Researchers



Results 21-40 of 356
Issue DateTitleAuthor(s)TypeМp-cat.
2025Hereditary neuropathies in Serbian populationVukojević, Milica  ; Marjanović, Ana ; Ivanović, Vukan ; Janković, Milena ; Kačar, Aleksandra  ; Basta, Ivana  ; Perić, Stojan  Conference Paper
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2025Empasiprubart in Multifocal Motor Neuropathy: Safety and Efficacy Data From the Phase 2 ARDA StudyQuerol, Luis; ...; Perić, Stojan  ; ...; (broj koautora 17)Conference Paper
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2025Secondary findings in 443 exome sequencing dataBranković, Marija  ; Han, Heonjong; Janković, Milena ; Marjanović, Ana ; Andrejić, Nikola; Gunjić, Ilija  ; Virić, Vanja  ; Palibrk, Aleksa; Lee, Hane; Perić, Stojan  Article
23M23
2025Video head impulse test findings in patients with peripheral myelin protein 22 related neuropathiesĆalić, Željka; Bjelica, Bogdan ; Perić, Stojan Z.  ; Vujnić, Milorad; Božović, Ivo ; Rakočević-Stojanović, Vidosava M. ; Bradshaw, Andrew; Welgampola, Miriam S.Article
21M21
2025Diagnosing missed cases of spinal muscular atrophy in genome, exome, and panel sequencing data setsWeisburd, Ben; ...; Perić, Stojan Z.  ; ...; (broj koautora 39)Article
21aM21a
2025Transcranial Brain Parenchyma Sonographic Findings in Familial and Sporadic Amyotrophic Lateral SclerosisBožović, Ivo ; Lična, Emir; Bjelica, Bogdan ; Milićević, Ognjen  ; Palibrk, Aleksa; Basta, Ivana  ; Perić, Stojan  ; Pavlović, Aleksandra  ; Stević, Zorica ; Mijajlović, Milija  Article
21aM21a
2025Adiponectin and Leptin-Considerations in Adult Patients with Spinal Muscular Atrophy Type 3Miletić, Marija; Stević, Zorica ; Perić, Stojan Z  ; Tančić-Gajić, Milina  ; Rakočević, Jelena  ; Stojanović, Miloš  ; Marković, Bojan; Žarković, Miloš  Article
21M21
2025APOE, ATXN1 and ATXN2 genetic analysis in ALS/FTD patientsMarjanović, Ana ; Virić, Vanja  ; Mandić, Gorana  ; Stojković, Tanja  ; Perić, Stojan  ; Basta, Ivana  ; Janković, Milena ; Stojadinović, Lenka ; Jovanović, Emilija; Branković, Marija  ;
Novaković, Ivana  ; Stević, Zorica ; Stefanova, Elka ;
Conference Paper
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2025Disease burden in Serbian patients with facioscapulohumeral muscular dystrophyRalić, Branislav; Albano, N.; Virić, Vanja  ; Nuredini, A.; Azanjac, Ana  ; Rajić, Sonja  ; Marjanović, Ana ; Tupler, R.; Heatwole, C.; Perić, Stojan  Conference Paper
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2025Baseline Characteristics of the First 100 Study Participants with Multifocal Motor Neuropathy in the iMMersioN studyHewamadduma, Channa; Perić, Stojan Z.  ; Claeys, Kristl; Querol, Luis; Altamimi, Sadiq; Van de Walle, Inge; Persson, Emma; Van Hoomissen, Iris; Szmyd, Gabriela; Vujcic, Miodrag;
Cadour, Stephanie; Van de Steen, Olivier; Arvin-Berod, Clemence; Allen, Jeffrey A.;
Conference Paper
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2025Causal Variants in CHRNA1 and CHRNB1 Genes for Anti-acetylcholine Receptor Antibody Positive Myasthenia Gravis: Evidence from Bayesian Fine-Mapping and Genetic Association StudyGarai, Nemanja  ; Petrović, Kristina  ; Perić, Stojan  ; Đorđević, Ivana; Pešović, Jovan  ; Brkušanin, Miloš  ; Brajušković, Goran  ; Lavrnić, Dragana ; Apostolski, Slobodan ; Basta, Ivana  ;
Jovanović, Vladimir M.  ; Savić-Pavićević, Dušanka  ;
Article
21M21
2025Novel HSPB8 mutations in severe early-onset myopathy with involvement of respiratory and cardiac muscles cause proteostasis defects in cell modelsTedesco, Barbara; Perić, Stojan  ; ...; Rakočević-Stojanović, Vidosava ; Milenković, Sanja  ; ...; Ivanović, Vukan ; ...; (broj koautora 23)Article
21M21
2025Oligoclonal bands in blood and cerebrospinal fluid of patients with immune-mediated neuropathiesSekulić, A.; Božović, Ivo ; Palibrk, Aleksa; Janković, Mladen; Perić, Stojan  ; Drulović, Jelena ; Basta, Ivana  Conference Paper
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2025Screening for Pompe disease in Serbian patients with limb-girdle muscle weaknessSekulić, Aleksandar; Virić, Vanja  ; Todorović, Teodora; Pešović, Jovan  ; Branković, Marija  ; Andrejić, Nikola; Palibrk, Aleksa; Božović, Ivo ; Ivanović, Vukan ; Basta, Ivana Z.  ;
Perić, Stojan Z.  ;
Article
22M22
2025Empasiprubart Versus Intravenous Immunoglobulin in Multifocal Motor Neuropathy Phase 3 Study Design: EMPASSIONQuerol, Luis; Perić, Stojan Z.  ; Cadour, Stephanie; Rigby, Simon; Van de Walle, Inge; Persson, Emma; Vujcic, Miodrag; Van de Steen, Olivier; Mashchenko, Oleksandr; Van Hoomissen, Iris;
Allen, Jeffrey A.; Katzberg, Hans; Kuwabara, Satoshi; Stettner, Mark; Rinaldi, Simon; Van der Pol, W Ludo;
Conference Paper
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2024Screening for Pompe disease and its differential diagnosesSekulić, A.; Todorović, T.; Perić, Stojan  ; Basta, Ivana  ; Ivanović, Vukan ; Rakočević-Stojanović, Vidosava M. ; Božović, Ivo ; Palibrk, Aleksa; Virić, Vanja  Conference Paper
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2024Bulbar-onset amyotrophic lateral sclerosis in a patient with genetically confirmed Huntington's disease: a case studyBožović, Ivo ; Gluščević, Sanja; Kezić, Ivana; Ivanovic, Vukan ; Palibrk, Aleksa; Perić, Stojan  ; Basta, Ivana  ; Stević, Zorica Article
Mp. category will be shown later
2024The GENESIS database and tools: A decade of discovery in Mendelian genomicsDanzi, Matt C.; ...; Perić, Stojan Z.  ; ...; (broj koautora 37)Article
21M21
2024Impact of discontinuation and reintroduction of alglucoidase alpha in patients with late-onset Pompe diseaseAndrejić, Nikola; Virić, Vanja  ; Andabaka, Marko ; Božović, Ivo ; Palibrk, Aleksa; Ivanović, Vukan ; Basta, Ivana  ; Stević, Zorica ; Perić, Stojan  Conference Paper
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2024Whole exome sequencing in Serbian patients with hereditary spastic paraplegiaBranković, Marija  ; Ivanović, Vukan ; Basta, Ivana  ; Khang, Rin; Lee, Eugene; Stević, Zorica ; Ralić, Branislav; Tubić, Radoje  ; Seo, GoHun; Marković, Vladana  ;
Božović, Ivo ; Svetel, Marina ; Marjanović, Ana ; Veselinović, Nikola; Mesaroš, Šarlota  ; Janković, Milena ; Savić-Pavićević, Dušanka  ; Jovin, Zita; Novaković, Ivana  ; Lee, Hane; Perić, Stojan  ;
Article
22M22