Naziv |
Akcije |
Šušnjar, Iva
Huntingtonova bolest / Perković, Olivio ; Sorta-Bilajac Turina, Iva (mentor);
Rijeka, Fakultet zdravstvenih studija, . 2019 |
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Ristić, Smiljana ; Starčević Čizmarević, Nada ; Lavtar, Polona ; Lovrečić, Luca ; Perković, Olivio ; Sepčić, Juraj ; Šega Jazbec, Saša ; Kapović, Miljenko ; Peterlin, Borut.
Angiotensin-converting enzyme insertion/deletion gene polymorphism and interferon-β treatment response in multiple sclerosis patients: a preliminary report. // Pharmacogenetics and genomics, 27 (2017), 6; 232-235 |
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Bucuk, Mira ; Gašparović, Iva ; Sonnenschein, Ivan ; Perković, Olivio
A patient with myasthenia gravis and a large arachnoid cyst – report of a case // Wiener klinische Wochenschrift, 129 (2017), 9-10; 366-368. doi: 10.1007/s00508-017-1177-z |
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Ristić, Smiljana ; Starčević Čizmarević, Nada ; Lavtar, Polona ; Lovrečić, Luca ; Perković, Olivio ; Sepčić, Juraj ; Šega Jazbec, Saša ; Kapović, Miljenko ; Peterlin, Borut.
Angiotensin-converting enzyme (ACE) I/D gene polymorphism and IFN-β treatment response in multiple sclerosis patients. // 10th ISABS Conference on Forensic and Anthropologic Genetics. 2017. str. 295-295 |
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Gašparović, Iva
Polimorfizmi gena sustava matriks metaloproteinaza i fibrinolize u multiploj sklerozi. / Ristić, Smiljana ; Perković, Olivio (mentor);
Rijeka, Medicinski fakultet u Rijeci, . 2015 |
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Gašparović, Iva ; Starčević-Čizmarević, Nada ; Perković, Olivio ; Lovrečić, Luca ; Miljenko, Kapović ; Peterlin, Borut ; Ristić, Smiljana
Polimorfizmi gena matriksmetaloproteinaze-2 i matriksmetaloproteinaze-9 u multiploj sklerozi // Knjiga sažetaka VI hrvatskog kongresa humane genetike s međunarodnim sudjelovanjem. 2015. str. 86-86 |
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Gasparović, Iva ; Starčević Čizmarević, Nada ; Lovrečić, Luca ; Perković, Olivio ; Lavtar, Polona ; Sepčić, Juraj ; Šega Jazbec, Saša ; Kapović, Miljenko ; Peterlin, Borut ; Ristić, Smiljana
MMP-2-1575 G/A polymorphism modifiesthe 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 |
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Živković, Maja ; Starčević Čizmarević, Nada ; Lovrečić, Luca ; Klupka-Sarić, Inge ; Stanković, Aleksandra ; Gašparović, Iva ; Lavtar, Polona ; Dinčić, Evica ; Stojković, Ljiljana ; Rudolf, Gorazd et al.
The Role of TPA I/D and PAI-1 4G/5G Polymorphisms in Multiple Sclerosis // Disease markers, / (2014), 362780-1-362780-8. doi: 10.1155/2014/362708 |
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Sonnenschein, Ivan ; Tomić, Zoran ; Perković, Olivio ; Zadković, Barbara ; Bučuk, Mira
Diagnostic challenge of anti-GQ1b syndrome : differential diagnosis between Miller Fischer syndrome and Bickerstaff ’s brainstem encephalitis // Neurologia Croatica. Supplement, 63 (2014), S; 83-86 |
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Antulov, Ronald ; Holjar Erlić, Izidora ; Perković, Olivio ; Miletić, Damir ; Antončić, Igor
Susac's syndrome during pregnancy — The first Croatian case // Journal of the neurological sciences, 341 (2014), 1-2; 162-164. doi: 10.1016/j.jns.2014.04.010 |
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