Researchers
Janković, Milena
Rezultati 21-40 od 107
| Godina | Naslov | Autor(i) | Tip rezultata | Mp-kat. |
|---|---|---|---|---|
| 2024 | Clinical Characteristics and Whole Exome Sequencing Analysis in Serbian Cases of Clubfoot Deformity—Single Center Study![]() | Milanović, Filip; Dučić, Siniša | Article | 21M21 |
| 2024 | Secondary findings in 443 whole exome sequencing data![]() | Branković, Marija | Conference Paper | Mp. category will be shown later |
| 2024 | APOE genotype, ATXN1 and ATXN2 repeats size in C9orf72 expansion carriers![]() | Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2024 | Whole exome sequencing in Serbian patients with hereditary spastic paraplegia![]() | Branković, Marija | Article | 22M22 |
| 2024 | Analysis of clinical exome panel in rare movement and cognitive disorders![]() | Branković, Marija | Conference Paper | Mp. category will be shown later |
| 2024 | Exploring the Connection between Migraines and Pregnancy: The Impact of Physical Activity on Symptom Management![]() | Lacković, Milan | Article | 21M21 |
| 2023 | Basophilic peripheral nerve inclusions in a patient with L144F SOD1 amyotrophic lateral sclerosis![]() | Aleksić, Dejan | Article | 23M23 |
| 2023 | C9ORF72 intermediate repats in neurodegenerative disorders from Serbia![]() | Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2023 | Stroke vs. Preeclampsia: Dangerous Liaisons of Hypertension and Pregnancy![]() | Lacković, Milan | Article | 21M21 |
| 2023 | Novel GATOR1 variants in focal epilepsy![]() | Kovačević, Maša | Article | 22M22 |
| 2023 | Whole exome sequencing in Serbian patients with hereditary spastic paraplegia![]() | Ivanović, Vukan | Conference Paper | Mp. category will be shown later |
| 2023 | miRNAs as a Potential Biomarker in the COVID-19 Infection and Complications Course, Severity, and Outcome![]() | Janković, Milena | Article | 21M21 |
| 2023 | Novel variants in established epilepsy genes in focal epilepsy![]() | Kovačević, Maša | Article | 22M22 |
| 2023 | Analysis of clinical exome panel in rare neurodegenerative disorders in Serbian population![]() | Branković, Marija | Conference Paper | Mp. category will be shown later |
| 2023 | EPR-210 Whole exome sequencing in Serbian patients with hereditary spastic paraplegia![]() | Ivanović, Vukan | Conference Paper | Mp. category will be shown later |
| 2023 | Clinical and genetic features of Huntington’s disease patients from Serbia: A single-center experience![]() | Kresojević, Nikola | Article | 21M21 |
| 2023 | Reply to: “Differences in Sex‐Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism”![]() | Kresojević, Nikola | Article | 21a+M21a+ |
| 2023 | TREM2 R47H as a risk factor for Alzheimer's disease in Serbian patients![]() | Pešić, Milica | Conference Paper | Mp. category will be shown later |
| 2023 | The association of R47H variant in the TREM2 gene and genetic susceptibility to Alzheimer's disease in Serbian population![]() | Andrejić, Nikola; Pešić, Milica | Article | 53M53 |
| 2023 | Yield of GATOR1 gene sequencing in a Serbian focal epilepsy cohort![]() | Kovačević, Maša | Conference Paper | Mp. category will be shown later |
