Hasil Pencarian - Ivana Novaković

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  1. 1
    Genetic Aspects of Inflammation and Immune Response in Stroke

    Genetic Aspects of Inflammation and Immune Response in Stroke oleh Dejan Nikolic, Milena Jankovic, Bojana Petrovic, Ivana Novakovic

    Diterbitkan 2020-10-01
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  2. 2
    The Impact of the <i>IKBKG</i> Gene on the Appearance of the Corpus Callosum Abnormalities in Incontinentia Pigmenti

    The Impact of the <i>IKBKG</i> Gene on the Appearance of the Corpus Callosum Abnormalities in Incontinentia Pigmenti oleh Snežana Minić, Nataša Cerovac, Ivana Novaković, Slobodan Gazikalović, Svetlana Popadić, Dušan Trpinac

    Diterbitkan 2023-03-01
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  3. 3
    The Genetic Basis of Strokes in Pediatric Populations and Insight into New Therapeutic Options

    The Genetic Basis of Strokes in Pediatric Populations and Insight into New Therapeutic Options oleh Milena Jankovic, Bojana Petrovic, Ivana Novakovic, Slavko Brankovic, Natasa Radosavljevic, Dejan Nikolic

    Diterbitkan 2022-01-01
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  4. 4
    Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortion.

    Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortion. oleh Alenka Hodžić, Polona Lavtar, Momčilo Ristanović, Ivana Novaković, Jelena Dotlić, Borut Peterlin

    Diterbitkan 2018-01-01
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  5. 5
    Challenges in Rare Diseases Diagnostics: Incontinentia Pigmenti with Heterozygous <i>GBA</i> Mutation

    Challenges in Rare Diseases Diagnostics: Incontinentia Pigmenti with Heterozygous <i>GBA</i> Mutation oleh Snežana Minić, Dušan Trpinac, Ivana Novaković, Nataša Cerovac, Danijela Dobrosavljević Vukojević, Jérémie Rosain

    Diterbitkan 2022-07-01
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  6. 6
    miRNAs as a Potential Biomarker in the COVID-19 Infection and Complications Course, Severity, and Outcome

    miRNAs as a Potential Biomarker in the COVID-19 Infection and Complications Course, Severity, and Outcome oleh Milena Jankovic, Dejan Nikolic, Ivana Novakovic, Bojana Petrovic, Milan Lackovic, Milena Santric-Milicevic

    Diterbitkan 2023-03-01
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  7. 7
    Genetic variation in circadian rhythm genes CLOCK and ARNTL as risk factor for male infertility.

    Genetic variation in circadian rhythm genes CLOCK and ARNTL as risk factor for male infertility. oleh Alenka Hodžić, Momčilo Ristanović, Branko Zorn, Cane Tulić, Aleš Maver, Ivana Novaković, Borut Peterlin

    Diterbitkan 2013-01-01
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  8. 8
    Management of Pregnancy in a Patient with Familial Hypercholesterolemia and Previous Myocardial Infarction—Treatment with LDL Apheresis: A Case Report

    Management of Pregnancy in a Patient with Familial Hypercholesterolemia and Previous Myocardial Infarction—Treatment with LDL Apheresis: A Case Report oleh Milos Milincic, Jovana Todorovic, Stefan Dugalic, Ivana Novakovic, Maja Macura, Katarina Lalic, Miroslava Gojnic Dugalic

    Diterbitkan 2024-05-01
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  9. 9
    KCC2 rs2297201 Gene Polymorphism Might be a Predictive Genetic Marker of Febrile Seizures

    KCC2 rs2297201 Gene Polymorphism Might be a Predictive Genetic Marker of Febrile Seizures oleh Sanja Dimitrijevic, Biljana Jekic, Suzana Cvjeticanin, Aleksandra Tucovic, Tamara Filipovic, Ivana Novaković, Bojana Ivić, Dimitrije Nikolic

    Diterbitkan 2022-04-01
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  10. 10
    Association of PRDM16 rs12409277 and CtBP2 rs1561589 gene polymorphisms with lipid profile of adolescents

    Association of PRDM16 rs12409277 and CtBP2 rs1561589 gene polymorphisms with lipid profile of adolescents oleh Nela Maksimovic, Vanja Vidovic, Tatjana Damnjanovic, Biljana Jekic, Nada Majkic Singh, Slavko Simeunovic, Dara Savic Bozovic, Stojko Vidovic, Ivana Novakovic

    Diterbitkan 2021-01-01
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  11. 11
    C-5 Hydroxyethyl and Hydroxypropyl Acyclonucleosides as Substrates for Thymidine Kinase of Herpes Simplex Virus Type 1 (HSV-1 TK): Syntheses and Biological Evaluation

    C-5 Hydroxyethyl and Hydroxypropyl Acyclonucleosides as Substrates for Thymidine Kinase of Herpes Simplex Virus Type 1 (HSV-1 TK): Syntheses and Biological Evaluation oleh Silvana Raić-Malić, Simon M. Ametamey, Leonardo Scapozza, Davorka Završnik, Ursina Müller, Amar Osmanović, Ivana Novaković, Svjetlana Krištafor, Andrijana Meščić

    Diterbitkan 2013-05-01
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  12. 12
    Genetic and Epigenomic Modifiers of Diabetic Neuropathy

    Genetic and Epigenomic Modifiers of Diabetic Neuropathy oleh Milena Jankovic, Ivana Novakovic, Dejan Nikolic, Jasmina Mitrovic Maksic, Slavko Brankovic, Ivana Petronic, Dragana Cirovic, Sinisa Ducic, Mirko Grajic, Dragana Bogicevic

    Diterbitkan 2021-05-01
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  13. 13
    Current Concepts on Genetic Aspects of Mitochondrial Dysfunction in Amyotrophic Lateral Sclerosis

    Current Concepts on Genetic Aspects of Mitochondrial Dysfunction in Amyotrophic Lateral Sclerosis oleh Milena Jankovic, Ivana Novakovic, Phepy Gamil Anwar Dawod, Ayman Gamil Anwar Dawod, Aleksandra Drinic, Fayda I. Abdel Motaleb, Sinisa Ducic, Dejan Nikolic

    Diterbitkan 2021-09-01
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  14. 14
    Current State of Compulsory Basic and Clinical Courses in Genetics for Medical Students at Medical Faculties in Balkan Countries With Slavic Languages

    Current State of Compulsory Basic and Clinical Courses in Genetics for Medical Students at Medical Faculties in Balkan Countries With Slavic Languages oleh Nina Pereza, Nina Pereza, Rifet Terzić, Dijana Plaseska-Karanfilska, Olivera Miljanović, Olivera Miljanović, Ivana Novaković, Željka Poslon, Željka Poslon, Saša Ostojić, Saša Ostojić, Borut Peterlin

    Diterbitkan 2022-01-01
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  15. 15
    Analysis of the Association Between Polymorphisms within PAI-1 and ACE genes and Ischemic Stroke Outcome After rt-PA Therapy

    Analysis of the Association Between Polymorphisms within PAI-1 and ACE genes and Ischemic Stroke Outcome After rt-PA Therapy oleh Marija Dušanović Pjević, Ljiljana Beslac Bumbaširevic, Ljubica Vojvodic, Milka Grk, Nela Maksimović, Tatjana Damnjanović, Ivana Novaković, Katarina Kačar, Milica Pesic, Dijana Perovic, Milan Savic, Veljko Maksic, Jelena Trickovic, Biljana Jekic

    Diterbitkan 2019-04-01
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  16. 16
    Mutational Analysis and mtDNA Haplogroup Characterization in Three Serbian Cases of Mitochondrial Encephalomyopathies and Literature Review

    Mutational Analysis and mtDNA Haplogroup Characterization in Three Serbian Cases of Mitochondrial Encephalomyopathies and Literature Review oleh Phepy G. A. Dawod, Jasna Jancic, Ana Marjanovic, Marija Brankovic, Milena Jankovic, Janko Samardzic, Ayman Gamil Anwar Dawod, Ivana Novakovic, Fayda I. Abdel Motaleb, Vladimir Radlovic, Vladimir S. Kostic, Dejan Nikolic

    Diterbitkan 2021-10-01
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  17. 17
    A multicenter study of genetic testing for Parkinson’s disease in the clinical setting

    A multicenter study of genetic testing for Parkinson’s disease in the clinical setting oleh Anja Kovanda, Valentino Rački, Gaber Bergant, Dejan Georgiev, Dušan Flisar, Eliša Papić, Marija Brankovic, Milena Jankovic, Marina Svetel, Nataša Teran, Aleš Maver, Vladimir S. Kostic, Ivana Novakovic, Zvezdan Pirtošek, Martin Rakuša, Vladimira Vuletić, Borut Peterlin

    Diterbitkan 2022-11-01
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  18. 18
    Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis

    Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis oleh Ales Maver, Polona Lavtar, Smiljana Ristić, Sanja Stopinšek, Saša Simčič, Keli Hočevar, Juraj Sepčić, Jelena Drulović, Tatjana Pekmezović, Ivana Novaković, Hodžić Alenka, Gorazd Rudolf, Saša Šega, Nada Starčević-Čizmarević, Anja Palandačić, Gordana Zamolo, Miljenko Kapović, Tina Likar, Borut Peterlin

    Diterbitkan 2017-06-01
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  19. 19
    Phenotypic and Genetic Heterogeneity of Adult Patients with Hereditary Spastic Paraplegia from Serbia

    Phenotypic and Genetic Heterogeneity of Adult Patients with Hereditary Spastic Paraplegia from Serbia oleh Stojan Perić, Vladana Marković, Ayşe Candayan, Els De Vriendt, Nikola Momčilović, Andrija Savić, Nataša Dragašević-Mišković, Marina Svetel, Zorica Stević, Ivo Božović, Šarlota Mesaroš, Jelena Drulović, Ivana Basta, Igor Petrović, Olivera Tamaš, Milija Mijajlović, Ivana Novaković, Dragoslav Sokić, Albena Jordanova

    Diterbitkan 2022-09-01
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  20. 20
    Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients

    Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients oleh Konstantinos Mitropoulos, Eleni Merkouri Papadima, Georgia Xiromerisiou, Angeliki Balasopoulou, Kyriaki Charalampidou, Vasiliki Galani, Krystallia-Vassiliki Zafeiri, Efthymios Dardiotis, Styliani Ralli, Georgia Deretzi, Anne John, Kyriaki Kydonopoulou, Elpida Papadopoulou, Alba di Pardo, Fulya Akcimen, Annalisa Loizedda, Valerija Dobričić, Ivana Novaković, Vladimir S. Kostić, Clint Mizzi, Brock A. Peters, Nazli Basak, Sandro Orrù, Evangelos Kiskinis, David N. Cooper, Spyridon Gerou, Radoje Drmanac, Marina Bartsakoulia, Evangelia-Eirini Tsermpini, Georgios M. Hadjigeorgiou, Bassam R. Ali, Theodora Katsila, George P. Patrinos

    Diterbitkan 2017-12-01
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