Results 171 to 180 of about 272,074 (239)

Severe neuropsychiatric manifestations in a 17-year-old male with a 20p13 interstitial deletion encompassing CSNK2A1: a case report. [PDF]

J Med Case Rep
Laubach JP, Zeeb D, Weber S, Becker K, Seipelt P.   +4 more
europepmc   +1 more source

A Novel Variant of the <i>CHD8</i> Gene in a Patient with Autism Spectrum Disorder. [PDF]

Genes (Basel)
Falcone E, Bauleo A, De Stefano L, Brando R, Maietta S, Tabolacci E, Montesanto A, Pace V, Apa R, Puntorieri D, Cento L, Cuconato G, Muoio MG, Genuardi M.   +13 more
europepmc   +1 more source

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Infantile Autism in Kenya

Indian Journal of Pediatrics, 1982
Clinical features of infantile autism in three African children from Kenya are described. There is no essential difference in features of childhood autism as described in the west. In this prospective study the authors were able to confirm the onset of major symptoms of infantile autism before the age of three years and also an upper socio-economic ...
Dhadphale, M, Lukwago, M G, Gajjar, M
exaly   +3 more sources

Association Between Idiopathic Infantile Macrocephaly and Autism Spectrum Disorders

Lancet, The, 2001
We conducted a case-controlled, catch-up study of a cohort of boys born with macrocephaly in order to determine whether infantile macrocephaly is a risk marker for the later development of autism spectrum disorders.
Patrick Bolton, Andrew Pickles, P F Bolton   +2 more
exaly   +2 more sources

Infantile Autism

Neurologic Clinics, 1984
The authors define infantile autism, giving its time of manifestation, clinical development, differential diagnosis, management, and treatment. They hypothesize that the cause of autism probably will not be found in some consistent gross alteration in brain size or gross structure but that autistic children have some generalized deficit of neurologic ...
W, DeMyer, M, DeMyer
openaire   +2 more sources