Zobrazeno 1 - 10
of 48
pro vyhledávání: '"R. N. Dalton"'
Publikováno v:
Journal of Osteoporosis, Vol 2014 (2014)
Background. Vitamin D is important for bone health, although high loading doses have been associated with an increase in fracture risk. The mechanisms remain uncertain. Aim. We hypothesize that supraphysiological concentrations of 1,25 (OH)2 vitamin
Externí odkaz:
https://doaj.org/article/eb27113d4ba445d797d6cdc00fbb748b
Autor:
Andrew Sutton, Elizabeth Brettell, Kamlesh Khunti, F S Morris, Ryan S Ottridge, Jonathan Barratt, Alice J Sitch, Tracy Pellatt-Higgins, Paul Cockwell, Gillian Eaglestone, Maarten W. Taal, R A Jones, Edmund J. Lamb, Paul E. Stevens, Jonathan J Deeks, Philip A. Kalra, R N Dalton, Claire C. Sharpe
Publikováno v:
Annals of clinical biochemistry. 57(2)
Background Patients with chronic kidney disease often have increased plasma cardiac troponin concentration in the absence of myocardial infarction. Incidence of myocardial infarction is high in this population, and diagnosis, particularly of non ST-s
AIMS/HYPOTHESIS: Early detection of risk of microalbuminuria could prevent early renal damage. We investigated whether urine retinol binding protein and N-acetyl-glucosaminidase could predict the risk of microalbuminuria in a large cohort of children
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c04708043a8df46340b7091b2fd5f67a
https://ora.ox.ac.uk/objects/uuid:3f5a0272-6a65-4162-ade6-a1788c9c19de
https://ora.ox.ac.uk/objects/uuid:3f5a0272-6a65-4162-ade6-a1788c9c19de
OBJECTIVE: The early detection of a rise in albumin excretion within the normal range could permit early intervention to prevent the development of microalbuminuria (MA) in genetically susceptible subjects with type 1 diabetes. In the Oxford Regional
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cccd2ddfcc01ae589a29c6ffb6a7e4ee
https://doi.org/10.2337/diacare.23.12.1811
https://doi.org/10.2337/diacare.23.12.1811
Autor:
C. J. Schultz, R. N. Dalton, C. Turner, H. A. W. Neil, D. B. Dunger, for the Oxford Regional Prospective Group
Aims. Microalbuminuria and, to a lesser extent, renal tubular proteins are widely used in the early detection of incipient nephropathy in diabetes mellitus. Recent reports have indicated detrimental effects of storage at - 20°C on urine proteins. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27207cc239dd2b2d66053ce06032dc52
https://doi.org/10.1046/j.1464-5491.2000.00200.x
https://doi.org/10.1046/j.1464-5491.2000.00200.x
Autor:
Heather N. Reich, R. N. Dalton, Denis Daneman, Rahim Moineddin, Yesmino Elia, R. Dekker, Farid H. Mahmud, Etienne Sochett, David B. Dunger, James W. Scholey, David Z.I. Cherney
Publikováno v:
Diabetic Medicine. 29:1297-1302
Diabet. Med. 29, 1297–1302 (2012) Abstract Aims Patients with the highest albumin:creatinine ratio within the normal range are at an increased risk for developing microalbuminuria. The mechanistic basis for this is unknown, but may be related to re
Publikováno v:
Diabetic Medicine. 28:685-691
Diabet. Med. 28, 685–691 (2011) Abstract Aims Asymmetric dimethylarginine (ADMA) is an independent risk factor for cardiovascular disease and its concentrations are increased in several diseases, including diabetes. However, there is limited inform
Autor:
H. A. W. Neil, John A. Todd, Julie Edge, Barry Widmer, Carlo L. Acerini, Jason D. Cooper, R. N. Dalton, A. T. Prevost, C. P. Schwarze, M. L. Marcovecchio, Timothy Barrett, David B. Dunger, Julian P.H. Shield
Publikováno v:
Diabetologia. 52:1173-1181
AIMS/HYPOTHESIS: The relationship between BP and microalbuminuria in young people with type 1 diabetes is not completely clear. As microalbuminuria is preceded by a gradual rise in albumin excretion within the normal range, we hypothesised that ambul
Publikováno v:
Archives of Disease in Childhood. 94:258-262
To prospectively determine the change in prevalence of microalbuminuria in relation to changes in glycaemic control in children diagnosed with type 1 diabetes between 1986 and 1996.Prospective observational study of an inception cohort.The geographic
Autor:
M. Downing, G. T. N. Besley, M Cortina-Borja, J Leonard, J Oerton, M Henderson, Carol Dezateux, A Green, R N Dalton, Javaria M Khalid, Brage S. Andresen
Publikováno v:
Khalid, J M, Oerton, J, Cortina-Borja, M, Andresen, B S, Besley, G, Dalton, R N, Downing, M, Green, A, Henderson, M, Leonard, J, Dezateux, C & UK Collaborative Study of Newborn Screening for MCADD 2008, ' Ethnicity of children with homozygous c.985A >G medium-chain acyl-CoA dehydrogenase deficiency: findings from screening approximately 1.1 million newborn infants ', Journal of Medical Screening, vol. 15, no. 3, pp. 112-7 . https://doi.org/10.1258/jms.2008.008043
Objectives It has been suggested that homozygous c.985A>G medium-chain acyl-CoA dehydrogenase deficiency (MCADD) is a disease of White ethnic origin but little is known regarding its ethnic distribution. We estimated ethnic-specific homozygous c.985A