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Autori: Jankovic Milena Z

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Naslov Oligoclonal bands in the cerebrospinal fluid of patients with Guillain-Barre syndrome (Meeting Abstract)
Autori Kalac Aida  Basta Ivana Z  Bozovic Ivo  Jankovic Milena Z  Berisavac Iva I  Palibrk Aleksa  Stojiljkovic-Tamas Olivera  Jovanovic Dejana R  Stevic Zorica D  Rakocevic-Stojanovic Vidosava M  Lavrnic Dragana V  Peric Stojan Z 
Info EUROPEAN JOURNAL OF NEUROLOGY, (2020), vol. 27 br. , Suppl. 1, str. 948-948
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Quality of life in hereditary neuropathy with liability to pressure palsies is as impaired as in Charcot-Marie-Tooth disease type 1A (Meeting Abstract)
Autori Bjelica Bogdan  Peric Stojan Z  Bozovic Ivo  Basta Ivana Z  Kacar Aleksandra S  Jankovic Milena Z  Brankovic Marija  Palibrk Aleksa  Novakovic Ivana V  Lavrnic Dragana V  Stevic Zorica D  Rakocevic-Stojanovic Vidosava M 
Info EUROPEAN JOURNAL OF NEUROLOGY, (2020), vol. 27 br. , Suppl. 1, str. 400-400
Projekat Ministry of Education, Science and Technological Development of the Republic of Serbia [175083]
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Neuropathic pain in patients with Charcot-Marie-Tooth type 1A (Article)
Autori Bjelica Bogdan  Peric Stojan Z  Basta Ivana Z  Bozovic Ivo  Kacar Aleksandra S  Marjanovic Ana  Ivanovic Vukan  Marjanovic Ana  Jankovic Milena Z  Novakovic Ivana V  Rakocevic-Stojanovic Vidosava M 
Info NEUROLOGICAL SCIENCES, (2020), vol. 41 br. 3, str. 625-630
Projekat Ministarstvo Prosvete, Nauke i Tehnoloskog Razvoja [175083]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Whole mitochondrial genome analysis in carriers of mt3460 mutation with Leber's hereditary optic neuropathy (Meeting Abstract)
Autori Dawod Phepy GA  Rovcanin Branislav R  Marjanovic Ana  Marjanovic Ana  Jankovic Milena Z  Novakovic Ivana V  Motaleb Abdel F  Jancic Jasna B  Kostic Vladimir S 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 2, str. 1836-1837
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Analysis of ATXN1 and ATXN2 repeat length in C9ORF72 expansion carriers (Meeting Abstract)
Autori Marjanovic Ana  Dobricic Valerija S  Brankovic Marija  Jankovic Milena Z  Mandic Gorana B  Stefanova Elka D  Stevic Zorica D  Novakovic Ivana V  Kostic Vladimir S 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 961-961
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov NOTCH3 mutations in Serbian CADASIL patients (Meeting Abstract)
Autori Jankovic Milena Z  Dobricic Valerija S  Marjanovic Ana  Brankovic Marija  Pavlovic Aleksandra M  Dujmovic Irena  Mijajlovic Milija D  Novakovic Ivana V  Kostic Vladimir S 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 293-293
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Analysis of mtDNA mutations in Serbian patients with Leber hereditary optic neuropathy (Meeting Abstract)
Autori Dawod Phepy GA  Rovcanin Branislav R  Marjanovic Ana  Marjanovic Ana  Jankovic Milena Z  Novakovic Ivana V  Dujmovic Irena  Jancic Jasna B  Kostic Vladimir S 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 181-181
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Body composition analysis in patients with myotonic dystrophy types 1 and 2 (Article)
Autori Peric Stojan Z  Bozovic Ivo  Nisic Tanja  Banovic Marija  Vujnic Milorad  Svabic Tamara S  Pesovic Jovan  Brankovic Marija  Basta Ivana Z  Jankovic Milena Z  Savic-Pavicevic Dusanka Lj  Rakocevic-Stojanovic Vidosava M 
Info NEUROLOGICAL SCIENCES, (2019), vol. 40 br. 5, str. 1035-1040
Projekat Ministry of Education, Science and Technological Development of the Republic of Serbia [175083]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Identification of mutations in PARK2 gene in Serbian patients with Parkinson's disease (Meeting Abstract)
Autori Jankovic Milena Z  Dobricic Valerija S  Kresojevic Nikola D  Markovic Vladana V  Petrovic Igor N  Svetel Marina V  Pekmezovic Tatjana D  Novakovic Ivana V  Kostic Vladimir K 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2018), vol. 26 br. , Suppl. S, str. 410-411
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov C9ORF72 genetic screening in Serbian patients with neurodegenerative disorders (Meeting Abstract)
Autori Marjanovic Ana  Dobricic Valerija S  Marjanovic Ivan V  Brankovic Marija  Jankovic Milena Z  Mandic Gorana B  Stevic Zorica D  Novakovic Ivana V  Stefanova Elka D  Kostic Vladimir K 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2018), vol. 26 br. , Suppl. S, str. 376-376
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
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