Co-Authors
This is a "connection" page, showing publications co-authored by TETSUO ASHIZAWA and YADOLLAH HARATI.
Connection Strength
0.214
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Somatic instability of CTG repeat in myotonic dystrophy. Neurology. 1993 Dec; 43(12):2674-8.
Score: 0.116
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A "dystrophic" variant of autosomal recessive myotonia congenita caused by novel mutations in the CLCN1 gene. Neurology. 2000 Dec 12; 55(11):1697-703.
Score: 0.047
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Clinical features of Todd's post-epileptic paralysis. J Neurol Neurosurg Psychiatry. 1992 Jan; 55(1):63-4.
Score: 0.025
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A dominantly inherited syndrome with continuous motor neuron discharges. Ann Neurol. 1983 Mar; 13(3):285-90.
Score: 0.014
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Somatic sequence variation at the Friedreich ataxia locus includes complete contraction of the expanded GAA triplet repeat, significant length variation in serially passaged lymphoblasts and enhanced mutagenesis in the flanking sequence. Hum Mol Genet. 1999 Dec; 8(13):2425-36.
Score: 0.011