Ricker K - Search Results

1

Homozygosity for CCTG mutation in myotonic dystrophy type 2.

Schoser BG, Kress W, Walter MC, Halliger-Keller B, Lochmüller H, Ricker K. Schoser BG, et al. Among authors: ricker k. Brain. 2004 Aug;127(Pt 8):1868-77. doi: 10.1093/brain/awh210. Epub 2004 Jul 1. Brain. 2004. PMID: 15231584

2

Muscle pathology in 57 patients with myotonic dystrophy type 2.

Schoser BG, Schneider-Gold C, Kress W, Goebel HH, Reilich P, Koch MC, Pongratz DE, Toyka KV, Lochmüller H, Ricker K. Schoser BG, et al. Among authors: ricker k. Muscle Nerve. 2004 Feb;29(2):275-81. doi: 10.1002/mus.10545. Muscle Nerve. 2004. PMID: 14755494

3

Sudden cardiac death in myotonic dystrophy type 2.

Schoser BG, Ricker K, Schneider-Gold C, Hengstenberg C, Dürre J, Bültmann B, Kress W, Day JW, Ranum LP. Schoser BG, et al. Among authors: ricker k. Neurology. 2004 Dec 28;63(12):2402-4. doi: 10.1212/01.wnl.0000147335.10783.e4. Neurology. 2004. PMID: 15623712 Review.

4

Linkage of proximal myotonic myopathy to chromosome 3q.

Ricker K, Grimm T, Koch MC, Schneider C, Kress W, Reimers CD, Schulte-Mattler W, Mueller-Myhsok B, Toyka KV, Mueller CR. Ricker K, et al. Neurology. 1999 Jan 1;52(1):170-1. doi: 10.1212/wnl.52.1.170. Neurology. 1999. PMID: 9921867

5

Proximal myotonic myopathy: evidence for anticipation in families with linkage to chromosome 3q.

Schneider C, Ziegler A, Ricker K, Grimm T, Kress W, Reimers CD, Meinck H, Reiners K, Toyka KV. Schneider C, et al. Among authors: ricker k. Neurology. 2000 Aug 8;55(3):383-8. doi: 10.1212/wnl.55.3.383. Neurology. 2000. PMID: 10932272

6

A sporadic case of rippling muscle disease caused by a de novo caveolin-3 mutation.

Vorgerd M, Ricker K, Ziemssen F, Kress W, Goebel HH, Nix WA, Kubisch C, Schoser BG, Mortier W. Vorgerd M, et al. Among authors: ricker k. Neurology. 2001 Dec 26;57(12):2273-7. doi: 10.1212/wnl.57.12.2273. Neurology. 2001. PMID: 11756609

7

Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrum.

Day JW, Ricker K, Jacobsen JF, Rasmussen LJ, Dick KA, Kress W, Schneider C, Koch MC, Beilman GJ, Harrison AR, Dalton JC, Ranum LP. Day JW, et al. Among authors: ricker k. Neurology. 2003 Feb 25;60(4):657-64. doi: 10.1212/01.wnl.0000054481.84978.f9. Neurology. 2003. PMID: 12601109

8

Myotonic dystrophy type 2: human founder haplotype and evolutionary conservation of the repeat tract.

Liquori CL, Ikeda Y, Weatherspoon M, Ricker K, Schoser BG, Dalton JC, Day JW, Ranum LP. Liquori CL, et al. Among authors: ricker k. Am J Hum Genet. 2003 Oct;73(4):849-62. doi: 10.1086/378720. Epub 2003 Sep 22. Am J Hum Genet. 2003. PMID: 14505273 Free PMC article.

9

Proof of genetic heterogeneity in the proximal myotonic myopathy syndrome (PROMM) and its relationship to myotonic dystrophy type 2 (DM2).

Kress W, Mueller-Myhsok B, Ricker K, Schneider C, Koch MC, Toyka KV, Mueller CR, Grimm T. Kress W, et al. Among authors: ricker k. Neuromuscul Disord. 2000 Oct;10(7):478-80. doi: 10.1016/s0960-8966(00)00129-2. Neuromuscul Disord. 2000. PMID: 10996776

10

Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9.

Liquori CL, Ricker K, Moseley ML, Jacobsen JF, Kress W, Naylor SL, Day JW, Ranum LP. Liquori CL, et al. Among authors: ricker k. Science. 2001 Aug 3;293(5531):864-7. doi: 10.1126/science.1062125. Science. 2001. PMID: 11486088

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