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A genome-wide survey and functional brain imaging study identify CTNNBL1 as a memory-related gene.
Papassotiropoulos A, Stefanova E, Vogler C, Gschwind L, Ackermann S, Spalek K, Rasch B, Heck A, Aerni A, Hanser E, Demougin P, Huynh KD, Luechinger R, Klarhöfer M, Novakovic I, Kostic V, Boesiger P, Scheffler K, de Quervain DJ. Papassotiropoulos A, et al. Among authors: novakovic i. Mol Psychiatry. 2013 Feb;18(2):255-63. doi: 10.1038/mp.2011.148. Epub 2011 Nov 22. Mol Psychiatry. 2013. PMID: 22105620 Free PMC article.
Epilepsy in a child with Wolf-Hirschhorn syndrome.
Mitić V, Cuturilo G, Novaković I, Dimitrijević N, Damnjanović T, Dimitrijević A, Dobricić V, Kostić V, Radlović N. Mitić V, et al. Among authors: novakovic i. Srp Arh Celok Lek. 2011 Nov-Dec;139(11-12):795-9. Srp Arh Celok Lek. 2011. PMID: 22338478 Free article.
A novel Notch3 Gly89Cys mutation in a Serbian CADASIL family.
Pavlovic AM, Dobricic V, Semnic R, Lackovic V, Novakovic I, Bajcetic M, Sternic N. Pavlovic AM, et al. Among authors: novakovic i. Acta Neurol Belg. 2013 Sep;113(3):299-302. doi: 10.1007/s13760-012-0174-2. Epub 2013 Jan 15. Acta Neurol Belg. 2013. PMID: 23319290
Transcranial sonography in patients with Parkinson's disease with glucocerebrosidase mutations.
Kresojević N, Mijajlović M, Perić S, Pavlović A, Svetel M, Janković M, Dobričić V, Novaković I, Lakočević MB, Klein C, Kostić VS. Kresojević N, et al. Among authors: novakovic i. Parkinsonism Relat Disord. 2013 Apr;19(4):431-5. doi: 10.1016/j.parkreldis.2012.12.006. Epub 2013 Jan 16. Parkinsonism Relat Disord. 2013. PMID: 23332636
166 results