Zerres K - Search Results

1

A point mutation in the human connexin32 promoter P2 does not correlate with X-linked dominant Charcot-Marie-Tooth neuropathy in Germany.

Bergmann C, Schröder JM, Rudnik-Schöneborn S, Zerres K, Senderek J. Bergmann C, et al. Among authors: zerres k. Brain Res Mol Brain Res. 2001 Mar 31;88(1-2):183-5. doi: 10.1016/s0169-328x(01)00040-7. Brain Res Mol Brain Res. 2001. PMID: 11295246

2

Phenotypic variation of a novel nonsense mutation in the P0 intracellular domain.

Senderek J, Ramaekers VT, Zerres K, Rudnik-Schöneborn S, Schröder JM, Bergmann C. Senderek J, et al. Among authors: zerres k. J Neurol Sci. 2001 Nov 15;192(1-2):49-51. doi: 10.1016/s0022-510x(01)00591-3. J Neurol Sci. 2001. PMID: 11701152

3

Allelic variants in the 5' non-coding region of the connexin32 gene: possible pitfalls in the diagnosis of X linked Charcot-Marie-Tooth neuropathy (CMTX).

Bergmann C, Zerres K, Rudnik-Schöneborn S, Eggermann T, Schröder JM, Senderek J. Bergmann C, et al. Among authors: zerres k. J Med Genet. 2002 Sep;39(9):e58. doi: 10.1136/jmg.39.9.e58. J Med Genet. 2002. PMID: 12205128 Free PMC article. No abstract available.

4

Autosomal recessive polycystic kidney disease does not map to the second gene locus for autosomal dominant polycystic kidney disease on chromosome 4.

Zerres K, Mücher G, Rudnik-Schöneborn S. Zerres K, et al. Hum Genet. 1994 Jun;93(6):697-8. doi: 10.1007/BF00201574. Hum Genet. 1994. PMID: 8005596

5

Pregnancy and delivery in Charcot-Marie-Tooth disease type 1.

Rudnik-Schöneborn S, Röhrig D, Nicholson G, Zerres K. Rudnik-Schöneborn S, et al. Among authors: zerres k. Neurology. 1993 Oct;43(10):2011-6. doi: 10.1212/wnl.43.10.2011. Neurology. 1993. PMID: 8413959

6

Current status of DNA diagnosis for hereditary nephropathies.

Zerres K, Rudnik-Schöneborn S. Zerres K, et al. Kidney Blood Press Res. 1996;19(3-4):209-14. doi: 10.1159/000174076. Kidney Blood Press Res. 1996. PMID: 8887263 Review.

7

[Genetically-induced kidney diseases].

Zerres K, Rudnik-Schöneborn S. Zerres K, et al. Internist (Berl). 1999 May;40(5):534-42. doi: 10.1007/s001080050367. Internist (Berl). 1999. PMID: 10407763 Review. German. No abstract available.

8

DNA diagnosis in hereditary nephropathies.

Zerres K, Eggermann T, Rudnik-Schöneborn S. Zerres K, et al. Clin Nephrol. 2001 Sep;56(3):181-92. Clin Nephrol. 2001. PMID: 11597032

9

Diagnostic algorithms in Charcot-Marie-Tooth neuropathies: experiences from a German genetic laboratory on the basis of 1206 index patients.

Rudnik-Schöneborn S, Tölle D, Senderek J, Eggermann K, Elbracht M, Kornak U, von der Hagen M, Kirschner J, Leube B, Müller-Felber W, Schara U, von Au K, Wieczorek D, Bußmann C, Zerres K. Rudnik-Schöneborn S, et al. Among authors: zerres k. Clin Genet. 2016 Jan;89(1):34-43. doi: 10.1111/cge.12594. Epub 2015 Apr 29. Clin Genet. 2016. PMID: 25850958

10

Childhood onset autosomal dominant polycystic kidney disease in sibs: clinical picture and recurrence risk. German Working Group on Paediatric Nephrology (Arbeitsgemeinschaft für Pädiatrische Nephrologie.

Zerres K, Rudnik-Schöneborn S, Deget F. Zerres K, et al. J Med Genet. 1993 Jul;30(7):583-8. doi: 10.1136/jmg.30.7.583. J Med Genet. 1993. PMID: 8411032 Free PMC article.

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