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J Neurophysiol. 2018; 120(6):2788-2795.
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Expert Opin Pharmacother. 2014; 15(18):2653-71.
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Clin Neurophysiol. 2014; 126(3):626-33.
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IKAP deficiency in an FD mouse model and in oligodendrocyte precursor cells results in downregulation of genes involved in oligodendrocyte differentiation and myelin formation.
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Disturbances in affective touch in hereditary sensory & autonomic neuropathy type III.
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Int J Psychophysiol. 2014; 93(1):56-61.
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Relationship between proprioception at the knee joint and gait ataxia in HSAN III.
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Mov Disord. 2013; 28(6):823-7.
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Cardiac-locked bursts of muscle sympathetic nerve activity are absent in familial dysautonomia.
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Can loss of muscle spindle afferents explain the ataxic gait in Riley-Day syndrome?.
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Brain. 2011; 134(Pt 11):3198-208.
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The molecular basis of familial dysautonomia: overview, new discoveries and implications for directed therapies.
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A world without pain or tears.
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