Sarnat HB. New insights into the pathogenesis of congenital myopathies. J Child Neurol. 1994;9:193-201.
Schapira D, Swash W. Neonatal spinal muscular atrophy presenting as respiratory distress: a clinical variant. Muscle Nerve. 1985;8:661-663.
Shelbourne P, Davies J, Buxton J, et al. Direct diagnosis of myotonic dystrophy with a disease-specific DNA marker. N Eng J Med. 1993;328:471-475.
Sladky JT, Brown MJ, Berman PH. Chronic inflammatory demyelinating polyneuropathy of infancy: a corticosteroid-responsive disorder. Ann Neurol. 1986;20:76-81.
Thompson JA, Glasgow LA, Warpinski JR, et al. Infant botulism: clinical spectrum and epidemiology. Pediatrics. 1980;66:936-942.
Volpe JJ. Neuromuscular disorders: motor system, evaluation, and arthrogryposis multiplex congenita. In: Neurology of the Newborn. Philadelphia, Penn: WB Saunders Co; 1995a:585-605.
Volpe JJ. Neuromuscular disorders: levels above the lower motor neuron to the neuromuscular junction. In: Neurology of the Newborn. Philadelphia, Penn: WB Saunders CO; 1995b:606-633.
Zellweger H, Afifi A, McCormick WF, et al. Severe congenital muscular dystrophy. Am J Dis Child. 1967;114:591-602.