Researchers
Perić, Stojan
Results 241-260 of 351
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2016 | Evaluation of the adequacy of requests for electrodiagnostic examination in a tertiary referral center![]() | Nikolić, Ana | Article | 22M22 |
| 2016 | Guillain-Barré syndrome in elderly![]() | Perić, Stojan Z. | Conference Paper | Mp. category will be shown later |
| 2016 | Executive dysfunction and survival in patients with amyotrophic lateral sclerosis: Preliminary report from a Serbian centre for motor neuron disease![]() | Stojković, Tanja | Article | 22M22 |
| 2016 | 18F-FDG-PET Study in patients with myotonic dystrophy type 1 and 2![]() | Stojanović, Vidosava | Conference Paper | Mp. category will be shown later |
| 2016 | Myotonic dystrophy type 2 significantly affects quality of life![]() | Vujnić, Milorad; Perić, Stojan | Conference Paper | Mp. category will be shown later |
| 2016 | Recurrent Guillain-Barre Syndrome - Case Series![]() | Basta, Ivana Z. | Conference Paper | Mp. category will be shown later |
| 2016 | Comparison of temporal and stride characteristics in myotonic dystrophies type 1 and 2 during dual-task walking![]() | Radovanović, Saša M. | Article | 21aM21a |
| 2016 | Guillain-Barré syndrome in the elderly![]() | Perić, Stojan | Article | 21M21 |
| 2016 | Prognostic factors and survival of ALS patients from Belgrade, Serbia![]() | Stević, Zorica | Article | 22M22 |
| 2016 | Application of exome sequencing technologies: A case study of patients with unexplained limb-girdle muscle weakness harbouring GAA mutations![]() | Johnson, Katherine; Bertoli, Marta; Phillips, Lauren; Töpf, Ana; Claeys, Kristl; Rakočević-Stojanović, Vidosava M.
Akay, Ela; Bastian, Alexandra E.; Lusakowska, Anna; Lek, Monkol; Xu, Liwen; MacArthur, Daniel; Straub, Volker;
| Conference Paper | Mp. category will be shown later |
| 2015 | Varijantni ponovci kao mogući genetički modifikatori DM1![]() | Pešović, Jovan | Conference Paper | Mp. category will be shown later |
| 2015 | MuSK autoantibodies in myasthenia gravis detected by cell based assay — A multinational study![]() | Tsonis, A.I.; Zisimopoulou, P.; Lazaridis, K.; Tzartos, J.; Matsigkou, E.; Zouvelou, V.; Mantegazza, R.; Antozzi, C.; Andreetta, F.; Evoli, A.;
Deymeer, F.; Saruhan-Direskeneli, G.; Durmus, H.; Brenner, T.; Vaknin, A.; Berrih-Aknin, S.; Behin, A.; Sharshar, T.; De Baets, M.; Losen, M.; Martinez-Martinez, P.; Kleopa, K.A.; Zamba-Papanicolaou, E.; Kyriakides, T.; Kostera-Pruszczyk, A.; Szczudlik, P.; Szyluk, B.; Lavrnić, Dragana
| Article | 22M22 |
| 2015 | Echocardiography in patients with myotonic dystrophy type 1![]() | Perić, Stojan Z. | Conference Paper | Mp. category will be shown later |
| 2015 | Association between the SMN2 gene copy number and clinical characteristics of patients with spinal muscular atrophy with homozygous deletion of exon 7 of the SMN1 gene![]() | Žarkov, Marija | Article | 23M23 |
| 2015 | Variant repeats in DM1 patients might be associated with milder clinical presentation![]() | Pešović, Jovan | Conference Paper | Mp. category will be shown later |
| 2015 | Udruženost Devic-ove bolesti i miotoniĉnih distrofija (DM) tip 1 i tip 2 - prikaz porodice![]() | Stojanović, Vidosava | Conference Paper | Mp. category will be shown later |
| 2015 | Variant repeats as genetic modifiers of DM1 – a case report![]() | Pešović, Jovan | Conference Paper | Mp. category will be shown later |
| 2015 | Variability of multisystemic features in myotonic dystrophy type 1 – lessons from Serbian registry![]() | Rakočević-Stojanović, Vidosava | Article | 22M22 |
| 2015 | Mreža za neuromišićne bolesti Srbije (NMD-SerbNet)![]() | Brkušanin, Miloš | Conference Paper | Mp. category will be shown later |
| 2015 | Brain sonography insight into the midbrain in myotonic dystrophy type 2![]() | Rakočević-Stojanović, Vidosava | Article | 22M22 |
