Researchers
Janković, Milena
Rezultati 61-80 od 107
| Godina | Naslov | Autor(i) | Tip rezultata | Mp-kat. |
|---|---|---|---|---|
| 2021 | Etiology of status epilepticus in Neurological Intensive Care Unit![]() | Radišić, Vanja | Conference Paper | Mp. category will be shown later |
| 2020 | Quality of life in hereditary neuropathy with liability to pressure palsies is as impaired as in Charcot-Marie-Tooth disease type 1A![]() | Bjelica, Bogdan | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2020 | Oligoclonal bands in the cerebrospinal fluid of patients with Guillain-Barre syndrome![]() | Kalač, Aida; Basta, Ivana Z. | Conference Paper | Mp. category will be shown later |
| 2020 | Neuropathic pain in patients with Charcot-Marie-Tooth type 1A![]() | Bjelica, Bogdan | Article | 22M22 |
| 2020 | Genetic Aspects of Inflammation and Immune Response in Stroke![]() | Nikolić, Dejan | Article | 21M21 |
| 2020 | Oligoclonal bands in the cerebrospinal fluid of patients with chronic inflammatory demyelinating polyradiculoneuropathy![]() | Basta, Ivana Z. | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2020 | Whole Mitochondrial Genome Analysis in Serbian Cases of Leber’s Hereditary Optic Neuropathy![]() | Dawod, Phepy G. A.; Jančić, Jasna | Naučni članak | 21M21 - Vodeći međunarodni časopis kategorije M21 |
| 2020 | Yield of the PMP22 deletion analysis in patients with compression neuropathies![]() | Ivanović, Vukan | Научни чланак | 21M21 - Водећи међународни часопис категорије M21 |
| 2019 | Body composition analysis in patients with myotonic dystrophy types 1 and 2![]() | Perić, Stojan | Научни чланак | 22M22 - Међународни часопис категорије M22 |
| 2019 | Phenotypic and genetic spectrum of patients with limb-girdle muscular dystrophy type 2A from Serbia![]() | Perić, Stojan | Naučni članak | Mp kategorija će biti prikazana naknadno. |
| 2019 | Analysis of ATXN1 and ATXN2 repeat length in C9ORF72 expansion carriers![]() | Marjanović, Ana | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2019 | Results of clinical exome analysis in rare neurodegenerative disorders in Serbian population![]() | Branković, Marija | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2019 | KRIT1 Gene Analysis In Serbian Patients With Familial Cerebral Cavernous Malformation![]() | Branković, Marija | Conference Paper | Mp. category will be shown later |
| 2019 | NOTCH3 mutations in Serbian CADASIL patients![]() | Janković, Milena Z. | Conference Paper | Mp. category will be shown later |
| 2019 | Whole mitochondrial genome analysis in carriers of mt3460 mutation with Leber's hereditary optic neuropathy![]() | Dawod, Phepy G. A.; Rovčanin, Branislav R. | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2019 | Analysis of mtDNA mutations in Serbian patients with Leber hereditary optic neuropathy![]() | Dawod, Phepy G. A.; Rovčanin, Branislav R.; Branković, Marija | Конференцијски рад | Мп категорија ће бити приказана накнадно. |
| 2019 | Angiogenin gene mutations in patients with amyotrophic lateral sclerosis from tertiary center in Belgrade![]() | Janković, Milena | Конференцијски рад | Мп категорија ће бити приказана накнадно. |
| 2019 | Molecular genetic testing of Huntington’s disease and genetic counselling![]() | Mandić, Ratka; Marjanović, Ana | Конференцијски рад | Мп категорија ће бити приказана накнадно. |
| 2019 | Genetika amiotrofične lateralne skleroze![]() | Stević, Zorica | Conference Paper | Mp. category will be shown later |
| 2019 | Spectrum of mutations in presenilin 1 gene in patients with early onset Alzheimer disease![]() | Andabaka, Marko | Conference Paper | Mp. category will be shown later |
