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Development and internal validation of a model for postoperative morbidity in adults undergoing major elective colorectal surgery: the peri‐operative quality improvement programme (PQIP) colorectal risk model

Anaesthesia, 2022-12, Vol.77 (12), p.1356-1367

2022

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Development of a scoring system for survival following surgery for metastatic bone disease

The bone & joint journal, 2021-11, Vol.103-B (11), p.1725-1730

2021

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Epidermal Growth Factor Receptor, Protein Kinase B/Akt, and Glioma Response to Erlotinib

JNCI : Journal of the National Cancer Institute, 2005-06, Vol.97 (12), p.880-887

2005

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Pre-hospital management of burns by the UK fire service

Emergency medicine journal : EMJ, 2005-03, Vol.22 (3), p.205-208

2005

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Recognition and management of haemophagocytic lymphohistiocytosis on the ICU: a case series

Critical care (London, England), 2012-01, Vol.16 (S1), p.P441-P441, Article P441

2012

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Neck Ultrasound Prior to Percutaneous Tracheostomy: Should this Now be a Standard of Practice?

Journal of the Intensive Care Society, 2011-10, Vol.12 (4), p.342-342

2011

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Pregnancy outcome in a woman with spina bifida and a ventriculo-peritoneal shunt

Journal of obstetrics and gynaecology, 1999, Vol.19 (3), p.304-305

1999

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Occludin phosphorylation: identification of an occludin kinase in brain and cell extracts as CK2

FEBS letters, 2003-06, Vol.545 (2), p.161-166

2003

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Hereditary elliptocytosis complicating pregnancy

Journal of obstetrics and gynaecology, 1999, Vol.19 (3), p.308-309

1999

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Sequence variants in the genes for the interleukin-23 receptor (IL23R) and its ligand (IL12B) confer protection against psoriasis

Human genetics, 2007-09, Vol.122 (2), p.201-206

2007

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Delivery of drinking, eating and mobilising (DrEaMing) and its association with length of hospital stay after major noncardiac surgery: observational cohort study

British journal of anaesthesia : BJA, 2022-07, Vol.129 (1), p.114-126

2022

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Methylation of the PTEN promoter defines low-grade gliomas and secondary glioblastoma

Neuro-oncology (Charlottesville, Va.), 2007-07, Vol.9 (3), p.271-279

2007

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Predicting severe pain after major surgery: a secondary analysis of the Peri-operative Quality Improvement Programme (PQIP) dataset

Anaesthesia, 2023-07, Vol.78 (7), p.840-852

2023

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Assessing resilience to underpin implementation of Land Degradation Neutrality: A case study in the rangelands of western New South Wales, Australia

Environmental science & policy, 2019-10, Vol.100, p.37-46

2019

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Identification of a novel mutation disrupting the DNA binding activity of GCM2 in autosomal recessive familial isolated hypoparathyroidism

Journal of medical genetics, 2005-05, Vol.42 (5), p.443-448

2005

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A genome-wide scan and HCRTR2 candidate gene analysis in a European cluster headache cohort

Neurology, 2006-06, Vol.66 (12), p.1888-1893

2006

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Sperm Mitochondrial Function is Affected by Stallion Age and Predicts Post-Thaw Motility

Journal of equine veterinary science, 2017-03, Vol.50, p.52-61

2017

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Research priorities in single-ventricle heart conditions: a United Kingdom national study

Cardiology in the young, 2019-03, Vol.29 (3), p.303-309

2019

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Kangaroos in the rangelands: opportunities for landholder collaboration

The Rangeland journal, 2009, Vol.31 (1), p.161

2009

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Sharing Skippy: how can landholders be involved in kangaroo production in Australia?

The Rangeland journal, 2009, Vol.31 (3), p.283

2009

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Low prevalence of MYOC mutations in UK primary open-angle glaucoma patients limits the utility of genetic testing

Human genetics, 2004-10, Vol.115 (5), p.428-431

2004

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A novel locus for Meckel-Gruber syndrome, MKS3, maps to chromosome 8q24

Human genetics, 2002-10, Vol.111 (4-5), p.456-461

2002

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Corrigendum: Mutations in FRMD7 , a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

Nature genetics, 2011-07, Vol.43 (7), p.720-720

2011

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Erratum: Corrigendum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

Nature genetics, 2011-06, Vol.43 (7), p.720-720

2011

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Correction: Corrigendum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

Nature genetics, 2011, Vol.43 (7), p.720-720

2011

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Development and internal validation of a model for postoperative morbidity in adults undergoing major elective colorectal surgery: the peri‐operative quality improvement programme (PQIP) colorectal risk model

Development of a scoring system for survival following surgery for metastatic bone disease

Epidermal Growth Factor Receptor, Protein Kinase B/Akt, and Glioma Response to Erlotinib

Pre-hospital management of burns by the UK fire service

Recognition and management of haemophagocytic lymphohistiocytosis on the ICU: a case series

Neck Ultrasound Prior to Percutaneous Tracheostomy: Should this Now be a Standard of Practice?

Pregnancy outcome in a woman with spina bifida and a ventriculo-peritoneal shunt

Occludin phosphorylation: identification of an occludin kinase in brain and cell extracts as CK2

Hereditary elliptocytosis complicating pregnancy

Sequence variants in the genes for the interleukin-23 receptor (IL23R) and its ligand (IL12B) confer protection against psoriasis

Delivery of drinking, eating and mobilising (DrEaMing) and its association with length of hospital stay after major noncardiac surgery: observational cohort study

Methylation of the PTEN promoter defines low-grade gliomas and secondary glioblastoma

Predicting severe pain after major surgery: a secondary analysis of the Peri-operative Quality Improvement Programme (PQIP) dataset

Assessing resilience to underpin implementation of Land Degradation Neutrality: A case study in the rangelands of western New South Wales, Australia

Identification of a novel mutation disrupting the DNA binding activity of GCM2 in autosomal recessive familial isolated hypoparathyroidism

A genome-wide scan and HCRTR2 candidate gene analysis in a European cluster headache cohort

Sperm Mitochondrial Function is Affected by Stallion Age and Predicts Post-Thaw Motility

Research priorities in single-ventricle heart conditions: a United Kingdom national study

Kangaroos in the rangelands: opportunities for landholder collaboration

Sharing Skippy: how can landholders be involved in kangaroo production in Australia?

Low prevalence of MYOC mutations in UK primary open-angle glaucoma patients limits the utility of genetic testing

A novel locus for Meckel-Gruber syndrome, MKS3, maps to chromosome 8q24

Corrigendum: Mutations in FRMD7 , a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

Erratum: Corrigendum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

Correction: Corrigendum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

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