RALF KRAHE to Aged
This is a "connection" page, showing publications RALF KRAHE has written about Aged.
Connection Strength
0.060
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Mutant (CCTG)n expansion causes abnormal expression of zinc finger protein 9 (ZNF9) in myotonic dystrophy type 2. Am J Pathol. 2010 Dec; 177(6):3025-36.
Score: 0.016
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Effect of myotonic dystrophy trinucleotide repeat expansion on DMPK transcription and processing. Genomics. 1995 Jul 01; 28(1):1-14.
Score: 0.005
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De novo myotonic dystrophy mutation in a Nigerian kindred. Am J Hum Genet. 1995 May; 56(5):1067-74.
Score: 0.005
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Most expression and splicing changes in myotonic dystrophy type 1 and type 2 skeletal muscle are shared with other muscular dystrophies. Neuromuscul Disord. 2014 Mar; 24(3):227-40.
Score: 0.005
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Joint effects of germ-line TP53 mutation, MDM2 SNP309, and gender on cancer risk in family studies of Li-Fraumeni syndrome. Hum Genet. 2011 Jun; 129(6):663-73.
Score: 0.004
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Myotonic dystrophy type 2 found in two of sixty-three persons diagnosed as having fibromyalgia. Arthritis Rheum. 2008 Nov; 58(11):3627-31.
Score: 0.003
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High frequency of co-segregating CLCN1 mutations among myotonic dystrophy type 2 patients from Finland and Germany. J Neurol. 2008 Nov; 255(11):1731-6.
Score: 0.003
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Similar brain tau pathology in DM2/PROMM and DM1/Steinert disease. Neurology. 2005 Nov 22; 65(10):1636-8.
Score: 0.003
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Proximal myotonic dystrophy mimicking progressive muscular atrophy. Eur J Neurol. 2005 Feb; 12(2):160-1.
Score: 0.003
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POLG mutations in neurodegenerative disorders with ataxia but no muscle involvement. Neurology. 2004 Oct 12; 63(7):1251-7.
Score: 0.003
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New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2). Neuromuscul Disord. 2004 Apr; 14(4):274-83.
Score: 0.002
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Executive dysfunction and avoidant personality trait in myotonic dystrophy type 1 (DM-1) and in proximal myotonic myopathy (PROMM/DM-2). Neuromuscul Disord. 2003 Dec; 13(10):813-21.
Score: 0.002
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Multiple founder effects and geographical clustering of BRCA1 and BRCA2 families in Finland. Eur J Hum Genet. 2000 Oct; 8(10):757-63.
Score: 0.002
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Proximal myotonic dystrophy--a family with autosomal dominant muscular dystrophy, cataracts, hearing loss and hypogonadism: heterogeneity of proximal myotonic syndromes? Neuromuscul Disord. 1997 Jun; 7(4):217-28.
Score: 0.002
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Myotonic dystrophy phenotype without expansion of (CTG)n repeat: an entity distinct from proximal myotonic myopathy (PROMM)? J Neurol. 1996 Oct; 243(10):715-21.
Score: 0.001