Christine P. Burren

Bristol, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 37 publications

The lived experience of adolescents with X-linked hypophosphataemia treated with burosumab at end of skeletal growth: a mixed-methods analysis.

The lived experience of adolescents with X-linked hypophosphataemia treated with burosumab at end of skeletal growth: a mixed-methods analysis.

Journal: PloS one

Published: September 24, 2025

Adolescents' experience of living with X-linked hypophosphataemia (XLH): a mixed-methods analysis of those who continued and discontinued burosumab treatment after end of skeletal growth.

Adolescents' experience of living with X-linked hypophosphataemia (XLH): a mixed-methods analysis of those who continued and discontinued burosumab treatment after end of skeletal growth.

Journal: Orphanet journal of rare diseases

Published: September 04, 2025

Congenital hallux valgus occurs in Fibrodysplasia Ossificans Progressiva and BMPR1B-associated dysplasia: an important distinction.

Congenital hallux valgus occurs in Fibrodysplasia Ossificans Progressiva and BMPR1B-associated dysplasia: an important distinction.

Journal: BMC medical genomics

Published: January 12, 2024

Growth reference charts for children with hypochondroplasia.

Growth reference charts for children with hypochondroplasia.

Journal: American journal of medical genetics. Part A

Published: September 04, 2023

Effective Long-term Pediatric Pegvisomant Monotherapy to Final Height in X-linked Acrogigantism.

Effective Long-term Pediatric Pegvisomant Monotherapy to Final Height in X-linked Acrogigantism.

Journal: JCEM case reports

Published: November 13, 2022

Rapid-onset obesity, hypothalamic dysfunction, hypoventilation, and autonomic dysregulation syndrome - neuro-endocrine tumours (ROHHAD-NET): case series and learning points.

Rapid-onset obesity, hypothalamic dysfunction, hypoventilation, and autonomic dysregulation syndrome - neuro-endocrine tumours (ROHHAD-NET): case series and learning points.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: July 29, 2022

Patient-reported experience of clinical care of osteogenesis imperfecta (OI) during the COVID-19 pandemic.

Patient-reported experience of clinical care of osteogenesis imperfecta (OI) during the COVID-19 pandemic.

Journal: Frontiers in public health

Published: July 19, 2022

A systematic analysis of splicing variants identifies new diagnoses in the 100,000 Genomes Project.

A systematic analysis of splicing variants identifies new diagnoses in the 100,000 Genomes Project.

Journal: Genome medicine

Published: February 02, 2022

Infigratinib in children with achondroplasia: the PROPEL and PROPEL 2 studies.

Infigratinib in children with achondroplasia: the PROPEL and PROPEL 2 studies.

Journal: Therapeutic advances in musculoskeletal disease

Published: December 22, 2021

Mutations That Affect the Surface Expression of TRPV6 Are Associated with the Upregulation of Serine Proteases in the Placenta of an Infant.

Mutations That Affect the Surface Expression of TRPV6 Are Associated with the Upregulation of Serine Proteases in the Placenta of an Infant.

Journal: International journal of molecular sciences

Published: November 05, 2021

Monitoring Skull Base Abnormalities in Children with Osteogenesis Imperfecta - Review of Current Practice and a Suggested Clinical Pathway.

Monitoring Skull Base Abnormalities in Children with Osteogenesis Imperfecta - Review of Current Practice and a Suggested Clinical Pathway.

Journal: Bone

Published: August 08, 2021

Non-collagen pathogenic variants resulting in the osteogenesis imperfecta phenotype in children: a single-country observational cohort study.

Non-collagen pathogenic variants resulting in the osteogenesis imperfecta phenotype in children: a single-country observational cohort study.

Journal: Archives of disease in childhood

Published: July 27, 2021

Showing 1-12 of 37

Last Updated: 09/26/2026