Does the CCR5-Δ32 mutation explain the variable coronavirus-2019 pandemic statistics in Europe?

por Starčević Čizmarević, Nada, Tota, Marin, Ristić, Smiljana
Publicado 2020

In reply:

por Starčević Čizmarević, Nada, Tota, Marin, Ristić, Smiljana
Publicado 2021

Could angiotensin-converting enzyme 1 I/D polymorphism be a modificator of COVID-19 response in different populations, diseases, and/or conditions?

por Dević Pavlić, Sanja, Nadalin, Sergej, Starčević Čizmarević, Nada, Buretić-Tomljanović, Alena, Radojčić Badovinac, Anđelka, Ristić, Smiljana
Publicado 2020

The Role of Iron and Iron Overload in Chronic Liver Disease

por Milic, Sandra, Mikolasevic, Ivana, Orlic, Lidija, Devcic, Edita, Starcevic-Cizmarevic, Nada, Stimac, Davor, Kapovic, Miljenko, Ristic, Smiljana
Publicado 2016

Low frequency of HFE gene mutations in Croatian patients suspected of having hereditary hemochromatosis

por Milić, Sandra, Ristić, Smiljana, Starčević-Čizmarević, Nada, Brajenović-Milić, Bojana, Crnić-Martinović, Marija, Kapović, Miljenko, Peterlin, Borut, Štimac, Davor
Publicado 2011

Functional Inference of Methylenetetrahydrofolate Reductase Gene Polymorphisms on Enzyme Stability as a Potential Risk Factor for Down Syndrome in Croatia

por Vraneković, Jadranka, Babić Božović, Ivana, Starčević Čizmarević, Nada, Buretić-Tomljanović, Alena, Ristić, Smiljana, Petrović, Oleg, Kapović, Miljenko, Brajenović-Milić, Bojana
Publicado 2010

The lack of association between angiotensin‐converting enzyme gene insertion/deletion polymorphism and nicotine dependence in multiple sclerosis

por Nadalin, Sergej, Buretić‐Tomljanović, Alena, Lavtar, Polona, Starčević Čizmarević, Nada, Hodžić, Alenka, Sepčić, Juraj, Kapović, Miljenko, Peterlin, Borut, Ristić, Smiljana
Publicado 2016

The effects of microbiota abundance on symptom severity in Parkinson’s disease: A systematic review

por Papić, Eliša, Rački, Valentino, Hero, Mario, Tomić, Zoran, Starčević-Čižmarević, Nada, Kovanda, Anja, Kapović, Miljenko, Hauser, Goran, Peterlin, Borut, Vuletić, Vladimira
Publicado 2022

Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis

por Lavtar, Polona, Rudolf, Gorazd, Maver, Aleš, Hodžić, Alenka, Starčević Čizmarević, Nada, Živković, Maja, Šega Jazbec, Saša, Klemenc Ketiš, Zalika, Kapović, Miljenko, Dinčić, Evica, Raičević, Ranko, Sepčić, Juraj, Lovrečić, Luca, Stanković, Aleksandra, Ristić, Smiljana, Peterlin, Borut
Publicado 2018

The Role of TPA I/D and PAI-1 4G/5G Polymorphisms in Multiple Sclerosis

por Živković, Maja, Starčević Čizmarević, Nada, Lovrečić, Luca, Klupka-Sarić, Inge, Stanković, Aleksandra, Gašparović, Iva, Lavtar, Polona, Dinčić, Evica, Stojković, Ljiljana, Rudolf, Gorazd, Šega Jazbec, Saša, Perković, Olivio, Sinanović, Osman, Sepčić, Juraj, Kapović, Miljenko, Peterlin, Borut, Ristić, Smiljana
Publicado 2014

Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis

por Maver, Ales, Lavtar, Polona, Ristić, Smiljana, Stopinšek, Sanja, Simčič, Saša, Hočevar, Keli, Sepčić, Juraj, Drulović, Jelena, Pekmezović, Tatjana, Novaković, Ivana, Alenka, Hodžić, Rudolf, Gorazd, Šega, Saša, Starčević-Čizmarević, Nada, Palandačić, Anja, Zamolo, Gordana, Kapović, Miljenko, Likar, Tina, Peterlin, Borut
Publicado 2017