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Profil bibliographique

Mark Harris

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

77Publications signalées
8175Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Computer Graphics and Visualization TechniquesParallel Computing and Optimization Techniques3D Shape Modeling and AnalysisAdvanced Data Storage TechnologiesScoliosis diagnosis and treatment

Les publications récentes

Accès ouvert 2025 book-chapter OpenAlex

Context Beyond Simple Rules: Deploying an Automated NLP-Based Pipeline for Sentiment and Theme Prediction in Paediatric Healthcare Setting

Caroline Baumgartner, Ewart Jonny Sheldon, Sebin Sabu, Jaskaran Singh Kawatra et autres

The National Health Service (NHS) uses the Friends and Family Test (FFT) to gather patient feedback aimed at improving service quality and satisfaction. The current workflow involves FFT feedback processed manually by the Patient Experience team to identify sentiment and theme, which …

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0 citations Frontiers in artificial intelligence and applications
Accès ouvert 2025 conference-abstract OpenAlex

96 Context beyond simple rules: enhancing the natural language processing pipeline for sentiment and theme prediction in family and friends test feedback

Caroline Baumgartner, Sebin Sabu, Jaskaran Singh Kawatra, Pavithra Rajendran et autres

Background In this work, we present our outcomes on operationalising a Natural Language Processing (NLP) pipeline which helps the Patient Experience team by reducing their efforts towards a time-consuming manual approach. Our pipeline automates and provides an accurate summary of NHS Friends …

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0 citations
Accès ouvert 2025 conference-abstract OpenAlex

155 The surgical and anaesthetic management in scoliosis correction in tuberous scoliosis complex (Bourneville’s disease)

Aman Sharma, Priyanka Nageswaran, Edel Broomfield, Daniel Fontannaz et autres

Introduction Tuberous Sclerosis Complex (TSC) is a rare autosomal dominant disease with an incidence of 1:8000 and manifests with cutaneous, cerebral, cardiac, ophthalmic and renal tuberous growth. The scoliosis in TSC patients is very rare with only 2 deformity corrections reported. We …

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0 citations
Accès ouvert 2024 article OpenAlex

Retrospective analysis of medium-term outcomes following anterior lumbar interbody fusion surgery performed in a tertiary spinal surgical centre

T. Srirangarajan, Kelechi Eseonu, B Fakouri, Panagiotis Liantis et autres

INTRODUCTION: Anterior lumbar interbody fusion (ALIF) can treat spondylolisthesis, degenerative disc disease and pseudoarthrosis. This approach facilitates complete discectomy, disc space distraction, indirect decompression of neural foramina and placement of large interbody devices. Several intra- and postoperative complications can be attributed to …

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4 citations Annals of The Royal College of Surgeons of England
Accès ouvert 2023 conference-paper OpenAlex

47 Operationalising a friends and family test natural language processing pipeline

Victor Banda, William Bryant, Suzanne Collin, Taraben Kapadia et autres

Background To manage the workload of data entry, manual sentence splitting and redaction of patient feedback that comes in form of 2000 comments per month, the patient experience team have worked with multiple data teams at GOSH to automate the process through …

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0 citations Poster presentations
2021 conference-paper OpenAlex

48 Enhanced recovery after surgery for patients with adolescent idiopathic scoliosis (AIS) undergoing posterior spinal fusion

Lauren Wilson, Marina George, Edel Broomfield, Mark Harris et autres

Background The benefits of using an Enhanced Recovery after Surgery (ERAS) protocol are recognised in adults but, until recently, there has been little evidence in paediatrics. Posterior spinal fusion (PSF) for adolescent idiopathic scoliosis (AIS) can be associated with significant pain and …

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1 citation Digital posters
Accès ouvert 2020 conference-paper OpenAlex

65 Management of early-onset scoliosis in patients with Prader Willi syndrome with magnetic growth rods – a case series review

Henry Bowyer, Amir Ahmadzadeh Amiri, Mark Harris

Background Prader Willi syndrome (PWS) is a rare genetic disorder characterised by developmental delay and hyperphagia. It is strongly associated with scoliosis, largely attributed to hypotonia and ligamentous laxity. Management of scoliosis in these patients can be challenging due to early onset …

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0 citations

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