Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Stephen M P O'Riordan"'
Publikováno v:
Endocrine Abstracts.
Autor:
Mehul T. Dattani, D. P. R. Muller, Gayatri Sharma, Kevin Mills, Sinead Bryan, Peter Hindmarsh, Stephen M. P. O'Riordan
Publikováno v:
Free Radical Biology & Medicine
Increased oxidative stress has been implicated in both the onset and the progression of diabetes mellitus and its complications. The development of easy to measure biomarkers of oxidative stress would, therefore, help in determining in a prospective
Autor:
Li F. Chan, Stephen M. P. O'Riordan, Heiko Krude, Colm Costigan, Martin O. Savage, Adrian J. L. Clark, Paolo Cavarzere, Colin Ball, Louise A. Metherell, Sally Ann Lynch
Publikováno v:
Clinical Endocrinology
Summary Objective Familial glucocorticoid deficiency (FGD) is a rare auto- somal recessive disease characterized by isolated glucocorticoid deficiency with preserved mineralocorticoid secretion. Mutations in the ACTH receptor (MC2R) account for appro
Publikováno v:
Pediatric Diabetes. 9:338-344
The Developmental Endocrinology Research Group, The Institute of Child Health, University College London, London, UK; Department of Respiratory Medicine, The Children’s Hospital at Westmead, University of Sydney, Sydney, Australia; Institute of End
Autor:
Hilary Hoey, S. George, Nathan R. Hill, Nuala Murphy, Edna Roche, Gerard J. Canny, Peter Hindmarsh, Colm Costigan, Stephen M. P. O'Riordan, Dubhfeasa Slattery, David R. Matthews, Peter Greally
Publikováno v:
Diabetes Care. 32:1020-1022
OBJECTIVE To validate continuous glucose monitoring (CGM) in children and adolescents with cystic fibrosis. RESEARCH DESIGN AND METHODS Paired oral glucose tolerance tests (OGTTs) and CGM monitoring was undertaken in 102 children and adolescents with
Autor:
Gayatri Sharma, Kevin Mills, Mehul T. Dattani, Sinead M Bryan, Peter C. Hindmarsh, Stephen M. P. O'Riordan, David P R Muller
Publikováno v:
Molecular nutritionfood research. 54(5)
Publikováno v:
Cystic Fibrosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06b101e3a401cfe14743553c965117eb
https://doi.org/10.1093/med/9780199582709.003.0007
https://doi.org/10.1093/med/9780199582709.003.0007
Publikováno v:
Pediatric diabetes. 10
TheDepartment of Pediatrics, University of Minnesota Children’sHospital, Minneapolis, USACorresponding author:Dr. Stephen MP O’Riordan MRCPI, MDThe Developmental Endocrinology and Research GroupThe Department of Clinical and Molecular GeneticsThe
Publikováno v:
Hormone research in paediatrics. 73(1)
Since the early 1990s the management of children with cystic fibrosis (CF) has come a long way and advances in both nutritional and medical care have resulted in a median age of survival of 30–35 years, as compared with a life expectancy of
Autor:
Stephen M P, O'Riordan, Peter, Hindmarsh, Nathan R, Hill, David R, Matthews, Sherly, George, Peter, Greally, Gerard, Canny, Dubhfeasa, Slattery, Nuala, Murphy, Edna, Roche, Colm, Costigan, Hilary, Hoey
Publikováno v:
Diabetes Care
OBJECTIVE To validate continuous glucose monitoring (CGM) in children and adolescents with cystic fibrosis. RESEARCH DESIGN AND METHODS Paired oral glucose tolerance tests (OGTTs) and CGM monitoring was undertaken in 102 children and adolescents with