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Showing 1 to 15 of 64 results
Patil, D.; Keown, P.; Scott, J. – Journal of Intellectual Disability Research, 2013
Background: It is unclear whether the substantial decline in number and duration of admissions for patients with intellectual disability (ID) have occurred uniformly over time with respect to age, gender, severity of disability, legal status and location of treatment. Method: A retrospective analysis of NHS (National Health Service) admissions for…
Descriptors: Foreign Countries, Mental Health, Mental Disorders, Comorbidity
Guest, J. F.; Bai, J. J.; Taylor, R. R.; Sladkevicius, E.; Lee, P. J.; Lachmann, R. H. – Journal of Intellectual Disability Research, 2013
Background: To quantify the costs and consequences of managing phenylketonuria (PKU) in the UK and to estimate the potential implications to the UK's National Health Service (NHS) of keeping patients on a phenylalanine-restricted diet for life. Methods: A computer-based model was constructed depicting the management of PKU patients over the…
Descriptors: Foreign Countries, Diseases, Metabolism, Dietetics
Wagemans, A.; van Schrojenstein Lantman-de Valk, H.; Proot, I.; Metsemakers, J.; Tuffrey-Wijne, I.; Curfs, L. – Journal of Intellectual Disability Research, 2013
Background: The aim of this study was to investigate the process of end-of-life decision-making regarding people with intellectual disabilities (ID) in the Netherlands, from the perspective of physicians. Methods: This qualitative study involved nine semi-structured interviews with ID physicians in the Netherlands after the deaths of patients with…
Descriptors: Foreign Countries, Death, Mental Retardation, Physicians
Corbani, S.; Chouery, E.; Fayyad, J.; Fawaz, A.; El Tourjuman, O.; Badens, C.; Lacoste, C.; Delague, V.; Megarbane, A. – Journal of Intellectual Disability Research, 2012
Background: Rett syndrome (RTT), an X-linked, dominant, neurodevelopment disorder represents 10% of female subjects with profound intellectual disability. Mutations in the "MECP2" gene are responsible for up to 95% of the classical RTT cases, and nearly 500 different mutations distributed throughout the gene have been reported. Methods: We report…
Descriptors: Mental Retardation, Genetic Disorders, Neurological Impairments, Genetics
Wieland, J.; Wardenaar, K. J.; Fontein, E.; Zitman, F. G. – Journal of Intellectual Disability Research, 2012
Background: Diagnostics and care for people with intellectual disabilities (ID) and psychiatric disorders need to be improved. This can be done by using assessment instruments to routinely measure the nature and severity of psychiatric symptoms. Up until now, in the Netherlands, assessment measures are seldom used in the psychiatric care for this…
Descriptors: Intelligence, Mental Retardation, Mental Disorders, Validity
Bonell, S.; Underwood, L.; Radhakrishnan, V.; McCarthy, J. – Journal of Intellectual Disability Research, 2012
Background: Patient experience of those accessing mental health services has been found to be different between ethnic groups. Although the needs of people with intellectual disabilities (ID) from different ethnic communities are being increasingly recognised, little has been published about their experiences of mental health services. The aim of…
Descriptors: Delphi Technique, Health Services, Mental Retardation, Ethnic Groups
Brown, M.; MacArthur, J.; McKechanie, A.; Mack, S.; Hayes, M.; Fletcher, J. – Journal of Intellectual Disability Research, 2012
Background: There have been significant concerns about the care and treatment of people with intellectual disabilities (ID) when attending general hospitals, which have led to inquiries that highlight service and systems failures. One response has been the development of Learning Disability Liaison Nursing (LDLN) Services across the UK that aim to…
Descriptors: Nursing, Health Needs, Program Effectiveness, Stakeholders
Iacono, T.; Carling-Jenkins, R. – Journal of Intellectual Disability Research, 2012
Background: The history of ethical guidelines addresses protection of human rights in the face of violations. Examples of such violations in research involving people with intellectual disabilities (ID) abound. We explore this history in an effort to understand the apparently stringent criteria for the inclusion of people with ID in research, and…
Descriptors: Guidelines, Civil Rights, Ethics, Foreign Countries
Gombos, F.; Bodizs, R.; Kovacs, I. – Journal of Intellectual Disability Research, 2011
Background: Williams syndrome (WS) is a neurodevelopmental genetic disorder characterised by physical abnormalities and a distinctive cognitive profile with intellectual disabilities (IDs) and learning difficulties. Methods: In our study, nine adolescents and young adults with WS and 9 age- and sex-matched typically developing (TD) participants…
Descriptors: Genetic Disorders, Learning Problems, Eye Movements, Mental Retardation
Lunsky, Y.; Gracey, C.; Bradley, E.; Koegl, C.; Durbin, J. – Journal of Intellectual Disability Research, 2011
Background: This study compares outpatients with intellectual disability (ID) receiving specialised services to outpatients with ID receiving general services in Ontario's tertiary mental healthcare system in terms of demographics, symptom profile, strengths and resources, and clinical service needs. Methods: A secondary analysis of Colorado…
Descriptors: Mental Retardation, Psychiatric Hospitals, Patients, Foreign Countries
Charlot, L.; Abend, S.; Ravin, P.; Mastis, K.; Hunt, A.; Deutsch, C. – Journal of Intellectual Disability Research, 2011
Background: Physical distress resulting from medical problems has been found to cause increased behaviour problems in patients with intellectual disabilities (ID). Despite this fact, little has been documented on the medical problems of individuals with ID admitted for inpatient psychiatric care. We conducted an exploratory investigation based on…
Descriptors: Age, Investigations, Autism, Symptoms (Individual Disorders)
Paton, C.; Flynn, A.; Shingleton-Smith, A.; McIntyre, S.; Bhaumik, S.; Rasmussen, J.; Hardy, S.; Barnes, T. – Journal of Intellectual Disability Research, 2011
Background: Antipsychotics are perceived to be over-used in the management of behavioural problems in people with an intellectual disability (ID). Published guidelines have set good practice standards for the use of these drugs for behavioural indications. We sought to identify the range of indications for which antipsychotic drugs are prescribed…
Descriptors: Standards, Severity (of Disability), Mental Retardation, Mental Disorders
Lunsky, Y.; White, S. E.; Palucka, A. M.; Weiss, J.; Bockus, S.; Gofine, T. – Journal of Intellectual Disability Research, 2010
Background: Limitations of general psychiatric services have led to the development of specialised psychiatric programmes for patients with intellectual disability (ID) and mental health needs. Few studies have examined treatment outcomes of specialised inpatient units, and no studies have explored how the effects of intervention may differ for…
Descriptors: Psychiatric Services, Health Needs, Mental Retardation, Mental Disorders
Oliver-Africano, P.; Dickens, S.; Ahmed, Z.; Bouras, N.; Cooray, S.; Deb, S.; Knapp, M.; Hare, M.; Meade, M.; Reece, B.; Bhaumik, S.; Harley, D.; Piachaud, J.; Regan, A.; Ade Thomas, D.; Karatela, S.; Rao, B.; Dzendrowskyj, T.; Lenotre, L.; Watson, J.; Tyrer, P. – Journal of Intellectual Disability Research, 2010
Background: Aggressive challenging behaviour in people with intellectual disability (ID) is frequently treated with antipsychotic drugs, despite a limited evidence base. Method: A multi-centre randomised controlled trial was undertaken to investigate the efficacy, adverse effects and costs of two commonly prescribed antipsychotic drugs…
Descriptors: Mental Retardation, Patients, Measures (Individuals), Drug Therapy
Copet, P.; Jauregi, J.; Laurier, V.; Ehlinger, V.; Arnaud, C.; Cobo, A. -M.; Molinas, C.; Tauber, M.; Thuilleaux, D. – Journal of Intellectual Disability Research, 2010
Background: Prader-Willi syndrome (PWS) is a rare genetic disorder characterised by developmental abnormalities leading to somatic and psychological symptoms. These include dysmorphic features, impaired growth and sexual maturation, hyperphagia, intellectual delay, learning disabilities and maladaptive behaviours. PWS is caused by a lack of…
Descriptors: Genetic Disorders, Intelligence, Body Composition, Mental Retardation

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