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M. Greenslade

North Bristol NHS Trust

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Multi site comparative study of three heparin induced thrombocytopenia (HIT) test methods and preliminary consideration of their utility in suspected vaccine induced thrombocytopenia and thrombosis (VITT)

2021 Transfusion Medicine
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Direct-Drive Linear Actuators for a Lower Extremity Exoskeleton

2017
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P.334 - Genetic diagnosis of inherited peripheral neuropathies using gene panel testing: The utility of follow up familial testing in 4 years of experience

2017 Neuromuscular Disorders
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GARS mutation Genotype phenotype correlation

2016
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A novel homozygous frameshift deletion in the SH3TC2 gene in a patient with Charcot–Marie–Tooth (CMT) type 4C and severe ataxia

2016 Neuromuscular Disorders
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Homozygous Familial Hypercholesterolaemia – Summary of cases detected at the Bristol Genetics Laboratory

2016 Atherosclerosis
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Modernising workflows for high throughput testing for Familial Hypercholesterolaemia: How to deliver a cost effective genetic testing service

2016 Atherosclerosis
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Implementation of a comprehensive gene screening test for familial hypercholesterolaemia using next generation sequencing

2013 Atherosclerosis
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(27) DNA sequence variant c.932A>C, p.Lys311Thr in LDLR gene in familial hypercholesterolaemia (FH): Observations from family studies

2012 Atherosclerosis
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3) Development of a single comprehensive gene screening test for familial hypercholesterolaemia using next generation sequencing

2012 Atherosclerosis
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