about
Vitamin D and skeletal health in infancy and childhood.Biallelic mutations in the 3' exonuclease TOE1 cause pontocerebellar hypoplasia and uncover a role in snRNA processing.Bone mass acquisition in healthy children.Generalized arterial calcification of infancy and pseudoxanthoma elasticum can be caused by mutations in either ENPP1 or ABCC6Differences in childhood adiposity influence upper limb fracture siteLongitudinal changes in lean mass predict pQCT measures of tibial geometry and mineralisation at 6-7 years.Skeletal morbidity in childhood acute lymphoblastic leukaemia.Tracking of 25-hydroxyvitamin D status during pregnancy: the importance of vitamin D supplementation.Validity of parental recall of children's fracture: implications for investigation of childhood osteoporosis.Children with nephrotic syndrome have greater bone area but similar volumetric bone mineral density to healthy controlsMaternal antenatal vitamin D status and offspring muscle development: findings from the Southampton Women's Survey.Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ.Seasonal variation in Internet searches for vitamin D.Energy expenditure, nutrition and growth.Investigation and management of hypercalcaemia in children.Investigation and management of short stature.Investigation and management of tall stature.Identifying targets to reduce the incidence of diabetic ketoacidosis at diagnosis of type 1 diabetes in the UK.Selective reduction in trabecular volumetric bone mineral density during treatment for childhood acute lymphoblastic leukemia.Pituitary function at long-term follow-up of childhood traumatic brain injury.Massive ovarian oedema: an unusual abdominal mass in infancy.Growth monitoring following traumatic brain injury.Approach to the Child with Hypercalcaemia.Diagnosis and management of Silver-Russell syndrome: first international consensus statement.Recognition and assessment of atypical and ambiguous genitalia in the newborn.Reduced cortical bone density with normal trabecular bone density in girls with Turner syndrome.Analysis of 17 α-hydroxyprogesterone in bloodspots by liquid chromatography tandem mass spectrometry.In vitro effects of combination chemotherapy on osteoblasts: implications for osteopenia in childhood malignancy.Hepatoblastoma in a child with a paternally-inherited ABCC8 mutation and mosaic paternal uniparental disomy 11p causing focal congenital hyperinsulinism.Bone Structural Characteristics and Response to Bisphosphonate Treatment in Children With Hajdu-Cheney Syndrome.Clinical features, diagnosis and molecular studies of familial central diabetes insipidus.Osteonecrosis following treatment for childhood acute lymphoblastic leukaemia: The Southampton Children's Hospital experience.Embedding electronic growth charts into clinical practice at a children's hospital.Iatrogenic injury in childhood staphylococcal scalded skin syndrome.Vitamin D and bone developmentElemental formula associated hypophosphataemic ricketsFurther defining the phenotypic spectrum of B4GALT7 mutationsManagement of Gonads in Adults with Androgen Insensitivity: An International SurveyHow close is the dose? Manipulation of 10 mg hydrocortisone tablets to provide appropriate doses to childrenLived experience of Silver-Russell syndrome: implications for management during childhood and into adulthood
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Justin H Davies
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Justin H Davies
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Justin H Davies
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0000-0001-7560-6320