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458 results
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Page 1
Salt wasting and deafness resulting from mutations in two chloride channels.
Schlingmann KP, Konrad M, Jeck N, Waldegger P, Reinalter SC, Holder M, Seyberth HW, Waldegger S. Schlingmann KP, et al. Among authors: konrad m. N Engl J Med. 2004 Mar 25;350(13):1314-9. doi: 10.1056/NEJMoa032843. N Engl J Med. 2004. PMID: 15044642 Free article. No abstract available.
Barttin mutations in antenatal Bartter syndrome with sensorineural deafness.
Ozlu F, Yapicioğlu H, Satar M, Narli N, Ozcan K, Buyukcelik M, Konrad M, Demirhan O. Ozlu F, et al. Among authors: konrad m. Pediatr Nephrol. 2006 Jul;21(7):1056-7. doi: 10.1007/s00467-006-0108-4. Epub 2006 May 24. Pediatr Nephrol. 2006. PMID: 16773427 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: konrad m. 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.
Mutations in CYP24A1 and idiopathic infantile hypercalcemia.
Schlingmann KP, Kaufmann M, Weber S, Irwin A, Goos C, John U, Misselwitz J, Klaus G, Kuwertz-Bröking E, Fehrenbach H, Wingen AM, Güran T, Hoenderop JG, Bindels RJ, Prosser DE, Jones G, Konrad M. Schlingmann KP, et al. Among authors: konrad m. N Engl J Med. 2011 Aug 4;365(5):410-21. doi: 10.1056/NEJMoa1103864. Epub 2011 Jun 15. N Engl J Med. 2011. PMID: 21675912 Free article.
Hereditary Hypokalemic Salt-losing Tubular Disorders.
Peters M, Konrad M, Seyberth HW. Peters M, et al. Among authors: konrad m. Saudi J Kidney Dis Transpl. 2003 Jul-Sep;14(3):386-97. Saudi J Kidney Dis Transpl. 2003. PMID: 17657111 Free article.
Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia.
Schlingmann KP, Sassen MC, Weber S, Pechmann U, Kusch K, Pelken L, Lotan D, Syrrou M, Prebble JJ, Cole DE, Metzger DL, Rahman S, Tajima T, Shu SG, Waldegger S, Seyberth HW, Konrad M. Schlingmann KP, et al. Among authors: konrad m. J Am Soc Nephrol. 2005 Oct;16(10):3061-9. doi: 10.1681/ASN.2004110989. Epub 2005 Aug 17. J Am Soc Nephrol. 2005. PMID: 16107578 Free article.
Insights into the molecular nature of magnesium homeostasis.
Konrad M, Schlingmann KP, Gudermann T. Konrad M, et al. 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.
458 results