Franklyn Howe
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Professor of Magnetic Resonance Imaging
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Professor Franklyn Howe is a faculty member at St. George's, University of London, specializing in Magnetic Resonance Imaging. His research interests encompass areas such as quasi-diffusion imaging, the characterization of bone marrow lesions in osteoarthritis, and the application of radiofrequency thalamotomy in tremor treatment. Professor Howe has contributed significantly to the understanding of diffusion imaging techniques and their clinical applications in neurology and osteoarthritis.
Recent Grants
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The use of multimodal MRI in clinical practice to aid diagnosis and prognosis for brain tumours
Open Date: 2021-01-01
Close Date: 2023-12-01
Grant: Close
Improving Brain Tumor Patient Outcomes through Patient Stratification & Novel Biomarkers
Open Date: 2017-10-01
Close Date: 2019-06-01
Grant: Close
Deep phenotyping to improve understanding of causal mechanisms and underlying gene mutations in primary lymphoedema and lymphatic malformations
Open Date: 2017-09-30
Close Date: 2022-09-29
Grant: Close
MRI biomarkers of low grade glioma growth and infiltration.
Open Date: 2012-06-01
Close Date: 2017-05-31
Grant: Close
MRI biomarkers of tumour response to anti-vascular therapy
Open Date: 2009-04-01
Close Date: 2012-09-30
Articles (8)
Year:
2025
Year:
2024
Radiofrequency thalamotomy is a neurosurgical management option for medically-refractory tremor. In this observational study, we evaluate the MRI features of the resultant lesion, their temporal dynamics, and how they vary depending on surgical factors. We report on lesion characteristics including size and location, as well as how these vary over time and across different MRI sequences. Data from 12 patients (2 essential tremor, 10 Parkinson’s disease) who underwent unilateral radiofrequency thalamotomy for tremor were analysed. Lesion characteristics were compared across five structural sequences. Volumetric analysis of lesion features was performed at early (<5 weeks) and late (>5 months) timepoints by manual segmentation. Lesion location was determined after registration of lesions to standard space. All patients showed tremor improvement (clinical global impressions scale) postoperatively. Chronic side-effects included balance disturbances (n = 4) and worsening mobility due to parkinsonism progression (n = 1). Early lesion features including a necrotic core, cytotoxic oedema and perilesional oedema were best demarcated on T2-weighted sequences. Multiple lesions were associated with greater cytotoxic oedema compared with single lesions (T2-weighted mean volume: 537 ± 112 mm³ versus 302 ± 146 mm³, P = 0.028). Total lesion volume reduced on average by 90% between the early and late scans (T2-weighted mean volume: 918 ± 517 versus 75 ± 50 mm³, t = 3.592, P = 0.023, n = 5), with comparable volumes demonstrated at ∼6 months after surgery. Lesion volumes on susceptibility-weighted images were larger than those of T2-weighted images at later timepoints. Radiofrequency thalamotomy produces focused and predictable lesion imaging characteristics over time. T2-weighted scans distinguish between the early lesion core and oedema characteristics, while lesions may remain more visible on susceptibility-weighted images in the months following surgery. Scanning patients in the immediate postoperative period and then at 6 months is clinically meaningful for understanding the anatomical basis of the transient and permanent effects of thalamotomy.
Year:
2023
Year:
2022
Year:
2022
Year:
2021
Year:
2020
Year:
2020
Collaborators (8)
Erlick A Pereira
University College London
Catherine Spilling
King’s College London
Nidhi Sofat
Professor of Rheumatology
St George’s, University of London
Thomas Barrick
Reader in Magnetic Resonance Imaging
St George’s, University of London
Daniel McWilliams
-
Matt Hall
University College London
David Walsh
Professor of Rheumatology
University of Nottingham
FRANCESCA MORGANTE
Reader in Neurology
St George’s, University of London
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