about
Germline or somatic GPR101 duplication leads to X-linked acrogigantism: a clinico-pathological and genetic study.Risedronate in children with osteogenesis imperfecta: a randomised, double-blind, placebo-controlled trial.Mitochondrial dysfunction in patients with primary congenital insulin resistance.Attitudes to Exercise and Diabetes in Young People with Type 1 Diabetes Mellitus: A Qualitative Analysis.Improving patient outcomes in fibrous dysplasia/McCune-Albright syndrome: an international multidisciplinary workshop to inform an international partnership.Gonadotrophin abnormalities in an infant with Lowe syndrome.Identification of 70 calcium-sensing receptor mutations in hyper- and hypo-calcaemic patients: evidence for clustering of extracellular domain mutations at calcium-binding sites.Care of children with diabetes as inpatients: frequency of admissions, clinical care and patient experience.Hartsfield syndrome associated with a novel heterozygous missense mutation in FGFR1 and incorporating tumoral calcinosis.Diagnostic and management challenges from childhood, puberty through to transition in severe insulin resistance due to insulin receptor mutations.Pamidronate "zebra lines": A treatment timeline.TRPV6 compound heterozygous variants result in impaired placental calcium transport and severe undermineralization and dysplasia of the fetal skeletonBritish Paediatric and Adolescent Bone Group's position statement on vitamin D deficiencyHow does physical activity and fitness influence glycaemic control in young people with Type 1 diabetes?Evaluation and management of bone health in children with epilepsy on long-term antiepileptic drugs: United Kingdom survey of paediatric neurologistsInpatient care for children with diabetes: are standards being met?Clinical report follow up: Type 1 Collagenopathy presenting with a Russell-Silver phenotypePost-mortem histology in transient receptor potential cation channel subfamily V member 6 (TRPV6) under-mineralising skeletal dysplasia suggests postnatal skeletal recovery: a case reportPAPSS2-related brachyolmia: Clinical and radiological phenotype in 18 new casesChallenges of delivery of dental care and dental pathologies in children and young people with osteogenesis imperfecta
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Christine P Burren
@ast
Christine P Burren
@en
Christine P Burren
@es
Christine P Burren
@nl
type
label
Christine P Burren
@ast
Christine P Burren
@en
Christine P Burren
@es
Christine P Burren
@nl
prefLabel
Christine P Burren
@ast
Christine P Burren
@en
Christine P Burren
@es
Christine P Burren
@nl
P106
P1153
6603729237
P21
P31
P496
0000-0002-3778-2945