Mark E Roberts
Overview
Explore the profile of Mark E Roberts including associated specialties, affiliations and a list of published articles.
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Articles
39
Citations
917
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Recent Articles
1.
Wu C, Ding J, Tindall G, Pittman Z, Thies M, Roberts M
Molecules
. 2024 Aug;
29(16).
PMID: 39202958
Over the past decade, the production of biofuels from lignocellulosic biomass has steadily increased to offset the use of fuels from petroleum. To make biofuels cost-competitive, however, it is necessary...
2.
Monceau A, Nath R, Suarez-Calvet X, Musumeci O, Toscano A, Kierdaszuk B, et al.
Brain
. 2024 Jul;
147(12):4213-4226.
PMID: 39045638
Late-onset Pompe disease (LOPD) is a rare genetic disorder caused by the deficiency of acid alpha-glucosidase leading to progressive cellular dysfunction owing to the accumulation of glycogen in the lysosome....
3.
Roberts M, Rahman N, Maskell N, Bibby A, Blyth K, Corcoran J, et al.
Thorax
. 2023 Aug;
78(11):1143-1156.
PMID: 37553157
No abstract available.
4.
Roberts M, Rahman N, Maskell N, Bibby A, Blyth K, Corcoran J, et al.
Thorax
. 2023 Jul;
78(Suppl 3):s1-s42.
PMID: 37433578
No abstract available.
5.
Williams A, Emmett R, Roberts M
Phys Chem Chem Phys
. 2023 Jun;
25(24):16222-16226.
PMID: 37288877
The zinc iodine (ZI) redox flow battery (RFB) has emerged as a promising candidate for grid-scale electrical energy storage owing to its high energy density, low cost and environmental friendliness....
6.
Rautemaa V, Roberts M, Bentley A, Felton T
ERJ Open Res
. 2021 Jul;
7(3).
PMID: 34322542
Type 1 myotonic dystrophy (DM1) causes sleep disordered breathing and respiratory failure due to a combination of obstructive sleep apnoea, reduced central drive and respiratory muscle weakness. Noninvasive ventilation (NIV)...
7.
Chaddha U, Agrawal A, Feller-Kopman D, Kaul V, Shojaee S, Maldonado F, et al.
Lancet Respir Med
. 2021 Feb;
9(9):1050-1064.
PMID: 33545086
Although our understanding of the pathogenesis of empyema has grown tremendously over the past few decades, questions still remain on how to optimally manage this condition. It has been almost...
8.
Ng Y, Thompson K, Loher D, Hopton S, Falkous G, Hardy S, et al.
Front Genet
. 2020 Mar;
11:24.
PMID: 32158465
Mitochondrial complex I deficiency is associated with a diverse range of clinical phenotypes and can arise due to either mitochondrial DNA (mtDNA) or nuclear gene defects. We investigated two adult...
9.
Molenaar J, Verhoeven J, Rodenburg R, Kamsteeg E, Erasmus C, Vicart S, et al.
Brain
. 2020 Feb;
143(2):452-466.
PMID: 32040565
Brody disease is an autosomal recessive myopathy characterized by exercise-induced muscle stiffness due to mutations in the ATP2A1 gene. Almost 50 years after the initial case presentation, only 18 patients...
10.
Bhatnagar R, Piotrowska H, Laskawiec-Szkonter M, Kahan B, Luengo-Fernandez R, Pepperell J, et al.
JAMA
. 2019 Dec;
323(1):60-69.
PMID: 31804680
Importance: Malignant pleural effusion (MPE) is challenging to manage. Talc pleurodesis is a common and effective treatment. There are no reliable data, however, regarding the optimal method for talc delivery,...