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Pregled prema Projekat Parkinson"

Prikaz rezultata 1 do 14 od 14
GodinaNaslovAutor(i)Tip rezultataMp-kat.
2022A multiplex pedigree with pathologically confirmed multiple system atrophy and Parkinson's disease with dementiaFanciulli, Alessandra; ...; Stankovic, Iva; ...; (broj, koautora 26)Naučni članak
21M21 - Vodeći međunarodni časopis kategorije M21
2016An expanded evaluation of protein function prediction methods shows an improvement in accuracyJiang, Yuxiang; Gemović, Branislava S.  ; Glišić, Sanja  ; Perović, Vladimir R.  ; Veljković, Veljko ; Veljković, Nevena V.  Naučni članak
21a+M21a+ - Vodeći međunarodni časopis kategorije M21a+
2024ANO10-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case SeriesMilovanović, 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+
2024Contribution of MRI for the Early Diagnosis of Parkinsonism in Patients with Diagnostic UncertaintyChougar, 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 StudiesLill, 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;
Naučna kritika i polemika
21aM21a - Vodeći međunarodni časopis kategorije M21a
2024Genotype-phenotype correlation in PRKN-associated Parkinson's diseaseMenon, Poornima Jayadev; ...; Jovanović, Čarna; Svetel, Marina V. ; ...; (broj koautora 53)Naučni članak
21aM21a - Vodeći međunarodni časopis kategorije M21a
2012Genotype-phenotype correlations in THAP1 dystonia: Molecular foundations and description of new casesLeDoux, 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, YuArticle
21M21
2016Guidelines 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  Naučni članak
21aM21a - Vodeći međunarodni časopis kategorije M21a
2024IMMUnity Unveiled: A Translational NETwork for tackling PARKinson's Disease – IMMUPARKNETGugu, 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;
Naučni članak
Mp kategorija će biti prikazana naknadno.
2010Low-frequency repetitive transcranial magnetic stimulation and off-phase motor symptoms in Parkinson's diseaseFilipović, Saša  ; Rothwell, John C.; Bhatia, KailashNaučni članak
22M22 - Međunarodni časopis kategorije M22
2012Novel PRRT2 mutation in an African-American family with paroxysmal kinesigenic dyskinesiaHedera, Peter; Xiao, Jianfeng; Puschmann, Andreas; Momcilovic, Dragana R; Wu, Steve W; LeDoux, Mark SNaučni članak
21M21 - Vodeći međunarodni časopis kategorije M21
2024Predictors of Care Home Admission and Survival Rate in Patients With Syndromes Associated With Frontotemporal Lobar Degeneration in EuropeBorroni, Barbara; ...; Stefanova, Elka ; ...; Mandić-Stojmenović, Gorana  ; ...; (broj koautora 30)Article
21a+M21a+
2010Slow (1 Hz) repetitive transcranial magnetic stimulation (rTMS) induces a sustained change in cortical excitability in patients with Parkinson's diseaseFilipović, Saša  ; Rothwell, John C.; Bhatia, KailashArticle
21M21
2013Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 geneLohmann, Katja; ...; Kostic, Vladimir S; ...; (broj, koautora 29)Article
21a+M21a+