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Détail de l'auteur
Auteur A. CLARKE |
Documents disponibles écrits par cet auteur (2)
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Intracranial Calcification and Seizures: a Case of Central Neurofibromatosis / A. CLARKE in Developmental Medicine & Child Neurology, 32-8 (August 1990)
[article]
Titre : Intracranial Calcification and Seizures: a Case of Central Neurofibromatosis Type de document : Texte imprimé et/ou numérique Auteurs : A. CLARKE, Auteur ; W. CHURCH, Auteur ; David GARDNER-MEDWIN, Auteur ; R. SENGUPTA, Auteur Année de publication : 1990 Article en page(s) : p.729-732 Langues : Anglais (eng) Index. décimale : PER Périodiques Résumé : Calcifications intra-craniennes et crises: un cas de neurofibromatose centrale
Une calcification péri-ventriculaire a été trouvée chez un garcon de huit ans présentant des crises comitiales. Le diagnostic de sclérose tubéreuse fut envisagé (comme sa mère) il présentait une neurofibromatose centrale. Cette affection doit être envisagée dans le diagnostic différentiel des enfants présentant à la fois calcifications intra-craniennes et crises comitiales.Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=134
in Developmental Medicine & Child Neurology > 32-8 (August 1990) . - p.729-732[article] Intracranial Calcification and Seizures: a Case of Central Neurofibromatosis [Texte imprimé et/ou numérique] / A. CLARKE, Auteur ; W. CHURCH, Auteur ; David GARDNER-MEDWIN, Auteur ; R. SENGUPTA, Auteur . - 1990 . - p.729-732.
Langues : Anglais (eng)
in Developmental Medicine & Child Neurology > 32-8 (August 1990) . - p.729-732
Index. décimale : PER Périodiques Résumé : Calcifications intra-craniennes et crises: un cas de neurofibromatose centrale
Une calcification péri-ventriculaire a été trouvée chez un garcon de huit ans présentant des crises comitiales. Le diagnostic de sclérose tubéreuse fut envisagé (comme sa mère) il présentait une neurofibromatose centrale. Cette affection doit être envisagée dans le diagnostic différentiel des enfants présentant à la fois calcifications intra-craniennes et crises comitiales.Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=134 A national survey of Rett syndrome: behavioural characteristics / R. CIANFAGLIONE in Journal of Neurodevelopmental Disorders, 7-1 (December 2015)
[article]
Titre : A national survey of Rett syndrome: behavioural characteristics Type de document : Texte imprimé et/ou numérique Auteurs : R. CIANFAGLIONE, Auteur ; A. CLARKE, Auteur ; M. KERR, Auteur ; R. P. HASTINGS, Auteur ; C. OLIVER, Auteur ; J. MOSS, Auteur ; M. HEALD, Auteur ; D. FELCE, Auteur Article en page(s) : p.11 Langues : Anglais (eng) Mots-clés : Behavioural characteristics Great Britain Intellectual disabilities Rett syndrome Index. décimale : PER Périodiques Résumé : BACKGROUND: The aim was to gain a UK national sample of people with Rett syndrome (RTT) across the age range and compare their characteristics using a variety of relevant behavioural measures with a well-chosen contrast group. METHODS: The achieved sample was 91 girls and women, aged from 4 to 47 years, of whom 71 were known to be MECP2 positive. The contrast group (n = 66), matched for age, gender, language and self-help skills, comprised individuals with six other syndromes associated with intellectual disability. Parental questionnaire measures of RTT specific characteristics, impulsivity, overactivity, mood, interest and pleasure, repetitive behaviour and self-injury were administered. RESULTS: Hand stereotypies, breathing irregularities, night-time unrest and anxiety or inappropriate fear were commonly reported among the RTT sample. Problems of low mood were also reported as common. However, mood and interest and pleasure were no lower than found in the contrast group. In addition, self-injury was lower than in the contrast group and was associated with factors found to predict self-injury in other groups of people with severe intellectual disabilities. CONCLUSIONS: There is variability in the manifestation of problem behaviours potentially associated with the syndrome across individuals, with some more severely affected in most areas than others. Some of this variability appears to be underpinned by genetic mutation. En ligne : http://dx.doi.org/10.1186/s11689-015-9104-y Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=347
in Journal of Neurodevelopmental Disorders > 7-1 (December 2015) . - p.11[article] A national survey of Rett syndrome: behavioural characteristics [Texte imprimé et/ou numérique] / R. CIANFAGLIONE, Auteur ; A. CLARKE, Auteur ; M. KERR, Auteur ; R. P. HASTINGS, Auteur ; C. OLIVER, Auteur ; J. MOSS, Auteur ; M. HEALD, Auteur ; D. FELCE, Auteur . - p.11.
Langues : Anglais (eng)
in Journal of Neurodevelopmental Disorders > 7-1 (December 2015) . - p.11
Mots-clés : Behavioural characteristics Great Britain Intellectual disabilities Rett syndrome Index. décimale : PER Périodiques Résumé : BACKGROUND: The aim was to gain a UK national sample of people with Rett syndrome (RTT) across the age range and compare their characteristics using a variety of relevant behavioural measures with a well-chosen contrast group. METHODS: The achieved sample was 91 girls and women, aged from 4 to 47 years, of whom 71 were known to be MECP2 positive. The contrast group (n = 66), matched for age, gender, language and self-help skills, comprised individuals with six other syndromes associated with intellectual disability. Parental questionnaire measures of RTT specific characteristics, impulsivity, overactivity, mood, interest and pleasure, repetitive behaviour and self-injury were administered. RESULTS: Hand stereotypies, breathing irregularities, night-time unrest and anxiety or inappropriate fear were commonly reported among the RTT sample. Problems of low mood were also reported as common. However, mood and interest and pleasure were no lower than found in the contrast group. In addition, self-injury was lower than in the contrast group and was associated with factors found to predict self-injury in other groups of people with severe intellectual disabilities. CONCLUSIONS: There is variability in the manifestation of problem behaviours potentially associated with the syndrome across individuals, with some more severely affected in most areas than others. Some of this variability appears to be underpinned by genetic mutation. En ligne : http://dx.doi.org/10.1186/s11689-015-9104-y Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=347