[1]
Popielarska A., Popielarska M.: Psychiatria wieku rozwojowego. PZWL,
Warszawa 2000.
[2]
Goodman R., Scott S.: Psychiatria dzieci i młodzieży. Urban & Partner,
Wrocław 2000.
[3]
Wolańczyk T., Komender J.: Zaburzenia emocjonalne i behawioralne u
dzieci. PZWL, Warszawa 2005.
[4]
Michałowicz R., Jóźwiak S.: Neurologia dziecięca. Urban & Partner,
Wrocław 2000.
[5]
Pisula E.: Małe dziecko z autyzmem. Gdańskie wydawnictwo
psychologiczne, Gdańsk 2005.
[6]
Yates K., Le Couteur A.: Diagnosing autism. Paediatrics and Child Health
2009; 19: 55-59.
[7]
Bryson S.E.: Brief report: Epidemiology of autism. Journal of autism and
Developmental Disorders 1996; 26: 165-167.
[8]
Baird G., Simonoff E., Pickles A., et al.: Prevalence of disorders of the
autism spectrum in the population cohort of children in south Thames:
the Special Needs and autism Project (SNAP). Lancet 2006; 368: 210-
215.
[9]
Plauche Johnson C., Myers S.M.: Council on Children with Disabilities:
Identification and evaluation of children with autism spectrum disorders.
Pediatrics 2007; 120: 1183-1215.
[10]
Paya Gonzalez B., Fuentes Menchaca N. et al.: Neurobiology of autism:
neuropathology and neuroimaging studies. Actas Esp. Psiquiatr. 2007;
35: 271-276.
[11]
Hardan A.Y., Muddasani S., Vemulapalli M. et al.: An MRI study of
increased cortical thickness in autism. Am. J. Psychiatry 2006; 163:
1290-1292.
[12]
McAlonan G.M., Cheung V., Cheung C. et al.: Maping the brain in autism.
A voxel-based MRI study of volumetric and intercorrelations in autism.
Brain 2005; 128: 268-276.
[13]
Bigler E.D., Tate D.F., Neeley E.S. et al.: Temporal lobe, autism, and
macrocephaly. AJNR Am. J. Neuroradiol. 2003; 24: 2066-2076.
[14]
Palmen S.J., van Engeland H., Hot P.R. et al.: Neuropathological findings
in autism. Brain 2004; 127: 2572-2583.
[15]
Williams JH., Whiten A., Suddendorf T.,et al.: Imitation, mirror neurons
and autism. Neurosci Biobehav Rev. 2001; 25: 287 – 295.
[16]
Cattaneo L., Rizzolatti G.,: The mirror neuron system. Arch Neurol. 2009;
66: 557-560.
[17]
Reddy K.S.: Cytogenetic abnormalities and fragile – X syndrome in
Autism Spectrum Disorder. BMC Med. Genet. 2005; 18: 3-6.
[18]
Christian S.L., Brune C.W., Sudi J. Et al.: Novel submicroscopic
chromosomal abnormalities detected in autism spectrum disorder. Biol.
Psychiatry 2008; 63: 1111-1117.
[19]
Weiss L.A., Shen Y., Korn J.M. et al.: Association between microdeletion
and microduplication at 16p11.2 and autism. N. Engl. J. Med. 2008; 358:
667-675.
[20]
Morrow B.: Identifying autism loci and genes by tracing recent shared
ancestry. Science 2008; 321: 218-223.
[21]
Jamain S., Radyushkin K., Hammerschmidt K. et al.: Reduced social
interaction and ultrasonic communication in a mouse model of monogenic
heritable autism. Proc. Natl. Acad. Sci. USA 2008; 105: 1710-1715.
[22]
Janusonis S.: Origin of the blood hyperserotonemia of autism. Theor.
Biol. Med. Model 2008; 22: 5-10.
[23]
Melke J., Goubran Botros H., Chaste P. et al.: Abnormal melatonin
synthesis in autism spectrum disorders. Mol. Psychiatry 2008; 13: 90-
98.
[24]
Wing L.: The history of ideas on autism. Autism 1997; 1: 12-21.
[25]
Rutter M.: Aetiology of autism: findings and guestions. J. IntellectDisabil.
Res. 2005;49: 231-238.
[26]
Dover C.J., Le Couteur A.: How to diagnose autism. Arch. Dis. Child.
2007; 92: 540-545.
[27]
Bryson S.E.: Rogers S.J., Fombonne E.: Autism spectrum disorders:
Early detection, intervention, education, and psychopharmacological
management. Can. J. Psychiatry 2003; 48: 506-516.