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Items: 1 to 50 of 63

1.

Investigation of metabolic properties and effects of 17β-carboxamide glucocorticoids on human peripheral blood leukocytes.

Dobričić V, Drvenica I, Stančić A, Mihailović M, Čudina O, Bugarski D, Ilić V.

Arch Pharm (Weinheim). 2018 Apr 16:e1700371. doi: 10.1002/ardp.201700371. [Epub ahead of print]

PMID:
29660818
2.

WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype.

Kulikovskaja L, Sarajlija A, Savic-Pavicevic D, Dobricic V, Klein C, Westenberger A.

Neurol Genet. 2018 Mar 27;4(2):e227. doi: 10.1212/NXG.0000000000000227. eCollection 2018 Apr. No abstract available.

3.

Design and Synthesis of Novel Deuterated Ligands Functionally Selective for the γ-Aminobutyric Acid Type A Receptor (GABAAR) α6 Subtype with Improved Metabolic Stability and Enhanced Bioavailability.

Knutson DE, Kodali R, Divović B, Treven M, Stephen MR, Zahn NM, Dobričić V, Huber AT, Meirelles MA, Verma RS, Wimmer L, Witzigmann C, Arnold LA, Chiou LC, Ernst M, Mihovilovic MD, Savić MM, Sieghart W, Cook JM.

J Med Chem. 2018 Mar 22;61(6):2422-2446. doi: 10.1021/acs.jmedchem.7b01664. Epub 2018 Mar 6.

PMID:
29481759
4.

Alkyl polyglucoside vs. ethoxylated surfactant-based microemulsions as vehicles for two poorly water-soluble drugs: physicochemical characterization and in vivo skin performance.

Pajić NZB, Todosijević MN, Vuleta GM, Cekić ND, Dobričić VD, Vučen SR, Čalija BR, Lukić MŽ, Ilić TM, Savić SD.

Acta Pharm. 2017 Dec 20;67(4):415-439. doi: 10.1515/acph-2017-0036.

PMID:
29337676
5.

Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients.

Mitropoulos K, Merkouri Papadima E, Xiromerisiou G, Balasopoulou A, Charalampidou K, Galani V, Zafeiri KV, Dardiotis E, Ralli S, Deretzi G, John A, Kydonopoulou K, Papadopoulou E, di Pardo A, Akcimen F, Loizedda A, Dobričić V, Novaković I, Kostić VS, Mizzi C, Peters BA, Basak N, Orrù S, Kiskinis E, Cooper DN, Gerou S, Drmanac R, Bartsakoulia M, Tsermpini EE, Hadjigeorgiou GM, Ali BR, Katsila T, Patrinos GP.

Hum Genomics. 2017 Dec 8;11(1):30. doi: 10.1186/s40246-017-0126-2.

6.

GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia.

Dobričić V, Tomić A, Branković V, Kresojević N, Janković M, Westenberger A, Rašić VM, Klein C, Novaković I, Svetel M, Kostić VS.

Parkinsonism Relat Disord. 2017 Dec;45:81-84. doi: 10.1016/j.parkreldis.2017.09.017. Epub 2017 Sep 18.

PMID:
28958832
7.

Evaluation of Biological Activity and Computer-Aided Design of New Soft Glucocorticoids.

Dobričić V, Jaćević V, Vučićević J, Nikolic K, Vladimirov S, Čudina O.

Arch Pharm (Weinheim). 2017 May;350(5). doi: 10.1002/ardp.201600383. Epub 2017 Apr 18.

PMID:
28418199
8.

Application of biopartitioning micellar chromatography and QSRR modeling for prediction of gastrointestinal absorption and design of novel β-hydroxy-β-arylalkanoic acids.

Dobričić V, Savić J, Nikolic K, Vladimirov S, Vujić Z, Brborić J.

Eur J Pharm Sci. 2017 Mar 30;100:280-284. doi: 10.1016/j.ejps.2017.01.023. Epub 2017 Jan 23.

PMID:
28126559
9.

Novel GNB1 mutations disrupt assembly and function of G protein heterotrimers and cause global developmental delay in humans.

Lohmann K, Masuho I, Patil DN, Baumann H, Hebert E, Steinrücke S, Trujillano D, Skamangas NK, Dobricic V, Hüning I, Gillessen-Kaesbach G, Westenberger A, Savic-Pavicevic D, Münchau A, Oprea G, Klein C, Rolfs A, Martemyanov KA.

Hum Mol Genet. 2017 Mar 15;26(6):1078-1086. doi: 10.1093/hmg/ddx018.

PMID:
28087732
10.

In vitro prediction of gastrointestinal absorption of novel β-hydroxy-β-arylalkanoic acids using PAMPA technique.

Savić J, Dobričić V, Nikolic K, Vladimirov S, Dilber S, Brborić J.

Eur J Pharm Sci. 2017 Mar 30;100:36-41. doi: 10.1016/j.ejps.2017.01.005. Epub 2017 Jan 7.

PMID:
28077276
11.

A pilot study on predictors of brainstem raphe abnormality in patients with major depressive disorder.

Kostić M, Munjiza A, Pesic D, Peljto A, Novakovic I, Dobricic V, Tosevski DL, Mijajlovic M.

J Affect Disord. 2017 Feb;209:66-70. doi: 10.1016/j.jad.2016.11.034. Epub 2016 Nov 22.

PMID:
27888722
12.

Seemingly dominant inheritance of a recessive ANO10 mutation in romani families with cerebellar ataxia.

Mišković ND, Domingo A, Dobričić V, Max C, Braenne I, Petrović I, Grütz K, Pawlack H, Tournev I, Kalaydjieva L, Svetel M, Lohmann K, Kostić VS, Westenberger A.

Mov Disord. 2016 Dec;31(12):1929-1931. doi: 10.1002/mds.26816. Epub 2016 Oct 27. No abstract available.

PMID:
27787937
13.

Transcranial sonography in dopa-responsive dystonia.

Svetel M, Tomić A, Mijajlović M, Dobričić V, Novaković I, Pekmezović T, Brajković L, Kostić VS.

Eur J Neurol. 2017 Jan;24(1):161-166. doi: 10.1111/ene.13172. Epub 2016 Oct 12.

PMID:
27731537
14.

Five-year study of quality of life in myotonic dystrophy.

Peric S, Vujnic M, Dobricic V, Marjanovic A, Basta I, Novakovic I, Lavrnic D, Rakocevic-Stojanovic V.

Acta Neurol Scand. 2016 Nov;134(5):346-351. doi: 10.1111/ane.12549. Epub 2015 Dec 21.

PMID:
27696366
15.

Excellent outcome of pallidal deep brain stimulation in DYT6 dystonia: A case report.

Vuletic V, Chudy D, Almahariq F, Dobricic V, Kostic V, Bogdanovic N.

J Neurol Sci. 2016 Jul 15;366:18-19. doi: 10.1016/j.jns.2016.04.032. Epub 2016 Apr 19. No abstract available.

PMID:
27288769
16.

Multidimensional aspects of pain in myotonic dystrophies.

Peric M, Peric S, Rapajic N, Dobricic V, Savic-Pavicevic D, Nesic I, Radojicic S, Novakovic I, Lavrnic D, Rakocevic-Stojanovic V.

Acta Myol. 2015 Dec;34(2-3):126-32.

17.

HPCA-related dystonia: Too rare to be found?

Dobričić V, Kresojević N, Marjanović A, Tomić A, Svetel M, Novaković I, Kostić VS.

Mov Disord. 2016 Jul;31(7):1071. doi: 10.1002/mds.26634. Epub 2016 May 4. No abstract available.

PMID:
27145302
18.

Comparison of temporal and stride characteristics in myotonic dystrophies type 1 and 2 during dual-task walking.

Radovanović S, Perić S, Savić-Pavićević D, Dobričić V, Pešović J, Kostić V, Rakočević-Stojanović V.

Gait Posture. 2016 Feb;44:194-9. doi: 10.1016/j.gaitpost.2015.12.020. Epub 2015 Dec 20.

PMID:
27004657
19.

The cumulative effect of genetic polymorphisms on depression and brain structural integrity.

Kostic M, Canu E, Agosta F, Munjiza A, Novakovic I, Dobricic V, Maria Ferraro P, Miler Jerkovic V, Pekmezovic T, Lecic Tosevski D, Filippi M.

Hum Brain Mapp. 2016 Jun;37(6):2173-84. doi: 10.1002/hbm.23165. Epub 2016 Mar 9.

PMID:
26956059
20.

Subtelomeric screening in Serbian children with dysmorphic features and unexplained developmental delay/intellectual disabilities.

Damnjanovic T, Cuturilo G, Maksimovic N, Dimitrijevic N, Mitic V, Jekic B, Lukovic L, Bunjevacki V, Varljen T, Dobricic V, Jovanovic I, Kostic V, Novakovic I.

Turk J Pediatr. 2015 Mar-Apr;57(2):154-60.

PMID:
26690596
21.

Evaluation of critical formulation parameters in design and differentiation of self-microemulsifying drug delivery systems (SMEDDSs) for oral delivery of aciclovir.

Janković J, Djekic L, Dobričić V, Primorac M.

Int J Pharm. 2016 Jan 30;497(1-2):301-11. doi: 10.1016/j.ijpharm.2015.11.011. Epub 2015 Dec 1.

PMID:
26611669
22.

Modified local diatomite as potential functional drug carrier--A model study for diclofenac sodium.

Janićijević J, Krajišnik D, Čalija B, Vasiljević BN, Dobričić V, Daković A, Antonijević MD, Milić J.

Int J Pharm. 2015 Dec 30;496(2):466-74. doi: 10.1016/j.ijpharm.2015.10.047. Epub 2015 Oct 21.

PMID:
26498370
23.

Screening for C9orf72 Expansion Mutation in Serbian Patients with Early-Onset Dementia.

Mandic-Stojmenovic G, Stefanova E, Dobricic V, Novakovic I, Stojkovic T, Jesic A, Kostic V.

Dement Geriatr Cogn Disord. 2015;40(5-6):358-65. doi: 10.1159/000438748. Epub 2015 Sep 25.

PMID:
26401819
24.

Phenotype of non-c.907_909delGAG mutations in TOR1A: DYT1 dystonia revisited.

Dobričić V, Kresojević N, Žarković M, Tomić A, Marjanović A, Westenberger A, Cvetković D, Svetel M, Novaković I, Kostić VS.

Parkinsonism Relat Disord. 2015 Oct;21(10):1256-9. doi: 10.1016/j.parkreldis.2015.08.001. Epub 2015 Aug 10.

PMID:
26297380
25.

Influence of Solid Drug Delivery System Formulation on Poorly Water-Soluble Drug Dissolution and Permeability.

Krstić M, Popović M, Dobričić V, Ibrić S.

Molecules. 2015 Aug 13;20(8):14684-98. doi: 10.3390/molecules200814684.

26.

Are Leber's mitochondial DNA mutations associated with aquaporin-4 autoimmunity?

Dujmovic I, Jancic J, Dobricic V, Jankovic M, Novakovic I, Comabella M, Drulovic J.

Mult Scler. 2016 Mar;22(3):393-4. doi: 10.1177/1352458515590649. Epub 2015 Jul 24. No abstract available.

PMID:
26209590
27.

Variability of multisystemic features in myotonic dystrophy type 1--lessons from Serbian registry.

Rakocevic-Stojanovic V, Peric S, Basta I, Dobricic V, Ralic V, Kacar A, Peric M, Novakovic I.

Neurol Res. 2015 Nov;37(11):939-44. doi: 10.1179/1743132815Y.0000000068. Epub 2015 Jul 17.

PMID:
26184384
28.

Presenting symptoms of GBA-related Parkinson's disease.

Kresojević N, Janković M, Petrović I, Kumar KR, Dragašević N, Dobričić V, Novaković I, Svetel M, Klein C, Pekmezović T, Kostić VS.

Parkinsonism Relat Disord. 2015 Jul;21(7):804-7. doi: 10.1016/j.parkreldis.2015.04.028. Epub 2015 May 1.

PMID:
25957717
29.

Identification of novel variants in LRRK2 gene in patients with Parkinson's disease in Serbian population.

Janković MZ, Kresojević ND, Dobričić VS, Marković VV, Petrović IN, Novaković IV, Kostić VS.

J Neurol Sci. 2015;353(1-2):59-62. doi: 10.1016/j.jns.2015.04.002. Epub 2015 Apr 12.

PMID:
25899316
30.

Pattern of disease progression in atypical form of pantothenate-kinase-associated neurodegeneration (PKAN) - Prospective study.

Tomić A, Petrović I, Svetel M, Dobričić V, Dragašević Mišković N, Kostić VS.

Parkinsonism Relat Disord. 2015 May;21(5):521-4. doi: 10.1016/j.parkreldis.2015.02.006. Epub 2015 Feb 17.

PMID:
25724846
31.

Prediction of blood-brain barrier permeation of α-adrenergic and imidazoline receptor ligands using PAMPA technique and quantitative-structure permeability relationship analysis.

Vucicevic J, Nikolic K, Dobričić V, Agbaba D.

Eur J Pharm Sci. 2015 Feb 20;68:94-105. doi: 10.1016/j.ejps.2014.12.014. Epub 2014 Dec 24.

PMID:
25542610
32.

Metabolic syndrome in patients with myotonic dystrophy type 1.

Vujnic M, Peric S, Popovic S, Raseta N, Ralic V, Dobricic V, Novakovic I, Rakocevic-Stojanovic V.

Muscle Nerve. 2015 Aug;52(2):273-7. doi: 10.1002/mus.24540. Epub 2015 Jun 19.

PMID:
25487787
33.

Novel GNAL mutations in two German patients with sporadic dystonia.

Ziegan J, Wittstock M, Westenberger A, Dobričić V, Wolters A, Benecke R, Klein C, Kamm C.

Mov Disord. 2014 Dec;29(14):1833-4. doi: 10.1002/mds.26066. Epub 2014 Nov 7. No abstract available.

PMID:
25382112
34.

Frontostriatal dysexecutive syndrome: a core cognitive feature of myotonic dystrophy type 2.

Peric S, Mandic-Stojmenovic G, Stefanova E, Savic-Pavicevic D, Pesovic J, Ilic V, Dobricic V, Basta I, Lavrnic D, Rakocevic-Stojanovic V.

J Neurol. 2015 Jan;262(1):142-8. doi: 10.1007/s00415-014-7545-y. Epub 2014 Oct 28.

PMID:
25346064
35.

Mutations in Niemann Pick type C gene are risk factor for Alzheimer's disease.

Kresojević N, Dobričić V, Svetel M, Kostić V.

Med Hypotheses. 2014 Nov;83(5):559-62. doi: 10.1016/j.mehy.2014.08.025. Epub 2014 Sep 6.

PMID:
25220527
36.

Significant impact of behavioral and cognitive impairment on quality of life in patients with myotonic dystrophy type 1.

Rakocevic-Stojanovic V, Peric S, Madzarevic R, Dobricic V, Ralic V, Ilic V, Basta I, Nikolic A, Stefanova E.

Clin Neurol Neurosurg. 2014 Nov;126:76-81. doi: 10.1016/j.clineuro.2014.08.021. Epub 2014 Aug 30.

PMID:
25215445
37.

Design, synthesis, and local anti-inflammatory activity of 17β-carboxamide derivatives of glucocorticoids.

Dobričić V, Marković B, Milenković N, Savić V, Jaćević V, Rančić N, Vladimirov S, Cudina O.

Arch Pharm (Weinheim). 2014 Nov;347(11):786-97. doi: 10.1002/ardp.201400165. Epub 2014 Aug 27.

PMID:
25159891
38.

Shorter CTG repeats length in an oligodendroglioma from a myotonic dystrophy type 1 patient.

Rakocevic-Stojanovic V, Peric S, Ralic V, Milicevic M, Dobricic V.

Acta Neurol Belg. 2015 Sep;115(3):505-7. doi: 10.1007/s13760-014-0336-5. Epub 2014 Aug 6. No abstract available.

PMID:
25096749
39.

Inorganically modified diatomite as a potential prolonged-release drug carrier.

Janićijević J, Krajišnik D, Calija B, Dobričić V, Daković A, Krstić J, Marković M, Milić J.

Mater Sci Eng C Mater Biol Appl. 2014 Sep;42:412-20. doi: 10.1016/j.msec.2014.05.052. Epub 2014 Jun 2.

PMID:
25063135
40.

C9orf72 expansion as a possible genetic cause of Huntington disease phenocopy syndrome.

Kostić VS, Dobričić V, Stanković I, Ralić V, Stefanova E.

J Neurol. 2014 Oct;261(10):1917-21. doi: 10.1007/s00415-014-7430-8. Epub 2014 Jul 18.

PMID:
25034271
41.

De novo mutation in the GNAL gene causing seemingly sporadic dystonia in a Serbian patient.

Dobričić V, Kresojević N, Westenberger A, Svetel M, Tomić A, Ralić V, Petrović I, Lukić MJ, Lohmann K, Novaković I, Klein C, Kostić VS.

Mov Disord. 2014 Aug;29(9):1190-3. doi: 10.1002/mds.25876. Epub 2014 Apr 13.

PMID:
24729450
42.

Biopartitioning micellar chromatography as a predictive tool for skin and corneal permeability of newly synthesized 17β-carboxamide steroids.

Dobričić V, Nikolic K, Vladimirov S, Čudina O.

Eur J Pharm Sci. 2014 Jun 2;56:105-12. doi: 10.1016/j.ejps.2014.02.007. Epub 2014 Mar 4.

PMID:
24607748
43.

Transcranial sonography in patients with myotonic dystrophy type 1.

Peric S, Pavlovic A, Ralic V, Dobricic V, Basta I, Lavrnic D, Rakocevic Stojanovic V.

Muscle Nerve. 2014 Aug;50(2):278-82. doi: 10.1002/mus.24162. Epub 2014 May 15.

PMID:
24395217
44.

17β-carboxamide steroids--in vitro prediction of human skin permeability and retention using PAMPA technique.

Dobričić V, Marković B, Nikolic K, Savić V, Vladimirov S, Čudina O.

Eur J Pharm Sci. 2014 Feb 14;52:95-108. doi: 10.1016/j.ejps.2013.10.017. Epub 2013 Nov 12.

PMID:
24239478
45.

No association between brain-derived neurotrophic factor G196A polymorphism and clinical features of Parkinson's disease.

Svetel M, Pekmezovic T, Markovic V, Novaković I, Dobričić V, Djuric G, Stefanova E, Kostić V.

Eur Neurol. 2013;70(5-6):257-62. doi: 10.1159/000352033. Epub 2013 Sep 17.

PMID:
24051673
46.

Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice.

Keller A, Westenberger A, Sobrido MJ, García-Murias M, Domingo A, Sears RL, Lemos RR, Ordoñez-Ugalde A, Nicolas G, da Cunha JE, Rushing EJ, Hugelshofer M, Wurnig MC, Kaech A, Reimann R, Lohmann K, Dobričić V, Carracedo A, Petrović I, Miyasaki JM, Abakumova I, Mäe MA, Raschperger E, Zatz M, Zschiedrich K, Klepper J, Spiteri E, Prieto JM, Navas I, Preuss M, Dering C, Janković M, Paucar M, Svenningsson P, Saliminejad K, Khorshid HR, Novaković I, Aguzzi A, Boss A, Le Ber I, Defer G, Hannequin D, Kostić VS, Campion D, Geschwind DH, Coppola G, Betsholtz C, Klein C, Oliveira JR.

Nat Genet. 2013 Sep;45(9):1077-82. doi: 10.1038/ng.2723. Epub 2013 Aug 4.

PMID:
23913003
47.

Mutational analysis of ATP7B gene and the genotype-phenotype correlation in patients with Wilson's disease in Serbia.

Tomić A, Dobricić V, Novaković I, Svetel M, Pekmezović T, Kresojević N, Potrebić A, Kostić VS.

Vojnosanit Pregl. 2013 May;70(5):457-62.

PMID:
23789284
48.

A common polymorphism in the brain-derived neurotrophic factor gene in patients with adult-onset primary focal and segmental dystonia.

Svetel MV, Djuric G, Novakovic I, Dobricic V, Stefanova E, Kresojevic N, Tomic A, Jankovic M, Petrovic I, Pekmezovic T, Kostic VS.

Acta Neurol Belg. 2013 Sep;113(3):243-5. doi: 10.1007/s13760-013-0183-9. Epub 2013 Feb 5.

PMID:
23381842
49.

Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification.

Hsu SC, Sears RL, Lemos RR, Quintáns B, Huang A, Spiteri E, Nevarez L, Mamah C, Zatz M, Pierce KD, Fullerton JM, Adair JC, Berner JE, Bower M, Brodaty H, Carmona O, Dobricić V, Fogel BL, García-Estevez D, Goldman J, Goudreau JL, Hopfer S, Janković M, Jaumà S, Jen JC, Kirdlarp S, Klepper J, Kostić V, Lang AE, Linglart A, Maisenbacher MK, Manyam BV, Mazzoni P, Miedzybrodzka Z, Mitarnun W, Mitchell PB, Mueller J, Novaković I, Paucar M, Paulson H, Simpson SA, Svenningsson P, Tuite P, Vitek J, Wetchaphanphesat S, Williams C, Yang M, Schofield PR, de Oliveira JR, Sobrido MJ, Geschwind DH, Coppola G.

Neurogenetics. 2013 Feb;14(1):11-22. doi: 10.1007/s10048-012-0349-2. Epub 2013 Jan 20.

50.

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.

Parkinsonism Relat Disord. 2013 Apr;19(4):431-5. doi: 10.1016/j.parkreldis.2012.12.006. Epub 2013 Jan 16.

PMID:
23332636

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