Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Milena, Jankovic"'
Autor:
Filip Milanovic, Sinisa Ducic, Milena Jankovic, Sanja Sindjic-Antunovic, Emilija Dubljanin-Raspopović, Milica Aleksic, Goran Djuricic, Dejan Nikolic
Publikováno v:
Children, Vol 11, Iss 6, p 647 (2024)
Background: Recognized as one of the most serious musculoskeletal deformities, occurring in 1–2 per 1000 newborns, 80% of clubfeet are idiopathic while 20% present with associated malformations. The etiopathogenesis of clubfoot is described as mult
Externí odkaz:
https://doaj.org/article/777272c979544468be7020d075fad6aa
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
Publikováno v:
Medicina, Vol 60, Iss 1, p 49 (2023)
Migraine is a prevalent neurological disorder that significantly impacts the quality of life for affected individuals. The pathogenesis behind migraines is not yet fully understood, but hormonal changes, especially fluctuations in, estrogen and proge
Externí odkaz:
https://doaj.org/article/eb79a2dfa7784bb89b128d43365a78ca
Publikováno v:
Medicina, Vol 59, Iss 10, p 1707 (2023)
Stroke during pregnancy and preeclampsia are two distinct but interrelated medical conditions, sharing a common denominator—blood control failure. Along with cardiovascular diseases, diabetes, dyslipidemia, and hypercoagulability, hypertension is u
Externí odkaz:
https://doaj.org/article/a41f7d9d06b14fbfb593e3f6cf651b1a
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:
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:
Dejan Aleksic, Sanja Milenkovic, Milena Jankovic, Zorica Stevic, Vidosava Rakocevic-Stojanovic, Stojan Peric
Publikováno v:
Vojnosanitetski pregled. 80:87-89
Introduction. Histopathological findings of various inclusions were reported in the central nervous system of amyotrophic lateral sclerosis (ALS) patients but not in the peripheral nerves. Case report. We present a 66-year-old man with lower limb wea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::344785c9051074c45d2cf9f517d6fde3
https://doi.org/10.2298/vsp210717097a
https://doi.org/10.2298/vsp210717097a
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1be4636fdd1cb20440f15e5d053af03
https://doi.org/10.2298/gensr2203313m
https://doi.org/10.2298/gensr2203313m
Autor:
Marija Brankovic, Natasa Dragasevic, Valerija Dobricic, Ales Maver, Gaber Bergant, Igor Petrovic, Stojan Peric, Ana Marjanovic, Milena Jankovic, Jasna Jancic, Ivana Novakovic, Borut Peterlin, Marina Svetel, Vladimir Kostic
Publikováno v:
Genetika. 54:395-409
The aim of the study was to analyze the genetic basis of a various range of neurodegenerative disorders manifesting by movement disorders (MD) using next generation sequencing (NGS) clinical exome panel. The study included a total number of 42 cases,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db08887abdf6f748232da74c4b462d51
https://doi.org/10.2298/gensr2201395b
https://doi.org/10.2298/gensr2201395b
Autor:
Ivana Novakovic, Radoje Tubic, Stojan Peric, Milena Jankovic, Aleksandra Kacar, Marija Branković, Ana Marjanovic, Vidosava Rakocevic-Stojanovic, Bogdan Bjelica, Vukan Ivanovic
Publikováno v:
Journal of Neurology. 267:3617-3623
Hereditary neuropathy with liability to pressure palsies (HNPP) is a rare neuromuscular disorder, mostly caused by PMP22 deletion. To determine a yield of the genetic analysis of PMP22 gene deletion in patients with compression neuropathies. We inclu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdef97e406e816a752f2f7bb1b857754
https://doi.org/10.1007/s00415-020-10052-w
https://doi.org/10.1007/s00415-020-10052-w