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Recommendations for the Diagnosis and Management of Prader-Willi Syndrome

The journal of clinical endocrinology and metabolism, 2008-11, Vol.93 (11), p.4183-4197

2008

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The presentation, course and outcome of COVID-19 infection in people with Prader-Willi syndrome: unexpected findings from an international survey

Orphanet journal of rare diseases, 2022-02, Vol.17 (1), p.69-69, Article 69

2022

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The CaSR Modulator NPS-2143 Reduced UV-Induced DNA Damage in Skh:hr1 Hairless Mice but Minimally Inhibited Skin Tumours

International journal of molecular sciences, 2023-03, Vol.24 (5), p.4921

2023

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Patient journey mapping to investigate quality and cultural safety in burn care for Aboriginal and Torres Strait Islander children and families - development, application and implications

BMC health services research, 2022-11, Vol.22 (1), p.1428-1428, Article 1428

2022

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Systemic long-term metabolic effects of acute non-severe paediatric burn injury

Scientific reports, 2022-07, Vol.12 (1), p.13043-13043, Article 13043

2022

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Factors that impact access to ongoing health care for First Nation children with a chronic condition

BMC health services research, 2018-06, Vol.18 (1), p.448-448, Article 448

2018

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Gene expression profiling in the adult Down syndrome brain

Genomics (San Diego, Calif.), 2007-12, Vol.90 (6), p.647-660

2007

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Development of the eating behaviour in Prader–Willi Syndrome: advances in our understanding

International Journal of Obesity, 2011-02, Vol.35 (2), p.188-197

2011

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The phenomenology and diagnosis of psychiatric illness in people with Prader–Willi syndrome

Psychological medicine, 2008-10, Vol.38 (10), p.1505-1514

2008

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Appetite hormones and the transition to hyperphagia in children with Prader-Willi syndrome

International Journal of Obesity, 2012-12, Vol.36 (12), p.1564-1570

2012

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Factors contributing to longer length of stay in Aboriginal and Torres Strait Islander children hospitalised for burn injury

Injury epidemiology, 2020-10, Vol.7 (1), p.52-11, Article 52

2020

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Population prevalence and estimated birth incidence and mortality rate for people with Prader-Willi syndrome in one UK Health Region

Journal of medical genetics, 2001-11, Vol.38 (11), p.792-798

2001

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Recurrent and metastatic congenital mesoblastic nephroma: where does the evidence stand?

Pediatric surgery international, 2017-11, Vol.33 (11), p.1183-1188

2017

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Duty of care and autonomy: how support workers managed the tension between protecting service users from risk and promoting their independence in a specialist group home

Journal of intellectual disability research, 2011-09, Vol.55 (9), p.873-884

2011

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A longitudinal follow-up study of people with Prader–Willi syndrome with psychosis and those at increased risk of developing psychosis due to genetic subtype

Psychological medicine, 2014-08, Vol.44 (11), p.2431-2435

2014

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Novel insights into maladaptive behaviours in Prader-Willi syndrome: serendipitous findings from an open trial of vagus nerve stimulation

Journal of intellectual disability research, 2016-02, Vol.60 (2), p.149-155

2016

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Indigenous research methodology - weaving a research interface

International journal of social research methodology, 2020-05, Vol.23 (3), p.255-267

2020

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The impact of general anesthesia on child development and school performance: a population‐based study

Pediatric anesthesia, 2018-06, Vol.28 (6), p.528-536

2018

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The course and outcome of psychiatric illness in people with Prader-Willi syndrome: implications for management and treatment

Journal of intellectual disability research, 2007-01, Vol.51 (1), p.32-42

2007

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Changes in appetite, food preference, and eating habits in frontotemporal dementia and Alzheimer’s disease

Journal of neurology, neurosurgery and psychiatry, 2002-10, Vol.73 (4), p.371-376

2002

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Hypothesis: arterial glycocalyx dysfunction is the first step in the atherothrombotic process

QJM, 2008-07, Vol.101 (7), p.513-518

2008

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Prune belly syndrome

Pediatric surgery international, 2012-03, Vol.28 (3), p.219-228

2012

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1,25-Dihydroxyvitamin D3 Suppresses UV-Induced Poly(ADP-Ribose) Levels in Primary Human Keratinocytes, as Detected by a Novel Whole-Cell ELISA

International journal of molecular sciences, 2024-05, Vol.25 (11), p.5583

2024

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Living 'a life like ours': support workers' accounts of substitute decision-making in residential care homes for adults with intellectual disabilities

Journal of intellectual disability research, 2010-02, Vol.54 (2), p.144-160

2010

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Behavioural phenotypes associated with specific genetic disorders: evidence from a population-based study of people with Prader-Willi syndrome

Psychological medicine, 2003-01, Vol.33 (1), p.141-153

2003

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Recommendations for the Diagnosis and Management of Prader-Willi Syndrome

The presentation, course and outcome of COVID-19 infection in people with Prader-Willi syndrome: unexpected findings from an international survey

The CaSR Modulator NPS-2143 Reduced UV-Induced DNA Damage in Skh:hr1 Hairless Mice but Minimally Inhibited Skin Tumours

Patient journey mapping to investigate quality and cultural safety in burn care for Aboriginal and Torres Strait Islander children and families - development, application and implications

Systemic long-term metabolic effects of acute non-severe paediatric burn injury

Factors that impact access to ongoing health care for First Nation children with a chronic condition

Gene expression profiling in the adult Down syndrome brain

Development of the eating behaviour in Prader–Willi Syndrome: advances in our understanding

The phenomenology and diagnosis of psychiatric illness in people with Prader–Willi syndrome

Appetite hormones and the transition to hyperphagia in children with Prader-Willi syndrome

Factors contributing to longer length of stay in Aboriginal and Torres Strait Islander children hospitalised for burn injury

Population prevalence and estimated birth incidence and mortality rate for people with Prader-Willi syndrome in one UK Health Region

Recurrent and metastatic congenital mesoblastic nephroma: where does the evidence stand?

Duty of care and autonomy: how support workers managed the tension between protecting service users from risk and promoting their independence in a specialist group home

A longitudinal follow-up study of people with Prader–Willi syndrome with psychosis and those at increased risk of developing psychosis due to genetic subtype

Novel insights into maladaptive behaviours in Prader-Willi syndrome: serendipitous findings from an open trial of vagus nerve stimulation

Indigenous research methodology - weaving a research interface

The impact of general anesthesia on child development and school performance: a population‐based study

The course and outcome of psychiatric illness in people with Prader-Willi syndrome: implications for management and treatment

Changes in appetite, food preference, and eating habits in frontotemporal dementia and Alzheimer’s disease

Hypothesis: arterial glycocalyx dysfunction is the first step in the atherothrombotic process

Prune belly syndrome

1,25-Dihydroxyvitamin D3 Suppresses UV-Induced Poly(ADP-Ribose) Levels in Primary Human Keratinocytes, as Detected by a Novel Whole-Cell ELISA

Living 'a life like ours': support workers' accounts of substitute decision-making in residential care homes for adults with intellectual disabilities

Behavioural phenotypes associated with specific genetic disorders: evidence from a population-based study of people with Prader-Willi syndrome

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