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Developmental Medicine and Child Neurology|June 1, 1988
The basic care needs of profoundly mentally retarded children with multiple handicapsB Hagberg, K Edebol-Tysk, B EdströmJournal of Medical Genetics|September 1, 1996
Rett syndrome, classical and atypical: genealogical support for common originH O Akesson, B Hagberg, J WahlströmBrain & Development|May 1, 1992
Tokyo symposium on the Rett syndrome: neurobiological approach--concluding remarks and epilogueB Hagberg, S Naidu, A K PercyElectroencephalography and Clinical Neurophysiology|January 1, 1989
EEG development in Rett syndrome. A study of 30 casesI Hagne, I Witt-Engerström, B HagbergAmerican Journal of Medical Genetics|March 3, 1997
Identification of mutations in the CACNL1A3 gene in 13 families of Scandinavian origin having hypokalemic periodic paralysis and evidence of a founder effect in Danish familiesA Sillén, T Sørensen, I Kantola, et al.Neuropediatrics|February 1, 1989
Epidemiology of spastic tetraplegic cerebral palsy in Sweden. II. Prevalence, birth data and originK Edebol-Tysk, B Hagberg, G HagbergHuman Genetics|January 1, 1980
Y-to-X chromosome translocation observed in two generationsH O Akesson, B Hagberg, J WahlströmAmerican Journal of Medical Genetics|March 1, 1993
New X-linked syndrome with severe mental retardation, severely impaired vision, severe hearing defect, epileptic seizures, spasticity, restricted joint mobility, and early deathK H Gustavson, G Annerén, H Malmgren, et al.Clinical Genetics|May 1, 1985
Effect of folic acid treatment in the fragile X syndromeK H Gustavson, K Dahlbom, A Flood, et al.Journal of Intellectual Disability Research : JIDR|September 11, 2004
Mild intellectual disability in children in Lahore, Pakistan: aetiology and risk factorsM Yaqoob, A Bashir, S Zaman, et al.Pageof 27