Article)
Autori Kecmanovic Miljana  Ristic Aleksandar J  Sokic Dragoslav V  Keckarevic-Markovic Milica  Vojvodic Nikola M  Ercegovac Marko D  Jankovic Slavko M  Keckarevic Dusan P  Savic-Pavicevic Dusanka Lj  Romac Stanka P 
Info EPILEPSIA, (2009), vol. 50 br. 6, str. 1612-1615
Projekat Ministry of Science, Republic of Serbia [145057-D, 143013]
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 Mutations in NHLRC1 gene are predominant cause of Lafora disease in Serbian population (Meeting Abstract)
Autori Kecmanovic Miljana  Jovic ND  Keckarevic-Markovic Milica  Dobricic Valerija S  Keckarevic Dusan P  Ignjatovic PM  Romac Stanka P 
Info JOURNAL OF NEUROLOGY, (2008), vol. 255 br. , Suppl. Suppl. 2, str. 102-103
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
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 HD phenocopies - Possible role of saitohin gene (Article)
Autori Jankovic N  Kecmanovic Miljana  Dimitrijevic Rajna D  Keckarevic-Markovic Milica  Dobricic Valerija S  Savic-Pavicevic Dusanka Lj  Romac Stanka P 
Info INTERNATIONAL JOURNAL OF NEUROSCIENCE, (2008), vol. 118 br. 3, str. 391-397
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov MECP2 mutations in Serbian Rett syndrome patients (Editorial Material)
Autori Djarmati Ana  Dobricic Valerija S  Kecmanovic Miljana  Marsh P  Jancic-Stefanovic Jasna B  Klein Christine  Djuric Milena Lj  Romac Stanka P 
Info ACTA NEUROLOGICA SCANDINAVICA, (2007), vol. 116 br. 6 , Suppl. , str. 413 -419
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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