Hageman A, Gabreels F, Liem KD, et al. Congenital myotonic dystrophy: report on 13 cases and a review of the literature. J Neurol Sci. 1993;115:95-101.
Hakamada S, Kumagai T, Hara K. Congenital hypomyelination neuropathy in a newborn. Neuropediatrics. 1983;14:182-183.
Hart ZH, Chang CH, DiMauro S, et al. Muscle carnitine deficiency and fatal cardiomyopathy. Neurology. 1978;28:147-151.
Heckmatt JZ, Sewry CA, Hodes D, et al. Congenital centronuclear (myotubular) myopathy. A clinical, pathological and genetic study in eight children. Brain. 1985;108:941-964.
Hogan GR, Gutmann I, Schmidt R, et al. Pompe’s disease. Neurology. 1969;19:894-900.
Jones HR JR, Bulton CF, Harper CM Jr. Pediatric Clinical Electromyography. Philadelphia, Penn: Lippincott-Raven; 1996.
Lipsitz PJ, English IC. Hypermagnesemia in the newborn infant. Pediatrics. 1967;40:856-862.
McMenamin JB, Becker LE, Murphy EG. Congenital muscular dystrophy: a clinicopathologic report of 24 cases. J Pediatr. 1982;100:692-697.
Munsat TL, Piper D, Cancilla P. Inflammatory myopathy with facioscapulohumeral distribution. Neurology. 1972;22:335-347.
Namba T, Brown SB, Grob D. Neonatal myasthenia gravis: report of two cases and review of the literature. Pediatrics. 1970;45:488-504.
Ouvrier RA. Giant axonal neuropathy. A review. Brain Dev. 1989;11:207-214.
Papazian O. Transient neonatal myasthenia gravis. J Child Neurol. 1992;7:135-141.
Pickett J, Berg B, Chaplin E, et al. Syndrome of botulism in infancy: clinical and electrophysiologic study. N Engl J Med. 1976;295:770-772.
Ptacek LJ, Johnson KJ, Griggs RC. Genetics and physiology of the myotonic muscle disorders. N Engl J Med. 1993;328:482-489.