Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Jovana Komazec"'
Autor:
Aleksa Jovanović, Nataša Tošić, Irena Marjanović, Jovana Komazec, Branka Zukić, Marina Nikitović, Rosanda Ilić, Danica Grujičić, Dragana Janić, Sonja Pavlović
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 24, p 17387 (2023)
Central nervous system (CNS) tumors comprise around 20% of childhood malignancies. Germline variants in cancer predisposition genes (CPGs) are found in approximately 10% of pediatric patients with CNS tumors. This study aimed to characterize variants
Externí odkaz:
https://doaj.org/article/bc989133d1c343419332a391d75b1f98
Autor:
Vesna Spasovski, Marina Andjelkovic, Marina Parezanovic, Jovana Komazec, Milena Ugrin, Kristel Klaassen, Maja Stojiljkovic
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 13, p 11212 (2023)
Systemic sclerosis (SSc) is a complex autoimmune inflammatory disorder with multiple organ involvement. Skin changes present the hallmark of SSc and coincide with poor prognosis. Interstitial lung diseases (ILD) are the most widely reported complicat
Externí odkaz:
https://doaj.org/article/3999cbfb118e4ce9a16c0be8ece92a5c
Autor:
Sonja Pavlovic, Bojan Ristivojevic, Jovana Komazec, Branka Zukic, Vera Zdravkovic, Milena Ugrin, Teodora Karan-Djurasevic
Publikováno v:
Molecular Biology Reports. 47:6759-6768
Maturity-onset diabetes of the young (MODY) is a form of monogenic diabetes caused by the variants in MODY-related genes. In addition to coding variants, variants in the promoter region of MODY-related genes can cause the disease as well. In this stu
Autor:
Marijana, Virijević, Irena, Marjanovic, Marina, Andjelkovic, Teodora, Karan-Djurasevic, Branka, Zukic, Jovana, Komazec, Ivana, Grubisa, Biljana, Stankovic, Andrija, Bogdanović, Sonja, Pavlovic
Publikováno v:
Genetics & Applications; 2024 Special Issue, p42-42, 1p
Autor:
Kristel, Klaassen, Sara, Stanković, Maja, Đorđević Milošević, Božica, Kecman, Marina, Andjelkovic, Anita, Skakić, Vesna, Spasovski, Milena, Ugrin, Jovana, Komazec, Marina, Parezanović, Nikola, Jocić, Nina, Stevanović, Sonja, Pavlovic, Maja, Stojiljković
Publikováno v:
Genetics & Applications; 2024 Special Issue, p41-41, 1p
Autor:
Anita Skakic, Maja Stojiljkovic, Iva Milacic, Sonja Pavlovic, Kristel Klaassen, Milena Ugrin, Jovana Komazec
Publikováno v:
Genetika, Vol 49, Iss 2, Pp 457-467 (2017)
Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is one of the most common endocrine diseases, yet genetic diagnosis is among the most complicated of all monogenic disorders. It has an overall incidence of 1:10000-1:20000, it is
Autor:
Milan Rodic, Misa Vreca, Aleksandar Sovtic, Sonja Pavlovic, Predrag Minic, Marina Andjelkovic, Vesna Spasovski, Jovana Komazec
Publikováno v:
Srpski arhiv za celokupno lekarstvo (2019) 147(3-4):160-166
Srpski Arhiv za Celokupno Lekarstvo, Vol 147, Iss 3-4, Pp 160-166 (2019)
Srpski Arhiv za Celokupno Lekarstvo, Vol 147, Iss 3-4, Pp 160-166 (2019)
Introduction/Objective. Dysfunction of the axonemal structure leads to ciliopathies. Sensory and motile ciliopathies have been associated with numerous pediatric diseases, including respiratory diseases. Primary ciliary dyskinesia (PCD) is ciliopathy
Autor:
Sanja Stankovic, Mihailo Stjepanovic, Marina Andjelkovic, Sonja Pavlovic, Jovana Komazec, Ana Momcilovic, Violeta Mihailovic-Vucinic, Jelena Milin-Lazovic, Milena Santric-Milicevic, Vesna Spasovski, Vesna Skodric-Trifunovic
Publikováno v:
Archives of Medical Science : AMS
Introduction Sarcoidosis is a rare multisystem granulomatous disease with unknown etiology. The interplay of vitamin D deficiency and genetic polymorphisms in genes coding for the proteins relevant for metabolism of vitamin D is an important, but une
Autor:
Vera Zdravkovic, Maja Jesic, Milena Ugrin, Marina Andjelkovic, Jovana Komazec, Sonja Pavlovic, Silvija Sajic
Publikováno v:
Endokrynologia Polska. 70(1)
Introduction: Maturity onset diabetes of the young (MODY) is a rare form of monogenic diabetes. Being clinically and genetically heterogeneous, it is often misdiagnosed as type 1 or type 2 diabetes, leading to inappropriate therapy. MODY is caused by
Autor:
Jovanović, Aleksa1 (AUTHOR) aleksa.jovanovic@ncrc.ac.rs, Tošić, Nataša2 (AUTHOR) natasa.tosic@imgge.bg.ac.rs, Marjanović, Irena2 (AUTHOR) irena.marjanovic@imgge.bg.ac.rs, Komazec, Jovana2 (AUTHOR) jovana.komazec@imgge.bg.ac.rs, Zukić, Branka2 (AUTHOR) branka.zukic@imgge.bg.ac.rs, Nikitović, Marina3,4 (AUTHOR) marina.nikitovic@ncrc.ac.rs, Ilić, Rosanda4,5 (AUTHOR) gruj59@gmail.com, Grujičić, Danica4,5 (AUTHOR), Janić, Dragana1 (AUTHOR) dragana.janic@ncrc.ac.rs, Pavlović, Sonja2 (AUTHOR) sonya@imgge.bg.ac.rs
Publikováno v:
International Journal of Molecular Sciences. Dec2023, Vol. 24 Issue 24, p17387. 20p.