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Osveži iskanje
Raziskovalni
Avguštin Rotar N, Jerman A, Škoberne A, Borštnar Š, Kojc N, Lindič J.
The predictive value of urinary erythrocyte morphology for proliferative glomerular kidney disease.
Clinical nephrology. 2021, vol. 96, suppl. 1, str. s49-s55. ISSN 0301-0430.
0.9
Prikaz primera
Večerić‑Haler Ž, Borštnar Š, Luzar B, Jerše M and Kojc N.
Multiorgan failure with fatal outcome after stem cell tourism.
European journal of medical research. [Online ed.]. 2021, vol. 26, str. 1-5, ilustr. ISSN 2047-783X.
1.7
Pregledni
Vervaet BA, Nast CC, Schreurs G, Jayasumana C, Herath C, Kojc N, De Broe ME.
Chronic interstitial nephritis in agricultural communities: a new perspective on etiology, diagnosis and mechanism.
Nephrol Ther. 2021 Apr;17S:S45-S50.
0.7
Belčič Mikič T, Kojc N, Frelih M, Aleš-Rigler A, Večerić-Haler Ž.
Management of Anticoagulant-Related Nephropathy: A Single Center Experience.
J Clin Med. 2021 Feb 16;10(4):796.
3.8
Večerić-Haler Ž, Kojc N, Sever M, Zver S, Švajger U, Poženel P, Hartman K, Urdih T, Mlinšek G, Oblak M, Aleš Rigler A, Ihan A, Buturović Ponikvar J, Halloran Philip P, Arnol M.
Case Report: Capillary Leak Syndrome With Kidney Transplant Failure Following Autologous Mesenchymal Stem Cell Therapy: case report.
Frontiers in medicine. Jul. 2021, vol. 8, str. 1-7.
5.1
Boštjančič E, Večerić-Haler Ž, Kojc N.
The role of immune-related miRNAs in the pathology of kidney transplantation.
Biomolecules 2021; 11: 1-15.
4.9
Golobič V, Nosan G, Bertok S, Frelih M, Boštjančič E, Rus R.
A novel mutation of congenital nephrotic syndrome in a Slovenian child eventually receiving a renal transplant.
Croatian medical journal 2021; 62: 187-191.
1.4
Petek T, Frelih M, Marčun-Varda N.
Tubulointerstitial nephritis and uveitis syndrome in an adolescent female: a case report.
Journal of medical case reports. 2021, vol. 15, str. 1-17.
Oblak M, Mlinšek G, Kojc N, Frelih M, Buturović-Ponikvar J, Arnol M. Spot
Spot urine protein excretion in the first year following kidney transplantation associates with allograft rejection phenotype at 1-year surveillance biopsies: an observational national-cohort study.
Frontiers in medicine. Nov. 2021, vol. 8, str. 1-9.
Škoberne A, Škerget M, Kojc N, Frelih M, Aleš A, Večerić-Haler Ž, Borštnar Š, Avguštin Rotar N, Kovač D, Lindič J, Zver S.
Complement activation and cryoglobulinemia are common in monoclonal gammopathy of renal significance : data from a case series.
Clinical nephrology. 2021, vol. 96, suppl. 1, str. s16-s23. ISSN 0301-0430.
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