[1]
Hausmanowa-Petrusewicz I.: Elektromiografia kliniczna. PZWL,
Warszawa 1986: 134-185.
[2]
Hausmanowa-Petrusewicz I. (red).: Choroby nerwowo-mięśniowe.
Wydawnictwo Czelej, Lublin 2005: 35-140.
[3]
Jones H.R.Jr.: Pediatric Electromyography. [w:] Brown W., Botton C.
Clinical Electromyography. Second Edition, Butterworth-Heinemann,
Boston 1993, Chapter 25: 693-738.
[4]
Do Carmo R.J.: Motor unit action potential parameters in human newborn
infants. Arch Neurol 1960; 3: 136-140.
[5]
Sacco G., Buchthal F., Rosenfalck P.: Motor unit potentials at different
ages. Arch Neurol 1962; 6: 366-373.
[6]
Koenigsberger M.R., Patten B., Lovelace R.E.: Studies of neuromuscular
function in the newborn: A comparison of myoneural function in the full
term and the premature infant. Neuropaediatrie 1973; 4: 350-361.
[7]
Cornblath D.R.: Disorders of neuromuscular transmission in infants and
children. Muscle Nerve 1986; 9: 606-611.
[8]
Michałowicz R., Jóźwiak S. [red.]: Neurologia Dziecięca. Urban & Partner,
Wrocław 2000: 73-83.
[9]
Jóźwiak S.: Standardy postępowania w chorobach nerwowomięśniowych
u dzieci. Standardy Medyczne 2004; 6: 74-87.
[10]
Jones H.R.Jr.: EMG evaluation of the floppy infant: Differential diagnosis
and technical aspects. Muscle Nerve 1990; 13: 338-347.
[11]
Kroczka S.: Wskazania do nadania EMG w neuropediatrii. [w:] Kaciński
M. (red.) Neuropediatria. Wydawnictwo Lekarskie PZWL, Warszawa
2007: 448-451.
[12]
Packer R.J., Brown M.J., Berman P.H.: The diagnostic value of
electromyography in infantile hypotonia. Am J Dis Child 1982; 136:
1057-1059.
[13]
Miller V.S., Delgado M., Iannaccone S.T.: Neonatal hypotonia. Semin
Neurol 1993; 13: 73-83.
[14]
Buchthal F., Olsen P.Z.: Electromyography and muscle biopsy in infantile
spinal muscular atrophy. Brain 1970; 93: 15-30.
[15]
Hausmanowa-Petrusewicz I., Karwanska A.: Electromyographic findings
in different forms of infantile and juvenile proximal muscular atrophy.
Muscle Nerve 1986; 9: 37-46.
[16]
David W.S., Jones H.R.Jr.: Electromyographic evaluation of the floppy
infant. (abstr). Nerve Muscle 1990; 13: 857.
[17]
Kunz N.L., Daube J.R.: Electrophysiologic profile of childhood spinal
muscular atrophy. Muscle Nerve 1982; 5: S106.
[18]
Kaye E.M., Doll R.F., Natowicz M.R. et al.: Pelizaeus-Merzbacher disease
presenting as spinal muscular atrophy: clinical and molecular studies.
Ann Neurol 1994; 36: 916-919.
[19]
Kaiboriboon K., Hayat G.: Congenital cervical spinal atrophy: an
intrauterine hipoxic insult. Neuropediatrics 2001; 32: 330-334.
[20]
Ryniewicz B.: Dystrofie mięśniowe. Neurologica 2003; 2: 35-38.
[21]
Szapłyko W.: Badania elektroneurograficzne. [w:] Michałowicz R.,
Jóźwiak S. [red.] Neurologia dziecięca. Wydawnictwo Urban & Partner,
Wrocław 2000: 72-73.
[22]
Webster H.F., Favilla J.T.: Development of peripheral nerve fibers.
[w:] Dyck P.J., Thomas P.K., Lambert E.H., Bunge R. (ed.) Peripheral
neuropathy, vol.1, 2nd ed. Philadelphia: W.B. Saunders, 1984: 329-359.
[23]
Garcia A., Calleja J., Antolin F.M. et al.: Peripheral motor and sensory
nerve conduction studies in normal infants and children. Clin Neurophysiol
2000; 111: 513-520.
[24]
Cai F., Zhang J.: Study of nerve conduction and late responses in normal
Chinese infants, children and adults. J Child Neurol 1997; 12: 13-18.
[25]
Hyllienmark L., Ludvigsson J., Brismar T.: Normal values of nerve
conduction in children and adolescents. Electroecephalography and
Clinical Neurophysiology 1995; 97: 208-214.
[26]
Mayer R.F., Feldoman R.G.: Observations of the nature of the F-vawe in
man. Neurology 1967; 17: 147-156.
[27]
Yasumoto S., Mitsudome A.: F-waves in neonates: increased spinal
anterior horn motor neuron excitability. Brain Dev 2004; 26: 8-11.
[28]
Wagner A.L., Buchthal F.: Motor and sensory conduction in infancy and
childhood: reappraisal. Dev Med Child Neurol 1972; 14: 189-216.
[29]
Sladky J.T.: Guillain-Barre syndrome in children. J Child Neurol 2004; 19:
191-200.
[30]
Hiraga A., Mori M., Ogawara K. et al.: Differences in patterns of
progression in demyelinating and axonal Guillain-Barre syndromes.
Neurology 2003; 61: 471-474.
[31]
Ammache Z., Afifi A.K., Brown C.K. et al.: Childhood Guillain-Barre
syndrome: clinical and electrophysiologic features predictive of outcome.
J Child Neurol 2001; 16: 477-4783.
[32]
Pourmand R.: Evaluating patients with suspected peripheral neuropathy:
do the right think, not everything. Muscle Nerve 2002; 26: 288-290.
[33]
Nordwall M., Hyllienmark L., Ludvigsson J.: Early diabetic complications
in a population of young patients with type 1 diabetes mellitus despite
intensive treatment. J Pediatr Endocrinol Metab 2006; 19: 45-54.
[34]
Stickler D.E., Valenstein E., Neiberger R.E. et al.: Peripheral neuropathy in
genetic mitochondrial diseases. Pediatr Neurol 2006; 34: 127-131.