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Unravelling the myotonic dystrophy type 1 clinical spectrum: A systematic registry-based study with implications for disease classification

Revue neurologique, 2016-10, Vol.172 (10), p.572-580

2016

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Late-onset cervicoscapular muscle atrophy and weakness after radiotherapy for Hodgkin disease: a case series

Journal of neurology, neurosurgery and psychiatry, 2010, Vol.81 (1), p.101-104

2010

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Motor and respiratory decline in patients with late onset Pompe disease after cessation of enzyme replacement therapy during COVID‐19 pandemic

European journal of neurology, 2022-04, Vol.29 (4), p.1181-1186

2022

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Clinical improvement of DM1 patients reflected by reversal of disease-induced gene expression in blood

BMC medicine, 2022-11, Vol.20 (1), p.1-395, Article 395

2022

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Assessment of calf muscle contraction by diffusion tensor imaging

European radiology, 2008-10, Vol.18 (10), p.2303-2310

2008

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Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigations

Journal of neurology, 2019-12, Vol.266 (12), p.2987-2996

2019

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Myotonic dystrophy type 2 (DM2) and related disorders report of the 180th ENMC workshop including guidelines on diagnostics and management 3-5 December 2010, Naarden, The Netherlands

Neuromuscular disorders : NMD, 2011-06, Vol.21 (6), p.443-450

2011

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Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2

Neurology, 2003-06, Vol.60 (11), p.1854

2003

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Distinctive IFNγ signature in anti-synthetase syndrome and inclusion body myositis compared to dermatomyositis

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S203-S203

2016

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Retinal involvement in type 1 myotonic dystrophy: Literature review and presentation of a project based on the DM-Scope

Journal francais d'ophtalmologie, 2018-11, Vol.41 (9), p.e445

2018

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A large nationwide multicenter observational study: Characterizing myotonic dystrophy type 1 spectrum in pediatric patients

European journal of paediatric neurology, 2017-06, Vol.21, p.e229-e229

2017

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Multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of late-onset treatable metabolic disease

Revue neurologique, 2016-03, Vol.172 (3), p.231-241

2016

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Assessment of calf muscle contraction by diffusion tensor imaging

European radiology, 2008-10, Vol.18 (10), p.2303-2310

2008

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Correlation between mutation size and cardiac involvement in myotonic dystrophy type 1: An analysis of the DM1-heart registry

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S194-S194

2016

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140th ENMC International Workshop: Myotonic Dystrophy DM2/PROMM and other myotonic dystrophies with guidelines on management

Neuromuscular disorders : NMD, 2006-06, Vol.16 (6), p.403-413

2006

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G.P.133

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.840-841

2014

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O.6 Antisense approach for myotonic dystrophy

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.681-681

2011

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Severe cardiac arrhythmias in young patients with myotonic dystrophy type 1

Neurology, 2004-11, Vol.63 (10), p.1939

2004

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Clinical and histologic findings in autosomal centronuclear myopathy

Neurology, 2004-05, Vol.62 (9), p.1484

2004

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Detection of genomic viral RNA in nerve and muscle of patients with HCV neuropathy

Neurology, 2003-03, Vol.60 (5), p.808

2003

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P.18.1 The DM-Scope registry: Interfacing myotonic dystrophy clinical care and research

Neuromuscular disorders : NMD, 2013-10, Vol.23 (9), p.832-832

2013

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Central and peripheral components of exercise-related fatigability in myotonic dystrophy type 1

Acta neurologica Scandinavica, 2012-01, Vol.125 (1), p.38-46

2012

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P5.2 The DM-scope project: Promoting myotonic dystrophy care and research

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.724-724

2011

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VP.26 Potential of the MyoSuit, a lightweight wearable lower-limb cable-actuated exoskeleton in patients with neuromuscular disorders: preliminary findings

Neuromuscular disorders : NMD, 2022-10, Vol.32, p.S71-S72

2022

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VP.27 Potential of the Keeogo+, a lightweight wearable powered assistive exoskeleton in patients with neuromuscular disorders: preliminary findings

Neuromuscular disorders : NMD, 2022-10, Vol.32, p.S72

2022

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Unravelling the myotonic dystrophy type 1 clinical spectrum: A systematic registry-based study with implications for disease classification

Late-onset cervicoscapular muscle atrophy and weakness after radiotherapy for Hodgkin disease: a case series

Motor and respiratory decline in patients with late onset Pompe disease after cessation of enzyme replacement therapy during COVID‐19 pandemic

Clinical improvement of DM1 patients reflected by reversal of disease-induced gene expression in blood

Assessment of calf muscle contraction by diffusion tensor imaging

Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigations

Myotonic dystrophy type 2 (DM2) and related disorders report of the 180th ENMC workshop including guidelines on diagnostics and management 3-5 December 2010, Naarden, The Netherlands

Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2

Distinctive IFNγ signature in anti-synthetase syndrome and inclusion body myositis compared to dermatomyositis

Retinal involvement in type 1 myotonic dystrophy: Literature review and presentation of a project based on the DM-Scope

A large nationwide multicenter observational study: Characterizing myotonic dystrophy type 1 spectrum in pediatric patients

Multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of late-onset treatable metabolic disease

Assessment of calf muscle contraction by diffusion tensor imaging

Correlation between mutation size and cardiac involvement in myotonic dystrophy type 1: An analysis of the DM1-heart registry

140th ENMC International Workshop: Myotonic Dystrophy DM2/PROMM and other myotonic dystrophies with guidelines on management

G.P.133

O.6 Antisense approach for myotonic dystrophy

Severe cardiac arrhythmias in young patients with myotonic dystrophy type 1

Clinical and histologic findings in autosomal centronuclear myopathy

Detection of genomic viral RNA in nerve and muscle of patients with HCV neuropathy

P.18.1 The DM-Scope registry: Interfacing myotonic dystrophy clinical care and research

Central and peripheral components of exercise-related fatigability in myotonic dystrophy type 1

P5.2 The DM-scope project: Promoting myotonic dystrophy care and research

VP.26 Potential of the MyoSuit, a lightweight wearable lower-limb cable-actuated exoskeleton in patients with neuromuscular disorders: preliminary findings

VP.27 Potential of the Keeogo+, a lightweight wearable powered assistive exoskeleton in patients with neuromuscular disorders: preliminary findings

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