R A Chalmers
Overview
Explore the profile of R A Chalmers including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
172
Citations
1052
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0
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Recent Articles
11.
Lord J, Thomason M, Littlejohns P, Chalmers R, Bain M, Addison G, et al.
J Epidemiol Community Health
. 1999 Jul;
53(3):179-86.
PMID: 10396496
Study Objective: To estimate the net financial benefit of neonatal screening for phenylketonuria (PKU): by a simple pooling of cost data from the literature; and by a more complex modelling...
12.
Halket J, Przyborowska A, Stein S, Mallard W, Down S, Chalmers R
Rapid Commun Mass Spectrom
. 1999 Mar;
13(4):279-84.
PMID: 10097403
The National Institute of Standards and Technology (NIST) Automated Mass Spectral Deconvolution and Identification System (AMDIS) is applied to a selection of data files obtained from the gas chromatography/mass spectrometry...
13.
Bax B, Bain M, Talbot P, PARKER-WILLIAMS E, Chalmers R
Clin Sci (Lond)
. 1999 Jan;
96(2):171-8.
PMID: 9918897
Erythrocytes offer the exciting opportunity of being used as carriers of therapeutic agents. Encapsulation within erythrocytes will give the therapeutic agent a clearance equivalent to the normal life of the...
14.
van der Knaap M, Jakobs C, Hoffmann G, Nyhan W, Renier W, Smeitink J, et al.
Ann Neurol
. 1999 Jan;
45(1):111-9.
PMID: 9894884
D-2-Hydroxyglutaric aciduria has been observed in patients with extremely variable clinical symptoms, creating doubt about the existence of a disease entity related to the biochemical finding. An international survey of...
15.
Thomason M, Lord J, Bain M, Chalmers R, Littlejohns P, Addison G, et al.
J Public Health Med
. 1998 Oct;
20(3):331-43.
PMID: 9793900
Background: Developments in screening technology and increased understanding of the natural history and treatment of inborn errors of metabolism (IEMs) have produced pressure to extend neonatal screening programmes. This review...
16.
Coughlin E, Christensen E, Kunz P, Krishnamoorthy K, Walker V, Dennis N, et al.
Mol Genet Metab
. 1998 Jun;
63(4):254-62.
PMID: 9635293
Fumarase deficiency is a rare autosomal recessive disorder of the citric acid cycle causing severe neurological impairment. The cDNA for both the rat and human enzymes has been cloned previously...
17.
Burns S, Holmes H, Chalmers R, Johnson A, Iles R
Biochim Biophys Acta
. 1998 Jun;
1406(3):274-82.
PMID: 9630673
Proton NMR spectra of urine from subjects with multiple acyl-CoA dehydrogenase deficiency, caused by defects in either the electron transport flavoprotein or electron transport flavoprotein ubiquinone oxidoreductase, provide a characteristic...
18.
Lee P, Harrison E, Jones M, Chalmers R, Leonard J, Whipp B
J Inherit Metab Dis
. 1998 May;
21(2):136-40.
PMID: 9584264
The effect of 4 weeks' treatment with oral-L-carnitine (100 mg/kg per day) on carnitine status and metabolic parameters during an incremental ramp exercise test in a 12-year-old girl with isovaleric...
19.
Chalmers R, Stanley C, English N, Wigglesworth J
J Pediatr
. 1997 Aug;
131(2):220-5.
PMID: 9290607
A breast-fed female infant died suddenly in the neonatal period at 31 hours of age with profound macrovesicular fatty infiltration of liver, kidney, and muscle on postmortem examination, suggestive of...
20.