Current developments in the understanding of mental retardation. Part I / Joel D. Bregman en Annual progress in child psychiatry and child develoment, Año 1992 ([11/11/2020])

Público ISBD [artículo]  inAnnual progress in child psychiatry and child develoment > Año 1992 [11/11/2020] . - pp. 285-312 Título : Current developments in the understanding of mental retardation. Part I : biological and phenomenological perspectives Tipo de documento: texto impreso Autores: Joel D. Bregman, Autor ; Roberth M. Hodapp, Autor Fecha de publicación: 2020 Artículo en la página: pp. 285-312 Idioma : Inglés (eng) Idioma original : Inglés (eng) Palabras clave: Daño cerebral crónico, Diagnóstico diferencial, Discapacidad intelectual, Trastornos neurocognitivos. Resumen: During the past decade, noteworthy advances have taken place within the field of mental retardation. The application of advanced biological techniques in such areas as molecular genetics and neuroimaging has substantially improved our ability to identify the biological factors that underlie the origin and pathogenesis of an increasing number of mental retardation syndromes. Link: ./index.php?lvl=notice_display&id=25223 [artículo] Current developments in the understanding of mental retardation. Part I : biological and phenomenological perspectives [texto impreso] / Joel D. Bregman, Autor ; Roberth M. Hodapp, Autor . - 2020 . - pp. 285-312. Idioma : Inglés (eng) Idioma original : Inglés (eng) in Annual progress in child psychiatry and child develoment > Año 1992 [11/11/2020] . - pp. 285-312 Palabras clave: Daño cerebral crónico, Diagnóstico diferencial, Discapacidad intelectual, Trastornos neurocognitivos. Resumen: During the past decade, noteworthy advances have taken place within the field of mental retardation. The application of advanced biological techniques in such areas as molecular genetics and neuroimaging has substantially improved our ability to identify the biological factors that underlie the origin and pathogenesis of an increasing number of mental retardation syndromes. Link: ./index.php?lvl=notice_display&id=25223

Fragile-X syndrome / Joel D. Bregman en Annual progress in child psychiatry and child develoment, Año 1988 ([23/11/2020])

Público ISBD [artículo]  inAnnual progress in child psychiatry and child develoment > Año 1988 [23/11/2020] . - pp. 468-491 Título : Fragile-X syndrome : variability of phenotypic expression Tipo de documento: texto impreso Autores: Joel D. Bregman, Autor ; Elisabeth Dykens, Autor ; Michael Watson, Autor Fecha de publicación: 2020 Artículo en la página: pp. 468-491 Idioma : Inglés (eng) Idioma original : Inglés (eng) Palabras clave: Síndrome X frágil, Retraso mental ligado al cromosoma X, Autismo infantil, Trastorno por déficit de atención Resumen: Fragile-X syndrome is a recently described X-linked disorder that ranks second to Down syndrome as the most prevalent chromosomal form of mental retardation. Affected male individuals manifest a variable clinical phenotype that includes distinctive facial features, macroorchidism, cognitive and language impairments, and an impressive prevalence of attention deficit disorder and infantile autism. Link: ./index.php?lvl=notice_display&id=25334 [artículo] Fragile-X syndrome : variability of phenotypic expression [texto impreso] / Joel D. Bregman, Autor ; Elisabeth Dykens, Autor ; Michael Watson, Autor . - 2020 . - pp. 468-491. Idioma : Inglés (eng) Idioma original : Inglés (eng) in Annual progress in child psychiatry and child develoment > Año 1988 [23/11/2020] . - pp. 468-491 Palabras clave: Síndrome X frágil, Retraso mental ligado al cromosoma X, Autismo infantil, Trastorno por déficit de atención Resumen: Fragile-X syndrome is a recently described X-linked disorder that ranks second to Down syndrome as the most prevalent chromosomal form of mental retardation. Affected male individuals manifest a variable clinical phenotype that includes distinctive facial features, macroorchidism, cognitive and language impairments, and an impressive prevalence of attention deficit disorder and infantile autism. Link: ./index.php?lvl=notice_display&id=25334

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