Zobrazeno 1 - 10
of 66
pro vyhledávání: '"MARN, BORUT"'
Publikováno v:
Paediatria Croatica, Supplement. 2017 Supplement, Vol. 61, p163-169. 7p.
Autor:
MARN, BORUT1, BABIĆ, IRENA1, IVKOVIĆ, MLADEN1, VLAHOVIĆ, SANJA2, ŽULJ, IRIS3, DAWIDOWSKY, KRSTO4
Publikováno v:
Paediatria Croatica, Supplement. 2017 Supplement, Vol. 61, p142-146. 5p.
Autor:
Marn, Borut1 borut.marn@zg.t-com.hr, Kekić, Branko2
Publikováno v:
Paediatria Croatica. 2016, Vol. 60 Issue 1, p9-15. 7p.
Autor:
Bošnjak-Nađ, Katarina, Popović-Miočinović, Ljiljana, Ivkić, Mirjana, Zadro, Anka, Marn, Borut
Oštećenja sluha (periferna i centralna, supkortikalna) češća su u neurorizične djece nego u općoj populaciji. Cilj rada: ispitati učestalost oštećenja sluha u neurorizične djece te ispitati perinatalne čimbenike visokog rizika na ošteće
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::975391aac611cba84d5bcda8836875f5
https://www.bib.irb.hr/1052571
https://www.bib.irb.hr/1052571
Autor:
Krakar, Goran, Marn, Borut, Pustišek, Nives, Ulamec, Monika, Gojmerac, Tomislav, Mejaški Bošnjak, Vlatka
Objective: We report a case of Melkersson- Rosenthal syndrome (MRS) associated with oligodontia in 15 years old girl. Background: MRS is a rare neuromucocutaneous disorder of uncertain etiology causing localized edema, inflammation in the face and or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::7d1f7b6776ec50dead79023851c434ea
https://www.bib.irb.hr/682104
https://www.bib.irb.hr/682104
Predavanje razmatra rezultate sveobuhvatnog probira novorođenčadi na oštećenje sluha u RH od 2002. do 2011.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::571d63b146b2464a3f130d8a4d30a3f5
https://www.bib.irb.hr/1101853
https://www.bib.irb.hr/1101853
Autor:
Sabol, Zlatko, Sabol, Filip, Kovač Šižgorić, Matilda, Kipke Sabol, Ljiljana, Bela Klancir, Svjetlana, Gjergja, Zdravka, Gjergja Juraški, Romana, Cvitanović Šojat, Ljerka, Krakar, Goran, Rešić, Biserka, Sasso, Antun, Hafner, Krasanka, Oršolić, Krešo, Marn, Borut, Petrinović Dorešić, Jelena, Barišić, Nina
Neurofibromatoza tip 2 neurokutana je bolest s autosomno dominantnim načinom nasljeđivanja. Gen NF2 tumorski je supresorski gen, lokaliziran na kromosomu 22q12.1 i kodira protein merlin ili švanomin. Karakteristične promjene u NF-u 2 su švanomi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::f9620233d26fa0383eae42eabbd4b180
https://www.bib.irb.hr/679557
https://www.bib.irb.hr/679557
Autor:
Gjurašin, Miroslav, Popović, Ljiljana, Mejaški Bošnjak, Vlatka, Moscatello, Đurđica, Marn, Borut, Župančić, Boris
Budu}; ; i da se pedijatri u svakodnevnom radu prvi susre}; ; u sa simptomima ili znakovima tegoba uzrokovanih pritiskom na vitalne strukture sredi{; ; njeg `iv~anog sustava u podru~ju kraniocervikalnog prijelaza, odlu~ili smo ispitati kakvo klini~ko
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::6766fc7cebd9747452c948266fc680dc
https://www.bib.irb.hr/682066
https://www.bib.irb.hr/682066
Autor:
Mejaški-Bošnjak, Vlatka, Đaković, Ivana, Đuranović, Vlasta, Lujić, Lucija, Krakar, Goran, Marn, Borut
Publikováno v:
Collegium antropologicum
Volume 35 supplement 1
Issue 1
Volume 35 supplement 1
Issue 1
Congenital cytomegalovirus (CMV) infection is the most common vertically transmitted disease with the rate of the infection ranging from 0.2 to 2.4% in newborn infants. Congenital CMV infection causes multiorgan affection, but the most severe and per
Autor:
Marn, Borut, Vlahović, Sanja
Objektivnim audiološkim pretragama želimo što ranije i točnije odrediti stupanja oštećenja sluha, krivulju praga sluha po frekvencijama i mjesto oštećenja. Bez obzira na ogroman napredak audioloških tehnika ovaj je zadatak još uvijek težak
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::5c0163cc1e8132f4f8fa5ec4b33b3be9
https://www.bib.irb.hr/728885
https://www.bib.irb.hr/728885