P Ian Andrews
Overview
Explore the profile of P Ian Andrews including associated specialties, affiliations and a list of published articles.
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15
Citations
268
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0
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Recent Articles
1.
Dale R, Thomas T, Patel S, Han V, Kothur K, Troedson C, et al.
Ann Clin Transl Neurol
. 2023 Jun;
10(8):1417-1432.
PMID: 37340737
Objective: Infection-triggered encephalopathy syndromes (ITES) are potentially devastating neuroinflammatory conditions. Although some ITES syndromes have recognisable MRI neuroimaging phenotypes, there are otherwise few biomarkers of disease. Early detection to enable...
2.
Yan J, Kothur K, Mohammad S, Chung J, Patel S, Jones H, et al.
EBioMedicine
. 2023 Apr;
91:104589.
PMID: 37119734
Background: Defining the presence of acute and chronic brain inflammation remains a challenge to clinicians due to the heterogeneity of clinical presentations and aetiologies. However, defining the presence of neuroinflammation,...
3.
Briest R, Cheung A, Kandula T, Cardamone M, Pillai S, Sampaio H, et al.
Dev Med Child Neurol
. 2022 Jun;
65(1):126-135.
PMID: 35661998
Aim: To improve delivery of acute therapies for acute ischaemic stroke (AIS). Method: We identified factors influencing the speed of diagnosis and delivery of acute therapies in a prospective cohort...
4.
Spinelli E, Christensen K, Bryant E, Schneider A, Rakotomamonjy J, Muir A, et al.
Ann Neurol
. 2021 Jun;
90(2):274-284.
PMID: 34185323
Objective: The MAST family of microtubule-associated serine-threonine kinases (STKs) have distinct expression patterns in the developing and mature human and mouse brain. To date, only MAST1 has been conclusively associated...
5.
Macdonald-Laurs E, Wenderoth J, Cardamone M, Sampaio H, Andrews P
Dev Med Child Neurol
. 2020 Jan;
62(10):1221-1223.
PMID: 31898325
Endovascular clot retrieval (ECR) is an emerging therapy for treatment of acute ischaemic stroke (AIS) in adults, including basilar artery occlusion (BAO). Its role in children is not well established....
6.
Mason S, Castilla-Vallmanya L, James C, Andrews P, Balcells S, Grinberg D, et al.
Medicine (Baltimore)
. 2019 Mar;
98(8):e14524.
PMID: 30813157
Rationale: Trio family-based whole exome sequencing (WES) is a powerful tool in the diagnosis of rare neurodevelopmental diseases, even in patients with the unclear diagnosis. There have been previous reports...
7.
Chan D, Young H, Palasanthiran P, Rawlinson W, Gray P, Andrews P
J Paediatr Child Health
. 2018 Jun;
54(11):1264-1267.
PMID: 29923642
No abstract available.
8.
Desai R, Frazier A, Durigon R, Patel H, Jones A, Dalla Rosa I, et al.
Brain
. 2017 May;
140(6):1595-1610.
PMID: 28549128
Although mitochondrial disorders are clinically heterogeneous, they frequently involve the central nervous system and are among the most common neurogenetic disorders. Identifying the causal genes has benefited enormously from advances...
9.
Teoh H, Mohammad S, Britton P, Kandula T, Lorentzos M, Booy R, et al.
JAMA Neurol
. 2016 Jan;
73(3):300-7.
PMID: 26785318
Importance: Enterovirus 71 (EV71) causes a spectrum of neurological complications with significant morbidity and mortality. Further understanding of the characteristics of EV71-related neurological disease, factors related to outcome, and potential...
10.
Guo Y, Menezes M, Menezes M, Liang J, Li D, Riley L, et al.
Neuromuscul Disord
. 2015 Jan;
25(3):257-61.
PMID: 25557462
Clinical phenotypes of congenital myasthenic syndromes and primary mitochondrial disorders share significant overlap in their clinical presentations, leading to challenges in making the correct diagnosis. Next generation sequencing is transforming...