Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Šućur, Nediljko"'
Autor:
Pećin, van, Merćep, Iveta, Bašić-Kes, Vanja, Bilić, Ervina, Borovečki, Fran, Bradamante, Mirna, Čikeš, Maja, Fumić, Ksenija, Hauptman, Ana Godan, Jelaković, Bojan, Leskovar, Dunja, Mihanović, Kristina Paponja, Perica, Dražen, Prgomet, Luka, Rački, Sanjin, Selthofer-Relatić, Kristina, Štanfel, Marija, Šućur, Nediljko, Vujičić, Božidar, Vukić, Tamara
Publikováno v:
Lijecnicki Vjesnik; 2024, Vol. 146 Issue 5/6, p157-169, 13p
Autor:
Pećin, Ivan *, Leskovar, Dunja, Šabić, Marina, Perica, Dražen, Šućur, Nediljko, Godan Hauptman, Ana, Merćep, Iveta, Borovečki, Fran, Premužić, Vedran, Jelaković, Bojan, Reiner, Željko
Publikováno v:
In Transfusion and Apheresis Science June 2022 61(3)
Autor:
Šućur, Nediljko, Pećin, Ivan, Ermacora, Lucija, Muačević-Katanec, Diana, Godan Hauptman, Ana, Perica, Dražen, Leskovar, Dunja, Fumić, Ksenija, Reiner, Željko
Publikováno v:
Liječnički vjesnik
Volume 142
Issue 11-12
Volume 142
Issue 11-12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::dae8cbc5a2b95cba5bd0e6c1baf295d1
https://hrcak.srce.hr/file/372900
https://hrcak.srce.hr/file/372900
Autor:
Muačević-Katanec, Diana, Pećin, Ivan, Šimić, Iveta, Fumić, Ksenija, Potočki, Kristina, Šućur, Nediljko, Reiner, Željko
Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome, MPS VI) is a progressive multisystemic lysosomal storage disease. Physical symptoms generally include growth retardation, and bone dysplasia. Enzyme replacement therapy is the treatment of choic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______579::cf032a2474486ca488a3c2aa38d68040
http://lijecnicki-vjesnik.hlz.hr/lijecnicki-vjesnik/smjernice-za-lijecenje-mukopolisaharidoze-mps-vi-u-odraslih-bolesnika/
http://lijecnicki-vjesnik.hlz.hr/lijecnicki-vjesnik/smjernice-za-lijecenje-mukopolisaharidoze-mps-vi-u-odraslih-bolesnika/
Autor:
Pećin, Ivan, Muačević-Katanec, Diana, Šimić, Iveta, Fumić, Ksenija, Potočki, Kristina, Šućur, Nediljko, Reiner, Željko
These guidelines provide a short summary of recommendations on Pompe disease, how to diagnose this disease, management of adult patients with this disease, follow-up of the patients and recommendations on therapy and genetic testing. Early diagnosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______579::aa2c738f707709a241f964cd2f87051b
http://lijecnicki-vjesnik.hlz.hr/lijecnicki-vjesnik/pompeova-bolest-smjernice-za-dijagnozu-i-lijecenje-odraslih-bolesnika/
http://lijecnicki-vjesnik.hlz.hr/lijecnicki-vjesnik/pompeova-bolest-smjernice-za-dijagnozu-i-lijecenje-odraslih-bolesnika/
Autor:
Merkler, Marijan, Šimić, Iveta, Pećin, Ivan, Muačević-Katanec, Diana, Šućur, Nediljko, Reiner, Željko
Gaucher disease is an autosomal recessive disorder, characterized by decreased levels of the lysosomal enzyme glucocerebrosidase. This deficiency results in a decreased breakdown of this glycosphingolipid glucocerebroside, which accumulates in the ly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______579::2bbd740e24074b0e9ab7635bc50d32ed
Autor:
Merkler, Marijan, Pećin, Ivan, Šimić, Iveta, Muačević-Katanec, Diana, Šućur, Nediljko, Reiner, Željko
Early diagnosis and management of patients with Fabry disease (FD) requires a multidisciplinary approach of several different experts. The aim of this document is to provide health care professionals with guidelines for management of adult patients w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______579::72ac81854856eb11d573db6de1770071
http://lijecnicki-vjesnik.hlz.hr/lijecnicki-vjesnik/fabryjeva-bolest-smjernice-za-dijagnozu-i-lijecenje-odraslih-bolesnika/
http://lijecnicki-vjesnik.hlz.hr/lijecnicki-vjesnik/fabryjeva-bolest-smjernice-za-dijagnozu-i-lijecenje-odraslih-bolesnika/
Autor:
Merkler, Marijan, Pećin, Ivan, Šimić, Iveta, Muačević-Katanec, Diana, Šućur, Nediljko, Reiner, Željko
Rano postavljanje dijagnoze i liječenje bolesnika s Fabryjevom bolesti zahtijeva multidisciplinarni pristup niza stručnjaka. Cilj je ovog dokumenta predstaviti našoj medicinskoj javnosti smjernice za dijagnozu i liječenje odraslih bolesnika s Fab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::e24f4ed58f895a9c1fd0a35e7d9a7c7c
https://www.bib.irb.hr/732141
https://www.bib.irb.hr/732141
Autor:
Šimić, Iveta [imi, Pećin, Ivan, Tedeschi-Reiner, Eugenia, Zrinšćak, Ozren, Šućur, Nediljko, Reiner, Željko
Publikováno v:
Collegium antropologicum
Volume 37
Issue 3
Volume 37
Issue 3
Diabetes mellitus is a metabolic disorder primarily characterized by elevated blood glucose levels and by microvas- cular and macrovascular complications which increase the morbidity and mortality.The aim of this study was to assess whether in high r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::6d468e1e29610a710c4e84b0bad4a32e
https://pubmed.ncbi.nlm.nih.gov/24308217
https://pubmed.ncbi.nlm.nih.gov/24308217
Familial hypercholesterolemia is the most common genetic metabolic disorder and is associated with significant morbidity and mortality from cardiovascular disease, in particular coronary heart disease (CHD). Gene mutations for LDL receptor, APOB or P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______579::6d9039f415d9af02bcb812967d1eb7f7
http://lijecnicki-vjesnik.hlz.hr/lijecnicki-vjesnik/porodicna-hiperkolesterolemija-mislimo-li-dovoljno-o-ovoj-teskoj-bolesti/
http://lijecnicki-vjesnik.hlz.hr/lijecnicki-vjesnik/porodicna-hiperkolesterolemija-mislimo-li-dovoljno-o-ovoj-teskoj-bolesti/