Seyberth HW - Search Results

1

Pharmacotyping of hypokalaemic salt-losing tubular disorders.

Reinalter SC, Jeck N, Peters M, Seyberth HW. Reinalter SC, et al. Among authors: seyberth hw. Acta Physiol Scand. 2004 Aug;181(4):513-21. doi: 10.1111/j.1365-201X.2004.01325.x. Acta Physiol Scand. 2004. PMID: 15283765 Review.

2

Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies.

Peters M, Jeck N, Reinalter S, Leonhardt A, Tönshoff B, Klaus G Gü, Konrad M, Seyberth HW. Peters M, et al. Among authors: seyberth hw. Am J Med. 2002 Feb 15;112(3):183-90. doi: 10.1016/s0002-9343(01)01086-5. Am J Med. 2002. PMID: 11893344

3

Salt handling in the distal nephron: lessons learned from inherited human disorders.

Jeck N, Schlingmann KP, Reinalter SC, Kömhoff M, Peters M, Waldegger S, Seyberth HW. Jeck N, et al. Among authors: seyberth hw. Am J Physiol Regul Integr Comp Physiol. 2005 Apr;288(4):R782-95. doi: 10.1152/ajpregu.00600.2004. Am J Physiol Regul Integr Comp Physiol. 2005. PMID: 15793031 Free article. Review.

4

Hypokalemic salt-losing tubulopathy with chronic renal failure and sensorineural deafness.

Jeck N, Reinalter SC, Henne T, Marg W, Mallmann R, Pasel K, Vollmer M, Klaus G, Leonhardt A, Seyberth HW, Konrad M. Jeck N, et al. Among authors: seyberth hw. Pediatrics. 2001 Jul;108(1):E5. doi: 10.1542/peds.108.1.e5. Pediatrics. 2001. PMID: 11433084

5

Evaluation of long-term treatment with indomethacin in hereditary hypokalemic salt-losing tubulopathies.

Reinalter SC, Gröne HJ, Konrad M, Seyberth HW, Klaus G. Reinalter SC, et al. Among authors: seyberth hw. J Pediatr. 2001 Sep;139(3):398-406. doi: 10.1067/mpd.2001.117007. J Pediatr. 2001. PMID: 11562620 Clinical Trial.

6

Hereditary hypokalemic salt-losing tubulopathies: Bartter-like syndromes.

Peters M, Jeck N, Seyberth HW, Konrad M. Peters M, et al. Among authors: seyberth hw. Contrib Nephrol. 2001;(136):157-73. doi: 10.1159/000060186. Contrib Nephrol. 2001. PMID: 11688378 Review. No abstract available.

7

Impaired response to furosemide in hyperprostaglandin E syndrome: evidence for a tubular defect in the loop of Henle.

Köckerling A, Reinalter SC, Seyberth HW. Köckerling A, et al. Among authors: seyberth hw. J Pediatr. 1996 Oct;129(4):519-28. doi: 10.1016/s0022-3476(96)70116-6. J Pediatr. 1996. PMID: 8859258 Clinical Trial.

8

Role of cyclooxygenase-2 in hyperprostaglandin E syndrome/antenatal Bartter syndrome.

Reinalter SC, Jeck N, Brochhausen C, Watzer B, Nüsing RM, Seyberth HW, Kömhoff M. Reinalter SC, et al. Among authors: seyberth hw. Kidney Int. 2002 Jul;62(1):253-60. doi: 10.1046/j.1523-1755.2002.00435.x. Kidney Int. 2002. PMID: 12081585 Free article.

9

Barttin increases surface expression and changes current properties of ClC-K channels.

Waldegger S, Jeck N, Barth P, Peters M, Vitzthum H, Wolf K, Kurtz A, Konrad M, Seyberth HW. Waldegger S, et al. Among authors: seyberth hw. Pflugers Arch. 2002 Jun;444(3):411-8. doi: 10.1007/s00424-002-0819-8. Epub 2002 Apr 9. Pflugers Arch. 2002. PMID: 12111250

10

Induction of microsomal prostaglandin E2 synthase in the macula densa in children with hypokalemic salt-losing tubulopathies.

Kömhoff M, Reinalter SC, Gröne HJ, Seyberth HW. Kömhoff M, et al. Among authors: seyberth hw. Pediatr Res. 2004 Feb;55(2):261-6. doi: 10.1203/01.PDR.0000101747.09626.6B. Epub 2003 Nov 19. Pediatr Res. 2004. PMID: 14630996

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