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Neurology|August 10, 2000
Proximal myotonic myopathy: evidence for anticipation in families with linkage to chromosome 3qC Schneider, A Ziegler, K Ricker, et al.Neurology|January 1, 1997
Proximal myotonic myopathy with MRI white matter abnormalities of the brainE Hund, O Jansen, M C Koch, et al.Neurology|January 5, 2002
A sporadic case of rippling muscle disease caused by a de novo caveolin-3 mutationM Vorgerd, K Ricker, F Ziemssen, et al.Science (New York, N.Y.)|August 4, 2001
Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9C L Liquori, K Ricker, M L Moseley, et al.The Journal of Clinical Investigation|April 20, 1999
Motor neuropathy in porphobilinogen deaminase-deficient mice imitates the peripheral neuropathy of human acute porphyriaR L Lindberg, R Martini, M Baumgartner, et al.Science (New York, N.Y.)|August 7, 1992
The skeletal muscle chloride channel in dominant and recessive human myotoniaM C Koch, K Steinmeyer, C Lorenz, et al.Journal of Medical Genetics|September 1, 1991
Confirmation of linkage of hyperkalaemic periodic paralysis to chromosome 17M C Koch, K Ricker, M Otto, et al.Human Genetics|November 1, 1991
Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17M C Koch, K Ricker, M Otto, et al.Neurology|December 30, 2004
Sudden cardiac death in myotonic dystrophy type 2B G H Schoser, K Ricker, C Schneider-Gold, et al.Neurology|January 28, 1999
Linkage of proximal myotonic myopathy to chromosome 3qK Ricker, T Grimm, M C Koch, et al.Pageof 10