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Détail de l'auteur
Auteur Stephan EHLERS |
Documents disponibles écrits par cet auteur (2)
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The Rett Syndrome Complex: Communicative Functions in Relation to Developmental Level and Autistic Features / Annika D. SANDBERG in Autism, 4-3 (September 2000)
[article]
Titre : The Rett Syndrome Complex: Communicative Functions in Relation to Developmental Level and Autistic Features Type de document : Texte imprimé et/ou numérique Auteurs : Annika D. SANDBERG, Auteur ; Stephan EHLERS, Auteur ; Bengt HAGBERG, Auteur ; Christopher GILLBERG, Auteur Article en page(s) : p.249-267 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Communicative functions and their relationship with overall developmental level and autistic features were studied in eight young women with disorders in the Rett syndrome complex, three with the classical variant and five with variants with partially preserved/regained speech. The Vineland Adaptive Behaviour Scales, individual structured observation, and a specially designed structured interview covering early pre-linguistic and linguistic development, current receptive and expressive language and non-verbal communication skills, were used. Autistic features were evaluated in accordance with the DSM-IV. Low levels of communicative abilities and overall functioning were demonstrated. In most cases, the communicative abilities did not reach the level expected on the basis of overall development. Joint attention behaviours and expressions of communicative intent were rare. However, six of the eight subjects showed clear examples of social interaction abilities.‘Eye pointing’, as distinct from ‘eye communication’, was demonstrated only in a minority of the cases. The level of communicative function at developmental arrest did not predict later language ability. It is suggested that intervention should focus on developing further the joint attention behaviours, intentional communications and communicative functions spontaneously used by individuals with disorders in the Rett syndrome complex. En ligne : http://dx.doi.org/10.1177/1362361300004003003 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=208
in Autism > 4-3 (September 2000) . - p.249-267[article] The Rett Syndrome Complex: Communicative Functions in Relation to Developmental Level and Autistic Features [Texte imprimé et/ou numérique] / Annika D. SANDBERG, Auteur ; Stephan EHLERS, Auteur ; Bengt HAGBERG, Auteur ; Christopher GILLBERG, Auteur . - p.249-267.
Langues : Anglais (eng)
in Autism > 4-3 (September 2000) . - p.249-267
Index. décimale : PER Périodiques Résumé : Communicative functions and their relationship with overall developmental level and autistic features were studied in eight young women with disorders in the Rett syndrome complex, three with the classical variant and five with variants with partially preserved/regained speech. The Vineland Adaptive Behaviour Scales, individual structured observation, and a specially designed structured interview covering early pre-linguistic and linguistic development, current receptive and expressive language and non-verbal communication skills, were used. Autistic features were evaluated in accordance with the DSM-IV. Low levels of communicative abilities and overall functioning were demonstrated. In most cases, the communicative abilities did not reach the level expected on the basis of overall development. Joint attention behaviours and expressions of communicative intent were rare. However, six of the eight subjects showed clear examples of social interaction abilities.‘Eye pointing’, as distinct from ‘eye communication’, was demonstrated only in a minority of the cases. The level of communicative function at developmental arrest did not predict later language ability. It is suggested that intervention should focus on developing further the joint attention behaviours, intentional communications and communicative functions spontaneously used by individuals with disorders in the Rett syndrome complex. En ligne : http://dx.doi.org/10.1177/1362361300004003003 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=208 The Syndromes Described by Kanner and Rett-Hagberg: Overlap in an Extended Family / Christopher GILLBERG in Developmental Medicine & Child Neurology, 32-3 (March 1990)
[article]
Titre : The Syndromes Described by Kanner and Rett-Hagberg: Overlap in an Extended Family Type de document : Texte imprimé et/ou numérique Auteurs : Christopher GILLBERG, Auteur ; Stephan EHLERS, Auteur ; Jan WAHLSTROM, Auteur Année de publication : 1990 Article en page(s) : p.258-261 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Les syndromes décrits par Kanner et Rett-Hagberg: chevauchement dans une même famille étendue
L'article rapporte le cas d'une famile étendue dans laquelle un syndrome de Rett-Hagberg, un autisme avec ataxie modérée et un autisme avec arriération mentale sévère s'observaient séparément chez trois filles cousines au deuxième degré. Les auteurs suggèrent des explications alternatives pour l'association possible entre un autisme et un syndrome de Rett-Hagberg: qu'ils soient reliés étroitement à un défaut génétique ou qu'ils constituent des phénotypes relativement homogènes avec plusieurs étiologies possibles.Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=133
in Developmental Medicine & Child Neurology > 32-3 (March 1990) . - p.258-261[article] The Syndromes Described by Kanner and Rett-Hagberg: Overlap in an Extended Family [Texte imprimé et/ou numérique] / Christopher GILLBERG, Auteur ; Stephan EHLERS, Auteur ; Jan WAHLSTROM, Auteur . - 1990 . - p.258-261.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 32-3 (March 1990) . - p.258-261
Index. décimale : PER Périodiques Résumé : Les syndromes décrits par Kanner et Rett-Hagberg: chevauchement dans une même famille étendue
L'article rapporte le cas d'une famile étendue dans laquelle un syndrome de Rett-Hagberg, un autisme avec ataxie modérée et un autisme avec arriération mentale sévère s'observaient séparément chez trois filles cousines au deuxième degré. Les auteurs suggèrent des explications alternatives pour l'association possible entre un autisme et un syndrome de Rett-Hagberg: qu'ils soient reliés étroitement à un défaut génétique ou qu'ils constituent des phénotypes relativement homogènes avec plusieurs étiologies possibles.Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=133