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Page 1
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: seyberth hw. 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.
Bartter's and Gitelman's syndrome.
Seyberth HW, Weber S, Kömhoff M. Seyberth HW, et al. Curr Opin Pediatr. 2017 Apr;29(2):179-186. doi: 10.1097/MOP.0000000000000447. Curr Opin Pediatr. 2017. PMID: 27906863 Review.
Genetics of hereditary disorders of magnesium homeostasis.
Schlingmann KP, Konrad M, Seyberth HW. Schlingmann KP, et al. Among authors: seyberth hw. Pediatr Nephrol. 2004 Jan;19(1):13-25. doi: 10.1007/s00467-003-1293-z. Epub 2003 Nov 22. Pediatr Nephrol. 2004. PMID: 14634861 Review.
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: seyberth hw. 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.
Hereditary Hypokalemic Salt-losing Tubular Disorders.
Peters M, Konrad M, Seyberth HW. Peters M, et al. Among authors: seyberth hw. Saudi J Kidney Dis Transpl. 2003 Jul-Sep;14(3):386-97. Saudi J Kidney Dis Transpl. 2003. PMID: 17657111
210 results