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Diabetic Medicine : a Journal of the British Diabetic Association|January 18, 2007
Incipient cardiovascular autonomic imbalance revealed by wavelet analysis of heart rate variability in Type 2 diabetic patientsV Urbancic-Rovan, B Meglic, A Stefanovska, et al.
Balkan Journal of Medical Genetics : BJMG|January 17, 2020
Clinical Next Generation Sequencing Reveals an <i>H3F3A</i> Gene as a New Potential Gene Candidate for Microcephaly Associated with Severe Developmental Delay, Intellectual Disability and Growth RetardationA Maver, G Čuturilo, Stojanović J Ruml, et al.
Clinical Genetics|February 1, 1997
Genetic epidemiology of Duchenne and Becker muscular dystrophy in SloveniaB Peterlin, J Zidar, M Meznaric-Petrusa, et al.
Annales De Genetique|June 9, 2004
Genealogical study of myotonic dystrophy in Istria (Croatia)I Medica, N Logar, D Leonardelli Mileta, et al.
Disease Markers|January 16, 2010
Genetic variation in osteopontin gene is associated with susceptibility to sarcoidosis in Slovenian populationA Maver, I Medica, B Salobir, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 22, 2010
Isolated bulbar paralysis in a patient with medullar tau pathology: a case reportJ Pretnar-Oblak, M Zaletel, T M Hajnsek, et al.
Human Reproduction (Oxford, England)|January 5, 2002
Screening for Y chromosome microdeletions in 226 Slovenian subfertile menB Peterlin, T Kunej, J Sinkovec, et al.
Acta Paediatrica (Oslo, Norway : 1992)|April 30, 2005
Carotid artery intima-media thickness and angiotensin-converting enzyme gene polymorphism in the offspring of parents with premature strokeN Marcun Varda, B Peterlin, S Umek Bradac, et al.
Genetics and Molecular Research : GMR|January 19, 2010
Lack of association of immune-response-gene polymorphisms with susceptibility to sarcoidosis in Slovenian patientsA Maver, I Medica, B Salobir, et al.
International Journal of Molecular Medicine|December 16, 1998
Autosomal dominant Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies: detection of the recombination in Slovene patients and exclusion of the potentially recessive Thr118Met PMP22 point mutationL Leonardis, J Zidar, A Ekici, et al.
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