Jeremy Allgrove | International and Private Care

Dr Jeremy Allgrove is a Consultant Paediatric Endocrinologist and is part of the multidisciplinary osteogenesis imperfecta service at Great Ormond Street Hospital (GOSH). He also runs a clinic for other metabolic bone and calcium disorders at GOSH.

使用语言：

English

Metabolic bone disease
Calcium and phosphate disorders
Osteoporosis in children
Osteogenesis imperfecta

Training:

MA
MD
FRCP
FRCPCH

Memberships:

Member European Society for Paediatric Endocrinology
Member British Society for Paediatric Endocrinology and Diabetes
Member British Paediatric and Adolescent Bone Group
Member Bone Research Society

Vitamin D
Parathyroid Hormone treatment of hypoparathyroidism

论文及文章发表

Allgrove, J., 2015. Voyages of Discovery. Endocr Dev 28:1-6. In: J. Allgrove and NJ. Shaw NJ, ed. 2nd Edition, Calcium and Bone Disorders in Children and Adolescents, Basel: Karger. Ch1.

Allgrove, J., 2015. Physiology of Calcium, Phosphate, Magnesium and Vitamin D. Endocr Dev 28:7-32. In: J. Allgrove and NJ. Shaw NJ, ed. 2nd Edition, Calcium and Bone Disorders in Children and Adolescents, Basel: Karger. Ch 2.

Allgrove, J., 2015 Classification of Disorders of Bone and Calcium Metabolism. Endocr Dev 28:291-318. In: J. Allgrove and NJ. Shaw NJ, ed. 2nd Edition, Calcium and Bone Disorders in Children and Adolescents,Basel: Karger. Ch 18.

Katugampola, H., Saraff, V., Kumaran, A., Allgrove, J., Shaw, N.J., 2015. Case Histories. Endocr Dev 28:319-413. In: J. Allgrove and NJ. Shaw NJ, ed. 2nd Edition, Calcium and Bone Disorders in Children and Adolescents, Basel: Karger. Ch. 19.

Formosa, N., Torpiano, J., Allgrove, J., Dattani, M.T., 2015. Anticonvulsant treatment associated with intractable hypocalcaemia in a female child with hypoparathyroidism. Horm Res Paediatr. 83 pp. 62-6.

Rogers, A., Nesbit, M.A., Hannan, F.M., Howles, S.A., Gorvin, C.M., Cranston, T., Allgrove, J., Bevan, J.S., Bano, G., Brain, C., Datta, V., Grossman, A.B., Hodgson, S.V., Izatt, L., Millar-Jones, L., Pearce, S.H., Robertson, L., Selby, P.L., Shine, B., Snape, K., Warner, J., Thakker, R.V. 2014. Mutational analysis of the adaptor protein 2 sigma subunit (AP2S1) gene: search for autosomal dominant hypocalcemia type 3 (ADH3).J Clin Endocrinol Metab. 99 pp. 1300-5.

Habel, A., Herriot, R., Kumararatne, D., Allgrove, J., Baker, K., Baxendale, H., Bu'Lock, F., Firth, H., Gennery, A., Holland, A., Illingworth, C., Mercer, N., Pannebakker, M., Parry, A., Roberts, A., Tsai-Goodman, B., 2014. Towards a safety net for management of 22q11.2 deletion syndrome: guidelines for our times. Eur J Pediatr. 173 pp. 757-65.

Alagaratnam, S., Brain, C., Spoudeas, H., Dattani, M.T., Hindmarsh, P., Allgrove, J., Van't Hoff, W., Kurzawinski, T.R., 2014. Surgical treatment of children with hyperparathyroidism: single centre experience. J Pediatr Surg. 49 pp. 1539-43.

Allgrove, J., Mughal, M.Z., 2014. Calcium deficiency rickets: extending the spectrum of 'nutritional' rickets. Arch Dis Child. 99 pp. 794-5.

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