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Publikováno v:
Journal of Cutaneous Pathology. Nov2023, Vol. 50 Issue 11, p1020-1026. 7p.
Autor:
Tokić, Tomislav1, Knez, Nora2, Lekić, Ante1, Pavlek, Mario3, Tokić, Lara Lalić3, Paar, Maja Hrabak4, Gašparović, Hrvoje1 hgasparovic@gmail.com
Publikováno v:
Rad Hrvatske Akademije Znanosti i Umjetnosti. Medicinske Znanosti. 2022, Vol. 553 Issue 60/61, p116-119. 4p.
Autor:
Knez, Nora1,2 (AUTHOR) noraknez6@gmail.com, Walkenhorst, Molly1 (AUTHOR) mwalkenhorst@kumc.edu, Haeri, Mohammad1 (AUTHOR) mhaeri@kumc.edu
Publikováno v:
Diagnostics (2075-4418). May2023, Vol. 13 Issue 9, p1628. 3p.
Publikováno v:
Liječnički vjesnik
Volume 145
Issue Supp 2
Volume 145
Issue Supp 2
INTRODUCTION/OBJECTIVES: Supracondylar humeral fractures (SHF) are the most common fractures associated with concomitant neurovascular injuries in children. Pink pulseless hand (PPH) labels SHF presenting without a pulse in a well- perfused hand. Man
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::660bff0a019e77bf6cea1fea2cd6b5c8
https://hrcak.srce.hr/file/437269
https://hrcak.srce.hr/file/437269
Publikováno v:
Liječnički vjesnik
Volume 144
Issue Supp 7
Volume 144
Issue Supp 7
Background: Endovascular aneurysm repair (EVAR) has become a well-established approach in the elective treatment of abdominal aortic aneurysms (AAA). It represents a treatment of choice for high-risk patients ineligible for open surgery due to the in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::668127c0505be271b58bb777a684b5eb
https://hrcak.srce.hr/file/422644
https://hrcak.srce.hr/file/422644
Introduction hereditary transthyretin amyloidosis (hATTR) is a rare progressive autosomal-dominant disorder of protein metabolism caused by the mutated transthyretin (TTR) gene. It is a systemic disease with a variable phenotype due to the more than
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::4779206bfa7b909502b80ccd434a040a
https://www.bib.irb.hr/1229809
https://www.bib.irb.hr/1229809
From simplex to complex – a case report of incidental peritoneal carcinomatosis during hernia repair
Introduction: Inguinal hernia is an extremely rare initial manifestation of gastrointestinal tumors. It is hypothesized that it is caused by increased intraabdominal pressure from malignancies. Hernia sac peritoneal carcinomatosis (PC) suggests advan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::ef9c8cb126b2e542f2c6975443d7b973
https://www.bib.irb.hr/1229804
https://www.bib.irb.hr/1229804
Autor:
Knez, Nora, Belina, Dražen
Pediatric subvalvular aortic stenosis (SAS) is a rare congenital heart defect caused by membrane below the aortic valve, resulting in an obstruction of the left ventricular outflow tract (LVOT). The asymptomatic course contributes to serous sequelae
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::4cf1605835585bd192e6e885fa013ae6
https://www.bib.irb.hr/1229638
https://www.bib.irb.hr/1229638
Publikováno v:
Liječnički vjesnik
Volume 144
Issue Supp 6
Volume 144
Issue Supp 6
INTRODUCTION: Although civility and politeness in the workplace are mainstays of modern cultural and societal norms, the healthcare system sometimes seems to be an exception to the rule. In an extremely dynamic, high-stakes environment that most hosp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::98233ae224ea8d43896e51054c02c141
https://hrcak.srce.hr/file/417199
https://hrcak.srce.hr/file/417199