Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Ajda Skarlovnik"'
Autor:
Ursa Sustar, Urh Groselj, Katarina Trebusak Podkrajsek, Matej Mlinaric, Jernej Kovac, Martin Thaler, Ana Drole Torkar, Ajda Skarlovnik, Tadej Battelino, Tinka Hovnik
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Lysosomal acid lipase deficiency (LAL-D) is an autosomal recessive lysosomal storage disorder, caused by homozygous or compound heterozygous pathogenic variants in the LIPA gene. Clinically, LAL-D is under- and misdiagnosed, due to similar clinical a
Externí odkaz:
https://doaj.org/article/c20ca39bf7dd4228aeefbb417a684df6
Autor:
Matej Mlinaric, Nevenka Bratanic, Vlasta Dragos, Ajda Skarlovnik, Matija Cevc, Tadej Battelino, Urh Groselj
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Homozygous familial hypercholesterolemia (HoFH) is a rare inherited metabolic disorder, frequently leading to an early cardiovascular death if not adequately treated. Since standard medications usually fail to reduce LDL-cholesterol (LDL-C) levels sa
Externí odkaz:
https://doaj.org/article/83a03f2fd9514ccabd6541fb923c582a
Publikováno v:
Zdravniški Vestnik, Vol 81, Iss 9 (2012)
Background: Structure and function of arterial system change with advancing age. The most important aging-induced changes of arterial system are: endothelial dysfunction, increased stiffness of arterial wall, an increase in arterial lumen size a
Externí odkaz:
https://doaj.org/article/152c1242b2534bbf8b6151da78720661
Publikováno v:
Zdravniški Vestnik, Vol 76, Iss 5 (2007)
Background: The aim of this study was to assess the incidence of malaria among the homogenous population of medical students and young doctors, specifically educated in tropical medicine, travelling to the third world countries for electives of two t
Externí odkaz:
https://doaj.org/article/f05d9ff21c8a4e0bbf858f3f0993e147
Autor:
Tadej Battelino, Ajda Skarlovnik, Vlasta Dragoš, Matija Cevc, Nevenka Bratanič, Urh Groselj, Matej Mlinaric
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Frontiers in Pediatrics
Frontiers in Pediatrics
Homozygous familial hypercholesterolemia (HoFH) is a rare inherited metabolic disorder, frequently leading to an early cardiovascular death if not adequately treated. Since standard medications usually fail to reduce LDL-cholesterol (LDL-C) levels sa
Publikováno v:
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research
Background Statin use is frequently associated with muscle-related symptoms. Coenzyme Q10 supplementation has yielded conflicting results in decreasing statin myopathy. Herein, we tested whether coenzyme Q10 supplementation could decrease statin-asso
Publikováno v:
Neurology, Psychiatry and Brain Research. 19:216-220
In this research, we observe volunteer's ability to recall visual stimuli in relation to their breathing phase at the time of presentation of those stimuli. To assess the ability to recall visual stimuli, we have exposed volunteers to a short term cu
Publikováno v:
Radiology and Oncology
Radiology and oncology (Ljubljana)
Radiology and oncology (Ljubljana)
Background. In current clinical practice lung scintigraphy is mainly used to exclude pulmonary embolism (PE). Modified diagnostic criteria for planar lung scintigraphy are considered, as newer scitigraphic methods, especially single photon emission c