Weber S - Search Results

1

Clinical course and NPHS2 analysis in patients with late steroid-resistant nephrotic syndrome.

Schwaderer P, Knüppel T, Konrad M, Mehls O, Schärer K, Schaefer F, Weber S. Schwaderer P, et al. Among authors: weber s. Pediatr Nephrol. 2008 Feb;23(2):251-6. doi: 10.1007/s00467-007-0653-5. Epub 2007 Nov 14. Pediatr Nephrol. 2008. PMID: 18000687

2

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. J Am Soc Nephrol. 2001 Sep;12(9):1872-1881. doi: 10.1681/ASN.V1291872. J Am Soc Nephrol. 2001. PMID: 11518780

3

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. J Am Soc Nephrol. 2001 Dec;12(12):2664-2672. doi: 10.1681/ASN.V12122664. J Am Soc Nephrol. 2001. PMID: 11729235

4

Recent advances in molecular genetics of hereditary magnesium-losing disorders.

Konrad M, Weber S. Konrad M, et al. Among authors: weber s. J Am Soc Nephrol. 2003 Jan;14(1):249-60. doi: 10.1097/01.asn.0000049161.60740.ce. J Am Soc Nephrol. 2003. PMID: 12506158 Review.

5

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: weber s. Kidney Int. 2003 Sep;64(3):923-32. doi: 10.1046/j.1523-1755.2003.00153.x. Kidney Int. 2003. PMID: 12911542 Free article.

6

NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.

Weber S, Gribouval O, Esquivel EL, Morinière V, Tête MJ, Legendre C, Niaudet P, Antignac C. Weber S, et al. Kidney Int. 2004 Aug;66(2):571-9. doi: 10.1111/j.1523-1755.2004.00776.x. Kidney Int. 2004. PMID: 15253708 Free article.

7

Hypomagnesemia with hypercalciuria and nephrocalcinosis: case report and a family study.

Tasic V, Dervisov D, Koceva S, Weber S, Konrad M. Tasic V, et al. Among authors: weber s. Pediatr Nephrol. 2005 Jul;20(7):1003-6. doi: 10.1007/s00467-005-1853-5. Epub 2005 Apr 26. Pediatr Nephrol. 2005. PMID: 15856319

8

Gene locus ambiguity in posterior urethral valves/prune-belly syndrome.

Weber S, Mir S, Schlingmann KP, Nürnberg G, Becker C, Kara PE, Ozkayin N, Konrad M, Nürnberg P, Schaefer F. Weber S, et al. Pediatr Nephrol. 2005 Aug;20(8):1036-42. doi: 10.1007/s00467-005-1977-7. Epub 2005 May 24. Pediatr Nephrol. 2005. PMID: 15912376

9

Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia.

Schlingmann KP, Sassen MC, Weber S, Pechmann U, Kusch K, Pelken L, Lotan D, Syrrou M, Prebble JJ, Cole DE, Metzger DL, Rahman S, Tajima T, Shu SG, Waldegger S, Seyberth HW, Konrad M. Schlingmann KP, et al. Among authors: weber s. J Am Soc Nephrol. 2005 Oct;16(10):3061-9. doi: 10.1681/ASN.2004110989. Epub 2005 Aug 17. J Am Soc Nephrol. 2005. PMID: 16107578

10

Recurrence of focal-segmental glomerulosclerosis in children after renal transplantation: clinical and genetic aspects.

Weber S, Tönshoff B. Weber S, et al. Transplantation. 2005 Sep 27;80(1 Suppl):S128-34. doi: 10.1097/01.tp.0000187110.25512.82. Transplantation. 2005. PMID: 16286890 Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

3,591 results

Search Page

Filters