Is there an increased prevalence of autistic spectrum disorders in people with 22q11 Deletion Syndrome? (English)
- New search for: Murphy, K. C.
- New search for: Sundram, F.
- New search for: Murphy, K. C.
- New search for: Sundram, F.
In:
Journal of Intellectual Disability Research
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52
, 10
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817
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2008
- Article (Journal) / Electronic Resource
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Title:Is there an increased prevalence of autistic spectrum disorders in people with 22q11 Deletion Syndrome?
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Contributors:Murphy, K. C. ( author ) / Sundram, F. ( author )
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Published in:Journal of Intellectual Disability Research ; 52, 10 ; 817
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Publisher:
- New search for: Blackwell Publishing Ltd
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Publication date:2008-10-01
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Size:1 pages
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Keywords:
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Source:
Table of contents – Volume 52, Issue 10
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 807
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Integrating levels of explanation in behavioural phenotype researchOliver, Chris / Woodcock, Kate et al. | 2008
- 810
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Sleep problems in developmental disabilities: Trends in research and treatmentDidden, R. et al. | 2008
- 810
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Elimination disorders in people with intellectual disabilityVan Laecke, E. et al. | 2008
- 810
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The neurobiology and genetics of eating and weight regulationHebebrand, J. et al. | 2008
- 810
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The Tom Oppe Lecture: Behavioural phenotypes and child psychiatrySteinhausen, H.‐C. et al. | 2008
- 811
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The Paradox of Prader Willi Syndrome: A genetic model of starvationHolland, A. J. et al. | 2008
- 812
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White matter microstructure in children with Velocardiofacial Syndrome: A Diffusion Tensor Imaging and Voxel Based Morphometry studySundram, F. / Murphy, D. G. / Murphy, K. C. et al. | 2008
- 812
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Abnormal protein glycoforms in Prader‐Willi syndromeBowling, F. G. / Munce, T. B. et al. | 2008
- 812
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The relationship between a deficit in attention switching and specific behaviours in Prader‐Willi syndromeWoodcock, K. A. / Oliver, C. / Humphreys, G. W. et al. | 2008
- 812
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Health management for people with intellectual disabilities in primary care; impact on basic physical functionsVan Schrojenstein Lantman‐de Valk, H. / Veenstra, M. / Straetmans, J. / Metsemakers, J. / Curfs, L. et al. | 2008
- 813
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Cognitive‐behavioural and autistic features of children with subtelomeric deletionsFisch, G. S. / Carey, J. / Youngblom, J. / Simensen, R. / Battaglia, A. et al. | 2008
- 813
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Physical and mental health of adults with Williams syndromeStinton, C. / Elison, S. / Udwin, O. / Howlin, P. et al. | 2008
- 813
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Pathogenetic mechanisms in Down SyndromeEinfeld, S. / Götz, J. / Holsinger, R. M. D. et al. | 2008
- 813
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Molecular karyotyping is important in determining the cause of behavioural phenotypesDe Ravel, T. J. L. / Swillen, A. / Willekens, D. / Descheemaeker, M.‐J. / Govers, V. / Borghgraef, M. / Vermeesch, J. R. / Fryns, J.‐P. et al. | 2008
- 814
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Melatonin is effective in treating sleep problems in Angelman syndrome but problems in metabolising melatonin may be part of the Angelman phenotypeBraam, W. / Smits, M. G. / Didden, R. / Curfs, L. M. G. et al. | 2008
- 814
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Hypersomnolence in Prader Willi SyndromeHeussler, H. / Harris, M. / Cooper, D. / Dakin, C. / Suresh, S. / Williams, G. et al. | 2008
- 814
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Trial of fenobam, an mGluR5 antagonist, in adults with Fragile X SyndromeHagerman, R. / Berry‐Kravis, E. / Hessl, D. / Coffey, S. / Schneider, A. / Nguyen, D. / Hervey, C. / Hutchison, J. / Snape, M. et al. | 2008
- 814
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Newborn screening in Fragile X syndromeTassone, F. / Hagerman, P. J. / Hagerman, R. J. et al. | 2008
- 815
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Investigating sleep architecture in Angelman, Cri du Chat and Cornelia de Lange syndromesPetty, J. / Oliver, C. / Moss, J. / Howlin, P. / Tunnicliffe, P. / Griffith, G. / Hastings, R. et al. | 2008
- 815
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Parental perception of sleep behaviour and sleep disorders in children with VCFS and their siblingsSwillen, A. / Berghs, I. / Schoeters, A. / Fryns, J.‐P. / Hellinkcx, W. / Devriendt, K. et al. | 2008
- 815
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Sleep Disordered Breathing in Prader‐Willi patients treated with rh GHNespoli, L. / Verri, A. / Nosetti, L. / Salvatoni, A. / Berini, J. / Chierici, V. / Niespolo, A. C. / Cremante, A. et al. | 2008
- 815
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Developmental aspects of sleep in Prader Willi SyndromeHeussler, H. / Suresh, S. / Harris, M. / Cooper, D. / Dakin, C. / Williams, G. / Wilson, S. et al. | 2008
- 816
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Psychiatric disorders in people with 22q11.2 Deletion Syndrome: A population‐based prevalence study in IrelandPrasad, S. E. / Howley, S. / Murphy, K. C. et al. | 2008
- 817
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Is there an increased prevalence of autistic spectrum disorders in people with 22q11 Deletion Syndrome?Murphy, K. C. / Sundram, F. et al. | 2008
- 817
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Genetics of autismFreitag, C. M. et al. | 2008
- 817
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Commonalities in the neurobiology between autism and fragile XHagerman, R. et al. | 2008
- 817
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Non‐syndromal autism: NeuropsychologyBolte, S. et al. | 2008
- 817
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Identifying effective interventions for young children with autism spectrum disordersHowlin, P. et al. | 2008
- 818
-
What can we learn from tuberous sclerosis complex (TSC) about autism?De Vries, P. J. et al. | 2008
- 818
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Rett Syndrome and long‐term disorder profileSmeets, E. / Schrander‐Stumpel, C. / Curfs, L. et al. | 2008
- 819
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Prevalence and risk factors of maladaptive behaviour in young children with Autistic DisorderHartley, S. L. / Sikora, D. M. / McCoy, R. et al. | 2008
- 830
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The behavioural phenotype of Smith–Magenis syndrome: evidence for a gene–environment interactionTaylor, L. / Oliver, C. et al. | 2008
- 842
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Early temperament and negative reactivity in boys with fragile X syndromeShanahan, M. / Roberts, J. / Hatton, D. / Reznick, J. / Goldsmith, H. et al. | 2008
- 855
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What clinical characteristics of children with autism influence their inclusion in regular classrooms?Yianni‐Coudurier, C. / Darrou, C. / Lenoir, P. / Verrecchia, B. / Assouline, B. / Ledesert, B. / Michelon, C. / Pry, R. / Aussilloux, C. / Baghdadli, A. et al. | 2008
- 864
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Factors associated with the risk of behaviour problems in adolescents with severe intellectual disabilitiesChadwick, O. / Kusel, Y. / Cuddy, M. et al. | 2008
- 877
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Behaviour problems and adults with Down syndrome: childhood risk factorsMcCarthy, J. et al. | 2008