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1. Management and efficacy of intensified insulin therapy starting in outpatients


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2. Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseases

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3390538
http://www.ncbi.nlm.nih.gov/pubmed/22675081  
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3. Genomic anatomy of the Tyrp1 (brown) deletion complex

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1450144
http://www.ncbi.nlm.nih.gov/pubmed/16505357  
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4. HTT-lowering reverses Huntington's disease immune dysfunction caused by NF kappa B pathway dysregulation


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5. HTT-lowering reverses Huntington's disease immune dysfunction caused by NF kappa B pathway dysregulation


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6. No association with common Caucasian genotypes in exons 8, 13 and 14 of the human cytoplasmic dynein heavy chain gene (DNCHC1) and familial motor neuron disorders


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7. Genomic anatomy of the Tyrp1 (brown) deletion complex


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