Publications by authors named "Timothy D Cheetham"

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L
Leptin and adiponectin in children and young persons with congenital adrenal hyperplasia.
Irina A Bacila, Neil R Lawrence, Sabah Alvi, Timothy D Cheetham, Elizabeth Crowne

Eur J Endocrinol· August 2025

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Sexual health and fertility in Duchenne muscular dystrophy-An exploratory study.
Janet Hoskin, Timothy D Cheetham, Rod T Mitchell, Sze Choong Wong, Claire L Wood

Muscle Nerve· September 2024

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Quality of Life in Children and Young People With Congenital Adrenal Hyperplasia-UK Nationwide Multicenter Assessment.
Neil Richard Lawrence, Irina Bacila, Jeremy Dawson, Sundus Mahdi, Sabah Alvi, Timothy D Cheetham

J Clin Endocrinol Metab· December 2023

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Is ongoing testosterone required after pubertal induction in Duchenne muscular dystrophy?
Claire L Wood, Kieren G Hollingsworth, Edrina Bokaie, Eric Hughes, Robert Muni-Lofra, Timothy D Cheetham

Endocr Connect· December 2023

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Expansion of the immature B lymphocyte compartment in Graves' disease.
Laura Claire Lane, Timothy David Cheetham, Salman Razvi, Kathleen Allinson, Simon Henry Schofield Pearce

Eur J Endocrinol· August 2023

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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.
Irina Bacila, Neil Richard Lawrence, Sundus Mahdi, Sabah Alvi, Timothy D Cheetham

Eur J Endocrinol· October 2022

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Initial response of young people with thyrotoxicosis to block and replace or dose titration thionamide.
Claire L Wood, Niamh Morrison, Michael Cole, Malcolm Donaldson, David B Dunger, Timothy D Cheetham

Eur Thyroid J· January 2022

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2022 European Thyroid Association Guideline for the management of pediatric Graves' disease.
Christiaan F Mooij, Timothy D Cheetham, Frederik A Verburg, Anja Eckstein, Simon H Pearce

Eur Thyroid J· January 2022

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The broad phenotypic spectrum of 17α-hydroxylase/17,20-lyase (CYP17A1) deficiency: a case series.
Min Sun, Jonathan W Mueller, Lorna C Gilligan, Angela E Taylor, Fozia Shaheen, Timothy D Cheetham

Eur J Endocrinol· October 2021

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Pubertal induction in adolescents with DMD is associated with high satisfaction, gonadotropin release and increased muscle contractile surface area.
Claire L Wood, Kieren G Hollingsworth, Eric Hughes, Sadhanandham Punniyakodi, Robert Muni-Lofra, Timothy D Cheetham

Eur J Endocrinol· January 2021

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Randomised trial of block and replace vs dose titration thionamide in young people with thyrotoxicosis.
Claire L Wood, Michael Cole, Malcolm Donaldson, David B Dunger, Ruth Wood, Timothy D Cheetham

Eur J Endocrinol· December 2020

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Predicted Benign and Synonymous Variants in Cause Primary Adrenal Insufficiency Through Missplicing.
Avinaash Maharaj, Federica Buonocore, Eirini Meimaridou, Gerard Ruiz-Babot, Leonardo Guasti, Timothy D Cheetham

J Endocr Soc· January 2019

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Catch-up growth and metabolic outcomes in adolescents born preterm.
Nicholas D Embleton, Murthy Korada, Claire L Wood, Mark S Pearce, Ravi Swamy, Timothy D Cheetham

Arch Dis Child· November 2016

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AIRE is not essential for the induction of human tolerogenic dendritic cells.
Katherine L Crossland, Mario Abinun, Peter D Arkwright, Timothy D Cheetham, Simon H Pearce

Autoimmunity· June 2016

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Should radioiodine be the first-line treatment for paediatric Graves' disease?
James D West, Timothy D Cheetham, Carole Dane, Anuja Natarajan

J Pediatr Endocrinol Metab· July 2015

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Growth and metabolic outcome in adolescents born preterm (GROWMORE): follow-up protocol for the Newcastle Preterm Birth GRowth study (PTBGS).
Claire L Wood, Robert J Tinnion, S Murthy Korada, Timothy D Cheetham, Caroline L Relton

BMC Pediatr· December 2013

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How do childhood diagnoses of type 1 diabetes cluster in time?
Colin R Muirhead, Timothy D Cheetham, Simon Court, Michael Begon, Richard J Q McNally

PLoS One· October 2013

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Rarer syndromes characterized by hypogonadotropic hypogonadism.
Majid Aminzadeh, Hyung-Goo Kim, Lawrence C Layman, Timothy D Cheetham

Front Horm Res· December 2010

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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.
Kyriaki S Alatzoglou, James P Turton, Daniel Kelberman, Peter E Clayton, Ameeta Mehta, Timothy D Cheetham

J Clin Endocrinol Metab· September 2009

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Genomic polymorphism at the interferon-induced helicase (IFIH1) locus contributes to Graves' disease susceptibility.
Alison Sutherland, Jocelyn Davies, Catherine J Owen, Suresh Vaikkakara, Christine Walker, Timothy D Cheetham

J Clin Endocrinol Metab· August 2007

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