References
- Burns J, Joseph PD, Rose KJ et al. 2009. Effect of oral curcumin on Dejerine-Sottas disease. Pediatric Neurology 41:305–308.
- Chung KW, Sunwoo IN, Kim SM et al. 2005. Two missense mutations of EGR2 R359W and GJB1 V136A in a Charcot-Marie-Tooth disease family. Neurogenetics 6:159–163.
- Donker ME, Eijckelhof BH, Tan GM et al. 2009. Serial postural and motor assessment of Fetal Akinesia Deformation Sequence (FADS). Early Human Development 85:785–790.
- Pearce JM. 2006. Dejerine-Sottas disease (progressive hypertrophic polyneuropathy). European Neurology 55:115–117.
- Ten Hof J, Nijhuis IJ, Mulder EJ et al. 2002. Longitudinal study of fetal body movements: Nomograms, intrafetal consistency, and relationship with episodes of heart rate patterns A and B. Pediatric Research 52:568–575.
- de Vries JI, Visser GH, Prechtl HF. 1982. The emergence of fetal behaviour. I. Qualitative aspects. Early Human Development 7:301–322.
- Wilmshurst JM, Pollard JD, Nicholson G et al. 2003. Peripheral neuropathies of infancy. Developmental Medicine & Child Neurology 45:408–414.