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

Year Number of Results
2002 3
2003 7
2004 4
2005 8
2006 5
2007 7
2008 12
2009 14
2010 12
2011 9
2012 8
2013 6
2014 12
2015 6
2016 6
2017 7
2018 15
2019 9
2020 9
2021 10
2022 10
2023 14
2024 3

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170 results

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Page 1
Physiology of a Forgotten Electrolyte-Magnesium Disorders.
Ray E, Mohan K, Ahmad S, Wolf MTF. Ray E, et al. Among authors: wolf mtf. Adv Kidney Dis Health. 2023 Mar;30(2):148-163. doi: 10.1053/j.akdh.2022.12.001. Adv Kidney Dis Health. 2023. PMID: 36868730 Free PMC article. Review.
Autosomal dominant tubulointerstitial kidney disease: diagnosis, classification, and management--A KDIGO consensus report.
Eckardt KU, Alper SL, Antignac C, Bleyer AJ, Chauveau D, Dahan K, Deltas C, Hosking A, Kmoch S, Rampoldi L, Wiesener M, Wolf MT, Devuyst O; Kidney Disease: Improving Global Outcomes. Eckardt KU, et al. Among authors: wolf mt. Kidney Int. 2015 Oct;88(4):676-83. doi: 10.1038/ki.2015.28. Epub 2015 Mar 4. Kidney Int. 2015. PMID: 25738250 Free article.
Nephronophthisis.
Wolf MT, Hildebrandt F. Wolf MT, et al. Pediatr Nephrol. 2011 Feb;26(2):181-94. doi: 10.1007/s00467-010-1585-z. Epub 2010 Jul 22. Pediatr Nephrol. 2011. PMID: 20652329 Free PMC article. Review.
Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly.
Braun DA, Rao J, Mollet G, Schapiro D, Daugeron MC, Tan W, Gribouval O, Boyer O, Revy P, Jobst-Schwan T, Schmidt JM, Lawson JA, Schanze D, Ashraf S, Ullmann JFP, Hoogstraten CA, Boddaert N, Collinet B, Martin G, Liger D, Lovric S, Furlano M, Guerrera IC, Sanchez-Ferras O, Hu JF, Boschat AC, Sanquer S, Menten B, Vergult S, De Rocker N, Airik M, Hermle T, Shril S, Widmeier E, Gee HY, Choi WI, Sadowski CE, Pabst WL, Warejko JK, Daga A, Basta T, Matejas V, Scharmann K, Kienast SD, Behnam B, Beeson B, Begtrup A, Bruce M, Ch'ng GS, Lin SP, Chang JH, Chen CH, Cho MT, Gaffney PM, Gipson PE, Hsu CH, Kari JA, Ke YY, Kiraly-Borri C, Lai WM, Lemyre E, Littlejohn RO, Masri A, Moghtaderi M, Nakamura K, Ozaltin F, Praet M, Prasad C, Prytula A, Roeder ER, Rump P, Schnur RE, Shiihara T, Sinha MD, Soliman NA, Soulami K, Sweetser DA, Tsai WH, Tsai JD, Topaloglu R, Vester U, Viskochil DH, Vatanavicharn N, Waxler JL, Wierenga KJ, Wolf MTF, Wong SN, Leidel SA, Truglio G, Dedon PC, Poduri A, Mane S, Lifton RP, Bouchard M, Kannu P, Chitayat D, Magen D, Callewaert B, van Tilbeurgh H, Zenker M, Antignac C, Hildebrandt F. Braun DA, et al. Among authors: wolf mtf. Nat Genet. 2017 Oct;49(10):1529-1538. doi: 10.1038/ng.3933. Epub 2017 Aug 14. Nat Genet. 2017. PMID: 28805828 Free PMC article.
Nephronophthisis: a pathological and genetic perspective.
Wolf MTF, Bonsib SM, Larsen CP, Hildebrandt F. Wolf MTF, et al. Pediatr Nephrol. 2023 Nov 6. doi: 10.1007/s00467-023-06174-8. Online ahead of print. Pediatr Nephrol. 2023. PMID: 37930417 Review.
Uromodulin in mineral metabolism.
Wolf MTF, Zhang J, Nie M. Wolf MTF, et al. Curr Opin Nephrol Hypertens. 2019 Sep;28(5):481-489. doi: 10.1097/MNH.0000000000000522. Curr Opin Nephrol Hypertens. 2019. PMID: 31205055 Free PMC article. Review.
Nephronophthisis and related syndromes.
Wolf MT. Wolf MT. Curr Opin Pediatr. 2015 Apr;27(2):201-11. doi: 10.1097/MOP.0000000000000194. Curr Opin Pediatr. 2015. PMID: 25635582 Free PMC article. Review.
Distinguishing species.
Müller T, Philippi N, Dandekar T, Schultz J, Wolf M. Müller T, et al. Among authors: wolf m. RNA. 2007 Sep;13(9):1469-72. doi: 10.1261/rna.617107. Epub 2007 Jul 24. RNA. 2007. PMID: 17652131 Free PMC article.
Paramecium: RNA sequence-structure phylogenetics.
Weimer M, Vďačný P, Wolf M. Weimer M, et al. Among authors: wolf m. Int J Syst Evol Microbiol. 2023 Apr;73(4). doi: 10.1099/ijsem.0.005744. Int J Syst Evol Microbiol. 2023. PMID: 37022772
Pediatric Gastric Mucosal Calcinosis.
Ngai D, Wolf M, Kelley S, Goyal A. Ngai D, et al. Among authors: wolf m. JPGN Rep. 2022 Jul 25;3(3):e212. doi: 10.1097/PG9.0000000000000212. eCollection 2022 Aug. JPGN Rep. 2022. PMID: 37168627 Free PMC article.
170 results