Iskalni niz:
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Jezik:
Št. zadetkov: 15
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)
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
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
Pregledni znanstveni članek
Oznake: citomegalovirus;krvne komponente;testiranje;odstranjevanje levkocitov;inaktiviranje patogenov;preprečevanje prenosa;
Leto: 2013 Vir: dLib.si Digitalna knjižnica Slovenije
Magistrsko delo
Oznake: čustvena inteligentnost;čustvena kompetentnost;učitelji;specialni pedagogi;šola;otroci s posebnimi potrebami;
Leto: 2020 Vir: Pedagoška fakulteta (UP PEF)
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)
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)
Izvirni znanstveni članek
Oznake: elektrokemoterapija;elektroporacija;bleomycin;electrochemotherapy;electroporation;
Bleomycin concentration in patientsʹ plasma and tumors after electrochemotherapy
Leto: 2021 Vir: Onkološki inštitut Ljubljana (OI)
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)
Št. zadetkov: 15
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