Publications by authors named "Paul Arundel"

25Publications

High-resolution peripheral quantitative computed tomography in children with osteogenesis imperfecta.

Pediatr Radiol 2020 11 1;50(12):1781-1787. Epub 2020 Jul 1.

Academic Unit of Child Health, University of Sheffield, Damer Street, Sheffield, S10 2TH, UK.

View Article and Find Full Text PDF
November 2020

Autism and heritable bone fragility: A true association?

Bone Rep 2018 Jun 18;8:156-162. Epub 2018 Apr 18.

Academic Unit of Child Health, University of Sheffield, UK.

View Article and Find Full Text PDF
June 2018

Type V osteogenesis imperfecta undergoing surgical correction for scoliosis.

Eur Spine J 2018 09 19;27(9):2079-2084. Epub 2018 Feb 19.

Sheffield Children's Hospital, Sheffield, UK.

View Article and Find Full Text PDF
September 2018

Atypical osteogenesis imperfecta caused by a 17q21.33 deletion involving COL1A1.

Clin Dysmorphol 2017 Oct;26(4):228-230

aYorkshire Regional Genetics Service, Chapel Allerton Hospital, Leeds Teaching Hospitals NHS Trust, Leeds bClinical Genetics Service, City Hospital Campus cDepartment of Cytogenetics, Nottingham University Hospitals NHS Trust, Nottingham dDepartment of Paediatric Psychology eHighly Specialised Severe, Complex and Atypical OI Service fSheffield Clinical Genetics Service, Sheffield Children's NHS Foundation Trust gAcademic Unit of Child Health, University of Sheffield, Sheffield, UK.

View Article and Find Full Text PDF
October 2017

The Effect of Whole Body Vibration Training on Bone and Muscle Function in Children With Osteogenesis Imperfecta.

J Clin Endocrinol Metab 2017 08;102(8):2734-2743

Department of Endocrinology & Diabetes, Birmingham Children's Hospital, Birmingham B4 6NH, United Kingdom.

View Article and Find Full Text PDF
August 2017

Phenotypic variability in patients with osteogenesis imperfecta caused by BMP1 mutations.

Am J Med Genet A 2016 12 30;170(12):3150-3156. Epub 2016 Aug 30.

Highly Specialised Severe, Complex and Atypical OI Service, Sheffield Children's NHS Foundation Trust, Sheffield, UK.

View Article and Find Full Text PDF
December 2016

Copy number variants in association with type 1 collagenopathy: Atypical osteogenesis imperfecta.

Am J Med Genet A 2016 Feb 15;170A(2):476-481. Epub 2015 Oct 15.

Academic Unit of Child Health, University of Sheffield, United Kingdom.

View Article and Find Full Text PDF
February 2016

Primary Osteoporosis.

Endocr Dev 2015 12;28:162-75. Epub 2015 Jun 12.

Academic Unit of Child Health, University of Sheffield, Sheffield Children's Hospital, Sheffield, UK.

View Article and Find Full Text PDF
November 2016

CRTAP mutation in a patient with Cole-Carpenter syndrome.

Am J Med Genet A 2015 Mar 21;167A(3):587-91. Epub 2015 Jan 21.

Sheffield Clinical Genetics Service, Sheffield Children's NHS Foundation Trust, UK.

View Article and Find Full Text PDF
March 2015

Ultrastructural and histological findings on examination of skin in osteogenesis imperfecta: a novel study.

Clin Dysmorphol 2015 Apr;24(2):45-54

aSheffield Clinical Genetics Service bDepartment of Histopathology cSheffield Diagnostic Genetics Service, Sheffield Children's NHS Foundation Trust dElectron Microscopy Unit, Department of Histopathology, Royal Hallamshire Hospital eNational EDS Service fAcademic Unit of Child Health, University of Sheffield, Sheffield, UK.

View Article and Find Full Text PDF
April 2015

Fracture prediction and the definition of osteoporosis in children and adolescents: the ISCD 2013 Pediatric Official Positions.

J Clin Densitom 2014 Apr-Jun;17(2):275-80. Epub 2014 Mar 14.

Department of Endocrinology and Diabetes, Birmingham Children's Hospital, Birmingham, UK.

View Article and Find Full Text PDF
August 2014

Genotype-phenotype study in type V osteogenesis imperfecta.

Clin Dysmorphol 2013 Jul;22(3):93-101

Sheffield Clinical Genetics Service, Sheffield Children's NHS Foundation Trust, Sheffield, UK.

View Article and Find Full Text PDF
July 2013