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B Jarząb
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D Handkiewicz-Junak
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J Włoch
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ng/ml at the same time. The rhTSH group had significantly fewer hypothyroid symptoms and better quality of life, as measured by the Billewicz scoring system and Short Form-36 instrument respectively. In addition to the multicenter study, at

Article Type:
Review Article
DOI:
https://doi.org/10.1677/erc.1.00880
Volume/Issue:
Volume 12: Issue 4
Free access
Sasha R Howard Centre for Endocrinology, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, Charterhouse Square, London, UK
Department of Paediatric Endocrinology, Barts Health NHS Trust, London, UK

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Sarah Freeston Whipps Cross Hospital, Barts Health NHS Trust, London, UK

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Barney Harrison Retired Endocrine Surgeon, Sheffield, UK

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Louise Izatt Department of Clinical and Cancer Genetics, Guy’s and St Thomas’ NHS Foundation Trust, London, UK

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Sonali Natu Department of Pathology, University Hospital of North Tees and Hartlepool NHS Foundation Trust, Stockton-on-Tees, UK

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Kate Newbold Department of Clinical Oncology, Royal Marsden Hospital Foundation Trust, London, UK

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Sabine Pomplun Department of Pathology, University College London Hospital NHS Foundation Trust, London, UK

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Helen A Spoudeas Department of Paediatric Endocrinology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK

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Sophie Wilne Department of Paediatric Oncology, Nottingham University Hospital’s NHS Trust, Nottingham, UK

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Tom R Kurzawinski Department of Endocrine Surgery, University College London Hospitals NHS Foundation Trust, London, UK
Department of Paediatric Endocrine Surgery, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK

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Mark N Gaze Department of Clinical Oncology, University College London Hospitals NHS Foundation Trust, London, UK
Department of Clinical Oncology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK

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CYP-specific scoring system, the GDG recommends following Royal College of Pathologists guidelines. It is important to note that age is an important predictor of CYP in that most, albeit low quality, studies show that young children have a worse

Article Type:
Other
DOI:
https://doi.org/10.1530/ERC-22-0035
Volume/Issue:
Volume 29: Issue 11
Open access
Catherine Goudie Division of Hematology-Oncology, Department of Pediatrics, The Hospital for Sick Children, Toronto, Canada

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Fady Hannah-Shmouni Section on Endocrinology and Genetics The Eunice Kennedy Shriver Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA

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Mahmure Kavak Department of Pharmacology and Toxicology, University of Toronto, Toronto, Canada

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Constantine A Stratakis Section on Endocrinology and Genetics The Eunice Kennedy Shriver Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA

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William D Foulkes Department of Human Genetics, Research Institute of the McGill University Health Centre, and Lady Davis Institute, Jewish General Hospital, McGill University, Montreal, Canada

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et al . 1993 ). The clinical features of BWS are presented in Table 1 . Recently, a comprehensive consensus statement including a scoring system for genetic testing in patients with clinical features of BWS was presented by Brioude et al . (2018

Article Type:
Review Article
DOI:
https://doi.org/10.1530/ERC-18-0160
Volume/Issue:
Volume 25: Issue 8
Free access