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The UPTAKE study: implications for the future of COVID-19 vaccination trial recruitment in UK and beyond

Trials, 2021-04, Vol.22 (1), p.296-296, Article 296

2021

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The UPTAKE study: a cross-sectional survey examining the insights and beliefs of the UK population on COVID-19 vaccine uptake and hesitancy

BMJ open, 2021-06, Vol.11 (6), p.e048856-e048856

2021

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Steroid Sulfatase Deficiency and Androgen Activation Before and After Puberty

The journal of clinical endocrinology and metabolism, 2016-06, Vol.101 (6), p.2545-2553

2016

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Reductions in Basal Metabolic Rate and Physical Activity Contribute to Hypothalamic Obesity

The journal of clinical endocrinology and metabolism, 2008-07, Vol.93 (7), p.2588-2593

2008

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The relationship between bone mass and body composition in children with hypothalamic and simple obesity

Clinical endocrinology (Oxford), 2014-01, Vol.80 (1), p.85-91

2014

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Links Between Granuloma Annulare, Necrobiosis Lipoidica Diabeticorum and Childhood Diabetes: A Matter of Time?

Pediatric dermatology, 2010-03, Vol.27 (2), p.178-181

2010

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Hyperleptinaemia rather than fasting hyperinsulinaemia is associated with obesity following hypothalamic damage in children

European journal of endocrinology, 2008-12, Vol.159 (6), p.791-797

2008

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Response to Letter to the Editor From Arroyo et al: “Timing of Puberty, Pubertal Growth, and Adult Height in Short Children Born Small for Gestational Age Treated With Growth Hormone”

The journal of clinical endocrinology and metabolism, 2023-09, Vol.108 (10), p.e1161-e1161

2023

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Clinical characteristics and treatment requirements of children with autosomal recessive pseudohypoaldosteronism

European journal of endocrinology, 2021-05, Vol.184 (5), p.K15-K20

2021

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Idiopathic gonadotrophin deficiency: genetic questions addressed through phenotypic characterization

Clinical endocrinology (Oxford), 2001-08, Vol.55 (2), p.163-174

2001

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Causes, patterns and severity of androgen excess in 487 consecutively recruited pre- and post-pubertal children

European journal of endocrinology, 2019-03, Vol.180 (3), p.213-221

2019

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KLB, encoding β‐Klotho, is mutated in patients with congenital hypogonadotropic hypogonadism

EMBO molecular medicine, 2017-10, Vol.9 (10), p.1379-1397

2017

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Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humans

The Journal of clinical investigation, 2006-09, Vol.116 (9), p.2442-2455

2006

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Functional Consequences of Seven Novel Mutations in the CYP11B1 Gene: Four Mutations Associated with Nonclassic and Three Mutations Causing Classic 11β-Hydroxylase Deficiency

The journal of clinical endocrinology and metabolism, 2010-02, Vol.95 (2), p.779-788

2010

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Phenotypic variability in 17β-hydroxysteroid dehydrogenase-3 deficiency and diagnostic pitfalls

Clinical endocrinology (Oxford), 2007-07, Vol.67 (1), p.20-28

2007

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Septo-Optic Dysplasia: Antenatal Risk Factors and Clinical Features in a Regional Study

Hormone research in paediatrics, 2012-01, Vol.78 (2), p.81-87

2012

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An association of craniopharyngioma in Turner syndrome

Pediatric blood & cancer, 2013-06, Vol.60 (6), p.E7-E9

2013

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Estradiol: micrograms or milligrams

Endocrinology, diabetes & metabolism case reports, 2016-02, Vol.2016, p.150096-150096

2016

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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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Functional Consequences of Seven Novel Mutations in the CYP11B1 Gene: Four Mutations Associated with Nonclassic and Three Mutations Causing Classic 11β-Hydroxylase Deficiency

Endocrinology (Philadelphia), 2010-02, Vol.151 (2), p.839-839

2010

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Impact of disordered puberty on bone density in β‐thalassaemia major

British journal of haematology, 2003-01, Vol.120 (2), p.353-358

2003

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Acute Fatty Liver Disease after Suprasellar Tumor Resection

Journal of pediatric gastroenterology and nutrition, 2004-09, Vol.39 (3), p.288-291

2004

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Thyroxine: cause and cure for headache

Acta pædiatrica (Oslo), 2006-05, Vol.95 (5), p.632-633

2006

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Thyroxine: Cause and cure for headache

Acta Paediatrica, 2006-05, Vol.95 (5), p.632-633

2006

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Abnormal growth in noonan syndrome: the challenge of optimal therapy

Pediatric endocrinology reviews : PER, 2009-06, Vol.6 Suppl 4, p.523

2009

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The UPTAKE study: implications for the future of COVID-19 vaccination trial recruitment in UK and beyond

The UPTAKE study: a cross-sectional survey examining the insights and beliefs of the UK population on COVID-19 vaccine uptake and hesitancy

Steroid Sulfatase Deficiency and Androgen Activation Before and After Puberty

Reductions in Basal Metabolic Rate and Physical Activity Contribute to Hypothalamic Obesity

The relationship between bone mass and body composition in children with hypothalamic and simple obesity

Links Between Granuloma Annulare, Necrobiosis Lipoidica Diabeticorum and Childhood Diabetes: A Matter of Time?

Hyperleptinaemia rather than fasting hyperinsulinaemia is associated with obesity following hypothalamic damage in children

Response to Letter to the Editor From Arroyo et al: “Timing of Puberty, Pubertal Growth, and Adult Height in Short Children Born Small for Gestational Age Treated With Growth Hormone”

Clinical characteristics and treatment requirements of children with autosomal recessive pseudohypoaldosteronism

Idiopathic gonadotrophin deficiency: genetic questions addressed through phenotypic characterization

Causes, patterns and severity of androgen excess in 487 consecutively recruited pre- and post-pubertal children

KLB, encoding β‐Klotho, is mutated in patients with congenital hypogonadotropic hypogonadism

Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humans

Functional Consequences of Seven Novel Mutations in the CYP11B1 Gene: Four Mutations Associated with Nonclassic and Three Mutations Causing Classic 11β-Hydroxylase Deficiency

Phenotypic variability in 17β-hydroxysteroid dehydrogenase-3 deficiency and diagnostic pitfalls

Septo-Optic Dysplasia: Antenatal Risk Factors and Clinical Features in a Regional Study

An association of craniopharyngioma in Turner syndrome

Estradiol: micrograms or milligrams

Clinical characteristics and management of cranial diabetes insipidus in infants

Functional Consequences of Seven Novel Mutations in the CYP11B1 Gene: Four Mutations Associated with Nonclassic and Three Mutations Causing Classic 11β-Hydroxylase Deficiency

Impact of disordered puberty on bone density in β‐thalassaemia major

Acute Fatty Liver Disease after Suprasellar Tumor Resection

Thyroxine: cause and cure for headache

Thyroxine: Cause and cure for headache

Abnormal growth in noonan syndrome: the challenge of optimal therapy

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