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Št. zadetkov: 22
Klinični pomen določanja F-PSA in F-PSA
Mojca Grošelj, Mirko Čeh, Črtomir Stropnik
Diplomsko delo
Oznake: PSA;PSA gen;T-PSA;F-PSA;biosinteza;tkivna specifičnost;
Klinični pomen določanja F-PSA in F-PSA : diplomsko delo visokega strokovnega študijskega programa
Leto: 1999 Vir: Fakulteta za kemijo in kemijsko tehnologijo (UM FKKT)
Nekrotizirajoči enterokolitis
Maja Pavčnik Arnol, Mojca Grošelj-Grenc, Diana Gvardijančič
Pregledni znanstveni članek
Oznake: nekrotizirajoči enterokolitis;novorojenček;nedonošenost;perforacija črevesa,;kirurško zdravljenje;prognoza;
Nekrotizirajoči enterokolitis je ishemična in vnetna nekroza črevesa, ki prizadene predvsem nedonošenčke. Je pomemben vzrok obolevnosti in umrljivosti v enotah intenzivne terapije novorojenčkov. V patogenezo nekrotizirajočega enterokolitisa so vpleteni številni dejavniki, kot so genetska dovzetnost, ...
Leto: 2012 Vir: dLib.si Digitalna knjižnica Slovenije
Obravnava novorojenčkov s prirojeno srčno napako, ki potrebujejo zdravljenje s prostaglandinom E1 - slovenske smernice
Mojca Grošelj-Grenc, Maja Pavčnik Arnol, Gorazd Kalan, Tomaž Podnar, Ivan Vidmar
Strokovni članek
Oznake:
Background: Early recognition of duct-dependent congenital heart disease in newborns with duct-dependent pulmonary or systemic blood flow or transpositionof the great arteries is critical for early introduction of prostaglandin E1 (PGE1), which allows stabilization of the newborn till cardiac cathet ...
Leto: 2012 Vir: dLib.si Digitalna knjižnica Slovenije
Smernice za preprečevanje prenosa CMV s transfuzijo krvnih komponent
Marko Cukjati, Vladan Rajić, Darja Paro Panjan, Tanja Premru-Sršen, Irena Štucin Gantar, Mojca Grošelj-Grenc, Urška Rahne-Potokar, Samo Zver
Pregledni znanstveni članek
Oznake: citomegalovirus;krvne komponente;testiranje;odstranjevanje levkocitov;inaktiviranje patogenov;preprečevanje prenosa;
Leto: 2013 Vir: dLib.si Digitalna knjižnica Slovenije
Mnenja pedagogov o pomenu čustvene inteligentnosti pri delu z otroki s posebnimi potrebami
Petra Grošelj, Mojca Kukanja-Gabrijelčič
Magistrsko delo
Oznake: čustvena inteligentnost;čustvena kompetentnost;učitelji;specialni pedagogi;šola;otroci s posebnimi potrebami;
Leto: 2020 Vir: Pedagoška fakulteta (UP PEF)
Ethical considerations and multidisciplinary care for pediatric patients with hypoplastic left heart syndrome
Mojca Železnik, Urh Grošelj, Petja Fister
Pregledni znanstveni članek
Oznake: hypoplastic left heart syndrome;congenital heart defect;prenatal diagnosis;neonatal care;palliative surgery;medical ethic;multidisciplinary care;decision making;
Background: Hypoplastic left heart syndrome (HLHS) was a fatal congenital heart defect (CHD) until the 1980s. Introduction of the Norwood procedure and subsequent Fontan operation significantly improved survival by creating a single-ventricle circulation. Due to the high mortality associated with th ...
Leto: 2025 Vir: Digitalni repozitorij raziskovalnih organizacij Slovenije
Towards a comprehensive strategy for the management of rare diseases in Slovenia
Dalibor Stanimirović, Eva Murko, Tadej Battelino, Urh Grošelj, Mojca Žerjav-Tanšek
Izvirni znanstveni članek
Oznake: redke bolezni;obravnava pacienta;javno zdravje;slovenski zdravstveni sistem;zdravljenje;
Rare diseases (RDs), with distinctive and complex features, pose a serious public health concern and represent a considerable challenge for the Slovenian healthcare system. One of the potential approaches to tackling this problem and treating patients with RDs in a quality and effective manner is to ...
Leto: 2021 Vir: Medicinska fakulteta (UL MF)
Hypercholesterolemia in two siblings with resistance to thyroid hormones due to disease-causing variant in thyroid hormone receptor (THRB) gene
Maja Jakič, Magdalena Avbelj, Katarina Trebušak Podkrajšek, Jasna Šuput, Mojca Žerjav-Tanšek, Tadej Battelino, Urh Grošelj
Izvirni znanstveni članek
Oznake: thyroid;resistance to thyroid hormones;RTHB;hyroid hormone receptor;THRB;hypothyroidism;hypercholesterolemia;
Resistance to thyroid hormone beta (RTHβ) is a syndrome characterized by a reduced response of target tissues to thyroid hormones. In 85% of cases, a pathogenic mutation in the thyroid hormone receptor beta (THRB) gene is found. The clinical picture of RTHβ is very diverse; the most common findings ...
Leto: 2020 Vir: Medicinska fakulteta (UL MF)
Data highlighting effects of Ketogenic diet on cardiomyopathy and hepatopathy in Glycogen storage disease Type IIIA
Tatiana Marusic, Mojca Žerjav-Tanšek, Andreja Širca-Čampa, Ajda Mezek, Pavel Berden, Tadej Battelino, Urh Grošelj
Izvirni znanstveni članek
Oznake: inborn genetic diseases;glycogen storage disease;glycogen storage disease type III;cardiomyopathy;hypertrophic diet;ketogenic;
Datasets highlighting effects of ketogenic diet (KD) in a glycogen storage disease type IIIa patient is presented with the longest patient follow up report to date. Now a 15-year old girl with GSD type IIIa, diagnosed at 1 year of age, had initially introduced treatment with diet high carbohydrates, ...
Leto: 2020 Vir: Medicinska fakulteta (UL MF)
Palliative care for children and adults with inherited metabolic disease in Europe
Anja Lee, Yngve Thomas Bliksrud, Michela Onali, Julia Neugebauer, Francois Eyskens, Urh Grošelj, Mojca Žerjav-Tanšek
Izvirni znanstveni članek
Oznake: palliative care;quality of life;patients;paediatric palliative care;inherited metabolic diseases;genetic disorders;MetabERN;The European Reference Network for Hereditary Metabolic Disorders;
Palliative care should be an integral part of follow-up for patients with life-limiting/life-threatening conditions, irrespective of age and diagnosis. Many patients with inherited metabolic disorders (IMD) have palliative care needs due to multi-systemic conditions without curative treatment option ...
Leto: 2025 Vir: Digitalni repozitorij raziskovalnih organizacij Slovenije
Št. zadetkov: 22
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