Search Results - "Starcevic-Cizmarevic, Nada" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

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

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

by 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
Published in PloS one (11.01.2018)

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ACE I/D polymorphism and epidemiological findings for COVID-19: One year after the pandemic outbreak in Europe

ACE I/D polymorphism and epidemiological findings for COVID-19: One year after the pandemic outbreak in Europe

by Ristić, Smiljana, Pavlić, Sanja Dević, Nadalin, Sergej, Čizmarević, Nada Starčević
Published in The Journal of infection (01.09.2021)

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CCR5 Δ32 and CTLA-4 +49 A/G Gene Polymorphisms and Interferon-β Treatment Response in Croatian and Slovenian Multiple Sclerosis Patients

CCR5 Δ32 and CTLA-4 +49 A/G Gene Polymorphisms and Interferon-β Treatment Response in Croatian and Slovenian Multiple Sclerosis Patients

by Nekić, Jasna, Stanković Matić, Ivana, Rački, Valentino, Janko Labinac, Dolores, Vuletić, Vladimira, Kapović, Miljenko, Ristić, Smiljana, Peterlin, Borut, Starčević Čizmarević, Nada
Published in International journal of molecular sciences (05.07.2024)

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Applicability of clinical genetic testing for deep brain stimulation treatment in monogenic Parkinson’s disease and monogenic dystonia: a multidisciplinary team perspective

Applicability of clinical genetic testing for deep brain stimulation treatment in monogenic Parkinson’s disease and monogenic dystonia: a multidisciplinary team perspective

by Rački, Valentino, Hero, Mario, Papić, Eliša, Rožmarić, Gloria, Čizmarević, Nada Starčević, Chudy, Darko, Peterlin, Borut, Vuletić, Vladimira
Published in Frontiers in neuroscience (10.11.2023)

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Potential protective role of a NOD2 polymorphism in the susceptibility to multiple sclerosis is not associated with interferon therapy

Potential protective role of a NOD2 polymorphism in the susceptibility to multiple sclerosis is not associated with interferon therapy

by Zeckanovic, Aida, Maver, Ales, Ristic, Smiljana, Cizmarevic, Nada Starcevic, Peterlin, Borut, Lovrecic, Luca
Published in Biomedical reports (01.12.2021)

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The Influence of Hemochromatosis Gene (HFE) Mutations on SARS-CoV-2 Susceptibility and COVID-19 Severity

The Influence of Hemochromatosis Gene (HFE) Mutations on SARS-CoV-2 Susceptibility and COVID-19 Severity

by Ristić, Smiljana, Milić, Sandra, Tatalović, Tanja, Bilobrk, Matea, Rončević, Dobrica, Ćurko-Cofek, Božena, Barac-Latas, Vesna, Čizmarević, Nada Starčević
Published in Balkan medical journal (08.05.2023)

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Lack of association between C282Y and H63D polymorphisms in the hemochromatosis gene and risk of multiple sclerosis: A meta-analysis

Lack of association between C282Y and H63D polymorphisms in the hemochromatosis gene and risk of multiple sclerosis: A meta-analysis

by Starčević Čizmarević, Nada, Ćurko-Cofek, Božena, Barac-Latas, Vesna, Peterlin, Borut, Ristić, Smiljana
Published in Biomedical reports (01.02.2022)

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MTHFR C677T and A1298C polymorphisms as a risk factor for congenital heart defects in Down syndrome

MTHFR C677T and A1298C polymorphisms as a risk factor for congenital heart defects in Down syndrome

by Babic Bozovic, Ivana, Vranekovic, Jadranka, StarcevicCizmarevic, Nada, Mahulja-Stamenkovic, Vesna, Prpic, Igor, Brajenovic-Milic, Bojana
Published in Pediatrics international (01.08.2011)

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The Role of Iron and Iron Overload in Chronic Liver Disease

The Role of Iron and Iron Overload in Chronic Liver Disease

by Milic, Sandra, Mikolasevic, Ivana, Orlic, Lidija, Devcic, Edita, Starcevic-Cizmarevic, Nada, Stimac, Davor, Kapovic, Miljenko, Ristic, Smiljana
Published in Medical science monitor (22.06.2016)

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

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

by Nadalin, Sergej, Buretić‐Tomljanović, Alena, Lavtar, Polona, Starčević Čizmarević, Nada, Hodžić, Alenka, Sepčić, Juraj, Kapović, Miljenko, Peterlin, Borut, Ristić, Smiljana
Published in Brain and behavior (01.01.2017)

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A rare Y-autosome translocation found in a patient with nonobstructive azoospermia: Case report

A rare Y-autosome translocation found in a patient with nonobstructive azoospermia: Case report

by Barišić, Anita, Buretić Tomljanović, Alena, Starčević Čizmarević, Nada, Ostojić, Saša, Romac, Pavle, Vraneković, Jadranka
Published in Systems biology in reproductive medicine (04.07.2021)

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Angiotensin-converting enzyme gene polymorphism in patients with multiple sclerosis from Bosnia and Herzegovina

Angiotensin-converting enzyme gene polymorphism in patients with multiple sclerosis from Bosnia and Herzegovina

by Klupka-Sarić, Inge, Peterlin, Borut, Lovrečić, Luca, Sinanović, Osman, Vidović, Mirjana, Sehanović, Aida, Cizmarević, Nada Starčević, Sepčić, Juraj, Kapović, Miljenko, Ristić, Smiljana
Published in Genetic testing and molecular biomarkers (01.11.2011)

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Chronic iron overload induces gender-dependent changes in iron homeostasis, lipid peroxidation and clinical course of experimental autoimmune encephalomyelitis

Chronic iron overload induces gender-dependent changes in iron homeostasis, lipid peroxidation and clinical course of experimental autoimmune encephalomyelitis

by Ćurko-Cofek, Božena, Kezele, Tanja Grubić, Marinić, Jelena, Tota, Marin, Čizmarević, Nada Starčević, Milin, Čedomila, Ristić, Smiljana, Radošević-Stašić, Biserka, Barac-Latas, Vesna
Published in Neurotoxicology (Park Forest South) (01.12.2016)

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Angiotensin-converting enzyme insertion/deletion gene polymorphism in multiple sclerosis: a meta-analysis

Angiotensin-converting enzyme insertion/deletion gene polymorphism in multiple sclerosis: a meta-analysis

by Ristić, Smiljana, Čizmarević, Nada Starčević, Sepčić, Juraj, Kapović, Miljenko, Peterlin, Borut
Published in Neurological sciences (01.12.2016)

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MMP-2 −1575G/A polymorphism modifies the onset of optic neuritis as a first presenting symptom in MS?

MMP-2 −1575G/A polymorphism modifies the onset of optic neuritis as a first presenting symptom in MS?

by Gašparović, Iva, Čizmarević, Nada Starčević, Lovrečić, Luca, Perković, Olivio, Lavtar, Polona, Sepčić, Juraj, Jazbec, Saša Šega, Kapović, Miljenko, Peterlin, Borut, Ristić, Smiljana
Published in Journal of neuroimmunology (15.09.2015)

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MMP-2 − 1575 G/A polymorphism modifies the onset of optic neuritis as a first presenting symptom in MS?

MMP-2 − 1575 G/A polymorphism modifies the onset of optic neuritis as a first presenting symptom in MS?

by Gašparović, Iva, Čizmarević, Nada Starčević, Lovrečić, Luca, Perković, Olivio, Lavtar, Polona, Sepčić, Juraj, Jazbec, Saša Šega, Kapović, Miljenko, Peterlin, Borut, Ristić, Smiljana
Published in Journal of neuroimmunology (15.09.2015)

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CTLA-4 +49 and TNF-alpha-308 gene polymorphisms in celiac patients with exocrine pancreatic insufficiency

CTLA-4 +49 and TNF-alpha-308 gene polymorphisms in celiac patients with exocrine pancreatic insufficiency

by Licul, Vanja, Cizmarević, Nada Starcević, Ristić, Smiljana, Mikolasević, Ivana, Mijandrusić, Brankica Sincić
Published in Collegium antropologicum (01.12.2013)

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

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

by Klupka-Sarić, Inge, Lovrečić, Luca, Starčević Čizmarević, Nada, Živković, Maja, 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
Published in Disease markers (01.01.2014)

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

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

by 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
Published in Scientific reports (16.06.2017)

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Does the CCR5-[DELTA]32 mutation explain the variable coronavirus-2019 pandemic statistics in Europe?

Does the CCR5-[DELTA]32 mutation explain the variable coronavirus-2019 pandemic statistics in Europe?

by Cizmarevic, Nada Starcevic, Tota, Marin, Ristic, Smiljana
Published in Croatian medical journal (01.12.2020)

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