Konrad M - Search Results

1

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: konrad m. Am J Med. 2002 Feb 15;112(3):183-90. doi: 10.1016/s0002-9343(01)01086-5. Am J Med. 2002. PMID: 11893344

2

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: konrad m. 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

3

Hereditary Hypokalemic Salt-losing Tubular Disorders.

Peters M, Konrad M, Seyberth HW. Peters M, et al. Among authors: konrad m. Saudi J Kidney Dis Transpl. 2003 Jul-Sep;14(3):386-97. Saudi J Kidney Dis Transpl. 2003. PMID: 17657111

4

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

Jeck N, Konrad M, Hess M, Seyberth HW. Jeck N, et al. Among authors: konrad m. 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.

5

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

6

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: konrad m. J Pediatr. 2001 Sep;139(3):398-406. doi: 10.1067/mpd.2001.117007. J Pediatr. 2001. PMID: 11562620 Clinical Trial.

7

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

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

8

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

9

Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.

Weber S, Schneider L, Peters M, Misselwitz J, Rönnefarth G, Böswald M, Bonzel KE, Seeman T, Suláková T, Kuwertz-Bröking E, Gregoric A, Palcoux JB, Tasic V, Manz F, Schärer K, Seyberth HW, Konrad M. Weber S, et al. Among authors: konrad m. J Am Soc Nephrol. 2001 Sep;12(9):1872-1881. doi: 10.1681/ASN.V1291872. J Am Soc Nephrol. 2001. PMID: 11518780

10

Primary gene structure and expression studies of rodent paracellin-1.

Weber S, Schlingmann KP, Peters M, Nejsum LN, Nielsen S, Engel H, Grzeschik KH, Seyberth HW, Gröne HJ, Nüsing R, Konrad M. Weber S, et al. Among authors: konrad m. J Am Soc Nephrol. 2001 Dec;12(12):2664-2672. doi: 10.1681/ASN.V12122664. J Am Soc Nephrol. 2001. PMID: 11729235

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