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Arnaud Lacour

university of lille

94

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1145

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Electro-clinical presentation of hereditary transthyretin related amyloidosis when presenting as a polyneuropathy of unknown origin in northern France.

2021 Revue Neurologique
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Clinical and Molecular Spectrum Associated with COL6A3 c.7447A>G p.(Lys2483Glu) Variant: Elucidating its Role in Collagen VI-related Myopathies.

2021 Journal of neuromuscular diseases
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Confounding clinical presentation and different disease progression in CMT4B1

2020 Neuromuscular Disorders
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Intravenous immunoglobulin for treatment of chronic inflammatory demyelinating polyneuropathy and multifocal motor neuropathy in France: are daily practices in accordance with guidelines?

2019 European Journal of Neurology
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Hereditary neuropathy with liability to pressure palsy in patients under 30 years old: Neurophysiological data and proposed electrodiagnostic criteria

2018 Muscle & Nerve
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Skin biopsy findings in patients with CMT1A: Baseline data from the CLN-PXT3003-01 study provide new insights into the pathophysiology of the disorder

2018 Journal of Neuropathology and Experimental Neurology
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JCV serology in time: 3 years of follow‐up

2017 Acta Neurologica Scandinavica
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Bent spine syndrome as the initial symptom of late-onset Pompe disease

2017 Muscle & Nerve
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Home care organization impacts patient management and survival in ALS

2017 Amyotrophic Lateral Sclerosis
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Mutations in GFPT1-related congenital myasthenic syndromes are associated with synaptic morphological defects and underlie a tubular aggregate myopathy with synaptopathy

2017 Journal of Neurology
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