Zobrazeno 1 - 10
of 234
pro vyhledávání: '"Ivana Novakovic"'
Autor:
Milos Milincic, Jovana Todorovic, Stefan Dugalic, Ivana Novakovic, Maja Macura, Katarina Lalic, Miroslava Gojnic Dugalic
Publikováno v:
Reports, Vol 7, Iss 2, p 39 (2024)
Familial hypercholesterolemia, a genetic disorder marked by elevated low-density lipoprotein cholesterol (LDL-C), poses significant risks for premature atherosclerosis and cardiovascular diseases, particularly during pregnancy. One of the safe method
Externí odkaz:
https://doaj.org/article/52527432e0654669b584ed0738dd316b
Autor:
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
Publikováno v:
npj Parkinson's Disease, Vol 8, Iss 1, Pp 1-4 (2022)
Abstract Parkinson’s disease (PD) guidelines lack clear criteria for genetic evaluation. We assessed the yield and rationale of genetic testing for PD in a routine clinical setting on a multicenter cohort of 149 early-onset and familial patients by
Externí odkaz:
https://doaj.org/article/8212afa2f27e4934942d7333f97b9926
Autor:
Nela Maksimovic, Vanja Vidovic, Tatjana Damnjanovic, Biljana Jekic, Nada Majkic Singh, Slavko Simeunovic, Dara Savic Bozovic, Stojko Vidovic, Ivana Novakovic
Publikováno v:
Archives of Medical Science, Vol 19, Iss 3, Pp 593-599 (2021)
Introduction Positive regulatory domain containing 16 (PRDM16) protein represents the key regulator of brown adipose tissue (BAT) development. It induces brown fat phenotype and represses white adipose tissue specific genes through the association wi
Externí odkaz:
https://doaj.org/article/160cb88bd27740d6b110cd35dd79238c
Autor:
Milena Jankovic, Dejan Nikolic, Ivana Novakovic, Bojana Petrovic, Milan Lackovic, Milena Santric-Milicevic
Publikováno v:
Diagnostics, Vol 13, Iss 6, p 1091 (2023)
During the last three years, since the emergence of the COVID-19 pandemic, a significant number of scientific publications have focused on resolving susceptibility to the infection, as well as the course of the disease and potential long-term complic
Externí odkaz:
https://doaj.org/article/bf97aa281cd54d89a967e35487bdc37d
Autor:
Milena Jankovic, Bojana Petrovic, Ivana Novakovic, Slavko Brankovic, Natasa Radosavljevic, Dejan Nikolic
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 3, p 1601 (2022)
Strokes within pediatric populations are considered to be the 10th leading cause of death in the United States of America, with over half of such events occurring in children younger than one year of life. The multifactorial etiopathology that has an
Externí odkaz:
https://doaj.org/article/6cbf2269dc5b4c0582768ed7bfab8646
Autor:
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
Publikováno v:
Diagnostics, Vol 11, Iss 11, p 1969 (2021)
Mitochondrial encephalomyopathies (MEMP) are heterogeneous multisystem disorders frequently associated with mitochondrial DNA (mtDNA) mutations. Clinical presentation varies considerably in age of onset, course, and severity up to death in early chil
Externí odkaz:
https://doaj.org/article/efad65c1e5054e169c32f3dbdc13deda
Autor:
Milena Jankovic, Ivana Novakovic, Phepy Gamil Anwar Dawod, Ayman Gamil Anwar Dawod, Aleksandra Drinic, Fayda I. Abdel Motaleb, Sinisa Ducic, Dejan Nikolic
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 18, p 9832 (2021)
Amyotrophic Lateral Sclerosis (ALS), neurodegenerative motor neuron disorder is characterized as multisystem disease with important contribution of genetic factors. The etiopahogenesis of ALS is not fully elucidate, but the dominant theory at present
Externí odkaz:
https://doaj.org/article/43ef9e8f3a1a4845bca3b862622cca44
Autor:
Milena Jankovic, Ivana Novakovic, Dejan Nikolic, Jasmina Mitrovic Maksic, Slavko Brankovic, Ivana Petronic, Dragana Cirovic, Sinisa Ducic, Mirko Grajic, Dragana Bogicevic
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 9, p 4887 (2021)
Diabetic neuropathy (DN), the most common chronic and progressive complication of diabetes mellitus (DM), strongly affects patients’ quality of life. DN could be present as peripheral, autonomous or, clinically also relevant, uremic neuropathy. The
Externí odkaz:
https://doaj.org/article/71bd904ed2064fac9455ddc580642136
Autor:
Jasmina Maksic, Nela Maksimovic, Lukas Rasulic, Olgica Milankov, Ana Marjanovic, Dragana Cvetkovic, Vidosava Rakocevic-Stojanovic, Ivana Novakovic
Publikováno v:
Vojnosanitetski pregled (2023) 80(3):201-207
Background/Aim. Duchenne muscular dystrophy (MD) and Becker MD are caused by mutations in the gene for dystrophin (DMD). They are X chromosome-linked recessive diseases where males are affected, and females are healthy carriers of the mutation in mos
Autor:
Ana Marjanovic, Valerija Dobricic, Milica Jecmenica-Lukic, Iva Stankovic, Ognjen Milicevic, Natasa Dragasevic-Miskovic, Marija Brankovic, Milena Jankovic, Ivana Novakovic, Marina Svetel, Elka Stefanova, Vladimir Kostic
Publikováno v:
Genetika. 54:1313-1330
These include, among others, two forms of atypical Parkinsonism, multiple system atrophy (MSA) and progressive supranuclear palsy (PSP). This study aimed to assess the potential role of C9orf72 repeat expansions among Serbian patients diagnosed with