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List of works by Andrew Biggin

20-year outcomes of childhood-onset type 1 diabetes: The CANDID incident cohort survey

scientific article published on 03 December 2020

A 21st century plague of biblical proportions

A Practical Approach to Children with Recurrent Fractures

scientific article published on 12 June 2015

Burosumab versus conventional therapy in children with X-linked hypophosphataemia: a randomised, active-controlled, open-label, phase 3 trial

scientific article published on 16 May 2019

Clinical Evidence for the Benefits of Burosumab Therapy for X-Linked Hypophosphatemia (XLH) and Other Conditions in Adults and Children

scientific article published on 28 May 2020

Consensus guidelines on the use of bisphosphonate therapy in children and adolescents.

scientific article published in March 2018

Detection of thirty novel FBN1 mutations in patients with Marfan syndrome or a related fibrillinopathy

scientific article published in January 2004

Effect of mutation type and location on clinical outcome in 1,013 probands with Marfan syndrome or related phenotypes and FBN1 mutations: an international study

scientific article

Evaluation of bone mineral density and morphology using pQCT in children after spinal cord injury

scientific article published on 11 March 2013

FBN1, TGFBR1, and the Marfan-craniosynostosis/mental retardation disorders revisited

scientific article published in May 2006

FGF23, Hypophosphatemia, and Emerging Treatments

scientific article published on 13 May 2019

Fracture during intravenous bisphosphonate treatment in a child with osteogenesis imperfecta: an argument for a more frequent, low-dose treatment regimen

scientific article published on 19 December 2013

Glibenclamide treatment in a Cantú syndrome patient with a pathogenic ABCC9 gain-of-function variant: Initial experience

scientific article published on 07 June 2019

Global consensus on nutritional rickets: Implications for Australia

scientific article published on 01 June 2020

Hemophagocytic Lymphohistiocytosis in Loeys-Dietz Syndrome

scientific article published on 09 March 2018

High Bone Mineral Density Osteogenesis Imperfecta in a Family with a Novel Pathogenic Variant in COL1A2

scientific article published on 11 September 2020

Homozygosity for frameshift mutations in XYLT2 result in a spondylo-ocular syndrome with bone fragility, cataracts, and hearing defects

scientific article

Intravenous zoledronic Acid given every 6 months in childhood osteoporosis

scientific article published on 18 September 2013

Long-Term Bisphosphonate Therapy in Osteogenesis Imperfecta

scientific article

Long-term Outcomes of Adolescent Anorexia Nervosa on Bone

scientific article published on 11 December 2018

Mutation screening of the mitochondrial genome using denaturing high-performance liquid chromatography.

scientific article published on 11 November 2004

Mutations in SLC34A3/NPT2c are associated with kidney stones and nephrocalcinosis

scientific article

Novel variant in Sp7/Osx associated with recessive osteogenesis imperfecta with bone fragility and hearing impairment

scientific article published on 27 January 2018

Osteogenesis imperfecta: diagnosis and treatment.

scientific article published on September 2014

Positive impacts of changes to a tertiary hospital after-hours endocrine and diabetes on-call service

scientific article published on 17 December 2019

Response to growth hormone therapy and gonadal pathology in 45,X/46,XY females

scientific article published on 28 April 2015

Safety and effectiveness of stoss therapy in children with vitamin D deficiency

scientific article published on 28 May 2019

The long-term effects of switching from active intravenous bisphosphonate treatment to low-dose maintenance therapy in children with osteogenesis imperfecta

scientific article

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