еНаука - преглед
Преглед према Аутор Durr, Alexandra
Приказ резултата 1 до 4 од 4
Година | Наслов | Аутор(и) | Тип резултата | Мп-кат. |
---|---|---|---|---|
2017 | Nomenclature of genetic movement disorders: Recommendations of the International Parkinson and Movement Disorder Society task force | Marras, Connie; Lang, Anthony; van, de Warrenburg Bart P.; Sue, Carolyn M.; Tabrizi, Sarah J.; Bertram, Lars; Mercimek-Mahmutoglu, Saadet; Ebrahimi-Fakhari, Darius; Warner, Thomas T.; Durr, Alexandra; | Научни чланак | 21aM21a - Рад у међ. часопису изузетних вредности |
2016 | Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force | Marras, Connie; Lang, Anthony E; van, de Warrenburg Bart P; Sue, Carolyn M; Tabrizi, Sarah J; Bertram, Lars; Mercimek-Mahmutoglu, Saadet; Ebrahimi-Fakhari, Darius; Warner, Thomas T; Durr, Alexandra;
Assmann, Birgit; Lohmann, Katja; Kostic, Vladimir K; Klein, Christine;
| Научни чланак | 21aM21a - Рад у међ. часопису изузетних вредности |
2016 | Reply Letter to Jinnah "Locus Pocus" and Albanese "Complex Dystonia Is Not a Category in the New 2013 Consensus Classification": Necessary Evolution, No Magic! | Klein, Christine; Lang, Anthony E; van, de Warrenburg Bart P; Sue, Carolyn M; Tabrizi, Sarah J; Bertram, Lars; Mercimek-Mahmutoglu, Saadet; Ebrahimi-Fakhari, Darius; Warner, Thomas T; Durr, Alexandra;
Assmann, Birgit; Kostic, Vladimir K; Lohmann, Katja; Marras, Connie;
| Информативни прилог | 21aM21a - Рад у међ. часопису изузетних вредности |
2010 | Targeted Next-Generation Sequencing of a 12.5 Mb Homozygous Region Reveals ANO10 Mutations in Patients with Autosomal-Recessive Cerebellar Ataxia | Vermeer, Sascha; Hoischen, Alexander; Meijer, Rowdy P.P.; Gilissen, Christian; Neveling, Kornelia; Wieskamp, Nienke; de, Brouwer Arjan; Koenig, Michel; Anheim, Mathieu; Assoum, Mirna;
Drouot, Nathalie; Todorovic, Slobodanka; Milić Rašić, Vedrana
![]() ![]() | Научни чланак | 21aM21a - Рад у међ. часопису изузетних вредности |