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Functional fatigue in a sample of the UK myasthenic population

Neuromuscular disorders : NMD, 2017-03, Vol.27, p.S36-S37

2017

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SMA REACH UK: Relationship between the Revised Hammersmith Scale (RHS) and Revised Upper Limb Module (RULM) in a UK cohort of patients with SMA type 2 and 3

Neuromuscular disorders : NMD, 2017-03, Vol.27, p.S43-S43

2017

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P441 Difference in functional status and quality of life outcomes in a cohort of siblings with Charcot-Marie-Tooth disease children – a prospective study

Neuromuscular disorders : NMD, 2023-10, Vol.33, p.S188-S188

2023

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P209 Characteristics of patients with spinal muscular atrophy who have discontinued treatment with nusinersen: a multi-centre experience in the UK

Neuromuscular disorders : NMD, 2023-10, Vol.33, p.S87-S87

2023

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P136 Using the North Star and timed function test centiles in boys with Duchenne muscular dystrophy – a prospective study

Neuromuscular disorders : NMD, 2023-10, Vol.33, p.S81-S81

2023

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P.118 The effect of nusinersen on function and muscle strength in the upper limb in a cohort of children with spinal muscular atrophy (SMA) type 2 and 3

Neuromuscular disorders : NMD, 2022-10, Vol.32, p.S90-S91

2022

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P143 Centiles by age for the North Star ambulatory assessment and the associated timed items in glucocorticoid treated boys with Duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2023-10, Vol.33, p.S83-S83

2023

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P139 Correlation and validation of the North Star Ambulatory Assessment, timed test and motor function measure centiles for boys with Duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2023-10, Vol.33, p.S82-S82

2023

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The effect of orthosis and foot surgery in a cohort of Charcot-Marie-Tooth disease children

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S147-S148

2017

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P.170 - The effect of orthosis and foot surgery in a cohort of Charcot-Marie-Tooth disease children

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S147-S148

2017

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SMA: REGISTRIES, BIOMARKERS & OUTCOME MEASURES

Neuromuscular disorders : NMD, 2020-10, Vol.30, p.S102

2020

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HEREDITARY NEUROPATHIES & ALS

Neuromuscular disorders : NMD, 2020-10, Vol.30, p.S80

2020

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HEREDITARY NEUROPATHIES & ALS: P.117 The relationship between upper and lower limb function in a cohort of children with Charcot-Marie-Tooth (CMT) disease

Neuromuscular disorders : NMD, 2020-10, Vol.30, p.S80-S80

2020

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SMA: REGISTRIES, BIOMARKERS & OUTCOME MEASURES: P.190 Investigating temporal changes in percent predicted FVC and RULM score in non-ambulant SMA type III children

Neuromuscular disorders : NMD, 2020-10, Vol.30, p.S102-S102

2020

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P.423 - Functional fatigue in a sample of the UK myasthenic population

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S223-S223

2017

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Functional fatigue in a sample of the UK myasthenic population

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S223

2017

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SMA CLINICAL DATA, OUTCOME MEASURES AND REGISTRIES

Neuromuscular disorders : NMD, 2018-10, Vol.28, p.S53-S54

2018

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SMA CLINICAL DATA, OUTCOME MEASURES AND REGISTRIES: P.79The relationship between function and muscle strength in the upper limb in a cohort of children with spinal muscular atrophy type II and III – a prospective study

Neuromuscular disorders : NMD, 2018-10, Vol.28, p.S53-S54

2018

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P.227Secondary clinical outcomes of spinal surgery and satisfaction in patients with spinal muscular atrophy (SMA) II and non-ambulant III

Neuromuscular disorders : NMD, 2019-10, Vol.29, p.S133-S133

2019

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NMJ+C12 - Functional fatigue in a sample of the UK myasthenic population

Neuromuscular disorders : NMD, 2017-03, Vol.27, p.S36-S37

2017

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OD19 - SMA REACH UK: Relationship between the Revised Hammersmith Scale (RHS) and Revised Upper Limb Module (RULM) in a UK cohort of patients with SMA type 2 and 3

Neuromuscular disorders : NMD, 2017-03, Vol.27, p.S43-S43

2017

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P.220The revised Hammersmith scale (RHS) for spinal muscular atrophy: longitudinal trajectories in a large international cohort of patients with type 2 and 3 SMA

Neuromuscular disorders : NMD, 2019-10, Vol.29, p.S131-S131

2019

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Zur Deutung des sogenannten Akkomodations-Quotienten

Biomedizinische Technik, 1968, Vol.13 (1-6), p.240-243

MILEV, E.

1968

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Érythème borrélien de la face

Annales de dermatologie et de vénéréologie, 2008-12, Vol.135 (12), p.852-854

2008

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Visuomotor operation in transition from object fixation to prey shooting in chameleons

Biological cybernetics, 1994-07, Vol.71 (3), p.209-214

1994

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Functional fatigue in a sample of the UK myasthenic population

SMA REACH UK: Relationship between the Revised Hammersmith Scale (RHS) and Revised Upper Limb Module (RULM) in a UK cohort of patients with SMA type 2 and 3

P441 Difference in functional status and quality of life outcomes in a cohort of siblings with Charcot-Marie-Tooth disease children – a prospective study

P209 Characteristics of patients with spinal muscular atrophy who have discontinued treatment with nusinersen: a multi-centre experience in the UK

P136 Using the North Star and timed function test centiles in boys with Duchenne muscular dystrophy – a prospective study

P.118 The effect of nusinersen on function and muscle strength in the upper limb in a cohort of children with spinal muscular atrophy (SMA) type 2 and 3

P143 Centiles by age for the North Star ambulatory assessment and the associated timed items in glucocorticoid treated boys with Duchenne muscular dystrophy

P139 Correlation and validation of the North Star Ambulatory Assessment, timed test and motor function measure centiles for boys with Duchenne muscular dystrophy

The effect of orthosis and foot surgery in a cohort of Charcot-Marie-Tooth disease children

P.170 - The effect of orthosis and foot surgery in a cohort of Charcot-Marie-Tooth disease children

SMA: REGISTRIES, BIOMARKERS & OUTCOME MEASURES

HEREDITARY NEUROPATHIES & ALS

HEREDITARY NEUROPATHIES & ALS: P.117 The relationship between upper and lower limb function in a cohort of children with Charcot-Marie-Tooth (CMT) disease

SMA: REGISTRIES, BIOMARKERS & OUTCOME MEASURES: P.190 Investigating temporal changes in percent predicted FVC and RULM score in non-ambulant SMA type III children

P.423 - Functional fatigue in a sample of the UK myasthenic population

Functional fatigue in a sample of the UK myasthenic population

SMA CLINICAL DATA, OUTCOME MEASURES AND REGISTRIES

SMA CLINICAL DATA, OUTCOME MEASURES AND REGISTRIES: P.79The relationship between function and muscle strength in the upper limb in a cohort of children with spinal muscular atrophy type II and III – a prospective study

P.227Secondary clinical outcomes of spinal surgery and satisfaction in patients with spinal muscular atrophy (SMA) II and non-ambulant III

NMJ+C12 - Functional fatigue in a sample of the UK myasthenic population

OD19 - SMA REACH UK: Relationship between the Revised Hammersmith Scale (RHS) and Revised Upper Limb Module (RULM) in a UK cohort of patients with SMA type 2 and 3

P.220The revised Hammersmith scale (RHS) for spinal muscular atrophy: longitudinal trajectories in a large international cohort of patients with type 2 and 3 SMA

Zur Deutung des sogenannten Akkomodations-Quotienten

Érythème borrélien de la face

Visuomotor operation in transition from object fixation to prey shooting in chameleons

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