Author/Creator: Gillingwater, Thomas H - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Gillingwater, Thomas H

1. Anatomy: back in the public spotlight. Issue 9980 (9th May 2015)

Authors:: Gillingwater, Thomas H; Findlater, Gordon S
Journal:: Lancet
Issue:: Volume 385:Issue 9980(2015)
Page Start:: 1825
Record Type:: Journal Article
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2. Dawn of a new therapeutic era for spinal muscular atrophy. Issue 10063 (17th December 2016)

Authors:: Gillingwater, Thomas H
Journal:: Lancet
Issue:: Volume 388:Issue 10063(2016)
Page Start:: 2964
Record Type:: Journal Article
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3. Examining the impact of audience response systems on student performance in anatomy education: a randomised controlled trial. Issue 1 (February 2018)

Authors:: Fergusson, Stuart J; Aka, Justine J; Hennessy, Catherine M; Wilson, Andrew J; Parson, Simon H; Harrison, Ewen M; Finn, Gabrielle M; Gillingwater, Thomas H
Journal:: Scottish medical journal
Issue:: Volume 63:Issue 1(2018)
Page Start:: 16
Record Type:: Journal Article
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4. How far away is spinal muscular atrophy gene therapy?. (September 2015)

Authors:: Gillingwater, Thomas H; Murray, Lyndsay M
Journal:: Expert review of neurotherapeutics
Issue:: Volume 15:Number 9(2015)
Page Start:: 965
Record Type:: Journal Article
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5. How far away is spinal muscular atrophy gene therapy?. (September 2015)

Authors:: Gillingwater, Thomas H; Murray, Lyndsay M
Journal:: Expert review of neurotherapeutics
Issue:: Volume 15:Number 9(2015)
Page Start:: 965
Record Type:: Journal Article
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6. Lamin A/C dysregulation contributes to cardiac pathology in a mouse model of severe spinal muscular atrophy. (9th August 2019)

Authors:: Šoltić, Darija; Shorrock, Hannah K; Allardyce, Hazel; Wilson, Emma L; Holt, Ian; Synowsky, Silvia A; Shirran, Sally L; Parson, Simon H; Gillingwater, Thomas H; Fuller, Heidi R
Journal:: Human molecular genetics
Issue:: Volume 28:Number 21(2019)
Page Start:: 3515
Record Type:: Journal Article
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7. Maximising returns: combining newborn screening with gene therapy for spinal muscular atrophy. Issue 12 (28th July 2021)

Authors:: Gillingwater, Thomas H
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 92:Issue 12(2021)
Page Start:: 1252
Record Type:: Journal Article
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8. Motor neuron translatome reveals deregulation of SYNGR4 and PLEKHB1 in mutant TDP-43 amyotrophic lateral sclerosis models. (7th July 2020)

Authors:: Marques, Rita F; Engler, Jan B; Küchler, Katrin; Jones, Ross A; Lingner, Thomas; Salinas, Gabriela; Gillingwater, Thomas H; Friese, Manuel A; Duncan, Kent E
Journal:: Human molecular genetics
Issue:: Volume 29:Number 16(2020)
Page Start:: 2647
Record Type:: Journal Article
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9. Moving towards treatments for spinal muscular atrophy: hopes and limits. (September 2015)

Authors:: Wirth, Brunhilde; Barkats, Martine; Martinat, Cecile; Sendtner, Michael; Gillingwater, Thomas H
Journal:: Expert opinion on emerging drugs
Issue:: Volume 20:Number 3(2015:Sep.)
Page Start:: 353
Record Type:: Journal Article
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10. Pre-natal manifestation of systemic developmental abnormalities in spinal muscular atrophy. (9th July 2020)

Authors:: Motyl, Anna A L; Faller, Kiterie M E; Groen, Ewout J N; Kline, Rachel A; Eaton, Samantha L; Ledahawsky, Leire M; Chaytow, Helena; Lamont, Douglas J; Wishart, Thomas M; Huang, Yu-Ting; Gillingwater, Thomas H
Journal:: Human molecular genetics
Issue:: Volume 29:Number 16(2020)
Page Start:: 2674
Record Type:: Journal Article
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