Autori: Rakocevic-Stojanovic Vidosava M
Naslov | Novel HSPB8 mutations in severe early-onset myopathy with involvement of respiratory and cardiac muscles cause proteostasis defects in cell models (Article; Early Access) |
Autori | Tedesco Barbara Peric Stojan Z ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2025), vol. br. , str. - |
Projekat | Sanofi Genzyme; Ultragenyx; LGMD2I Research Fund; Samantha J Brazzo Foundation; LGMD2D Foundation; Kurt+Peter Foundation; Muscular Dystrophy UK; Coalition to Cure Calpain 3; National Human Genome Research Institute [R01 HG009141]; National Eye Institute; National Heart, Lung and Blood Institute [UM1 HG008900]; Ministry of Science of the Republic of Serbia [175083]; Fondazione Telethon, Italy [GGP19128]; Fondazione Italiana per la ricercasulla Sclerosi Laterale Amiotrofica (AriSLA), Italy; Association Francaise contre les Myopathies (AFM Telethon), France [23236]; Italian Ministry of University and Research (MIUR) [2017F2A2C5, 2022EFLFL8]; European Union-Next Generation EU [CN00000041, CUPB93D21010860004]; Progetto Dipartimenti di Eccellenza; Universita degli Studi di Milano; Agenzia Italiana del Farmaco (AIFA); National Institute Of Arthritis And Musculoskeletal And Skin Diseases of the National Institutes of Health [R21AR080407]; UCL/UCLH Biomedicine NIHR, UK; University of Antwerp (TOP-BOF) [38694, 41667]; Flanders Fund for Scientific Research (FWO-Flanders) [G040821N]; Solve-RD [779257] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: |
|
Naslov | Video head impulse test findings in patients with peripheral myelin protein 22 related neuropathies (Article) |
Autori | Calic Zeljka Bjelica Bogdan Peric Stojan Z ![]() |
Info | CLINICAL NEUROPHYSIOLOGY, (2025), vol. 175 br. , str. - |
Projekat | Garnett Passe and Rodney Williams Memorial Foundation |
Ispravka | Web of Science Članak Elečas Rang časopisa |
|
Naslov | Video head impulse gain is impaired in myotonic dystrophy types 1 and 2 (Article; Early Access) |
Autori | Calic Zeljka Peric Stojan Z ![]() |
Info | EUROPEAN JOURNAL OF NEUROLOGY, (2024), vol. br. , str. - |
Projekat | Garnett Passe and Rodney Williams Memorial Foundation Conjoint Grant |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: |
|
Naslov | Screening for Pompe disease and its differential diagnoses (Meeting Abstract) |
Autori | Sekulic Aleksandar Todorovic T Peric Stojan Z ![]() |
Info | NEUROMUSCULAR DISORDERS, (2024), vol. 43 br. , Suppl. 1, str. - |
Ispravka | Web of Science Članak Elečas Rang časopisa |
|
Naslov | Modal allele change as a predictor of skeletal muscle symptoms progression in myotonic dystrophy type 1 (Meeting Abstract) |
Autori | Radovanovic Nemanja Pesovic Jovan Peric Stojan Z ![]() ![]() ![]() |
Info | NEUROMUSCULAR DISORDERS, (2024), vol. 43 br. , Suppl. 1, str. - |
Ispravka | Web of Science Članak Elečas Rang časopisa |
|
Naslov | Transcranial brain parenchyma sonographic findings in patients with myotonic dystrophy type 1 and 2 (Article) |
Autori | Mijajlovic Milija D ![]() ![]() ![]() |
Info | HELIYON, (2024), vol. 10 br. 5, str. - |
Projekat | Ministry of Education and Science of the Republic of Serbia [200110, 175083] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: |
|
Naslov | Longitudinal analysis of CTG repeat somatic instability in myotonic dystrophy type 1 patients (Meeting Abstract) |
Autori | Radovanovic Nemanja Pesovic Jovan Peric Stojan Z ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 1, str. 517-518 |
Projekat | Science Fund of the Republic of Serbia [7754217] |
Ispravka | Web of Science Elečas Rang časopisa |
|
Naslov | Clinical and genetic features of congenital myasthenic syndrome in adult patients from Serbia (Meeting Abstract) |
Autori | Azanjac-Arsic Ana D ![]() ![]() |
Info | EUROPEAN JOURNAL OF NEUROLOGY, (2023), vol. 30 br. , Suppl. 1, str. 339-339 |
Ispravka | Web of Science Elečas Rang časopisa |
|
Naslov | Whole exome sequencing in Serbian patients with hereditary spastic paraplegia (Meeting Abstract) |
Autori | Ivanovic Vukan Brankovic Marija ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF NEUROLOGY, (2023), vol. 30 br. , Suppl. 1, str. 260-260 |
Ispravka | Web of Science Elečas Rang časopisa |
|
Naslov | The importance of direct genetic testing for determining female carriers of the mutation in dystrophinopathies (Article) |
Autori | Maksic Jasmina ![]() ![]() ![]() ![]() ![]() |
Info | VOJNOSANITETSKI PREGLED, (2023), vol. 80 br. 3, str. 201-207 |
Projekat | Serbian Ministry of Education, Science, and Technological Development [ON175091]; [ON175083] |
Ispravka | Web of Science Članak Elečas Rang časopisa |
|