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Year Number of Results
1997 1
2001 1
2007 1
2008 1
2009 1
2011 2
2012 3
2013 1
2014 1
2016 1
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2020 3
2021 1
2022 2
2023 4
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22 results

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Page 1
Clinical practice recommendations for primary hyperoxaluria: an expert consensus statement from ERKNet and OxalEurope.
Groothoff JW, Metry E, Deesker L, Garrelfs S, Acquaviva C, Almardini R, Beck BB, Boyer O, Cerkauskiene R, Ferraro PM, Groen LA, Gupta A, Knebelmann B, Mandrile G, Moochhala SS, Prytula A, Putnik J, Rumsby G, Soliman NA, Somani B, Bacchetta J. Groothoff JW, et al. Among authors: putnik j. Nat Rev Nephrol. 2023 Mar;19(3):194-211. doi: 10.1038/s41581-022-00661-1. Epub 2023 Jan 5. Nat Rev Nephrol. 2023. PMID: 36604599 Review.
[Transient pseudohypoaldosteronism].
Stajić N, Putnik J, Paripović A, Bogdanović R. Stajić N, et al. Among authors: putnik j. Srp Arh Celok Lek. 2011 Jan-Feb;139(1-2):37-43. doi: 10.2298/sarh1102037s. Srp Arh Celok Lek. 2011. PMID: 21568081 Free article. Serbian.
Modeling of ACTN4-Based Podocytopathy Using Drosophila Nephrocytes.
Odenthal J, Dittrich S, Ludwig V, Merz T, Reitmeier K, Reusch B, Höhne M, Cosgun ZC, Hohenadel M, Putnik J, Göbel H, Rinschen MM, Altmüller J, Koehler S, Schermer B, Benzing T, Beck BB, Brinkkötter PT, Habbig S, Bartram MP. Odenthal J, et al. Among authors: putnik j. Kidney Int Rep. 2022 Oct 31;8(2):317-329. doi: 10.1016/j.ekir.2022.10.024. eCollection 2023 Feb. Kidney Int Rep. 2022. PMID: 36815115 Free PMC article.
Exome sequencing in individuals with congenital anomalies of the kidney and urinary tract (CAKUT): a single-center experience.
Riedhammer KM, Ćomić J, Tasic V, Putnik J, Abazi-Emini N, Paripovic A, Stajic N, Meitinger T, Nushi-Stavileci V, Berutti R, Braunisch MC, Hoefele J. Riedhammer KM, et al. Among authors: putnik j. Eur J Hum Genet. 2023 Jun;31(6):674-680. doi: 10.1038/s41431-023-01331-x. Epub 2023 Mar 16. Eur J Hum Genet. 2023. PMID: 36922632 Free PMC article.
[Congenital nephrotic syndrome].
Stajić N, Putnik J, Paripović A, Djurić S, Bogdanović R. Stajić N, et al. Among authors: putnik j. Srp Arh Celok Lek. 2008 Dec;136 Suppl 4:307-11. doi: 10.2298/sarh08s4307s. Srp Arh Celok Lek. 2008. PMID: 20804100 Free article. Serbian.
The multifaceted phenotypic and genotypic spectrum of type-IV-collagen-related nephropathy-A human genetics department experience.
Ćomić J, Riedhammer KM, Günthner R, Schaaf CW, Richthammer P, Simmendinger H, Kieffer D, Berutti R, Tasic V, Abazi-Emini N, Nushi-Stavileci V, Putnik J, Stajic N, Lungu A, Gross O, Renders L, Heemann U, Braunisch MC, Meitinger T, Hoefele J. Ćomić J, et al. Among authors: putnik j. Front Med (Lausanne). 2022 Aug 31;9:957733. doi: 10.3389/fmed.2022.957733. eCollection 2022. Front Med (Lausanne). 2022. PMID: 36117978 Free PMC article.
22 results