Seyberth HW - Search Results

1

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.

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

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.

4

Late-onset manifestation of antenatal Bartter syndrome as a result of residual function of the mutated renal Na+-K+-2Cl- co-transporter.

Pressler CA, Heinzinger J, Jeck N, Waldegger P, Pechmann U, Reinalter S, Konrad M, Beetz R, Seyberth HW, Waldegger S. Pressler CA, et al. Among authors: seyberth hw. J Am Soc Nephrol. 2006 Aug;17(8):2136-42. doi: 10.1681/ASN.2005101071. Epub 2006 Jun 28. J Am Soc Nephrol. 2006. PMID: 16807401

5

Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype.

Jeck N, Konrad M, Peters M, Weber S, Bonzel KE, Seyberth HW. Jeck N, et al. Among authors: seyberth hw. Pediatr Res. 2000 Dec;48(6):754-8. doi: 10.1203/00006450-200012000-00009. Pediatr Res. 2000. PMID: 11102542

6

The diuretic- and Bartter-like salt-losing tubulopathies.

Jeck N, Konrad M, Hess M, Seyberth HW. Jeck N, et al. Among authors: seyberth hw. Nephrol Dial Transplant. 2000;15 Suppl 6:19-20. doi: 10.1093/ndt/15.suppl_6.19. Nephrol Dial Transplant. 2000. PMID: 11143975 No abstract available.

7

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

8

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.

9

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.

10

Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome.

Konrad M, Vollmer M, Lemmink HH, VAN DEN Heuvel LPWJ, Jeck N, Vargas-Poussou R, Lakings A, Ruf R, Deschênes G, Antignac C, Guay-Woodford L, Knoers NVAM, Seyberth HW, Feldmann D, Hildebrandt F. Konrad M, et al. Among authors: seyberth hw. J Am Soc Nephrol. 2000 Aug;11(8):1449-1459. doi: 10.1681/ASN.V1181449. J Am Soc Nephrol. 2000. PMID: 10906158

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