List of works - Philip G. Murray

60 YEARS OF NEUROENDOCRINOLOGY: The hypothalamo-GH axis: the past 60 years

scientific article

A recurrent mitochondrial p.Trp22Arg NDUFB3 variant causes a distinctive facial appearance, short stature and a mild biochemical and clinical phenotype

scientific article published on 18 April 2016

Associations with multiple pituitary hormone deficiency in patients with an ectopic posterior pituitary gland

scientific article published on 10 March 2008

Controversies in the diagnosis and management of growth hormone deficiency in childhood and adolescence

scientific article published on 07 July 2015

Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement

article by Giovanna Mantovani et al published August 2018 in Nature Reviews Endocrinology

Exome sequencing identifies CCDC8 mutations in 3-M syndrome, suggesting that CCDC8 contributes in a pathway with CUL7 and OBSL1 to control human growth

scientific article

Exploring the spectrum of 3-M syndrome, a primordial short stature disorder of disrupted ubiquitination.

scientific article published on September 2012

Growth hormone, the insulin-like growth factor axis, insulin and cancer risk.

scientific article published on 19 October 2010

Identifying biological pathways that underlie primordial short stature using network analysis

scientific article

Likelihood of persistent GH deficiency into late adolescence: relationship to the presence of an ectopic or normally sited posterior pituitary gland.

scientific article

Metabolites involved in glycolysis and amino acid metabolism are altered in short children born small for gestational age.

scientific article published on 08 April 2016

Pediatric perspective on pharmacogenomics.

scientific article

Pharmacogenomics related to growth disorders

scientific article

Recommendations for Diagnosis and Treatment of Pseudohypoparathyroidism and Related Disorders: An Updated Practical Tool for Physicians and Patients

scientific article published on 05 August 2020

Reduced appetite and body mass index with delayed puberty in a mother and son: association with a rare novel sequence variant in the leptin gene

article

The genetics of 3-M syndrome: unravelling a potential new regulatory growth pathway.

scientific article

The primordial growth disorder 3-M syndrome connects ubiquitination to the cytoskeletal adaptor OBSL1.

scientific article published on 28 May 2009

List of works by Philip G. Murray

60 YEARS OF NEUROENDOCRINOLOGY: The hypothalamo-GH axis: the past 60 years

A recurrent mitochondrial p.Trp22Arg NDUFB3 variant causes a distinctive facial appearance, short stature and a mild biochemical and clinical phenotype

Associations with multiple pituitary hormone deficiency in patients with an ectopic posterior pituitary gland

Controversies in the diagnosis and management of growth hormone deficiency in childhood and adolescence

Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement

Exome sequencing identifies CCDC8 mutations in 3-M syndrome, suggesting that CCDC8 contributes in a pathway with CUL7 and OBSL1 to control human growth

Exploring the spectrum of 3-M syndrome, a primordial short stature disorder of disrupted ubiquitination.

Growth hormone, the insulin-like growth factor axis, insulin and cancer risk.

Identifying biological pathways that underlie primordial short stature using network analysis

Likelihood of persistent GH deficiency into late adolescence: relationship to the presence of an ectopic or normally sited posterior pituitary gland.

Metabolites involved in glycolysis and amino acid metabolism are altered in short children born small for gestational age.

Pediatric perspective on pharmacogenomics.

Pharmacogenomics related to growth disorders

Recommendations for Diagnosis and Treatment of Pseudohypoparathyroidism and Related Disorders: An Updated Practical Tool for Physicians and Patients

Reduced appetite and body mass index with delayed puberty in a mother and son: association with a rare novel sequence variant in the leptin gene

The genetics of 3-M syndrome: unravelling a potential new regulatory growth pathway.

The primordial growth disorder 3-M syndrome connects ubiquitination to the cytoskeletal adaptor OBSL1.