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Characterization and optimization of a simple, repeatable system for the long term in vitro culture of aligned myotubes in 3D

Journal of cellular biochemistry, 2012-03, Vol.113 (3), p.1044-1053

2012

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Using stem cells and light to restore function to paralysed muscles

Neuromuscular disorders : NMD, 2017-03, Vol.27, p.S1-S1

2017

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Excitability properties of mouse and human skeletal muscle fibres compared by muscle velocity recovery cycles

Neuromuscular disorders : NMD, 2022-04, Vol.32 (4), p.347-357

2022

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The heat-shock response co-inducer arimoclomol protects against retinal degeneration in rhodopsin retinitis pigmentosa

Cell death & disease, 2014-05, Vol.5 (5), p.e1236-e1236

2014

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Characterisation of the heat shock response in primary and ES-cell derived spinal motor neurons and astrocytes exposed to cellular stress conditions modelling ALS

Neuromuscular disorders : NMD, 2017-03, Vol.27, p.S28-S28

2017

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In vitro models of Charcot-Marie-Tooth disease for investigating disease pathomechanisms

Neuromuscular disorders : NMD, 2017-03, Vol.27, p.S27-S28

2017

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Investigating inherent cellular changes in patient-derived mutant VCP fibroblasts as a model of inclusion body myopathy

Neuromuscular disorders : NMD, 2017-03, Vol.27, p.S38-S38

2017

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Longitudinal study of the neurodevelopmental characteristics of treated and untreated nonsyndromic craniosynostosis in infancy

Child's nervous system, 2013-06, Vol.29 (6), p.985-995

2013

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Absence of disturbed axonal transport in spinal and bulbar muscular atrophy

Human molecular genetics, 2011-05, Vol.20 (9), p.1776-1786

2011

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241st ENMC international workshop: Towards a European unifying lab for Kennedy's disease. 15–17th February, 2019 Hoofddorp, The Netherlands

Neuromuscular disorders : NMD, 2019-09, Vol.29 (9), p.716-724

2019

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Complete Correction of Severe Scaphocephaly : The Melbourne Method of Total Vault Remodeling

Plastic and reconstructive surgery (1963), 2008-04, Vol.121 (4), p.1300-1310

2008

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Mitochondrial dysfunction and abnormal calcium handling in cell models of Hereditary Sensory Neuropathy type I

Neuromuscular disorders : NMD, 2017-03, Vol.27, p.S25-S26

2017

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P55 Are axonal transport deficits present in a novel mouse model of spinal and bulbar muscular atrophy?

Neuromuscular disorders : NMD, 2014-03, Vol.24, p.S21-S22

2014

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P62 Investigating the effects of pharmacological up-regulation of the heat shock response in a transgenic mouse model of inclusion body myopathy

Neuromuscular disorders : NMD, 2014-03, Vol.24, p.S23-S23

2014

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Early postoperative efficacy of fibrin glue in face lifts: a prospective randomized trial

Plastic and reconstructive surgery (1963), 2005-03, Vol.115 (3), p.911-916

2005

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Investigating dysfunctional RNA processing in TDP-43 mouse mutants

Neuromuscular disorders : NMD, 2017-03, Vol.27, p.S32-S32

2017

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Modulation of cytoplasmic dynein and tubulin modification as potential therapeutic targets in SMA-LED

Neuromuscular disorders : NMD, 2017-03, Vol.27, p.S1-S1

2017

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Neuropathological findings from a human post mortem case of distal hereditary motor neuropathy (dHMN) due to p.Ser135Phe HSPB1 mutation and transgenic mice with mutant or wild-type HSP27 overexpression

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S283-S283

2015

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Inhibition of calpains, by treatment with leupeptin, improves motoneuron survival and muscle function in models of motoneuron degeneration

Neuroscience, 2004, Vol.125 (2), p.427-439

2004

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P49 Mitochondrial abnormalities and increased oxidative stress in HSBP1iinduced distal hereditary motor neuropathies

Neuromuscular disorders : NMD, 2014-03, Vol.24, p.S20-S20

2014

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P69 Investigating the effects of pharmacological up-regulation of the heat shock response in an in-vitro model of sporadic inclusion body myositis

Neuromuscular disorders : NMD, 2012-03, Vol.22, p.S26-S26

2012

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Long-term outcomes of surgical tongue reduction in Beckwith-Wiedemann syndrome

Plastic and reconstructive surgery (1963), 2007-03, Vol.119 (3), p.992-1002

2007

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Spreader graft placement: Location, location, location

Journal of plastic, reconstructive & aesthetic surgery, 2018-03, Vol.71 (3), p.448-449

2018

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S01 - Using stem cells and light to restore function to paralysed muscles

Neuromuscular disorders : NMD, 2017-03, Vol.27, p.S1-S1

2017

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271st ENMC international workshop: Towards a unifying effort to fight Kennedy's disease. 20-22 October 2023, Hoofddorp, Netherlands

Characterization and optimization of a simple, repeatable system for the long term in vitro culture of aligned myotubes in 3D

Using stem cells and light to restore function to paralysed muscles

Excitability properties of mouse and human skeletal muscle fibres compared by muscle velocity recovery cycles

The heat-shock response co-inducer arimoclomol protects against retinal degeneration in rhodopsin retinitis pigmentosa

Characterisation of the heat shock response in primary and ES-cell derived spinal motor neurons and astrocytes exposed to cellular stress conditions modelling ALS

In vitro models of Charcot-Marie-Tooth disease for investigating disease pathomechanisms

Investigating inherent cellular changes in patient-derived mutant VCP fibroblasts as a model of inclusion body myopathy

Longitudinal study of the neurodevelopmental characteristics of treated and untreated nonsyndromic craniosynostosis in infancy

Absence of disturbed axonal transport in spinal and bulbar muscular atrophy

241st ENMC international workshop: Towards a European unifying lab for Kennedy's disease. 15–17th February, 2019 Hoofddorp, The Netherlands

Complete Correction of Severe Scaphocephaly : The Melbourne Method of Total Vault Remodeling

Mitochondrial dysfunction and abnormal calcium handling in cell models of Hereditary Sensory Neuropathy type I

P55 Are axonal transport deficits present in a novel mouse model of spinal and bulbar muscular atrophy?

P62 Investigating the effects of pharmacological up-regulation of the heat shock response in a transgenic mouse model of inclusion body myopathy

Early postoperative efficacy of fibrin glue in face lifts: a prospective randomized trial

Investigating dysfunctional RNA processing in TDP-43 mouse mutants

Modulation of cytoplasmic dynein and tubulin modification as potential therapeutic targets in SMA-LED

Neuropathological findings from a human post mortem case of distal hereditary motor neuropathy (dHMN) due to p.Ser135Phe HSPB1 mutation and transgenic mice with mutant or wild-type HSP27 overexpression

Inhibition of calpains, by treatment with leupeptin, improves motoneuron survival and muscle function in models of motoneuron degeneration

P49 Mitochondrial abnormalities and increased oxidative stress in HSBP1iinduced distal hereditary motor neuropathies

P69 Investigating the effects of pharmacological up-regulation of the heat shock response in an in-vitro model of sporadic inclusion body myositis

Long-term outcomes of surgical tongue reduction in Beckwith-Wiedemann syndrome

Spreader graft placement: Location, location, location

S01 - Using stem cells and light to restore function to paralysed muscles

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