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Tim Lavin

Showing results (1-10 of 10) with videos related to

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Disability and Rehabilitation|December 17, 2019
Living with Polyneuropathy Organomegaly Endocrinopathy Monoclonal gammopathy Skin changes (POEMS) syndrome: a case study of healthcare experiences and quality of lifeJessica Twigg, Abigail Methley, Tim Lavin, et al.
British Journal of Hospital Medicine (London, England : 2005)|February 7, 2022
Hereditary transthyretin amyloidosis presenting with neuropathy and a bullous rashRyan Ys Keh, David Fitzgerald, Ruth Green, et al.
Muscle & Nerve|April 28, 2025
Feasibility and Tolerability of Subcutaneous Immunoglobulin via Manual Push Pre-Filled Syringes for Inflammatory Neuropathies: A Retrospective Cohort StudyHannah Smith, Susan Cooper, Ryan Yann Shern Keh, et al.
Practical Neurology|June 22, 2021
<i>The Last Act of Love</i>Christopher Hutchcroft, Matthew Jones, Tim Lavin, et al.
Practical Neurology|July 19, 2022
Pragmatic guide to peripheral nerve disease and the role of clinical biomarkersRyan Yann Shern Keh, Sachit Shah, James B Lilleker, et al.
Journal of the Peripheral Nervous System : JPNS|October 3, 2022
Rasch-built overall disability scale for POEMS syndrome (POEMS-RODS)Ryan Yann Shern Keh, James B Lilleker, Tim Lavin, et al.
Neuro-Oncology Advances|March 19, 2026
A systematic review and meta-analysis of outcomes following active surveillance, surgery and radiotherapy of meningiomas in NF2-related schwannomatosisJack Sheppard, Siddarth Kannan, Jane Halliday, et al.
Journal of the Peripheral Nervous System : JPNS|April 10, 2025
Diagnosis and Management of Multifocal Motor Neuropathy in the United Kingdom: A Multicentre SurveyYusuf A Rajabally, Christina Englezou, Grace Cluett, et al.
Journal of Medical Genetics|June 26, 2024
<i>NF2</i>-related schwannomatosis and other schwannomatosis: an updated genetic and epidemiological studyClaire Forde, Miriam J Smith, George J Burghel, et al.
Brain : a Journal of Neurology|February 9, 2021
An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathyAlistair T Pagnamenta, Rauan Kaiyrzhanov, Yaqun Zou, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Disability and Rehabilitation|December 17, 2019
Living with Polyneuropathy Organomegaly Endocrinopathy Monoclonal gammopathy Skin changes (POEMS) syndrome: a case study of healthcare experiences and quality of lifeJessica Twigg, Abigail Methley, Tim Lavin, et al.
British Journal of Hospital Medicine (London, England : 2005)|February 7, 2022
Hereditary transthyretin amyloidosis presenting with neuropathy and a bullous rashRyan Ys Keh, David Fitzgerald, Ruth Green, et al.
Muscle & Nerve|April 28, 2025
Feasibility and Tolerability of Subcutaneous Immunoglobulin via Manual Push Pre-Filled Syringes for Inflammatory Neuropathies: A Retrospective Cohort StudyHannah Smith, Susan Cooper, Ryan Yann Shern Keh, et al.
Practical Neurology|June 22, 2021
<i>The Last Act of Love</i>Christopher Hutchcroft, Matthew Jones, Tim Lavin, et al.
Practical Neurology|July 19, 2022
Pragmatic guide to peripheral nerve disease and the role of clinical biomarkersRyan Yann Shern Keh, Sachit Shah, James B Lilleker, et al.
Journal of the Peripheral Nervous System : JPNS|October 3, 2022
Rasch-built overall disability scale for POEMS syndrome (POEMS-RODS)Ryan Yann Shern Keh, James B Lilleker, Tim Lavin, et al.
Neuro-Oncology Advances|March 19, 2026
A systematic review and meta-analysis of outcomes following active surveillance, surgery and radiotherapy of meningiomas in NF2-related schwannomatosisJack Sheppard, Siddarth Kannan, Jane Halliday, et al.
Journal of the Peripheral Nervous System : JPNS|April 10, 2025
Diagnosis and Management of Multifocal Motor Neuropathy in the United Kingdom: A Multicentre SurveyYusuf A Rajabally, Christina Englezou, Grace Cluett, et al.
Journal of Medical Genetics|June 26, 2024
<i>NF2</i>-related schwannomatosis and other schwannomatosis: an updated genetic and epidemiological studyClaire Forde, Miriam J Smith, George J Burghel, et al.
Brain : a Journal of Neurology|February 9, 2021
An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathyAlistair T Pagnamenta, Rauan Kaiyrzhanov, Yaqun Zou, et al.
Pageof 1