M. Rouanet

Axonal sensory motor neuropathy in copper‐deficient Wilson's disease

W. Meissner, F. Tison, A. Foubert-Samier, 2009, Muscle & nerve.

Hyperacute Guillain-Barré syndrome mimicking stroke: report of 3 cases: Guillain-Barré and stroke.

I. Sibon, P. Renou, O. Fleury, 2014, The American journal of emergency medicine.

Acute Brachial Radiculoplexopathy and Giant Cell Arteritis

Nathalie Damon-Perrière, G. Solé, F. Leger, 2018, The neurologist.

Acute tibial neuropathy in an elderly

G. L. Masson, F. Duval, S. Mathis, 2017, Journal of Clinical Neuroscience.

A new mutation of the lamin A/C gene leading to autosomal dominant axonal neuropathy, muscular dystrophy, cardiac disease, and leuconychia

G. Másson, C. Goizet, X. Ferrer, 2004, Journal of Medical Genetics.

A French family with Charcot–Marie–Tooth disease related to simultaneous heterozygous MFN2 and GDAP1 mutations

F. Tison, P. Latour, C. Goizet, 2012, Neuromuscular Disorders.

An in-frame deletion in BICD2 associated with a non-progressive form of SMALED

A. Durr, G. Stevanin, P. Pennamen, 2018, Clinical Neurology and Neurosurgery.

Head drops are also observed in advanced Huntington disease.

U. Spampinato, A. Danek, F. Tison, 2013, Parkinsonism & related disorders.

Mild recurrent neuropathy in CMT1B with a novel nonsense mutation in the extracellular domain of the MPZ gene

P. Latour, X. Ferrer, A. Vital, 2001, Journal of neurology, neurosurgery, and psychiatry.

Autosomal Dominant MPAN: Mosaicism Expands the Clinical Spectrum to Atypical Late‐Onset Phenotypes

P. Fergelot, G. Stevanin, B. Desnous, 2023, Movement disorders : official journal of the Movement Disorder Society.