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Browsing by Project University College London Hospitals Biomedical Research Centre
Showing results 1 to 7 of 7
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2025 | Biallelic variants in COX18 cause a mitochondrial disorder primarily manifesting as peripheral neuropathy | Armirola-Ricaurte, Camila; ...; Tomic, Aleksandra; ...; Milic-Rasic, Vedrana; (broj, koautora 20) | Article | 21a+M21a+ |
| 2023 | Clinical characteristics and management of neurocysticercosis patients: a retrospective assessment of case reports from Europe | Stelzle, Dominik; Abraham, Annette; Kaminski, Miriam; Schmidt, Veronika; De Meijere, Robert; Bustos, Javier A; Garcia, Hector Hugo; Sahu, Priyadarshi Soumyaranjan; Bobić, Branko   ; Cretu, Carmen;
Chiodini, Peter; Dermauw, Veronique; Devleesschauwer, Brecht; Dorny, Pierre; Fonseca, Ana; Gabriël, Sarah; Morales, Maria Ángeles Gómez; Laranjo-González, Minerva; Hoerauf, Achim; Hunter, Ewan; Jambou, Ronan; Jurhar-Pavlova, Maja; Reiter-Owona, Ingrid; Sotiraki, Smaragda; Trevisan, Chiara; Vilhena, Manuela; Walker, Naomi F; Zammarchi, Lorenzo; Winkler, Andrea Sylvia;
| Article | 21a+M21a+ |
| 2025 | European Academy of Neurology (EAN)/European Federation of Autonomic Societies (EFAS)/International Neuro-Urology Society (INUS) Guidelines for Practising Neurologists on the Assessment and Treatment of Neurogenic Urinary and Sexual Symptoms (NEUROGED Guidelines) | Panicker, Jalesh N; ...; Stankovic, Iva D; ...; (broj, koautora 36) | Article | 21aM21a |
| 2025 | Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORD | Cortese, Andrea; ...; Perić, Stojan ; ...; (broj koautora 81) | Article | 21a+M21a+ |
| 2018 | Prediction of a multiple sclerosis diagnosis in patients with clinically isolated syndrome using the 2016 MAGNIMS and 2010 McDonald criteria: a retrospective study | Filippi, Massimo; ...; Mesaroš, Šarlota T. ; ...; Drulović, Jelena S. ; ...; Dujmović-Bašuroski, Irena ; ...; (broj koautora 25) | Naučni članak | 21a+M21a+ - Vodeći međunarodni časopis kategorije M21a+ |
| 2025 | Recessive Variants in PIGG Cause a Motor Neuropathy with Variable Conduction Block, Childhood Tremor, and Febrile Seizures: Expanding the Phenotype | Record, Christopher J.; ...; Perić, Stojan ; ...; Ivanović, Vukan ; ...; (broj koautora 18) | Article | 21a+M21a+ |
| 2022 | The gene regulation knowledge commons: the action area of GREEKC | Kuiper, Martin; Bonello, Joseph; Fernández-Breis, Jesualdo T.; Bucher, Philipp; Futschik, Matthias E.; Gaudet, Pascale; Kulakovskiy, Ivan V.; Licata, Luana; Logie, Colin; Lovering, Ruth C.;
Makeev, Vsevolod J.; Orchard, Sandra; Panni, Simona; Perfetto, Livia; Sant, David; Schulz, Stefan; Vercruysse, Steven; Zerbino, Daniel R.; Lægreid, Astrid;
| Article | Mp. category will be shown later |