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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1972 1
1975 1
1996 3
1997 5
1998 4
1999 2
2000 3
2001 8
2002 6
2003 4
2004 6
2005 7
2006 10
2007 7
2008 9
2009 6
2010 8
2011 13
2012 18
2013 10
2014 7
2015 9
2016 7
2017 15
2018 11
2019 4
2020 2
2021 4
2022 6
2023 7
2024 3

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168 results

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Page 1
A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome.
Sadowski CE, Lovric S, Ashraf S, Pabst WL, Gee HY, Kohl S, Engelmann S, Vega-Warner V, Fang H, Halbritter J, Somers MJ, Tan W, Shril S, Fessi I, Lifton RP, Bockenhauer D, El-Desoky S, Kari JA, Zenker M, Kemper MJ, Mueller D, Fathy HM, Soliman NA; SRNS Study Group; Hildebrandt F. Sadowski CE, et al. Among authors: kemper mj. J Am Soc Nephrol. 2015 Jun;26(6):1279-89. doi: 10.1681/ASN.2014050489. Epub 2014 Oct 27. J Am Soc Nephrol. 2015. PMID: 25349199 Free PMC article.
Long-Term Efficacy and Safety of Repeated Rituximab to Maintain Remission in Idiopathic Childhood Nephrotic Syndrome: An International Study.
Chan EY, Yu ELM, Angeletti A, Arslan Z, Basu B, Boyer O, Chan CY, Colucci M, Dorval G, Dossier C, Drovandi S, Ghiggeri GM, Gipson DS, Hamada R, Hogan J, Ishikura K, Kamei K, Kemper MJ, Ma AL, Parekh RS, Radhakrishnan S, Saini P, Shen Q, Sinha R, Subun C, Teo S, Vivarelli M, Webb H, Xu H, Yap HK, Tullus K. Chan EY, et al. Among authors: kemper mj. J Am Soc Nephrol. 2022 Jun;33(6):1193-1207. doi: 10.1681/ASN.2021111472. Epub 2022 Mar 30. J Am Soc Nephrol. 2022. PMID: 35354600 Free PMC article.
Treatment of Genetic Forms of Nephrotic Syndrome.
Kemper MJ, Lemke A. Kemper MJ, et al. Front Pediatr. 2018 Mar 26;6:72. doi: 10.3389/fped.2018.00072. eCollection 2018. Front Pediatr. 2018. PMID: 29632851 Free PMC article. Review.
Pathogenesis, diagnosis and management of hyperkalemia.
Lehnhardt A, Kemper MJ. Lehnhardt A, et al. Among authors: kemper mj. Pediatr Nephrol. 2011 Mar;26(3):377-84. doi: 10.1007/s00467-010-1699-3. Epub 2010 Dec 22. Pediatr Nephrol. 2011. PMID: 21181208 Free PMC article. Review.
Effects of Burosumab Treatment on Mineral Metabolism in Children and Adolescents With X-linked Hypophosphatemia.
Ewert A, Rehberg M, Schlingmann KP, Hiort O, John-Kroegel U, Metzing O, Wühl E, Schaefer F, Kemper MJ, Derichs U, Richter-Unruh A, Patzer L, Albers N, Dunstheimer D, Haberland H, Heger S, Schröder C, Jorch N, Schmid E, Staude H, Weitz M, Freiberg C, Leifheit-Nestler M, Zivicnjak M, Schnabel D, Haffner D. Ewert A, et al. Among authors: kemper mj. J Clin Endocrinol Metab. 2023 Sep 18;108(10):e998-e1006. doi: 10.1210/clinem/dgad223. J Clin Endocrinol Metab. 2023. PMID: 37097907
Primary hyperoxaluria type 2.
Kemper MJ, Conrad S, Müller-Wiefel DE. Kemper MJ, et al. Eur J Pediatr. 1997 Jul;156(7):509-12. doi: 10.1007/s004310050649. Eur J Pediatr. 1997. PMID: 9243228 Review.
Commentary on "Pediatric Idiopathic Steroid-sensitive Nephrotic Syndrome Diagnosis and Therapy - Short version of the updated German Best Practice Guideline (S2e)".
Ehren R, Benz MR, Brinkkötter PT, Dötsch J, Eberl WR, Gellermann J, Hoyer PF, Jordans I, Kamrath C, Kemper MJ, Latta K, Müller D, Oh J, Tönshoff B, Weber S, Weber LT; German Society for Pediatric Nephrology. Ehren R, et al. Among authors: kemper mj. Pediatr Nephrol. 2021 Oct;36(10):2961-2966. doi: 10.1007/s00467-021-05136-2. Epub 2021 Jun 5. Pediatr Nephrol. 2021. PMID: 34091755 Free PMC article. No abstract available.
Body growth, upper arm fat area, and clinical parameters in children with nephropathic cystinosis compared with other pediatric chronic kidney disease entities.
Kluck R, Müller S, Jagodzinski C, Hohenfellner K, Büscher A, Kemper MJ, Oh J, Billing H, Thumfart J, Weber LT, Acham-Roschitz B, Arbeiter K, Tönshoff B, Hagenberg M, Kanzelmeyer N, Pavičić L, Haffner D, Zivicnjak M. Kluck R, et al. Among authors: kemper mj. J Inherit Metab Dis. 2022 Mar;45(2):192-202. doi: 10.1002/jimd.12473. Epub 2022 Jan 14. J Inherit Metab Dis. 2022. PMID: 34989402
A multicenter retrospective study of calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene variants.
Malakasioti G, Iancu D, Milovanova A, Tsygin A, Horinouchi T, Nagano C, Nozu K, Kamei K, Fujinaga S, Iijima K, Sinha R, Basu B, Morello W, Montini G, Waters A, Boyer O, Yıldırım ZY, Yel S, Dursun İ, McCarthy HJ, Vivarelli M, Prikhodina L, Besouw MTP, Chan EY, Huang W, Kemper MJ, Loos S, Prestidge C, Wong W, Zlatanova G, Ehren R, Weber LT, Chehade H, Hooman N, Tkaczyk M, Stańczyk M, Miligkos M, Tullus K; CNI in Monogenic SRNS Study Investigators. Malakasioti G, et al. Among authors: kemper mj. Kidney Int. 2023 May;103(5):962-972. doi: 10.1016/j.kint.2023.02.022. Epub 2023 Mar 8. Kidney Int. 2023. PMID: 36898413
168 results