Autori: Marjanovic Ana
Naslov | Frequency of C9orf72, GRN, and MAPT pathogenic variants in patients recruited at the Belgrade Memory Center (Article; Early Access) |
Autori | Stefanova Elka D ![]() ![]() ![]() |
Info | NEUROGENETICS, (2024), vol. br. , str. - |
Projekat | Ministarstvo Prosvete, Nauke i Tehnoloscaron;kog Razvoja |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: |
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Naslov | Whole exome sequencing in Serbian patients with hereditary spastic paraplegia (Article; Early Access) |
Autori | Brankovic Marija ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
Info | NEUROGENETICS, (2024), vol. br. , str. - |
Projekat | Yonsei University |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: |
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Naslov | RFC1 and FGF14 Repeat Expansions in Serbian Patients with Cerebellar Ataxia (Article; Early Access) |
Autori | Milovanovic Andona ![]() ![]() ![]() ![]() |
Info | MOVEMENT DISORDERS CLINICAL PRACTICE, (2024), vol. br. , str. - |
Projekat | Deutsche Forschungsgemeinschaft; University of Luebeck [FOR 2488]; German Research Foundation |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: |
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Naslov | ANO10-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series (Article; Early Access) |
Autori | Milovanovic Andona ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
Info | MOVEMENT DISORDERS, (2024), vol. br. , str. - |
Projekat | International Parkinson and Movement Disorder Society; The Parkinson's Foundation; University of Luebeck; Projekt DEAL |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: |
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Naslov | Clinical and Genetic Features of Huntington's Disease Patients From Republic of Serbia: A Single-Center Experience (Letter) |
Autori | Kresojevic Nikola D ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
Info | JOURNAL OF MOVEMENT DISORDERS, (2023), vol. 16 br. 3, str. 333-335 |
Projekat | Ministry of Education and Science of the Republic of Serbia [175090] |
Ispravka | Web of Science Članak Elečas Rang časopisa |
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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 |
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Naslov | Motor neuron involvement in facial muscles as characteristic of ANO10 mutation (Meeting Abstract) |
Autori | Dragasevic-Miskovic Natasa T Milovanovic Andona ![]() ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF NEUROLOGY, (2023), vol. 30 br. , Suppl. 1, str. 234-234 |
Ispravka | Web of Science Elečas Rang časopisa |
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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 |
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Naslov | Reply to: "Differences in Sex-Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism" (Letter) |
Autori | Kresojevic Nikola D ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
Info | MOVEMENT DISORDERS, (2023), vol. 38 br. 4, str. 712-713 |
Projekat | Ministry of Education and Science of the Republic of Serbia [175090] |
Ispravka | Web of Science Članak Elečas Rang časopisa |
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Naslov | C9orf72 Genetic Screening in Amyotrophic Lateral Sclerosis Patients from Serbia (Article) |
Autori | Marjanovic Ana ![]() ![]() ![]() ![]() ![]() ![]() |
Info | GENETIKA-BELGRADE, (2023), vol. 55 br. 1, str. 1-18 |
Projekat | Ministry of Education, Science and Technological Development, the Republic of Serbia [ON175090, ON175091, 200110] |
Ispravka | Web of Science Članak Elečas Rang časopisa |
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