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Outcomes of using flash glucose monitoring technology by children and young people with type 1 diabetes in a single arm study

Pediatric diabetes, 2018-11, Vol.19 (7), p.1294-1301

2018

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Activating germline mutations in STAT3 cause early-onset multi-organ autoimmune disease

Nature genetics, 2014-08, Vol.46 (8), p.812-814

2014

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Letter to the Editor: “Alemtuzumab-Induced Thyroid Dysfunction Exhibits Distinctive Clinical and Immunological Features”

The journal of clinical endocrinology and metabolism, 2019-09, Vol.104 (9), p.3624-3625

2019

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Permanent Decompensated Congenital Hypothyroidism in Newborns with Whole-Blood Thyroid-Stimulating Hormone Concentrations between 8 and 10 mU/L: The Case for Lowering the Threshold

Hormone research in paediatrics, 2018-01, Vol.89 (4), p.265-270

2018

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International Newborn Screening Practices for the Early Detection of Congenital Adrenal Hyperplasia

Hormone research in paediatrics, 2024, Vol.97 (2), p.113

2024

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A realist synthesis of multicentre comparative audit implementation: exploring what works and in which healthcare contexts

BMJ open quality, 2024-03, Vol.13 (1), p.e002629

2024

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Clinical and genetic heterogeneity of HNF4A/HNF1A mutations in a multicentre paediatric cohort with hyperinsulinaemic hypoglycaemia

European journal of endocrinology, 2022-04, Vol.186 (4), p.417

2022

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The presentation of congenital adrenal hyperplasia in an unscreened population

Journal of pediatric endocrinology & metabolism : JPEM, 2021-09, Vol.34 (9), p.1123

2021

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The Association of Vitamin D Status with Acute Respiratory Morbidity in Preterm Infants

The Journal of pediatrics, 2015-05, Vol.166 (5), p.1175-1180.e1

2015

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Vitamin D nutritional status in preterm infants and response to supplementation

British journal of nutrition, 2013-07, Vol.110 (1), p.156-163

2013

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Coeliac screening in a high-risk population: paediatric type 1 diabetes—a review of current guidelines and practice

Irish journal of medical science, 2019-02, Vol.188 (1), p.135-139

2019

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Next-Generation Sequencing Reveals Deep Intronic Cryptic ABCC8 and HADH Splicing Founder Mutations Causing Hyperinsulinism by Pseudoexon Activation

American journal of human genetics, 2013-01, Vol.92 (1), p.131-136

2013

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Expanding the clinical spectrum of chromosome 15q26 terminal deletions associated with IGF-1 resistance

European journal of pediatrics, 2017, Vol.176 (1), p.137-142

2017

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Vitamin D Status in Irish Children and Adolescents: Value of Fortification and Supplementation

Clinical pediatrics, 2014-12, Vol.53 (14), p.1345-1351

2014

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Randomized Cross-Over Trial of Insulin Glargine Plus Lispro or NPH Insulin Plus Regular Human Insulin in Adolescents With Type 1 Diabetes on Intensive Insulin Regimens

Diabetes care, 2003-03, Vol.26 (3), p.799-804

2003

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Secondary Hyperparathyroidism in Children with Mucolipidosis Type II (I-Cell Disease): Irish Experience

Journal of clinical medicine, 2022-03, Vol.11 (5), p.1366

2022

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Children and young people’s experiences and perceptions of self-management of type 1 diabetes: A qualitative meta-synthesis

Health Psychology Open, 2019-07, Vol.6 (2), p.205510291987710-2055102919877105

2019

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Spermatogenesis in a Prepubertal Boy

The Journal of pediatrics, 2012-08, Vol.161 (2), p.369-369.e1

2012

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Heritability of Childhood Weight Gain from Birth and Risk Markers for Adult Metabolic Disease in Prepubertal Twins

The journal of clinical endocrinology and metabolism, 2009-10, Vol.94 (10), p.3708-3713

2009

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Optimal Timing of Repeat Newborn Screening for Congenital Hypothyroidism in Preterm Infants to Detect Delayed Thyroid-Stimulating Hormone Elevation

The Journal of pediatrics, 2019-02, Vol.205, p.77-82

2019

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The Hypothalamic-Pituitary-Thyroid Axis in Preterm Infants; Changes in the First 24 Hours of Postnatal Life

The journal of clinical endocrinology and metabolism, 2004-06, Vol.89 (6), p.2824-2831

2004

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A Longitudinal Study of the Effects of a Gluten-Free Diet on Glycemic Control and Weight Gain in Subjects With Type 1 Diabetes and Celiac Disease

Diabetes care, 2002-07, Vol.25 (7), p.1117-1122

2002

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Triglyceride-rich lipoproteins inhibit cholesterol efflux to apolipoprotein (apo) A1 from human macrophage foam cells

Atherosclerosis, 2004-03, Vol.173 (1), p.27-38

2004

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Adolescent perspectives on negotiating self-management responsibilities for type 1 diabetes with their parents

Patient education and counseling, 2023-04, Vol.109, p.107629-107629, Article 107629

2023

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Sideroblastic anaemia and primary adrenal insufficiency due to a mitochondrial respiratory chain disorder in the absence of mtDNA deletion

BMJ case reports, 2015-02, Vol.2015 (feb26 1), p.bcr2014208514-bcr2014208514

2015

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Outcomes of using flash glucose monitoring technology by children and young people with type 1 diabetes in a single arm study

Activating germline mutations in STAT3 cause early-onset multi-organ autoimmune disease

Letter to the Editor: “Alemtuzumab-Induced Thyroid Dysfunction Exhibits Distinctive Clinical and Immunological Features”

Permanent Decompensated Congenital Hypothyroidism in Newborns with Whole-Blood Thyroid-Stimulating Hormone Concentrations between 8 and 10 mU/L: The Case for Lowering the Threshold

International Newborn Screening Practices for the Early Detection of Congenital Adrenal Hyperplasia

A realist synthesis of multicentre comparative audit implementation: exploring what works and in which healthcare contexts

Clinical and genetic heterogeneity of HNF4A/HNF1A mutations in a multicentre paediatric cohort with hyperinsulinaemic hypoglycaemia

The presentation of congenital adrenal hyperplasia in an unscreened population

The Association of Vitamin D Status with Acute Respiratory Morbidity in Preterm Infants

Vitamin D nutritional status in preterm infants and response to supplementation

Coeliac screening in a high-risk population: paediatric type 1 diabetes—a review of current guidelines and practice

Next-Generation Sequencing Reveals Deep Intronic Cryptic ABCC8 and HADH Splicing Founder Mutations Causing Hyperinsulinism by Pseudoexon Activation

Expanding the clinical spectrum of chromosome 15q26 terminal deletions associated with IGF-1 resistance

Vitamin D Status in Irish Children and Adolescents: Value of Fortification and Supplementation

Randomized Cross-Over Trial of Insulin Glargine Plus Lispro or NPH Insulin Plus Regular Human Insulin in Adolescents With Type 1 Diabetes on Intensive Insulin Regimens

Secondary Hyperparathyroidism in Children with Mucolipidosis Type II (I-Cell Disease): Irish Experience

Children and young people’s experiences and perceptions of self-management of type 1 diabetes: A qualitative meta-synthesis

Spermatogenesis in a Prepubertal Boy

Heritability of Childhood Weight Gain from Birth and Risk Markers for Adult Metabolic Disease in Prepubertal Twins

Optimal Timing of Repeat Newborn Screening for Congenital Hypothyroidism in Preterm Infants to Detect Delayed Thyroid-Stimulating Hormone Elevation

The Hypothalamic-Pituitary-Thyroid Axis in Preterm Infants; Changes in the First 24 Hours of Postnatal Life

A Longitudinal Study of the Effects of a Gluten-Free Diet on Glycemic Control and Weight Gain in Subjects With Type 1 Diabetes and Celiac Disease

Triglyceride-rich lipoproteins inhibit cholesterol efflux to apolipoprotein (apo) A1 from human macrophage foam cells

Adolescent perspectives on negotiating self-management responsibilities for type 1 diabetes with their parents

Sideroblastic anaemia and primary adrenal insufficiency due to a mitochondrial respiratory chain disorder in the absence of mtDNA deletion

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