Journal of Intellectual Disability Research

Integrating levels of explanation in behavioural phenotype research
pp. 807-809(3)

The neurobiology and genetics of eating and weight regulation
pp. 810-810(1)
Author: Hebebrand, J.

Elimination disorders in people with intellectual disability
pp. 810-810(1)
Author: Van Laecke, E.

Sleep problems in developmental disabilities: Trends in research and treatment
pp. 810-810(1)
Author: Didden, R.

The Tom Oppe Lecture: Behavioural phenotypes and child psychiatry
pp. 810-810(1)
Author: Steinhausen, H.-C.

The Paradox of Prader Willi Syndrome: A genetic model of starvation
pp. 811-811(1)
Author: Holland, A. J.

The relationship between a deficit in attention switching and specific behaviours in Prader-Willi syndrome
pp. 812-812(1)
Authors: Woodcock, K. A.; Oliver, C.; Humphreys, G. W.

Abnormal protein glycoforms in Prader-Willi syndrome
pp. 812-812(1)
Authors: Bowling, F. G.; Munce, T. B.

White matter microstructure in children with Velocardiofacial Syndrome: A Diffusion Tensor Imaging and Voxel Based Morphometry study
pp. 812-812(1)
Authors: Sundram, F.; Murphy, D. G.; Murphy, K. C.

Health management for people with intellectual disabilities in primary care; impact on basic physical functions
pp. 812-812(1)
Authors: van Schrojenstein Lantman-de Valk, H.; Veenstra, M.; Straetmans, J.; Metsemakers, J.; Curfs, L.

Physical and mental health of adults with Williams syndrome
pp. 813-813(1)
Authors: Stinton, C.; Elison, S.; Udwin, O.; Howlin, P.

Molecular karyotyping is important in determining the cause of behavioural phenotypes
pp. 813-813(1)
Authors: de Ravel, T. J. L.; Swillen, A.; Willekens, D.; Descheemaeker, M.-J.; Govers, V.; Borghgraef, M.; Vermeesch, J. R.; Fryns, J.-P.

Pathogenetic mechanisms in Down Syndrome
pp. 813-813(1)
Authors: Einfeld, S.; Götz, J.; Holsinger, R. M. D.

Cognitive-behavioural and autistic features of children with subtelomeric deletions
pp. 813-813(1)
Authors: Fisch, G. S.; Carey, J.; Youngblom, J.; Simensen, R.; Battaglia, A.

Newborn screening in Fragile X syndrome
pp. 814-814(1)
Authors: Tassone, F.; Hagerman, P. J.; Hagerman, R. J.

Melatonin is effective in treating sleep problems in Angelman syndrome but problems in metabolising melatonin may be part of the Angelman phenotype
pp. 814-814(1)
Authors: Braam, W.; Smits, M. G.; Didden, R.; Curfs, L. M. G.

Hypersomnolence in Prader Willi Syndrome
pp. 814-814(1)
Authors: Heussler, H.; Harris, M.; Cooper, D.; Dakin, C.; Suresh, S.; Williams, G.

Trial of fenobam, an mGluR5 antagonist, in adults with Fragile X Syndrome
pp. 814-814(1)
Authors: Hagerman, R.; Berry-Kravis, E.; Hessl, D.; Coffey, S.; Schneider, A.; Nguyen, D.; Hervey, C.; Hutchison, J.; Snape, M.

Developmental aspects of sleep in Prader Willi Syndrome
pp. 815-815(1)
Authors: Heussler, H.; Suresh, S.; Harris, M.; Cooper, D.; Dakin, C.; Williams, G.; Wilson, S.

Sleep Disordered Breathing in Prader-Willi patients treated with rh GH
pp. 815-815(1)
Authors: Nespoli, L.; Verri, A.; Nosetti, L.; Salvatoni, A.; Berini, J.; Chierici, V.; Niespolo, A. C.; Cremante, A.

Investigating sleep architecture in Angelman, Cri du Chat and Cornelia de Lange syndromes
pp. 815-815(1)
Authors: Petty, J.; Oliver, C.; Moss, J.; Howlin, P.; Tunnicliffe, P.; Griffith, G.; Hastings, R.

Parental perception of sleep behaviour and sleep disorders in children with VCFS and their siblings
pp. 815-815(1)
Authors: Swillen, A.; Berghs, I.; Schoeters, A.; Fryns, J.-P.; Hellinkcx, W.; Devriendt, K.

Psychiatric disorders in people with 22q11.2 Deletion Syndrome: A population-based prevalence study in Ireland
pp. 816-816(1)
Authors: Prasad, S. E.; Howley, S.; Murphy, K. C.

Genetics of autism
pp. 817-817(1)
Author: Freitag, C. M.

Non-syndromal autism: Neuropsychology
pp. 817-817(1)
Author: Bolte, S.

Identifying effective interventions for young children with autism spectrum disorders
pp. 817-817(1)
Author: Howlin, P.

Is there an increased prevalence of autistic spectrum disorders in people with 22q11 Deletion Syndrome?
pp. 817-817(1)
Authors: Murphy, K. C.; Sundram, F.

Commonalities in the neurobiology between autism and fragile X
pp. 817-817(1)
Author: Hagerman, R.

What can we learn from tuberous sclerosis complex (TSC) about autism?
pp. 818-818(1)
Author: de Vries, P. J.

Rett Syndrome and long-term disorder profile
pp. 818-818(1)
Authors: Smeets, E.; Schrander-Stumpel, C.; Curfs, L.

Prevalence and risk factors of maladaptive behaviour in young children with Autistic Disorder
pp. 819-829(11)
Authors: Hartley, S. L.; Sikora, D. M.; McCoy, R.

The behavioural phenotype of Smith-Magenis syndrome: evidence for a gene-environment interaction
pp. 830-841(12)
Authors: Taylor, L.; Oliver, C.

Early temperament and negative reactivity in boys with fragile X syndrome
pp. 842-854(13)
Authors: Shanahan, M.; Roberts, J.; Hatton, D.; Reznick, J.; Goldsmith, H.

What clinical characteristics of children with autism influence their inclusion in regular classrooms?
pp. 855-863(9)
Authors: Yianni-Coudurier, C.; Darrou, C.; Lenoir, P.; Verrecchia, B.; Assouline, B.; Ledesert, B.; Michelon, C.; Pry, R.; Aussilloux, C.; Baghdadli, A.

Factors associated with the risk of behaviour problems in adolescents with severe intellectual disabilities
pp. 864-876(13)
Authors: Chadwick, O.; Kusel, Y.; Cuddy, M.

Behaviour problems and adults with Down syndrome: childhood risk factors
pp. 877-882(6)
Author: McCarthy, J.