Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Moderately mentally retarded"'
Autor:
Ngcanga, Nosipho Margaret
The purpose of this study was to investigate the possibility of implementing community based care for moderately mentally retarded persons in a specific centre in the Port Elizabeth area. The objectives of the study were to identify • the needs of
Externí odkaz:
http://hdl.handle.net/10500/17566
Publikováno v:
Developmental Medicine & Child Neurology. 37:715-722
SUMMARY The present study represents the first effort to assess systematically the cognitive functioning of a population of individuals with Lesch-Nyhan syndrome using standardized psychometric instruments. Seven residents from a special hospital set
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91ac39430b2755e9e5ab82089ec14340
https://doi.org/10.1111/j.1469-8749.1995.tb15017.x
https://doi.org/10.1111/j.1469-8749.1995.tb15017.x
Publikováno v:
Journal of Intellectual Disability Research. 33:487-492
Effects of verbalization on discrimination reversal learning for moderately mentally retarded children were examined under three training conditions. Predicted results indicated that verbalization of both appropriate and inappropriate cues within rel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a813d22f9e68bec2f70716cdd9d0387
https://doi.org/10.1111/j.1365-2788.1989.tb01504.x
https://doi.org/10.1111/j.1365-2788.1989.tb01504.x
Publikováno v:
Clinical Genetics. 41:42-45
A mother of normal intelligence and her moderately mentally retarded son, both with the typical facial features of the Brachmann-de Lange syndrome, are reported. We discuss the variable expression of the Brachmann-de Lange syndrome by comparing the a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72b4dc78058c4666727b0370c9fc6a2b
https://doi.org/10.1111/j.1399-0004.1992.tb03628.x
https://doi.org/10.1111/j.1399-0004.1992.tb03628.x
Publikováno v:
Journal of Intellectual Disability Research. 34:29-40
In this paper, the authors report the results of a genetic-diagnostic survey of 262 instutionalized moderately mentally retarded patients and compare these data with their previous studies of the severely mentally retarded. Special attention is given
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cc773f0523d73c459bf49998551ae15
https://doi.org/10.1111/j.1365-2788.1990.tb01512.x
https://doi.org/10.1111/j.1365-2788.1990.tb01512.x
Publikováno v:
Journal of Intellectual Disability Research. 30:331-339
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::974029c1186a374d31ab744c2c7e5640
https://doi.org/10.1111/j.1365-2788.1986.tb01328.x
https://doi.org/10.1111/j.1365-2788.1986.tb01328.x
Publikováno v:
Clinical Genetics. 32:61-65
This report summarizes the clinical and cytogenetic findings in a 16-year-old moderately mentally retarded girl with 10q11.2----10q22 duplication. The phenotypic findings are identical to those found in one other patient with the same autosomal dupli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f1e4d86291deb36dbb13c38781ead6c
https://doi.org/10.1111/j.1399-0004.1987.tb03325.x
https://doi.org/10.1111/j.1399-0004.1987.tb03325.x
Publikováno v:
Neurology. 62:795-798
A pair of monozygotic male twins with tuberous sclerosis (TS) were followed between 18 months and 3 years of age. Twin A with 25 large cortical tubers and hence extensive brain involvement was moderately mentally retarded and met criteria for autism.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b8681082e7d9a1e7c4d1ca6e959c36f
https://doi.org/10.1212/01.wnl.0000113745.58425.ef
https://doi.org/10.1212/01.wnl.0000113745.58425.ef
Publikováno v:
Clinical Genetics. 26:445-447
Two fragile X chromosomes were found in 20% of the cells in a moderately mentally retarded patient with Klinefelter syndrome.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ebd1b272a4dc3ff7b7ef96d04ae5ec7
https://doi.org/10.1111/j.1399-0004.1984.tb01086.x
https://doi.org/10.1111/j.1399-0004.1984.tb01086.x
Publikováno v:
Clinical Genetics. 43:232-234
In this report we document male-to-male transmission in the hand-foot-genital syndrome. An affected father transmitted the syndrome to his three sons. A grade IV hypospadias, which was the most severe genital anomaly in affected males, was present in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab7eb59b7898c17382c448ca276d0bb1
https://doi.org/10.1111/j.1399-0004.1993.tb03808.x
https://doi.org/10.1111/j.1399-0004.1993.tb03808.x