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Diagnosis and management of Bartter syndrome: executive summary of the consensus and recommendations from the European Rare Kidney Disease Reference Network Working Group for Tubular Disorders.
Konrad M, Nijenhuis T, Ariceta G, Bertholet-Thomas A, Calo LA, Capasso G, Emma F, Schlingmann KP, Singh M, Trepiccione F, Walsh SB, Whitton K, Vargas-Poussou R, Bockenhauer D. Konrad M, et al. Among authors: schlingmann kp. Kidney Int. 2021 Feb;99(2):324-335. doi: 10.1016/j.kint.2020.10.035. Kidney Int. 2021. PMID: 33509356 Free article.
Insights into the molecular nature of magnesium homeostasis.
Konrad M, Schlingmann KP, Gudermann T. Konrad M, et al. Among authors: schlingmann kp. Am J Physiol Renal Physiol. 2004 Apr;286(4):F599-605. doi: 10.1152/ajprenal.00312.2003. Am J Physiol Renal Physiol. 2004. PMID: 15001450 Free article. Review.
TRPM6 and TRPM7--Gatekeepers of human magnesium metabolism.
Schlingmann KP, Waldegger S, Konrad M, Chubanov V, Gudermann T. Schlingmann KP, et al. Biochim Biophys Acta. 2007 Aug;1772(8):813-21. doi: 10.1016/j.bbadis.2007.03.009. Epub 2007 Apr 3. Biochim Biophys Acta. 2007. PMID: 17481860 Free article. Review.
The case | hypercalcemia in a 60-year-old male.
Helmuth A, Konrad M, Schlingmann KP, Pasch A. Helmuth A, et al. Among authors: schlingmann kp. Kidney Int. 2014 Jan;85(1):219-21. doi: 10.1038/ki.2013.184. Kidney Int. 2014. PMID: 24380919 Free article. No abstract available.
Polyhydramnios, Transient Antenatal Bartter's Syndrome, and MAGED2 Mutations.
Laghmani K, Beck BB, Yang SS, Seaayfan E, Wenzel A, Reusch B, Vitzthum H, Priem D, Demaretz S, Bergmann K, Duin LK, Göbel H, Mache C, Thiele H, Bartram MP, Dombret C, Altmüller J, Nürnberg P, Benzing T, Levtchenko E, Seyberth HW, Klaus G, Yigit G, Lin SH, Timmer A, de Koning TJ, Scherjon SA, Schlingmann KP, Bertrand MJ, Rinschen MM, de Backer O, Konrad M, Kömhoff M. Laghmani K, et al. Among authors: schlingmann kp. N Engl J Med. 2016 May 12;374(19):1853-63. doi: 10.1056/NEJMoa1507629. Epub 2016 Apr 27. N Engl J Med. 2016. PMID: 27120771 Free article.
Germline De Novo Mutations in ATP1A1 Cause Renal Hypomagnesemia, Refractory Seizures, and Intellectual Disability.
Schlingmann KP, Bandulik S, Mammen C, Tarailo-Graovac M, Holm R, Baumann M, König J, Lee JJY, Drögemöller B, Imminger K, Beck BB, Altmüller J, Thiele H, Waldegger S, Van't Hoff W, Kleta R, Warth R, van Karnebeek CDM, Vilsen B, Bockenhauer D, Konrad M. Schlingmann KP, et al. Am J Hum Genet. 2018 Nov 1;103(5):808-816. doi: 10.1016/j.ajhg.2018.10.004. Am J Hum Genet. 2018. PMID: 30388404 Free PMC article.
Juvenile onset IIH and CYP24A1 mutations.
Schlingmann KP, Cassar W, Konrad M. Schlingmann KP, et al. Bone Rep. 2018 Jun 21;9:42-46. doi: 10.1016/j.bonr.2018.06.005. eCollection 2018 Dec. Bone Rep. 2018. PMID: 30591926 Free PMC article.
70 results