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Browsing by Project Parkinson"
Showing results 1 to 14 of 14
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2022 | A multiplex pedigree with pathologically confirmed multiple system atrophy and Parkinson's disease with dementia | Fanciulli, Alessandra; ...; Stankovic, Iva; ...; (broj, koautora 26) | Article | 21M21 |
| 2016 | An expanded evaluation of protein function prediction methods shows an improvement in accuracy | Jiang, Yuxiang; Gemović, Branislava S.   ; Glišić, Sanja ; Perović, Vladimir R. ; Veljković, Veljko ; Veljković, Nevena V. | Article | 21a+M21a+ |
| 2024 | ANO10-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series | Milovanović, Andona ; Westenberger, Ana; Stanković, Iva D. ; Tamaš, Olivera S.; Branković, Marija ; Marjanović, Ana ; ...; Branković, Vesna; Novaković, Ivana V. ; Petrović, Igor N. ;
Svetel, Marina V.
; Klein, Christine; Kostić, Vladimir S. ; Dragašević-Mišković, Nataša T. ; (broj koautora 18); | Article | 21a+M21a+ |
| 2024 | Contribution of MRI for the Early Diagnosis of Parkinsonism in Patients with Diagnostic Uncertainty | Chougar, Lydia; Faucher, Alice; Faouzi, Johann; Lejeune, Francois Xavier; Gama, Lobo Goncalo; Jovanovic, Carna; Cormier, Florence; Dupont, Gwendoline; Vidailhet, Marie; Corvol, Jean Christophe;
Colliot, Olivier; Lehericy, Stephane; Grabli, David; Degos, Bertrand;
| Article | 21a+M21a+ |
| 2025 | (Dys)regulation of the Immune System in Parkinson's Disease: Methodologies, Techniques, and Key Findings from Human Studies | Lill, Christina M; di Flora, Alessia; Sechi, Leonardo A.; Pereira, Frederico C.; Moisoi, Nicoleta; Nikolovski, Neda ; Aktekin, Mustafa; Gursoy-Ozdemir, Yasemin; Deecke, Laura; Cossu, Davide;
Homann, Jan; Simula, Elena R.; Keskinoz, Elif Nedret; Oz-Arslan, Devrim; Muluk, Nuray Bayar; Gonçalves, Milene; Pirovano, Elenamaria; Comi, Cristoforo; Marino, Franca; on behalf of the IMMUPARKNET Consortium;
| Reviews | 21aM21a |
| 2024 | Genotype-phenotype correlation in PRKN-associated Parkinson's disease | Menon, Poornima Jayadev; ...; Jovanović, Čarna; Svetel, Marina V. ; ...; (broj koautora 53) | Article | 21aM21a |
| 2012 | Genotype-phenotype correlations in THAP1 dystonia: Molecular foundations and description of new cases | LeDoux, Mark S; Xiao, Jianfeng; Rudzinska, Monika; Bastian, Robert W; Wszolek, Zbigniew K; Van, Gerpen Jay A; Puschmann, Andreas; Momcilovic, Dragana R; Vemula, Satya R; Zhao, Yu | Article | 21M21 |
| 2016 | Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) | Bumbaširević, Vladimir ; Isaković, Aleksandra ; Kravić-Stevović, Tamara ; Marković, Ivanka ; Trajković, Vladimir ; Harhaji-Trajković, Ljubica ; Klionsky D. et al.; Ljujić, Mila | Article | 21aM21a |
| 2024 | IMMUnity Unveiled: A Translational NETwork for tackling PARKinson's Disease – IMMUPARKNET | Gugu, Mitilda; Acharya, Shubhra; Pira, Dogukan; Poletti, Simona; di Flora, Alessia; Saksida, Tamara ; Pilipenko, Vladimirs; Romero-Ramos, Marina; Marino, Franca; Munoz Delgado, Laura;
Nikolovski, Neda
; Gursoy Ozdemir, Yasemin; Lawson, Dale; Comi, Cristoforo; Figueira, ines; | Article | Mp. category will be shown later |
| 2010 | Low-frequency repetitive transcranial magnetic stimulation and off-phase motor symptoms in Parkinson's disease | Filipović, Saša ; Rothwell, John C.; Bhatia, Kailash | Article | 22M22 |
| 2012 | Novel PRRT2 mutation in an African-American family with paroxysmal kinesigenic dyskinesia | Hedera, Peter; Xiao, Jianfeng; Puschmann, Andreas; Momcilovic, Dragana R; Wu, Steve W; LeDoux, Mark S | Article | 21M21 |
| 2024 | Predictors of Care Home Admission and Survival Rate in Patients With Syndromes Associated With Frontotemporal Lobar Degeneration in Europe | Borroni, Barbara; ...; Stefanova, Elka ; ...; Mandić-Stojmenović, Gorana ; ...; (broj koautora 30) | Article | 21a+M21a+ |
| 2010 | Slow (1 Hz) repetitive transcranial magnetic stimulation (rTMS) induces a sustained change in cortical excitability in patients with Parkinson's disease | Filipović, Saša ; Rothwell, John C.; Bhatia, Kailash | Article | 21M21 |
| 2013 | Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene | Lohmann, Katja; ...; Kostic, Vladimir S; ...; (broj, koautora 29) | Article | 21a+M21a+ |