Jeck N - Search Results

1

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.

2

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.

3

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

4

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.

5

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: jeck n. Pflugers Arch. 2002 Jun;444(3):411-8. doi: 10.1007/s00424-002-0819-8. Epub 2002 Apr 9. Pflugers Arch. 2002. PMID: 12111250

6

Classification and rescue of ROMK mutations underlying hyperprostaglandin E syndrome/antenatal Bartter syndrome.

Peters M, Ermert S, Jeck N, Derst C, Pechmann U, Weber S, Schlingmann KP, Seyberth HW, Waldegger S, Konrad M. Peters M, et al. Among authors: jeck n. Kidney Int. 2003 Sep;64(3):923-32. doi: 10.1046/j.1523-1755.2003.00153.x. Kidney Int. 2003. PMID: 12911542 Free article.

7

A common sequence variation of the CLCNKB gene strongly activates ClC-Kb chloride channel activity.

Jeck N, Waldegger P, Doroszewicz J, Seyberth H, Waldegger S. Jeck N, et al. Kidney Int. 2004 Jan;65(1):190-7. doi: 10.1111/j.1523-1755.2004.00363.x. Kidney Int. 2004. PMID: 14675050 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

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

10

Loop disorders: insights derived from defined genotypes.

Jeck N, Seyberth HW. Jeck N, et al. Nephron Physiol. 2011;118(1):p7-14. doi: 10.1159/000320882. Epub 2010 Nov 11. Nephron Physiol. 2011. PMID: 21071987

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