List of works by Wolfgang Högler

A diagnosis not to be missed: nonclassic steroid 11β-hydroxylase deficiency presenting with premature adrenarche and hirsutism

scientific article published on 12 August 2013

Activating mutations in BRAF disrupt the hypothalamo-pituitary axis leading to hypopituitarism in mice and humans

scientific article published on 01 April 2021

Amalgamated Reference Data for Size-Adjusted Bone Densitometry Measurements in 3598 Children and Young Adults-the ALPHABET Study

scientific article

Bone Structural Characteristics and Response to Bisphosphonate Treatment in Children With Hajdu-Cheney Syndrome

scientific article published on 8 September 2017

Cardiac, bone and growth plate manifestations in hypocalcemic infants: revealing the hidden body of the vitamin D deficiency iceberg.

scientific article published on 26 June 2018

Complications of vitamin D deficiency from the foetus to the infant: One cause, one prevention, but who's responsibility?

scientific article published on 24 March 2015

ENDOCRINOLOGY AND ADOLESCENCE: Osteoporosis in children: diagnosis and management

scientific article published on 03 June 2015

Efficacy and treatment costs of zoledronate versus pamidronate in paediatric osteoporosis

scientific article published on 7 October 2017

Galactokinase deficiency in a patient with congenital hyperinsulinism

scientific article

Global Consensus Recommendations on Prevention and Management of Nutritional Rickets

scientific article published on 8 January 2016

IGFALS gene dosage effects on serum IGF-I and glucose metabolism, body composition, bone growth in length and width, and the pharmacokinetics of recombinant human IGF-I administration

scientific article published on 13 January 2014

New Developments in the Treatment of X-Linked Hypophosphataemia: Implications for Clinical Management

scientific article published on 01 April 2020

Oral Iron for Prevention and Treatment of Rickets and Osteomalacia in Autosomal Dominant Hypophosphatemia

scientific article published on 31 December 2019

Phenotypic Spectrum in Osteogenesis Imperfecta Due to Mutations in TMEM38B: Unraveling a Complex Cellular Defect

scientific article published on 16 March 2017

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

scientific article published on 30 August 2016

Skeletal and bone material phenotype in recessive osteogenesis imperfecta due to a novel homozygous point mutation in TMEM38B

article published in 2015

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

scientific article published on 3 May 2017