Št. zadetkov: 15
Magistrsko delo
Oznake:
arhitektura;magistrske naloge;bivanjske skupnosti;stanovanjske skupnosti;prazne vasi;prenove;starostniki;demenca;stanovanjske soseske;Pristava pri Štjaku;
Ne pozabi me
Leto:
2020
Vir:
Fakulteta za arhitekturo (UL FA)
Magistrsko delo
Oznake:
magistrske naloge;arhitektura;industrijske stavbe;prenove;skladišča;družbeni centri;izobraževalni centri;univerze;knjižnice;Liman;Novi Sad;
Češkoslovaško skladišče (Češki magacin) je industrijska stavba zaščitena kot spomenik kulture ki je zgrajena leta 1921 v takratni industrijski coni Veliki Liman v Novem Sadu. Danes stavba stoji obkrožena z tri študentska doma kateri jo ločujejo od prvotnega industrijskega okolja. “Ekstro-introvert” ...
Leto:
2023
Vir:
Fakulteta za arhitekturo (UL FA)
Diplomsko delo
Oznake:
motivacija;trgovina;izobraževanje;
Izobraževanja so v sodobnem svetu izjemno pomembna, tudi na trgu,na katerem deluje podjetje Menart Records d.o.o., zato je za konkurenčnost podjetja izjemno pomembno, da vodstvo z namenom učinkovitejšega poslovanja prepozna potencial izobraževanja ob delu. Pomemben faktor, ki pripomore k stalnemu iz ...
Leto:
2016
Vir:
Fakulteta za organizacijske vede (UM FOV)
Pregledni znanstveni članek
Oznake:
familial hypercholesterolemia;polygenic hypercholesterolemia;inflammation;atherosclerosis;carotid intima media thickness;cIMT;C-reactive protein;hsCRP;
Hypercholesterolemia is a major cause of atherosclerosis development and premature cardiovascular disease (CVD). It leads to inflammation, which further accelerates atherosclerosis progression. Familial hypercholesterolemia (FH) is an autosomal dominant disorder characterized by elevated serum LDL-c ...
Leto:
2020
Vir:
Medicinska fakulteta (UL MF)
Pregledni znanstveni članek
Oznake:
spol;tveganje za srčnožilna obolenja;sladkorna bolezen tipa 1;otroci;mladostniki;krvni tlak;hiperglikemija;dislipidemija;kajenje;infekcijske bolezni;
Cardiovascular disease (CVD) is the primary cause of higher and earlier morbidity and mortality in people with type 1 diabetes (T1D) compared to people without diabetes. In addition, women with T1D are at an even higher relative risk for CVD than men. However, the underlying pathophysiology is not w ...
Leto:
2021
Vir:
Medicinska fakulteta (UL MF)
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)
Kratki znanstveni prispevek
Oznake:
otroci;prekomerna teža;debelost;holesterol;
Leto:
2023
Vir:
Medicinska fakulteta (UL MF)
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)
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)
Kratki znanstveni prispevek
Oznake:
3-MGA-I;3-methylglutaconic aciduria type 1;precocious puberty;AUH gene;GnRH agonist;triptorelin;
3-methylglutaconic aciduria type 1 (3-MGA-I) (MIM ID #250950) is an ultra-rare, autosomal recessive organic aciduria, resulting from mutated AUH gene, leading to the deficient 3-methylglutaconyl-CoA hydratase (3-MGH). Only around 40 cases are previously reported, caused by a spectrum of 10 mutations ...
Leto:
2020
Vir:
Medicinska fakulteta (UL MF)