Jeck N - Search Results

1

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. Pediatrics. 2001 Jul;108(1):E5. doi: 10.1542/peds.108.1.e5. Pediatrics. 2001. PMID: 11433084

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: jeck n. 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

Antenatal Bartter syndrome with sensorineural deafness: refinement of the locus on chromosome 1p31.

Vollmer M, Jeck N, Lemmink HH, Vargas R, Feldmann D, Konrad M, Beekmann F, van Den Heuvel LP, Deschenes G, Guay-Woodford LM, Antignac C, Seyberth HW, Hildebrandt F, Knoers NV. Vollmer M, et al. Among authors: jeck n. Nephrol Dial Transplant. 2000 Jul;15(7):970-4. doi: 10.1093/ndt/15.7.970. Nephrol Dial Transplant. 2000. PMID: 10862633

4

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

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

5

Pharmacotyping of hypokalaemic salt-losing tubular disorders.

Reinalter SC, Jeck N, Peters M, Seyberth HW. Reinalter SC, et al. Among authors: jeck n. 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.

6

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: jeck n. J Am Soc Nephrol. 2000 Aug;11(8):1449-1459. doi: 10.1681/ASN.V1181449. J Am Soc Nephrol. 2000. PMID: 10906158

7

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: jeck n. Kidney Int. 2002 Jul;62(1):253-60. doi: 10.1046/j.1523-1755.2002.00435.x. Kidney Int. 2002. PMID: 12081585 Free article.

8

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: jeck n. 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.

9

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. 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.

10

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: jeck n. 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

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