• The University of Western Australia (M560), 35 Stirling Highway,

    6009 Perth

    Australia

  • 5737 Citations
  • 38 h-Index
20032023
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Research Output 2003 2020

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Review article
2020

The prevalence and phenotypic signatures of mental ill health for children and adolescents with a neurogenetic disorder associated with intellectual disability: a systematic review

Glasson, E., Buckley, N., Chen, W., Leonard, H., Epstein, A., Skoss, R., Jacoby, P., Blackmore, A. M., Bourke, J. & Downs, J., 2020, (Accepted/In press) In : Journal of the American Academy of Child & Adolescent Psychiatry.

Research output: Contribution to journalReview article

2019
2 Citations (Scopus)

Cannabis for refractory epilepsy in children: A review focusing on CDKL5 Deficiency Disorder

Dale, T., Downs, J., Olson, H., Bergin, A. M., Smith, S. & Leonard, H., Mar 2019, In : Epilepsy Research. 151, p. 31-39 9 p.

Research output: Contribution to journalReview article

5 Citations (Scopus)

Cyclin-Dependent Kinase-Like 5 Deficiency Disorder: Clinical Review

Olson, H. E., Demarest, S. T., Pestana-Knight, E. M., Swanson, L. C., Iqbal, S., Lal, D., Leonard, H., Cross, J. H., Devinsky, O. & Benke, T. A., 1 Aug 2019, In : Pediatric Neurology. 97, p. 18-25 8 p.

Research output: Contribution to journalReview article

Cyclin-Dependent Kinase 5
Phase III Clinical Trials
Muscle Hypotonia
Vision Disorders
Brain Diseases

Requirements for improving health and well-being of children with Prader-Willi syndrome and their families

Mackay, J., McCallum, Z., Ambler, G. R., Vora, K., Nixon, G., Bergman, P., Shields, N., Milner, K., Kapur, N., Crock, P., Caudri, D., Curran, J., Verge, C., Seton, C., Tai, A., Tham, E., Musthaffa, Y., Lafferty, A. R., Blecher, G., Harper, J. & 6 othersSchofield, C., Nielsen, A., Wilson, A., Leonard, H., Choong, C. S. & Downs, J., 30 Jun 2019, In : Journal of Paediatrics and Child Health.

Research output: Contribution to journalReview article

Open Access
Prader-Willi Syndrome
Growth Hormone
Health Services
Health
Quality of Life

The Brain Basis of Comorbidity in Neurodevelopmental Disorders

Licari, M. K., Finlay-Jones, A., Reynolds, J. E., Alvares, G. A., Spittle, A. J., Downs, J., Whitehouse, A. J. O., Leonard, H., Evans, K. L. & Varcin, K., Mar 2019, In : Current Developmental Disorders Reports. 6, 1, p. 9-18 10 p.

Research output: Contribution to journalReview article

2018
15 Citations (Scopus)

The prevalence of mental health disorders and symptoms in children and adolescents with cerebral palsy: a systematic review and meta-analysis

Downs, J., Blackmore, A. M., Epstein, A., Skoss, R., Langdon, K., Jacoby, P., Whitehouse, A. J. O., Leonard, H., Rowe, P. W., Glasson, E. J. & The Cerebral Palsy Mental Health Group, 1 Jan 2018, In : Developmental Medicine and Child Neurology. 60, 1, p. 30-38 9 p.

Research output: Contribution to journalReview article

Cerebral Palsy
Mental Disorders
Meta-Analysis
Mental Health
Confidence Intervals
5 Citations (Scopus)
Refugees
Parents
Intellectual Disability
Mothers
Attention Deficit Disorder with Hyperactivity

What effect does regular exercise have on oxidative stress in people with Down syndrome? A systematic review with meta-analyses

Shields, N., Downs, J., de Haan, J. B., Taylor, N. F., Torr, J., Fernhall, B., Kingsley, M., Mnatzaganian, G. & Leonard, H., 1 Jun 2018, In : Journal of Science and Medicine in Sport. 21, 6, p. 596-603 8 p.

Research output: Contribution to journalReview article

Down Syndrome
Meta-Analysis
Oxidative Stress
Biomarkers
Antioxidants
2009
25 Citations (Scopus)

Siblings of children with disabilities: challenges and opportunities

Dyke, P., Mulroy, S. & Leonard, H., 2009, In : Acta Paediatrica. 98, 1, p. 23-24

Research output: Contribution to journalReview article

2008
4 Citations (Scopus)

A guide for the assessment and management of vitamin D status in people with intellectual disability (developed as an AADDM Working Party initiative)

Vanlint, S., Nugent, M., Durvasula, S., Downs, J. & Leonard, H., 2008, In : Journal of Intellectual and Developmental Disability. 33, 2, p. 184 - 188

Research output: Contribution to journalReview article

53 Citations (Scopus)

Rare childhood diseases: How should we respond?

Zurynski, Y. A., Frith, K., Leonard, H. & Elliott, E. J., 2008, In : Archives of Disease in Childhood. 93, p. 1071-1074

Research output: Contribution to journalReview article

Rare Diseases
Health Services
Health Planning
Family Health
Research
2005
2 Citations (Scopus)
2004
7 Citations (Scopus)

Trisomy 21 and Rett syndrome: A double burden

Leonard, H., Weaving, L., Eastaugh, P., Smith, L., Delatycki, M., Engerstrom, I. W. & Christodoulou, J., 2004, In : Journal of Paediatrics and Child Health. 40, 7, p. 406-409

Research output: Contribution to journalReview article

Rett Syndrome
Down Syndrome
Methyl-CpG-Binding Protein 2
Hand
Dual (Psychiatry) Diagnosis
2003
69 Citations (Scopus)

Patients with the R133C mutation: is their phenotype different from patients with Rett syndrome with other mutations?

Leonard, H., Colvin, L., Christodoulou, J., Schiavello, T., Williamson, S., Davis, M., Ravine, D., Fyfe, S., De Klerk, N., Matsuishi, T., Kondo, I., Clarke, A., Hackwell, S. & Yamashita, Y., 2003, In : Journal of Medical Genetics. 40, 5, p. online - approx 5-10pp

Research output: Contribution to journalReview article