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Naslov Single Nucleotide Polymorphisms of Antioxidant Enzymes in Progressive Myoclonus Epilepsy (Meeting Abstract)
Autori Ercegovac Marko D  Jovic Nebojsa J  Sokic Dragoslav V  Simic Tatjana P  Savic-Radojevic Ana R  Coric Vesna M  Smiljic Jelena  Nikolic Dimitrije M  Kecmanovic Miljana  Pljesa-Ercegovac Marija S 
Info EPILEPSIA, (2016), vol. 57 br. , Suppl. 2, str. 123-123
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeats (Article)
Autori Gagic Milica  Keckarevic-Markovic Milica  Kecmanovic Miljana  Keckarevic Dusan P  Mladenovic Jelena M  Dackovic Jelena  Milic-Rasic Vedrana M  Romac Stanka P 
Info CLINICAL CHEMISTRY AND LABORATORY MEDICINE, (2016), vol. 54 br. 5, str. 773-780
Projekat Serbian Ministry of Education and Science [173016]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Clinical and genetic data on Lafora disease patients of Serbian/Montenegrin origin (Article)
Autori Kecmanovic Miljana  Jovic ND  Keckarevic-Markovic Milica  Keckarevic Dusan P  Stevanovic Galina B  Ignjatovic PM  Romac Stanka P 
Info CLINICAL GENETICS, (2016), vol. 89 br. 1, str. 104-108
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Is Adjunctive Perampanel An Option for Intractable Seizures in Lafora Disease? (Meeting Abstract)
Autori Genton Pierre  Jovic Nebojsa J  Lesca G  Kecmanovic Miljana 
Info EPILEPSIA, (2015), vol. 56 br. , Suppl. 1, str. 57-58
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov GSTA1, GSTM1, GSTP1 and GSTT1 polymorphisms in progressive myoclonus epilepsy: A Serbian case-control study (Article)
Autori Ercegovac Marko D  Jovic Nebojsa J  Sokic Dragoslav V  Savic-Radojevic Ana R  Coric Vesna M  Radic Tanja M  Nikolic Dimitrije M  Kecmanovic Miljana  Matic Marija G  Simic Tatjana P  Pljesa-Ercegovac Marija S 
Info SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, (2015), vol. 32 br. , str. 30-36
Projekat Serbian Ministry of Education, Science and Technological Development [175052]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov A Shared Haplotype Indicates a Founder Event in Unverricht-Lundborg Disease Patients from Serbia (Article)
Autori Kecmanovic Miljana  Ristic Aleksandar J  Ercegovac Marko D  Keckarevic-Markovic Milica  Keckarevic Dusan P  Sokic Dragoslav V  Romac Stanka P 
Info INTERNATIONAL JOURNAL OF NEUROSCIENCE, (2014), vol. 124 br. 2, str. 102-109
Projekat Ministry of Science, Republic of Serbia [173016]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Lafora disease: Severe phenotype associated with homozygous deletion of the NHLRC1 gene (Article)
Autori Kecmanovic Miljana  Jovic Nebojsa J  Cukic Mirjana  Keckarevic-Markovic Milica  Keckarevic Dusan P  Stevanovic Galina B  Romac Stanka P 
Info JOURNAL OF THE NEUROLOGICAL SCIENCES, (2013), vol. 325 br. 1-2, str. 170-173
Projekat Ministry of Science, Republic of Serbia [173016]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov An Algorithm for Genetic Testing of Serbian Patients with Demyelinating Charcot-Marie-Tooth (Article)
Autori Keckarevic-Markovic Milica  Dackovic Jelena  Mladenovic Jelena M  Milic-Rasic Vedrana M  Kecmanovic Miljana  Keckarevic Dusan P  Romac Stanka P 
Info GENETIC TESTING AND MOLECULAR BIOMARKERS, (2013), vol. 17 br. 1, str. 85-87
Projekat Serbian Ministry of Education and Science [173016]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov A founder R32G mutation in GJB1 gene of Serbian CMT patients (Meeting Abstract)
Autori Keckarevic-Markovic Milica  Kecmanovic Miljana  Keckarevic Dusan P  Mladenovic Jelena M  Milic-Rasic Vedrana M  Romac Stanka P 
Info EUROPEAN JOURNAL OF NEUROLOGY, (2012), vol. 19 br. , Suppl. 1, str. 783-783
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Over-representation of the L144F SOD1 mutation in Serbian ALS patients due to founder effect (Meeting Abstract)
Autori Keckarevic Dusan P  Stevic Zorica D  Keckarevic-Markovic Milica  Kecmanovic Miljana  Romac Stanka P 
Info EUROPEAN JOURNAL OF NEUROLOGY, (2012), vol. 19 br. , Suppl. 1, str. 272-272
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
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