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Congenital hypothyroidism in Northern Ireland: 40 years' experience of national screening programme

Clinical endocrinology (Oxford), 2023-10, Vol.99 (4), p.409-416

2023

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Fourteen-year-old girl with complicated hypothyroidism

Archives of disease in childhood. Education and practice edition, 2024-04, Vol.109 (2), p.95

2024

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Resolution of Consumptive Hypothyroidism Secondary to Infantile Hepatic Hemangiomatosis with a Combination of Propranolol and Levothyroxine

Journal of clinical research in pediatric endocrinology, 2018-09, Vol.10 (3), p.294-298

2018

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A novel IGSF1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF1 deficiency syndrome

Clinical endocrinology (Oxford), 2018-12, Vol.89 (6), p.813-823

2018

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Mortality in type 1 diabetes diagnosed in childhood in Northern Ireland during 1989‐2012: A population‐based cohort study

Pediatric diabetes, 2018-02, Vol.19 (1), p.166-170

2018

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Diagnostic value of exome and whole genome sequencing in craniosynostosis

Journal of medical genetics, 2017-04, Vol.54 (4), p.260

2017

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Clinical and metabolic effects of gluten free diet in children with type 1 diabetes and coeliac disease

Pediatric diabetes, 2011-06, Vol.12 (4pt1), p.322-325

2011

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Clinical Experience in the Screening and Management of a Large Kindred With Familial Isolated Pituitary Adenoma Due to an Aryl Hydrocarbon Receptor Interacting Protein (AIP) Mutation

The journal of clinical endocrinology and metabolism, 2014-04, Vol.99 (4), p.1122-1131

2014

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Mortality in type 1 diabetes diagnosed in childhood in Northern Ireland during 1989-2012: A population-based cohort study: MORGAN et al

Pediatric diabetes, 2018-02, Vol.19 (1), p.166-170

2018

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A novel IGSF 1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF 1 deficiency syndrome

Clinical endocrinology (Oxford), 2018-12, Vol.89 (6), p.813-823

2018

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Increased Population Risk of AIP‐Related Acromegaly and Gigantism in Ireland

Human mutation, 2017-01, Vol.38 (1), p.78-85

2017

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Thermal dysregulation in Prader-Willi syndrome: a potentially fatal complication in adolescence, not just in infancy

BMJ case reports, 2016-06, Vol.2016, p.bcr2016215344

2016

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The need for preoperative α-adrenergic blockade for ganglioneuroma excision

Pediatric anesthesia, 2014-03, Vol.24 (3), p.347-349

2014

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The need for preoperative [alpha]-adrenergic blockade for ganglioneuroma excision

Pediatric anesthesia, 2014-03, Vol.24 (3), p.347

2014

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Clinical characteristics and management of cranial diabetes insipidus in infants

Journal of Pediatric Endocrinology and Metabolism, 2013-11, Vol.26 (11), p.1041-1046

2013

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Differences in metabolic effects of twice daily versus multiple daily insulin injections in children with type 1 diabetes

Practical diabetes (2011), 2011-11, Vol.28 (9), p.384-387

2011

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The need for preoperative α-adrenergic blockade for ganglioneuroma excision

Paediatric anaesthesia, 2014, Vol.24 (3), p.347-349

2014

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Congenital hypothyroidism in Northern Ireland: 40 years' experience of national screening programme

Fourteen-year-old girl with complicated hypothyroidism

Resolution of Consumptive Hypothyroidism Secondary to Infantile Hepatic Hemangiomatosis with a Combination of Propranolol and Levothyroxine

A novel IGSF1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF1 deficiency syndrome

Mortality in type 1 diabetes diagnosed in childhood in Northern Ireland during 1989‐2012: A population‐based cohort study

Diagnostic value of exome and whole genome sequencing in craniosynostosis

Clinical and metabolic effects of gluten free diet in children with type 1 diabetes and coeliac disease

The Growth Hormone Deficiency

Clinical Experience in the Screening and Management of a Large Kindred With Familial Isolated Pituitary Adenoma Due to an Aryl Hydrocarbon Receptor Interacting Protein (AIP) Mutation

Mortality in type 1 diabetes diagnosed in childhood in Northern Ireland during 1989-2012: A population-based cohort study: MORGAN et al

A novel IGSF 1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF 1 deficiency syndrome

The Growth Hormone Deficiency (GHD) Reversal Trial: effect on final height of discontinuation versus continuation of growth hormone treatment in pubertal children with isolated GHD—a non-inferiority Randomised Controlled Trial (RCT)

Increased Population Risk of AIP‐Related Acromegaly and Gigantism in Ireland

Standardised practices in the networked management of congenital hyperinsulinism: a UK national collaborative consensus

Thermal dysregulation in Prader-Willi syndrome: a potentially fatal complication in adolescence, not just in infancy

The need for preoperative α-adrenergic blockade for ganglioneuroma excision

The need for preoperative [alpha]-adrenergic blockade for ganglioneuroma excision

Clinical characteristics and management of cranial diabetes insipidus in infants

Differences in metabolic effects of twice daily versus multiple daily insulin injections in children with type 1 diabetes

The need for preoperative α-adrenergic blockade for ganglioneuroma excision

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