Search Results - "Cheetham, Timothy D"
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Is ongoing testosterone required after pubertal induction in Duchenne muscular dystrophy?
Published in Endocrine Connections (01-09-2023)“…Glucocorticoids (GC) reduce inflammation and preserve muscle function in boys with Duchenne muscular dystrophy (DMD) but cause pubertal delay. Pubertal…”
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Genomic Polymorphism at the Interferon-Induced Helicase (IFIH1) Locus Contributes to Graves’ Disease Susceptibility
Published in The journal of clinical endocrinology and metabolism (01-08-2007)“…Context: A recent large-scale analysis of nonsynonymous coding polymorphisms showed strong evidence that an alanine to threonine amino acid change at codon 946…”
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3
Initial response of young people with thyrotoxicosis to block and replace or dose titration thionamide
Published in European thyroid journal (2022)“…Objective Patients with thyrotoxicosis are treated with anti-thyroid drug (ATD) using block and replace (BR) or a smaller, titrated dose of ATD (dose…”
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4
How do childhood diagnoses of type 1 diabetes cluster in time?
Published in PloS one (03-04-2013)“…Previous studies have indicated that type 1 diabetes may have an infectious origin. The presence of temporal clustering-an irregular temporal distribution of…”
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Catch-up growth and metabolic outcomes in adolescents born preterm
Published in Archives of disease in childhood (01-11-2016)“…BackgroundAccelerated infant weight gain in individuals born full term is linked to cardiovascular risk in adulthood, but data in those born preterm are…”
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Sexual health and fertility in Duchenne muscular dystrophy—An exploratory study
Published in Muscle & nerve (01-09-2024)“…Introduction/Aims Recent clinical guidelines recommend that adolescents with Duchenne muscular dystrophy (DMD) who are on daily glucocorticoid treatment should…”
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Quality of Life in Children and Young People With Congenital Adrenal Hyperplasia—UK Nationwide Multicenter Assessment
Published in The journal of clinical endocrinology and metabolism (21-12-2023)“…Abstract Context Quality of life (QoL) has been inconsistently reported in children and young people (CYP) with congenital adrenal hyperplasia (CAH). Objective…”
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Pubertal induction in adolescents with DMD is associated with high satisfaction, gonadotropin release and increased muscle contractile surface area
Published in European journal of endocrinology (01-01-2021)“…Background Pharmacological doses of glucocorticoids (GC) reduce inflammation and preserve muscle function in boys with Duchenne muscular dystrophy (DMD)…”
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Health status of children and young persons with congenital adrenal hyperplasia in the UK (CAH-UK): a cross-sectional multi-centre study
Published in European journal of endocrinology (01-10-2022)“…Objective There is limited knowledge on the onset of comorbidities in congenital adrenal hyperplasia (CAH) during childhood. We aimed to establish the health…”
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2022 European Thyroid Association Guideline for the management of pediatric Graves’ disease
Published in European thyroid journal (2022)“…Hyperthyroidism caused by Graves’ disease (GD) is a relatively rare disease in children. Treatment options are the same as in adults – antithyroid drugs (ATD),…”
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Randomised trial of block and replace vs dose titration thionamide in young people with thyrotoxicosis
Published in European journal of endocrinology (01-12-2020)“…Objective First-line treatment of thyrotoxicosis in young people is thionamide anti-thyroid drug (ATD) in a blocking dose with levothyroxine replacement (block…”
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The broad phenotypic spectrum of 17α-hydroxylase/17,20-lyase (CYP17A1) deficiency: a case series
Published in European journal of endocrinology (01-11-2021)“…Context 17α-Hydroxylase/17,20-lyase deficiency (17OHD) caused by mutations in the CYP17A1 gene is a rare form of congenital adrenal hyperplasia typically…”
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Expanding the Spectrum of Mutations in GH1 and GHRHR: Genetic Screening in a Large Cohort of Patients with Congenital Isolated Growth Hormone Deficiency
Published in The journal of clinical endocrinology and metabolism (01-09-2009)“…Context: It is estimated that 3–30% of cases with isolated GH deficiency (IGHD) have a genetic etiology, with a number of mutations being reported in GH1 and…”
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Should radioiodine be the first-line treatment for paediatric Graves' disease?
Published in Journal of pediatric endocrinology & metabolism : JPEM (01-07-2015)“…Debate exists regarding the optimal treatment strategy for paediatric Graves' disease with radioiodine (RAI), and surgery, usually reserved for failure of…”
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Predicted Benign and Synonymous Variants in CYP11A1 Cause Primary Adrenal Insufficiency Through Missplicing
Published in Journal of the Endocrine Society (01-01-2019)“…Abstract Primary adrenal insufficiency (PAI) is a potentially life-threatening condition that can present with nonspecific features and can be difficult to…”
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AIRE is not essential for the induction of human tolerogenic dendritic cells
Published in Autoimmunity (Chur, Switzerland) (18-05-2016)“…Loss-of-function mutations of the Autoimmune Regulator (AIRE) gene results in organ-specific autoimmunity and disease Autoimmune Polyendocrinopathy type 1…”
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Growth and metabolic outcome in adolescents born preterm (GROWMORE): follow-up protocol for the Newcastle Preterm Birth GRowth study (PTBGS)
Published in BMC pediatrics (20-12-2013)“…Preterm infants represent up to 10% of births worldwide and have an increased risk of adverse metabolic outcomes in later life. Early life exposures are key…”
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Establishing a registry of children and young people with diabetes in north east England and north Cumbria
Published in Practical diabetes (2011) (01-03-2013)“…The incidence of type 1 diabetes and type 2 diabetes in children and adolescents is rising. The associated public health burden is substantial with major…”
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Rarer syndromes characterized by hypogonadotropic hypogonadism
Published in Frontiers of hormone research (01-01-2010)“…Hypogonadotropic hypogonadism (HH) secondary to hypothalamic gonadotropin-releasing hormone deficiency is a notable feature of a number of rare syndromes,…”
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Hypertonic saline test for the investigation of posterior pituitary function
Published in Archives of disease in childhood (01-11-1998)“…The hypertonic saline test is a useful technique for distinguishing partial diabetes insipidus from psychogenic polydipsia, and for the diagnosis of complex…”
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