Items where Author is "Šupe, Svjetlana"

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Number of items: 6.

Article

Šupe, Svjetlana and Poljaković, Zdravka and Božina, Tamara and Ljevak, Josip and Macolić Šarinić, Viola and Božina, Nada (2015) Clinical application of genotype-guided dosing of warfarin in patients with acute stroke. Archives of Medical Research, 46 (4). pp. 265-273. ISSN 0188-4409

Šupe, Svjetlana and Božina, Nada and Matijević, Vesna and Bazina, Antonela and Mišmaš, Antonija and Ljevak, Josip and Alvir, Domagoj and Habek, Mario and Poljaković, Zdravka (2014) Prevalence of genetic polymorphisms of CYP2C9 and VKORC1 - implications for warfarin management and outcome in Croatian patients with acute stroke. Journal of the Neurological Sciences, 343 (1-2). pp. 30-35. ISSN 0022-510X

Matijević, Vesna and Alvir, Domagoj and Malojčić, Branko and Unušić, Lea and Šupe, Svjetlana and Boban, Marina and Bujan-Kovač, Andrea and Habek, Mario and Poljaković, Zdravka (2010) Systemic thrombolysis with recombinant tissue plasminogen activator in acute ischemic stroke: first Croatian experiences. Neurological Sciences, 31 (6). pp. 693-697. ISSN 1590-1874

Habek, Mario and Šupe, Svjetlana and Poljaković, Zdravka and Gelpi, Ellen and Alesch, François and Ozretić, David and Brinar, Vesna V. (2008) Subacute brainstem angioencephalopathy: favorable outcome with anticoagulation therapy. Journal of the Neurological Sciences, 275 (1-2). pp. 167-169. ISSN 0022-510X (In Press)

Petravić, Damir and Habek, Mario and Šupe, Svjetlana and Brinar, Vesna V. (2006) Recurrent optic neuromyelitis with endocrinopathies: a new syndrome or just a coincidence? Multiple Sclerosis, 12 (5). pp. 670-673. ISSN 1352-4585

Thesis

Šupe, Svjetlana (2011) Uloga genskog polimorfizma CYP2C9 i VKORC1 u individualizaciji terapije varfarinom kod pacijenata sa akutnim moždanim udarom [The role of genetic polymorphism of CYP2C9 and VKORC1 in the individualization of warfarin therapy in patients with acute stroke]. PhD thesis, Sveučilište u Zagrebu.

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