Philip Murray
Overview
Explore the profile of Philip Murray including associated specialties, affiliations and a list of published articles.
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Articles
14
Citations
315
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0
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Recent Articles
1.
Garner T, Clayton P, Hojby M, Murray P, Stevens A
J Clin Endocrinol Metab
. 2023 Dec;
109(5):1214-1221.
PMID: 38066644
Context: The pretreatment blood transcriptome predicts growth response to daily growth hormone (GH) therapy with high accuracy. Objective: Investigate response prediction using pretreatment transcriptome in children with GH deficiency (GHD)...
2.
Jain P, Badger D, Liang Y, Gebhard A, Santiago D, Murray P, et al.
Pept Sci (Hoboken)
. 2022 Jul;
113(3):e24199.
PMID: 35859761
HYD1 is an all D-amino acid linear 10-mer peptide that was discovered by one-bead-one-compound screening. HYD1 has five hydrophobic amino acids flanked by polar amino acids. Alanine scanning studies showed...
3.
Stevens A, Murray P, De Leonibus C, Garner T, Koledova E, Ambler G, et al.
Pharmacogenomics J
. 2021 May;
21(5):594-607.
PMID: 34045667
Recombinant human growth hormone (r-hGH) is used as a therapeutic agent for disorders of growth including growth hormone deficiency (GHD) and Turner syndrome (TS). Treatment is costly and current methods...
4.
Stevens A, Perchard R, Garner T, Clayton P, Murray P
Rev Endocr Metab Disord
. 2021 Mar;
22(1):135-143.
PMID: 33712998
We present current knowledge concerning the pharmacogenomics of growth hormone therapy in children with short stature. We consider the evidence now emerging for the polygenic nature of response to recombinant...
5.
van Trotsenburg P, Stoupa A, Leger J, Rohrer T, Peters C, Fugazzola L, et al.
Thyroid
. 2020 Dec;
31(3):387-419.
PMID: 33272083
An ENDO-European Reference Network (ERN) initiative was launched that was endorsed by the European Society for Pediatric Endocrinology and the European Society for Endocrinology with 22 participants from the ENDO-ERN...
6.
Mantovani G, Bastepe M, Monk D, de Sanctis L, Thiele S, Ahmed S, et al.
Horm Res Paediatr
. 2020 Aug;
93(3):182-196.
PMID: 32756064
Patients affected by pseudohypoparathyroidism (PHP) or related disorders are characterized by physical findings that may include brachydactyly, a short stature, a stocky build, early-onset obesity, ectopic ossifications, and neurodevelopmental deficits,...
7.
Yau D, Salomon-Estebanez M, Chinoy A, Grainger J, Craigie R, Padidela R, et al.
Endocrinol Diabetes Metab Case Rep
. 2019 Aug;
2019(1).
PMID: 31373474
Summary: Congenital hyperinsulinism (CHI) is an important cause of severe hypoglycaemia in infancy. To correct hypoglycaemia, high concentrations of dextrose are often required through a central venous catheter (CVC) with...
8.
Mantovani G, Bastepe M, Monk D, de Sanctis L, Thiele S, Usardi A, et al.
Nat Rev Endocrinol
. 2018 Jul;
14(8):476-500.
PMID: 29959430
This Consensus Statement covers recommendations for the diagnosis and management of patients with pseudohypoparathyroidism (PHP) and related disorders, which comprise metabolic disorders characterized by physical findings that variably include short...
9.
De Leonibus C, Murray P, Garner T, Hanson D, Clayton P, Stevens A
Pharmacogenomics J
. 2018 Jun;
19(2):200-210.
PMID: 29855605
Response to recombinant human growth hormone (r-hGH) in the first year of therapy has been associated with single-nucleotide polymorphisms (SNPs) in children with GH deficiency (GHD). Associated SNPs were screened...
10.
Stevens A, Murray P, Wojcik J, Raelson J, Koledova E, Chatelain P, et al.
Eur J Endocrinol
. 2016 Sep;
175(6):633-643.
PMID: 27651465
Objective: Single-nucleotide polymorphisms (SNPs) associated with the response to recombinant human growth hormone (r-hGH) have previously been identified in growth hormone deficiency (GHD) and Turner syndrome (TS) children in the...