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Naslov Founder c. 1048-1049delGA mutation in NHLRC1 gene in Lafora's disease patients from Serbia (Meeting Abstract)
Autori Kecmanovic Miljana  Jovic ND  Keckarevic-Markovic Milica  Keckarevic Dusan P  Stevanovic Galina B  Romac Stanka P 
Info EUROPEAN JOURNAL OF NEUROLOGY, (2012), vol. 19 br. , Suppl. 1, str. 236-236
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Glutathione Transferase Polymorphisms in Patients with Progressive Myoclonic Epilepsy (Meeting Abstract)
Autori Ercegovac Marko D  Coric Vesna M  Simic Tatjana P  Jovic Nebojsa J  Sokic Dragoslav V  Jakovljevic Jovana  Kecmanovic Miljana  Nikolic Dimitrije M  Jankovic Snezana D  Savic-Radojevic Ana R  Pljesa-Ercegovac Marija S 
Info EPILEPSIA, (2012), vol. 53 br. , Suppl. 5, str. 21-21
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov A novel P66S mutation in exon 3 of the SOD1 gene with early onset and rapid progression (Article)
Autori Keckarevic Dusan P  Stevic Zorica D  Keckarevic-Markovic Milica  Kecmanovic Miljana  Romac Stanka P 
Info AMYOTROPHIC LATERAL SCLEROSIS, (2012), vol. 13 br. 2, str. 237-240
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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 Clinical course of lafora disease associated with epm2b gene mutations in patients of serbian/montenegrin origin (Meeting Abstract)
Autori Jovic Nebojsa J  Kecmanovic Miljana 
Info EPILEPSIA, (2009), vol. 50 br. , Suppl. Suppl. 4, str. 207-207
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  
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