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Genetic aspects of congenital nephrotic syndrome: a consensus statement from the ERKNet-ESPN inherited glomerulopathy working group.
Lipska-Ziętkiewicz BS, Ozaltin F, Hölttä T, Bockenhauer D, Bérody S, Levtchenko E, Vivarelli M, Webb H, Haffner D, Schaefer F, Boyer O. Lipska-Ziętkiewicz BS, et al. Among authors: levtchenko e. Eur J Hum Genet. 2020 Oct;28(10):1368-1378. doi: 10.1038/s41431-020-0642-8. Epub 2020 May 28. Eur J Hum Genet. 2020. PMID: 32467597 Free PMC article.
Renal phenotype in Lowe Syndrome: a selective proximal tubular dysfunction.
Bockenhauer D, Bokenkamp A, van't Hoff W, Levtchenko E, Kist-van Holthe JE, Tasic V, Ludwig M. Bockenhauer D, et al. Among authors: levtchenko e. Clin J Am Soc Nephrol. 2008 Sep;3(5):1430-6. doi: 10.2215/CJN.00520108. Epub 2008 May 14. Clin J Am Soc Nephrol. 2008. PMID: 18480301 Free PMC article.
Improvement in the renal prognosis in nephropathic cystinosis.
Van Stralen KJ, Emma F, Jager KJ, Verrina E, Schaefer F, Laube GF, Lewis MA, Levtchenko EN. Van Stralen KJ, et al. Among authors: levtchenko en. Clin J Am Soc Nephrol. 2011 Oct;6(10):2485-91. doi: 10.2215/CJN.02000311. Epub 2011 Aug 25. Clin J Am Soc Nephrol. 2011. PMID: 21868618 Free PMC article.
Clinical utility gene card for: cystinosis.
Levtchenko E, van den Heuvel L, Emma F, Antignac C. Levtchenko E, et al. Eur J Hum Genet. 2014 May;22(5). doi: 10.1038/ejhg.2013.204. Epub 2013 Sep 18. Eur J Hum Genet. 2014. PMID: 24045844 Free PMC article. No abstract available.
Clinical utility gene card for: Dent disease (Dent-1 and Dent-2).
Ludwig M, Levtchenko E, Bökenkamp A. Ludwig M, et al. Among authors: levtchenko e. Eur J Hum Genet. 2014 Nov;22(11):1338. doi: 10.1038/ejhg.2014.33. Epub 2014 Mar 12. Eur J Hum Genet. 2014. PMID: 24619144 Free PMC article. No abstract available.
Clinical utility gene card for: Lowe syndrome.
Bökenkamp A, Levtchenko E, Recker F, Ludwig M. Bökenkamp A, et al. Among authors: levtchenko e. Eur J Hum Genet. 2015 Jun;23(6):889-. doi: 10.1038/ejhg.2014.177. Epub 2014 Sep 3. Eur J Hum Genet. 2015. PMID: 25182134 Free PMC article. No abstract available.
Treatment and long-term outcome in primary distal renal tubular acidosis.
Lopez-Garcia SC, Emma F, Walsh SB, Fila M, Hooman N, Zaniew M, Bertholet-Thomas A, Colussi G, Burgmaier K, Levtchenko E, Sharma J, Singhal J, Soliman NA, Ariceta G, Basu B, Murer L, Tasic V, Tsygin A, Decramer S, Gil-Peña H, Koster-Kamphuis L, La Scola C, Gellermann J, Konrad M, Lilien M, Francisco T, Tramma D, Trnka P, Yüksel S, Caruso MR, Chromek M, Ekinci Z, Gambaro G, Kari JA, König J, Taroni F, Thumfart J, Trepiccione F, Winding L, Wühl E, Ağbaş A, Belkevich A, Vargas-Poussou R, Blanchard A, Conti G, Boyer O, Dursun I, Pınarbaşı AS, Melek E, Miglinas M, Novo R, Mallett A, Milosevic D, Szczepanska M, Wente S, Cheong HI, Sinha R, Gucev Z, Dufek S, Iancu D; European dRTA Consortium; Kleta R, Schaefer F, Bockenhauer D. Lopez-Garcia SC, et al. Among authors: levtchenko e. Nephrol Dial Transplant. 2019 Jun 1;34(6):981-991. doi: 10.1093/ndt/gfy409. Nephrol Dial Transplant. 2019. PMID: 30773598
FGF23 and its role in X-linked hypophosphatemia-related morbidity.
Beck-Nielsen SS, Mughal Z, Haffner D, Nilsson O, Levtchenko E, Ariceta G, de Lucas Collantes C, Schnabel D, Jandhyala R, Mäkitie O. Beck-Nielsen SS, et al. Among authors: levtchenko e. Orphanet J Rare Dis. 2019 Feb 26;14(1):58. doi: 10.1186/s13023-019-1014-8. Orphanet J Rare Dis. 2019. PMID: 30808384 Free PMC article. Review.
Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia.
Haffner D, Emma F, Eastwood DM, Duplan MB, Bacchetta J, Schnabel D, Wicart P, Bockenhauer D, Santos F, Levtchenko E, Harvengt P, Kirchhoff M, Di Rocco F, Chaussain C, Brandi ML, Savendahl L, Briot K, Kamenicky P, Rejnmark L, Linglart A. Haffner D, et al. Among authors: levtchenko e. Nat Rev Nephrol. 2019 Jul;15(7):435-455. doi: 10.1038/s41581-019-0152-5. Nat Rev Nephrol. 2019. PMID: 31068690 Free PMC article.
287 results