日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Faecal inflammatory protein markers in children with autism spectrum disorder are comparable to their healthy siblings

自闭症谱系障碍儿童的粪便炎症蛋白标志物与其健康兄弟姐妹的水平相当。

Osredkar, Joško; Finderle, Petra; Godnov, Uroš; Jekovec-Vrhovšek, Maja; Vidova, Veronika; Elliott, James Price; Fabjan, Teja; Avguštin, Gorazd; Osredkar, Damjan; Kumer, Kristina

Proteomic analysis identifying proteins relevant for treatment success following experimental neonatal inflammation-sensitized hypoxia-ischemia

蛋白质组学分析鉴定与实验性新生儿炎症致敏缺氧缺血后治疗成功相关的蛋白质

Burkard, Hannah; Osredkar, Damjan; Maes, Elke; Bernis, Maria E; Bremer, Anna-Sophie; Zweyer, Margit; Dowling, Paul; Ohlendieck, Kay; Thoresen, Marianne; Sabir, Hemmen

An evolutionarily conserved role for CTNNB1/β-CATENIN in regulating the development of the corpus callosum.

CTNNB1/β-连环蛋白在调节胼胝体发育中发挥着进化保守的作用

Parichha Arpan, Datta Debarpita, Singh Amrita, Talwar Ishita, Yadav Shreya, Bose Mahima, Suresh Varun, Miroševič Špela, Žakelj Nina, Gosar David, Osredkar Damjan, Tole Shubha

Genotypic, functional, and phenotypic characterization in CTNNB1 neurodevelopmental syndrome.

CTNNB1神经发育综合征的基因型、功能和表型特征

Žakelj Nina, Gosar David, Miroševič Špela, Sanders Stephan J, Ljungdahl Alicia, Kohani Sayeh, Huang Shouhe, Leong Lok I, An Ying, Teo Miou-Jing, Moultrie Fiona, Jerala Roman, Lainšček Duško, Forstnerič Vida, Sušjan Petra, Lisowski Leszek, Perez-Iturralde Andrea, Mrak Jasna Oražem, Chan Ho Yin Edwin, Osredkar Damjan

Gene therapy of rare diseases as a milestone in medicine - overview of the field and report on initial experiences in Slovenia

罕见病基因疗法:医学发展史上的一个里程碑——该领域概述及斯洛文尼亚初步经验报告

Grošelj, Urh; Kavčič, Marko; Drole Torkar, Ana; Kafol, Jan; Lainšček, Duško; Jerala, Roman; Sever, Matjaž; Zver, Samo; Serša, Gregor; Čemažar, Maja; Strojan, Primož; Grošelj, Aleš; Žerjav Tanšek, Mojca; Miroševič, Špela; Ivančan, Simona; Prelog, Tomaž; Gosar, David; Oražem Mrak, Jasna; Mlinarič, Matej; Bertok, Sara; Kovač, Jernej; Kodrič, Jana; Battelino, Saba; Pokorn, Marko; Ihan, Alojz; Jazbec, Janez; Battelino, Tadej; Osredkar, Damjan

Unravelling genetic etiology of cerebral palsy: findings from a Slovenian pediatric cohort

揭示脑瘫的遗传病因:来自斯洛文尼亚儿科队列的研究结果

Arkar Silan, Ula; Trebše, Ana; Kovač, Jernej; Rogac, Mihael; Troha Gergeli, Anja; Šket, Robert; Bregant, Tina; Neubauer, David; Peterlin, Borut; Osredkar, Damjan

Corrigendum: Diagnostic Approach to Children with Unexplained Global Developmental Delay in Pediatric Neurology Outpatient Clinic

更正:儿科神经科门诊中不明原因全面发育迟缓儿童的诊断方法

Veronese, Airin; Osredkar, Damjan; Lovrečić, Luca; Troha Gergeli, Anja

Diagnostic Approach to Children with Unexplained Global Developmental Delay in Pediatric Neurology Outpatient Clinic

儿科神经科门诊不明原因全面发育迟缓患儿的诊断方法

Veronese, Airin; Osredkar, Damjan; Lovrečić, Luca; Troha Gergeli, Anja

Eculizumab for Thrombotic Microangiopathy Induced by Onasemnogene Abeparvovec in Spinal Muscular Atrophy

依库珠单抗治疗脊髓性肌萎缩症中由奥纳西姆诺基因阿贝帕沃韦引起的血栓性微血管病

Levart, Tanja Kersnik; Kar, Nina Olas; Pegan, Chiara Močnik; Vrščaj, Eva; Gergeli, Anja Troha; Loboda, Tanja; Osredkar, Damjan

Paving the way toward treatment solutions for CTNNB1 syndrome: a patient organization perspective

为CTNNB1综合征的治疗方案铺平道路:患者组织的视角

Miroševič, Špela; Khandelwal, Shivang; Amerson, Emily; Parks, Effie; Parks, Mariana; Cochran, Lauren; González Hernández, Ana; Ferraro, Mirela; Lisowski, Leszek; Perez-Iturralde, Andrea; Chung, Wendy; Jacob, Michele H; Žakelj, Nina; Lainšček, Duško; Forstnerič, Vida; Sušjan, Petra; Maruna, Matea; Jerala, Roman; Osredkar, Damjan