Pregled po CROSBI profilu: Smiljana Ristić (CROSBI Profil: 12702, MBZ: 142283)
Pronađeno 142 radova
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26.Angiotensin-converting enzyme insertion/deletion gene polymorphism in multiple sclerosis : a meta-analysis // Neurological sciences, 37 (2016), 12; 1955-1959 doi:10.1007/s10072-016-2698-3 (međunarodna recenzija, članak, znanstveni)
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27.Chronic iron overload induces gender-dependent changes in iron homeostasis, lipid peroxidation and clinical course of experimental autoimmune encephalomyelitis // Neurotoxicology, 57 (2016), 1-12 doi:10.1016/j.neuro.2016.08.014 (međunarodna recenzija, članak, znanstveni)
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28.Sequencing in patients with familial and sporadic multiple sclerosis reveals the possible etiological role of rare and highly penetrant genetic variation. // European Journal of Human Genetics
Barcelona, Španjolska, 2016. (poster, međunarodna recenzija, sažetak, znanstveni) -
29.Are rare coding mutations in the genes related to genetic peripheral neuropathies risk factors in multiple sclerosis (MS). // European Journal of Human Genetics
Barcelona, Španjolska, 2016. (poster, međunarodna recenzija, sažetak, znanstveni) -
30.Effect of genes in iron metabolism on multiple sclerosis development // European Journal of Human Genetics, Vol 24, Supplement 1
Barcelona, Španjolska: Nature publishing group, 2016. str. 200-200 (poster, međunarodna recenzija, sažetak, znanstveni) -
31.HLA-DQA1 i HLADQB1 geni u pacijenata s celijakijom // Medicina fluminensis, 52 (2016), 87-94 (podatak o recenziji nije dostupan, članak, znanstveni)
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32.Chronic iron overload induces gender-specific changes in iron homeostasis, lipid peroxidation and clinical course of experimental autoimmune encephalomyelitis // Interactive-program, The 10th International Congress on Autoimmunity, Leipzig
Leipzig, Njemačka, 2016. str. EP09 E-Posters (poster, međunarodna recenzija, sažetak, znanstveni) -
33.The Role of Iron And Iron Overload in Chronic Liver Disease // Medical science monitor, 22 (2016), 2144-2151 doi:10.12659/MSM.896494 (međunarodna recenzija, članak, znanstveni)
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34.Global DNA hypomethylation in white blood cells represents a feature of multiple sclerosis. // Book of abstracts, FEBS3+ Meeting „Molecules of Life“
Portorož, Slovenija, 2015. (poster, međunarodna recenzija, sažetak, znanstveni) -
35.Geni i celijakija // Paediatria Croatica, 59 (2015), 2; 88-94 (podatak o recenziji nije dostupan, pregledni rad, ostalo)
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36.Polimorfizmi gena sustava matriks metaloproteinaza i fibrinolize u multiploj sklerozi., 2015., doktorska disertacija, Medicinski fakultet, Rijeka
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37.Influence of CCR5Δ32 gene mutation on interferon-beta treatment response in multiple sclerosis // Book of abstracts, 11th Balkan Congress of Human Genetics
Beograd, Srbija, 2015. (poster, međunarodna recenzija, sažetak, znanstveni) -
38.Polimorfizmi gena matriksmetaloproteinaze-2 i matriksmetaloproteinaze-9 u multiploj sklerozi // Knjiga sažetaka VI hrvatskog kongresa humane genetike s međunarodnim sudjelovanjem
Split, Hrvatska, 2015. str. 86-86 (poster, domaća recenzija, sažetak, znanstveni) -
39.Utjecaj CCR5Δ32 mutacije na učinak terapije interferonom-beta u bolesnika s multiplom sklerozom, 2015., diplomski rad, preddiplomski, Fakultet zdravstvenih studija, Rijeka
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40.MMP-2-1575 G/A polymorphism modifies the onset of optic neuritis as a first presenting symptom in MS? // Journal of neuroimmunology, 286 (2015), 13-15 doi:10.1016/j.jneuroim.2015.06.014 (međunarodna recenzija, članak, znanstveni)
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41.The impact of ACE gene I/D polymorphism on plasma glucose and lipid concentrations in schizophrenia patients // Psychiatry research, 227 (2015), 1; 71-72 doi:10.1016/j.psychres.2015.03.014 (međunarodna recenzija, pismo, znanstveni)
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42.Polimorfizmi CTLA-4 i TNF-a gena u bolesnika s celijakijom // 2.Dani humane genetike - prof. dr. sc. Ljiljana Zergollern Čupak
Zagreb, Hrvatska, 2014. (predavanje, neobjavljeni rad, ostalo) -
43.CTLA-4 and TNF-a gene polymorphisms in celiac disease // Poster abstarcts Falk symposium 193
Amsterdam, 2014. str. 62-62 (poster, sažetak, ostalo) -
44.The Role of TPA I/D and PAI-1 4G/5G Polymorphisms in Multiple Sclerosis // Disease markers, / (2014), 362780-1 doi:10.1155/2014/362708 (međunarodna recenzija, članak, znanstveni)
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45.CTLA-4 +49 and TNF-alfa-308 Gene Polymorphisms in Celiac Patients with Exocrine Pancreatic Insufficiency // Collegium antropologicum, 37 (2013), 4; 1191-1194 (međunarodna recenzija, članak, znanstveni)
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46.Association of circadian rhythm genes ARNTL and CLOCK with multiple sclerosis (MS). // Book of abstracts / Lovrečić, Luca ; Maver, Aleš (ur.).
Ljubljana: Slovenian Association of Medical Genetics, 2013. str. 115-115 (poster, sažetak, ostalo) -
47.Signal transducers and activators of transcription genes (STAT genes)and Multiple sclerosis (MS). // Eur J Hum Genet
Pariz, Francuska: npg, 2013. str. 228-228 (poster, sažetak, znanstveni) -
48.Genetika neurodegenerativnih bolesti // Medicina Fluminensis, 49 (2013), 2; 144-156 (podatak o recenziji nije dostupan, pregledni rad, znanstveni)
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49.Tumor necrosis factor-alpha gene promoter -308 and -238 polymorphisms in patients with lung cancer as a second primary tumor // Book of abstracts / Lovrečić, Luca ; Maver, Aleš (ur.).
Ljubljana: Slovenian Association of Medical Genetics, 2013. str. 152-152 (poster, sažetak, znanstveni) -
50.Tumor necrosis factor-alpha gene promoter -308 and -238 polymorphisms in patients with lung cancer as a second primary tumor. // Medical science monitor, 19 (2013), 846-851 doi:10.12659/MSM.889554 (međunarodna recenzija, članak, znanstveni)
