Autori: Novakovic Ivana V
Naslov | Genetic variant rs16944 in IL1B gene is a risk factor for early-onset sepsis susceptibility and outcome in preterm infants (Article) |
Autori | Varljen Tatjana J ![]() ![]() ![]() ![]() ![]() |
Info | INFLAMMATION RESEARCH, (2020), vol. 69 br. 2, str. 155-157 |
Projekat | Ministarstvo Prosvete, Nauke i Tehnoloskog Razvoja [~175091] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
|
Naslov | phenotypic and genetic heterogeneity of adult patients with hereditary spastic paraplegia from Serbia (Meeting Abstract) |
Autori | Peric Stojan Z ![]() ![]() ![]() ![]() ![]() ![]() |
Info | JOURNAL OF THE NEUROLOGICAL SCIENCES, (2019), vol. 405 br. , Suppl. S, str. - |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
|
Naslov | Significance of KIT and PDGFRA mutations in gastric gastrointestinal stromal tumor imatinib-naive surgically treated patients (Article) |
Autori | Ebrahimi Keramatollah Sabljak Predrag V Simic Aleksandar P ![]() ![]() ![]() |
Info | VOJNOSANITETSKI PREGLED, (2019), vol. 76 br. 12, str. 1268-1273 |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
|
Naslov | GLUT1 deficiency syndrome: a case report with a novel SLC2A1 mutation (Article) |
Autori | Ivancevic Nikola ![]() ![]() ![]() ![]() ![]() ![]() |
Info | VOJNOSANITETSKI PREGLED, (2019), vol. 76 br. 5, str. 543-546 |
Projekat | Serbian Ministry of Education, Science and Technological Development [ON175091] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
|
Naslov | Clinical course of patients with pantothenate kinase-associated neurodegeneration (PKAN) before and after DBS surgery (Article) |
Autori | Svetel Marina V ![]() ![]() ![]() |
Info | JOURNAL OF NEUROLOGY, (2019), vol. 266 br. 12, str. 2962-2969 |
Projekat | Ministry of Education, Science and Technological Development of the Republic of Serbia [175090] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: 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 ![]() ![]() ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 2, str. 1836-1837 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
|
Naslov | Genetic variant rs16944 in IL1B gene is a risk factor for early onset sepsis susceptibility and outcome in preterm infants (Meeting Abstract) |
Autori | Maksimovic Nela S ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 2, str. 1364-1365 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science Scopus |
|
Naslov | Study of TNF, IL1B, and IL6 genes polymorphisms and susceptibility to bronchopulmonary dysplasia in premature neonates (Meeting Abstract) |
Autori | Damnjanovic Tatjana M ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 2, str. 1360-1360 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
|
Naslov | Analysis of ATXN1 and ATXN2 repeat length in C9ORF72 expansion carriers (Meeting Abstract) |
Autori | Marjanovic Ana ![]() ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 961-961 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science Scopus |
|
Naslov | Association of PRDM16 and CtBP2 genes polymorphisms with lipid profile of adolescents (Meeting Abstract) |
Autori | Maksimovic Nela S ![]() ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 658-658 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
|