Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Batnožić Varga, Mateja"'
Autor:
Held, Martina, Batnožić Varga, Mateja, Šestan, Mario, Šapina, Matej, Kifer, Nastasia, Grgurić, Danica, Crkvenac Gornik, Kristina, Frković, Marijan, Arvaj, Nena, Wagner, Jasenka, Jelušić Marija
IgA vasculitis (IgAV) is a desease in which genetic background also plays an important role. Some small studies have indicated the importance of variants in various non-HLA genes in the manifestation of different disease phenotypes. The aim of this r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::03a482bc162f997af88ff90d21b061ed
https://www.bib.irb.hr/1152410
https://www.bib.irb.hr/1152410
Autor:
Held, Martina, Batnožić Varga, Mateja, Šestan, Mario, Šapina, Matej, Kifer, Nastasia, Grgurić, Danica, Crkvenac Gornik, Kristina, Frković, Marijan, Arvaj, Nena, Wagner, Jasenka, Jelušić Marija.
Uvod. U manifestaciji različitih fenotipova IgA vaskulitisa (IgAV) važnu ulogu imaju i varijante gena izvan HLA sustava. Cilj je bio istražiti ulogu polimorfizama pojedinačnih nukleotida gena HMGB1 i AGER koji kodiraju za protein visoke pokretlji
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::747bdfc1e5426fcd0d3b0db58655ce94
https://www.bib.irb.hr/1152268
https://www.bib.irb.hr/1152268
Autor:
Šapina, Matej, Šestan, Mario, Kifer, Nastasia, Batnožić Varga, Mateja, Held, Martina, Sršen, Saša, Ovuka, Aleksandar, Frković, Marijan, Gagro, Alenka, Jelušić, Marija
Introduction: IgA vasculitis (IgAV) is the most common systemic vasculitis in children. The mandatory clinical feature of the disease is purpuric rash, which predominantly affects the lower extremities, accompanied by diffuse abdominal pain, joint in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::7fe49a483da693a65a70331e3c1c906c
https://www.bib.irb.hr/1168119
https://www.bib.irb.hr/1168119
Autor:
Batnožić Varga, Mateja, Šestan, Mario, Wagner, Jasenka, Crkvenac, Kristina, Kifer, Nastasia, Frković, Marijan, Štefinovec, Laura, Vučemilović Jurić, Valentina, Grgurić, Danica, Pušeljić, Silvija, Jelušić, Marija
IgA vasculitis (IgAV) or Henoch-Schönlein' s purpura is the most prevalent systemic small vessel vasculitis in childhood. High mobility group box-1 protein (HMBG1) is a pleiotropic cytokine that functions as a pro-inflammatory signal, important for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::e5918274d658bd1c6c778ac2c391624a
https://doi.org/10.1136/archdischild-2021-europaediatrics.442
https://doi.org/10.1136/archdischild-2021-europaediatrics.442
Autor:
Šestan, Mario, Kifer, Nastasia, Sršen, Saša, Ovuka, Aleksandar, Batnožić Varga, Mateja, Šapina, Matej, Held, Martina, Ban, Maja, Kozmar, Ana, ćorić, Marijana, Bulimbašić, Stela, Crkvenac, Kristina, Milošević, Danko, Frković, Marijan, Gagro, Alenka, Jelušić Marija
Indroduction: IgA vasculitis (IgAV) is the most common childhood-vasculitis in which more than 50% of children develop gastrointestinal (GI) symptoms. In 10-20% of patients serious complications such as intussusception, bowel perforation, and massive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::705eb63e152a6f76398441a5372a2115
https://www.bib.irb.hr/1152407
https://www.bib.irb.hr/1152407
Autor:
Šapina, Matej, Šestan, Mario, Kifer, Nastasia, Batnožić Varga, Mateja, Held, Martina, Sršen, Saša, Ovuka, Aleksandar, Frković, Marijan, Gagro, Alenka, Jelušić, Marija
Uvod. IgA vaskulitis (IgAV) najčešći je sistemski vaskulitis u djece. Ključno kliničko obilježje bolesti je purpu rični osip koji pretežno zahvaća donje ekstremitete popraćen difuznom boli u trbuhu, zahvaćanjem zglobova, nefritisom i/ili o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::678630e65e93c1b3b3a76c777863090e
https://www.bib.irb.hr/1152308
https://www.bib.irb.hr/1152308
Autor:
Held, Martina, Batnožić Varga, Mateja, Šestan, Mario, Šapina, Matej, Kifer, Nastasia, Grgurić, Danica, Crkvenac Gornik, Kristina, Frković, Marijan, Arvaj, Nena, Wagner, Jasenka, Jelušić, Marija
Introduction: The pathogenesis of IgA vasculitis (IgAV) is complex and still insufficiently elucidated. It is a multifactorial disease in the development of which, in addition to numerous environmental factors, the genetic background also plays an im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::7458a0816c44b3baf12afcf0f626ee87
https://doi.org/10.1186/s12969-021-00632-z
https://doi.org/10.1186/s12969-021-00632-z
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Sršen, Saša, Šapina, Matej, Batnožić Varga, Mateja, Šestan, Mario, Kifer, Nastasia, Ovuka, Aleksandar, Held, Martina, Ban, Maja, Kozmar, Ana, Ćorić, Marijana, Bulimbašić, Stela, Crkvenac Gornik, Kristina, Milošević, Danko, Frković, Marijan, Gagro, Alenka, Jelušić, Marija
The prevalence of generalized skin symptoms, as well as the most severe forms in childhood IgA vasculitis is much less than the classical findings. However, the more severe the skin symptoms are, the more severe the course of the disease is, and aggr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::e86247ca227d89a5ee8285f2a3b36563
https://doi.org/10.1186/s12969-020-00470-5
https://doi.org/10.1186/s12969-020-00470-5