International audienceObjective: The aim of this study was the comprehensive characterisation of longitudinal clinical, electrophysiological and neuroimaging measures in type III and IV adult spinal muscular atrophy (SMA) with a view to propose objective monitoring markers for future clinical trials. Methods: Fourteen type III or IV SMA patients underwent standardised assessments including muscle strength testing, functional evaluation (SMAFRS and MFM), MUNIX (abductor pollicis brevis, APB; abductor digiti minimi, ADM; deltoid; tibialis anterior, TA; trapezius) and quantitative cervical spinal cord MRI to appraise segmental grey and white matter atrophy. Patients underwent a follow-up assessment with the same protocol 24 months later. Longi...
Objective: We report natural history data in a large cohort of 199 patients with spinal muscular atr...
International audienceAbstract Objective To characterize the natural history of spinal muscular atro...
Outcome measures traditionally used in spinal muscular atrophy (SMA) clinical trials are inadequate ...
International audienceObjective: The aim of this study was the comprehensive characterisation of lon...
International audienceObjective : Objective of this study is the comprehensive characterisation of m...
peer reviewedSpinal muscular atrophy (SMA) is a monogenic disorder caused by loss of function mutati...
<div><p>Spinal muscular atrophy (SMA) is a monogenic disorder caused by loss of function mutations i...
OBJECTIVE: To characterize the natural history of spinal muscular atrophy (SMA) over 24 months using...
Objective: We report natural history data in a large cohort of 199 patients with spinal muscular atr...
International audienceAbstract Objective To characterize the natural history of spinal muscular atro...
Outcome measures traditionally used in spinal muscular atrophy (SMA) clinical trials are inadequate ...
International audienceObjective: The aim of this study was the comprehensive characterisation of lon...
International audienceObjective : Objective of this study is the comprehensive characterisation of m...
peer reviewedSpinal muscular atrophy (SMA) is a monogenic disorder caused by loss of function mutati...
<div><p>Spinal muscular atrophy (SMA) is a monogenic disorder caused by loss of function mutations i...
OBJECTIVE: To characterize the natural history of spinal muscular atrophy (SMA) over 24 months using...
Objective: We report natural history data in a large cohort of 199 patients with spinal muscular atr...
International audienceAbstract Objective To characterize the natural history of spinal muscular atro...
Outcome measures traditionally used in spinal muscular atrophy (SMA) clinical trials are inadequate ...