Journal of Intellectual Disability Research

Cover image for Vol. 52 Issue 10

October 2008

Volume 52, Issue 10

Pages 807–882

  1. Part 1: SSBP Abstracts, Guest Edited by Chris Oliver and Alexander von Gontard

    1. Top of page
    2. Part 1: SSBP Abstracts, Guest Edited by Chris Oliver and Alexander von Gontard
    3. Abstracts
    4. Part 1: SSBP Abstracts, Guest Edited by Chris Oliver and Alexander von Gontard
    5. Part 2: Original Articles
    1. Editorial

    2. Keynote Presentations

      The neurobiology and genetics of eating and weight regulation (page 810)

      J. Hebebrand

      Version of Record online: 6 OCT 2008 | DOI: 10.1111/j.1365-2788.2008.01118_1.x

    3. Elimination disorders in people with intellectual disability (page 810)

      E. Van Laecke

      Version of Record online: 6 OCT 2008 | DOI: 10.1111/j.1365-2788.2008.01118_2.x

    4. The Tom Oppe Lecture: Behavioural phenotypes and child psychiatry (page 810)

      H.-C. Steinhausen

      Version of Record online: 6 OCT 2008 | DOI: 10.1111/j.1365-2788.2008.01118_4.x

    5. The Paradox of Prader Willi Syndrome: A genetic model of starvation (page 811)

      A. J. Holland

      Version of Record online: 6 OCT 2008 | DOI: 10.1111/j.1365-2788.2008.01118_5.x

    6. Oral Presentations

      The relationship between a deficit in attention switching and specific behaviours in Prader-Willi syndrome (page 812)

      K. A. Woodcock, C. Oliver and G. W. Humphreys

      Version of Record online: 6 OCT 2008 | DOI: 10.1111/j.1365-2788.2008.01119_1.x

    7. Abnormal protein glycoforms in Prader-Willi syndrome (page 812)

      F. G. Bowling and T. B. Munce

      Version of Record online: 6 OCT 2008 | DOI: 10.1111/j.1365-2788.2008.01119_2.x

    8. Health management for people with intellectual disabilities in primary care; impact on basic physical functions (page 812)

      H. Van Schrojenstein Lantman-de Valk, M. Veenstra, J. Straetmans, J. Metsemakers and L. Curfs

      Version of Record online: 6 OCT 2008 | DOI: 10.1111/j.1365-2788.2008.01119_4.x

    9. Physical and mental health of adults with Williams syndrome (page 813)

      C. Stinton, S. Elison, O. Udwin and P. Howlin

      Version of Record online: 6 OCT 2008 | DOI: 10.1111/j.1365-2788.2008.01119_5.x

    10. Molecular karyotyping is important in determining the cause of behavioural phenotypes (page 813)

      T. J. L. De Ravel, A. Swillen, D. Willekens, M.-J. Descheemaeker, V. Govers, M. Borghgraef, J. R. Vermeesch and J.-P. Fryns

      Version of Record online: 6 OCT 2008 | DOI: 10.1111/j.1365-2788.2008.01119_6.x

    11. Pathogenetic mechanisms in Down Syndrome (page 813)

      S. Einfeld, J. Götz and R. M. D. Holsinger

      Version of Record online: 6 OCT 2008 | DOI: 10.1111/j.1365-2788.2008.01119_7.x

    12. Cognitive-behavioural and autistic features of children with subtelomeric deletions (page 813)

      G. S. Fisch, J. Carey, J. Youngblom, R. Simensen and A. Battaglia

      Version of Record online: 6 OCT 2008 | DOI: 10.1111/j.1365-2788.2008.01119_8.x

  2. Abstracts

    1. Top of page
    2. Part 1: SSBP Abstracts, Guest Edited by Chris Oliver and Alexander von Gontard
    3. Abstracts
    4. Part 1: SSBP Abstracts, Guest Edited by Chris Oliver and Alexander von Gontard
    5. Part 2: Original Articles
    1. Trial of fenobam, an mGluR5 antagonist, in adults with Fragile X Syndrome (page 814)

      R. Hagerman, E. Berry-Kravis, D. Hessl, S. Coffey, A. Schneider, D. Nguyen, C. Hervey, J. Hutchison and M. Snape

      Version of Record online: 6 OCT 2008 | DOI: 10.1111/j.1365-2788.2008.01119_9.x

  3. Part 1: SSBP Abstracts, Guest Edited by Chris Oliver and Alexander von Gontard

    1. Top of page
    2. Part 1: SSBP Abstracts, Guest Edited by Chris Oliver and Alexander von Gontard
    3. Abstracts
    4. Part 1: SSBP Abstracts, Guest Edited by Chris Oliver and Alexander von Gontard
    5. Part 2: Original Articles
    1. Oral Presentations

      Newborn screening in Fragile X syndrome (page 814)

      F. Tassone, P. J. Hagerman and R. J. Hagerman

      Version of Record online: 6 OCT 2008 | DOI: 10.1111/j.1365-2788.2008.01119_10.x

    2. Hypersomnolence in Prader Willi Syndrome (page 814)

      H. Heussler, M. Harris, D. Cooper, C. Dakin, S. Suresh and G. Williams

      Version of Record online: 6 OCT 2008 | DOI: 10.1111/j.1365-2788.2008.01119_12.x

    3. Developmental aspects of sleep in Prader Willi Syndrome (page 815)

      H. Heussler, S. Suresh, M. Harris, D. Cooper, C. Dakin, G. Williams and S. Wilson

      Version of Record online: 6 OCT 2008 | DOI: 10.1111/j.1365-2788.2008.01119_13.x

    4. Sleep Disordered Breathing in Prader-Willi patients treated with rh GH (page 815)

      L. Nespoli, A. Verri, L. Nosetti, A. Salvatoni, J. Berini, V. Chierici, A. C. Niespolo and A. Cremante

      Version of Record online: 6 OCT 2008 | DOI: 10.1111/j.1365-2788.2008.01119_14.x

    5. Investigating sleep architecture in Angelman, Cri du Chat and Cornelia de Lange syndromes (page 815)

      J. Petty, C. Oliver, J. Moss, P. Howlin, P. Tunnicliffe, G. Griffith and R. Hastings

      Version of Record online: 6 OCT 2008 | DOI: 10.1111/j.1365-2788.2008.01119_15.x

    6. Parental perception of sleep behaviour and sleep disorders in children with VCFS and their siblings (page 815)

      A. Swillen, I. Berghs, A. Schoeters, J.-P. Fryns, W. Hellinkcx and K. Devriendt

      Version of Record online: 6 OCT 2008 | DOI: 10.1111/j.1365-2788.2008.01119_16.x

    7. Psychiatric disorders in people with 22q11.2 Deletion Syndrome: A population-based prevalence study in Ireland (page 816)

      S. E. Prasad, S. Howley and K. C. Murphy

      Version of Record online: 6 OCT 2008 | DOI: 10.1111/j.1365-2788.2008.01119_17.x

    8. Educational Symposium

      Genetics of autism (page 817)

      C. M. Freitag

      Version of Record online: 6 OCT 2008 | DOI: 10.1111/j.1365-2788.2008.01120_1.x

    9. Non-syndromal autism: Neuropsychology (page 817)

      S. Bolte

      Version of Record online: 6 OCT 2008 | DOI: 10.1111/j.1365-2788.2008.01120_2.x

    10. Is there an increased prevalence of autistic spectrum disorders in people with 22q11 Deletion Syndrome? (page 817)

      K. C. Murphy and F. Sundram

      Version of Record online: 6 OCT 2008 | DOI: 10.1111/j.1365-2788.2008.01120_4.x

    11. Commonalities in the neurobiology between autism and fragile X (page 817)

      R. Hagerman

      Version of Record online: 6 OCT 2008 | DOI: 10.1111/j.1365-2788.2008.01120_5.x

    12. What can we learn from tuberous sclerosis complex (TSC) about autism? (page 818)

      P. J. De Vries

      Version of Record online: 6 OCT 2008 | DOI: 10.1111/j.1365-2788.2008.01120_6.x

    13. Rett Syndrome and long-term disorder profile (page 818)

      E. Smeets, C. Schrander-Stumpel and L. Curfs

      Version of Record online: 6 OCT 2008 | DOI: 10.1111/j.1365-2788.2008.01120_7.x

  4. Part 2: Original Articles

    1. Top of page
    2. Part 1: SSBP Abstracts, Guest Edited by Chris Oliver and Alexander von Gontard
    3. Abstracts
    4. Part 1: SSBP Abstracts, Guest Edited by Chris Oliver and Alexander von Gontard
    5. Part 2: Original Articles
    1. Early temperament and negative reactivity in boys with fragile X syndrome (pages 842–854)

      M. Shanahan, J. Roberts, D. Hatton, J. Reznick and H. Goldsmith

      Version of Record online: 21 MAY 2008 | DOI: 10.1111/j.1365-2788.2008.01074.x

    2. What clinical characteristics of children with autism influence their inclusion in regular classrooms? (pages 855–863)

      C. Yianni-Coudurier, C. Darrou, P. Lenoir, B. Verrecchia, B. Assouline, B. Ledesert, C. Michelon, R. Pry, C. Aussilloux and A. Baghdadli

      Version of Record online: 8 JUL 2008 | DOI: 10.1111/j.1365-2788.2008.01100.x

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