Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Višnja Prus"'
Autor:
Dijana Perković, Marko Barešić, Melanija Ražov Radas, Irena Jureković, Srđan Novak, Branimir Anić, jerka Karadža Lapić, Višnja Prus, Asja Stipić Marković
Publikováno v:
Liječnički vjesnik, Vol 144, Iss 11-12, Pp 411-415 (2022)
Hereditary angioedema (HAE) is a rare inherited disease characterized by recurrent attacks of painful swelling of the subcutaneous and submucosal tissues. Recurrent attacks of angioedema lead to functional impairment, reduced quality of life (QoL) an
Externí odkaz:
https://doaj.org/article/b567deafea504095b69fcdc61621d58c
Autor:
Dijana Perković, Simeon Grazio, Tatjana Kehler, Jadranka Morović Verglas, Srđan Novak, Višnja Prus, Branimir Anić
Publikováno v:
Liječnički vjesnik, Vol 143, Iss 3-4, Pp 130-138 (2021)
Giant cell arteritis (GCA) is the most common vasculitis of older age. It usually affects the branches of carotid arteries, especially temporal and ophthalmic artery. In addition to genetic predisposition, environmental factors also contribute to the
Externí odkaz:
https://doaj.org/article/05a8d20fc6eb4c8789175f7489c33413
Publikováno v:
Journal of Medical Case Reports, Vol 15, Iss 1, Pp 1-4 (2021)
Abstract Background Hereditary angioedema (HAE) is a rare disease characterized with recurrent swelling of subcutaneous or mucosal tissue that resolves in approximately 3 days. It can be presented with peripheral edema, abdominal and life-threatening
Externí odkaz:
https://doaj.org/article/01a74a8ba2244caf93045b22950968bf
Autor:
Mislav Radić, Srđan Novak, Marko Barešić, Ana Hećimović, Dijana Perković, Jasna Tekavec-Trkanjec, Miroslav Mayer, Višnja Prus, Jadranka Morović-Vergles, Daniela Marasović Krstulović, Mislav Cerovec, Ljiljana Bulat Kardum, Miroslav Samaržija, Branimir Anić
Publikováno v:
Biomedicines, Vol 10, Iss 12, p 3291 (2022)
The aim of this study was to develop a Croatian Delphi-based expert consensus for screening interstitial lung disease (ILD) associated with connective tissue disease (CTD). A systematic literature review was conducted on risk factors for the developm
Externí odkaz:
https://doaj.org/article/45df3ff3423f4449a21ba2e9ca2e4a33
Publikováno v:
Rheumatology International. 41:189-195
Behcet’s disease (BD) is vasculitis affecting vessels of variable sizes characterized with recurrent oral and/or genital aphthous ulcers accompanied by cutaneous, ocular, articular, gastrointestinal, and/or central nervous system inflammatory lesio
Publikováno v:
Journal of Medical Case Reports, Vol 15, Iss 1, Pp 1-4 (2021)
Journal of Medical Case Reports
Journal of Medical Case Reports
Background Hereditary angioedema (HAE) is a rare disease characterized with recurrent swelling of subcutaneous or mucosal tissue that resolves in approximately 3 days. It can be presented with peripheral edema, abdominal and life-threatening laryngea
Autor:
Ana Marija Lukinac, Kristina Kovačević Stranski, I. Kovacevic, Višnja Prus, Jasminka Milas Ahić, Željka Kardum, Ana Kovač
Publikováno v:
Reumatizam. 1
Autor:
Željka Kardum, Jasminka Milas Ahić, Ivana Kovačević, Ana Marija Lukinac, Ana Kovač, Kristina Kovačević Stranski, Višnja Prus
Publikováno v:
Reumatizam
Volume 66
Issue 1 (online first)
Volume 66
Issue 1 (online first)
Vaskulitis povezan s antineutrofilnim citoplazmatskim protutijelima (engl. Anti-neutrophil Cytoplasmatic Antibody – ANCA ) ili skraćeno ANCA vaskulitis (engl. ANCA-associated vasculitis – AAV ) jest vaskulitis malih krvnih žila karakteriziran n
Autor:
Joško Mitrović, Katarina Borić, Simeon Grazio, Frane Grubišić, Željka Kardum, Tatjana Kehler, Nikolina Ljubičić Marković, Daniela Marasović-Krstulović, Ksenija Maštrović-Radončić, Sonja Milanović, Višnja Prus, Ivana Tomljanović Rudar, Jadranka Morović-Vergles
Publikováno v:
Reumatizam
Volume 65
Issue suppl.1
Volume 65
Issue suppl.1
Background: Access to biologic treatment diff er in EU countries and is influenced by different factors. In CEE countries 1%–5% of all RA patients are treated with biological therapy. Factors influencing prescriptions of biologics in CEE are mostly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::819af999c26978ce41ba1f01e0dc262f
https://www.bib.irb.hr/1242715
https://www.bib.irb.hr/1242715
Autor:
Simeon Grazio, Srđan Novak, Nadica Laktašić-Žerjavić, Branimir Anić, Đurđica Babić-Naglić, Frane Grubišić, Nikolina Ljubičić Marković, Dušanka Martinović Kaliterna, Miroslav Mayer, Joško Mitrović, Višnja Prus, Tea Schnurrer-Luke-Vrbanić, Tonko Vlak
Publikováno v:
Reumatizam
Volume 64
Issue 2
Volume 64
Issue 2
Spondiloartritisi (SpA) grupa su upalnih reumatskih bolesti koje dijele zajednička etiopatogenetska, radiološka i klinička obilježja. Te su bolesti znatan teret za bolesnika i za društvo. Posljednjih godina dogodile su se velike novosti u klasif