J. Camdessanche

J. Antoine, J. Camdessanché, F. Cissé, 2012, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Trismus as the fi rst symptom of amyotrophic lateral sclerosis

J. Antoine, F. Cissé, G. Jousserand, 2012 .

[Update on fundamental and clinical research in amyotrophic lateral sclerosis].

A. Echaniz-Laguna, P. Cintas, P. Corcia, 2009, Revue neurologique.

Absence of Airway Secretion Accumulation Predicts Tolerance of Noninvasive Ventilation in Subjects With Amyotrophic Lateral Sclerosis

E. Broussolle, I. Court-Fortune, J. Antoine, 2013, Respiratory Care.

Fatigue and neuromuscular diseases.

P Calmels, G. Millet, L. Féasson, 2006, Annales de readaptation et de medecine physique : revue scientifique de la Societe francaise de reeducation fonctionnelle de readaptation et de medecine physique.

Devic disease and thymoma with anti-central nervous system and antithymus antibodies

L. Féasson, J. Antoine, J. Camdessanché, 2004, Neurology.

First clinical inflammatory demyelinating events of the central nervous system in a population aged over 70 years: A multicentre study.

B. Brochet, G. Edan, D. Brassat, 2019, Multiple sclerosis and related disorders.

Effectiveness of mycophenolate mofetil as first-line therapy in AQP4-IgG, MOG-IgG, and seronegative neuromyelitis optica spectrum disorders

S. Vukusic, B. Brochet, D. Brassat, 2017, Multiple sclerosis.

Paraneoplastic subacute sensory neuropathy with triple positive antineuronal antibodies associated with small-cell lung cancer

M. Killian, J. Camdessanché, P. Cathébras, 2020, BMJ Case Reports.

A clinical screening tool for objective and subjective cognitive disorders in multiple sclerosis.

D. Maucort-Boulch, C. Thomas-Antérion, S. Jacquin-Courtois, 2020, Annals of physical and rehabilitation medicine.

COVID-19 may induce Guillain–Barré syndrome

B. Pozzetto, J. Camdessanché, E. Botelho-Nevers, 2020, Revue Neurologique.

CLIPPERS and its mimics: evaluation of new criteria for the diagnosis of CLIPPERS

K. Hoang-Xuan, À. Rovira, N. Téllez, 2019, Journal of Neurology, Neurosurgery, and Psychiatry.

Unusual association of amyotrophic lateral sclerosis and myasthenia gravis: A dysregulation of the adaptive immune system?

V. Meininger, F. Salachas, M. Amador, 2016, Neuromuscular Disorders.

Relevance of anti-HNK1 antibodies in the management of anti-MAG neuropathies

J. Antoine, J. Camdessanché, A. Grapperon, 2019, Journal of Neurology.

Anti-MAG antibodies in 202 patients: clinicopathological and therapeutic features

A. Steck, A. Echaniz-Laguna, J. Antoine, 2017, Journal of Neurology, Neurosurgery, and Psychiatry.

[Myasthenia in elderly patients: a series of 23 cases].

F. Durand, J. Antoine, P. Cathébras, 2005, La Revue de medecine interne.

Is there a paraneoplastic ALS?

P. Corcia, P. Gordon, J. Camdessanché, 2015, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Heterozygous CLCN1 mutations can modulate phenotype in sodium channel myotonia

R. Touraine, B. Fontaine, S. Vicart, 2014, Neuromuscular Disorders.

CIDP Antibodies Target Junction Proteins and Identify Patient Subgroups

J. Antoine, O. Stoevesandt, C. Moritz, 2021, Neurology: Neuroimmunology & Neuroinflammation.

Antibodies against the node of Ranvier: a real-life evaluation of incidence, clinical features and response to treatment based on a prospective analysis of 1500 sera

L. Kremer, T. Maisonobe, A. Echaniz-Laguna, 2020, Journal of Neurology.

Completing the Immunological Fingerprint by Refractory Proteins: Autoantibody Screening via an Improved Immunoblotting Technique

J. Antoine, J. Camdessanché, C. Moritz, 2019, Proteomics. Clinical applications.

Pathophysiology and biomarkers in chronic inflammatory demyelinating polyradiculoneuropathies.

J. Antoine, J. Camdessanché, J. Svahn, 2014, Revue neurologique.

Tetraparesia with areflexia revealing cerebral venous thrombosis.

P. Garnier, M. Epinat, T. Atroun, 2013, Revue neurologique (Paris).

Comparison of spinal magnetic resonance imaging and classical clinical factors in predicting motor capacity in amyotrophic lateral sclerosis

Jeanne M. Miller, K. Dujardin, V. Marchand-Pauvert, 2023, Journal of Neurology.

[Research in amyotrophic lateral sclerosis: what is new in 2009?].

T. Perez, A. Echaniz-Laguna, P. Cintas, 2010, Revue neurologique (Paris).

[N-methyl-d-aspartate receptor antibody encephalitis: a treatable disorder involving B-lymphocytes. A report of two patients].

J. Antoine, J. Camdessanché, Fabien Forest, 2012, La Revue de medecine interne.

Clinical and electrophysiological characteristics of women with X-linked Charcot-Marie-Tooth disease.

A. Echaniz-Laguna, Y. Péréon, P. Latour, 2023, European journal of neurology.

CRMP5 Regulates Generation and Survival of Newborn Neurons in Olfactory and Hippocampal Neurogenic Areas of the Adult Mouse Brain

J. Honnorat, F. Jourdan, A. Veyrac, 2011, PLoS ONE.

Acute hemorrhagic leukoencephalopathy associated with influenza A (H1N1) virus

J. Antoine, J. Camdessanché, S. Pillet, 2011, Journal of Neurology.

Expression of the onconeural CV2/CRMP5 antigen in thymus and thymoma

J. Antoine, J. Camdessanché, D. Meyronet, 2006, Journal of Neuroimmunology.

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

J. Antoine, J. Camdessanché, N. Graveline, 2018, European journal of neurology.

Value of TENS for relief of chronic low back pain with or without radicular pain

B. Laurent, J. Camdessanché, M. Lanteri-Minet, 2012, European journal of pain.

Pregnancy and myopathies: Reciprocal impacts between pregnancy, delivery, and myopathies and their treatments. A clinical review.

L. Féasson, J. Camdessanché, B. Zagorda, 2021, Revue neurologique.

Proper definition of the set of autoantibody-targeted antigens relies on appropriate reference group selection.

J. Antoine, J. Camdessanché, O. Stoevesandt, 2020, New biotechnology.

Brain immunohistopathological study in a patient with anti‐NMDAR encephalitis

P. Convers, J. Honnorat, J. Antoine, 2011, European journal of neurology.

Electrophysiological features of chronic inflammatory demyelinating polyradiculoneuropathy associated with IgG4 antibodies targeting neurofascin 155 or contactin 1 glycoproteins

L. Kremer, David John Adams, T. Maisonobe, 2020, Clinical Neurophysiology.

[Review of the current use of rituximab during 4 years in a French university hospital].

M. Killian, J. Camdessanché, Q. Reynaud, 2015, La Revue de medecine interne.

[Internet and amyotrophic lateral sclerosis treatment: what is wrong?].

A. Destée, M. Giroud, V. Meininger, 2009, Revue neurologique (Paris).

Clinical characterisation of sensory neuropathy with anti-FGFR3 autoantibodies

A. Martinez, J. Antoine, J. Camdessanché, 2019, Journal of Neurology, Neurosurgery, and Psychiatry.

Anti-AGO1 Antibodies Identify a Subset of Autoimmune Sensory Neuronopathy

J. Antoine, M. Killian, S. Paul, 2023, Neurology: Neuroimmunology & Neuroinflammation.

Argonaute Autoantibodies as Biomarkers in Autoimmune Neurologic Diseases

M. Taussig, J. Honnorat, J. Antoine, 2021, Neurology: Neuroimmunology & Neuroinflammation.

Antifibroblast growth factor receptor 3 antibodies identify a subgroup of patients with sensory neuropathy

J. Honnorat, J. Antoine, J. Camdessanché, 2015, Journal of Neurology, Neurosurgery & Psychiatry.

Usefulness and prognostic value of diagnostic tests in patients with possible chronic inflammatory demyelinating polyradiculoneuropathy

P. Convers, S. Rheims, J. Antoine, 2022, Muscle & nerve.

Prognostic Factors and Treatment Efficacy in Spinal Cord Sarcoidosis

J. Dufour, B. Bonnotte, J. Antoine, 2022, Neurology.

TNF-α inhibitors used as steroid-sparing maintenance monotherapy in parenchymal CNS sarcoidosis

J. Camdessanché, C. Giannesini, A. Mékinian, 2021, Journal of Neurology, Neurosurgery, and Psychiatry.

Brain hemorrhage as a complication of type I cryoglobulinemia vasculopathy

L. Mazzola, F. Barral, D. Michel, 2003, Journal of Neurology.

Demyelinating polyradiculoneuropathy under combined BRAF/MEK inhibitors.

S. Dalle, J. Camdessanché, P. Devic, 2017, European journal of cancer.

Thrombolytic treatment in acute cerebral infarction

J. Camdessanché, J. Camdessanche, 2007 .

Acute neurological worsening after Rituximab treatment in patients with anti-MAG neuropathy

J. Antoine, J. Camdessanché, Emilie Sala, 2014, Journal of the Neurological Sciences.

Testing the validity of a set of diagnostic criteria for sensory neuronopathies: a francophone collaborative study

J. Lefaucheur, J. Pouget, T. Maisonobe, 2014, Journal of Neurology.

Proposition de critères diagnostiques de neuronopathie sensitive

J. Antoine, J. Camdessanché, C. Vial, 2009 .

Phrenic Nerve Conduction in Healthy Subjects

I. Court-Fortune, F. Costes, J. Antoine, 2019, Muscle & nerve.

Muscle Strength Recovery in Treated Guillain-Barré Syndrome: A Prospective Study for the First 18 Months After Onset

L. Féasson, J. Camdessanché, V. Gautheron, 2007, American journal of physical medicine & rehabilitation.

Somatosensory evoked potentials in the assessment of peripheral neuropathies: Commented results of a survey among French-speaking practitioners and recommendations for practice

D. Guehl, O. Etard, P. Convers, 2015, Neurophysiologie Clinique/Clinical Neurophysiology.

Added value of electromyography in the diagnosis of myopathy: A consensus exercise

A. Fuglsang-Frederiksen, M. Carvalho, I. Schofield, 2017, Clinical Neurophysiology.

Antiganglioside antibodies in paraneoplastic peripheral neuropathies

J. Antoine, C. Caudie, K. Férraud, 2004, Journal of Neurology, Neurosurgery & Psychiatry.

Mutation in the RRM2 domain of TDP-43 in Amyotrophic Lateral Sclerosis with rapid progression associated with ubiquitin positive aggregates in cultured motor neurons

P. Vourc'h, C. Andres, P. Corcia, 2018, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Solitary fibrous tumors of the central nervous system: report of five cases with unusual clinicopathological and outcome patterns

F. Vassal, C. Nuti, M. Péoc'h, 2011, Acta Neurochirurgica.

Vincristine‐induced neuropathy: Atypical electrophysiological patterns in children

Y. Péréon, L. Leclair-Visonneau, A. Magot, 2015, Muscle & nerve.

Visual Assessment of Age-Related White Matter Hyperintensities Using FLAIR Images at 3 T: Inter- and Intra-Rater Agreement

Jean-Philippe Camdessanché, Jean-Christophe Antoine, F. Schneider, 2015, Neurodegenerative Diseases.

Progress in hereditary neuropathies, myopathies and motoneuron disorders!

P. Laforêt, J. Camdessanché, J. Camdessanche, 2023, Revue neurologique.

N‐hexane exposure: a cause of small fiber neuropathy

J. Lefaucheur, T. Maisonobe, A. Metlaine, 2018, Journal of the peripheral nervous system : JPNS.

Current clinical management of CIDP with immunoglobulins in France: An expert opinion.

Y. Péréon, P. Cintas, M. Michaud, 2023, Revue neurologique.

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

A. Echaniz-Laguna, Y. Péréon, J. Antoine, 2018, Muscle & nerve.

[Paraneoplastic neurological syndromes].

J. Antoine, J. Camdessanché, J. Camdessanche, 2007, Presse medicale.

Clinical features and prognostic factors of spinal cord sarcoidosis: a multicenter observational study of 20 BIOPSY-PROVEN patients

D. Maucort-Boulch, J. Dufour, J. Antoine, 2016, Journal of Neurology.

Prevalence of fatigue and its explicative variables among people with multiple sclerosis.

G. Millet, J. Camdessanché, Nicolas Royer, 2022, NeuroRehabilitation.

Prognostic Factors and Treatments Efficacy in Spinal Cord Sarcoidosis: An Observational Cohort With Long-term Follow-up.

J. Dufour, B. Bonnotte, J. Antoine, 2022, Neurology.

Comparative efficacy of fingolimod vs natalizumab

P. Vermersch, S. Vukusic, B. Brochet, 2016, Neurology.

Assessment of implicit language and theory of mind in multiple sclerosis.

B. Laurent, C. Borg, J. Camdessanché, 2020, Annals of physical and rehabilitation medicine.

Anti-FGFR3 antibody epitopes are functional sites and correlate with the neuropathy pattern

J. Antoine, J. Camdessanché, C. Moritz, 2021, Journal of Neuroimmunology.

Stratégie diagnostique devant une neuronopathie sensitive

J. Antoine, J. Camdessanché, J. Camdessanche, 2014 .

Immunization and multiple sclerosis: Recommendations from the French Multiple Sclerosis Society.

C. Louapre, S. Vukusic, C. Mékiès, 2019, Revue neurologique.

Determination of normal values for an isocapnic hyperpnea endurance test in healthy individuals

I. Court-Fortune, F. Costes, S. Vergès, 2016, Respiratory Physiology & Neurobiology.

End-Plate Disorders in Intensive Care Unit.

J. Camdessanché, J. Camdessanche, 2020, Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society.

Amyotrophic lateral sclerosis or not: Keys for the diagnosis.

T. Lenglet, J. Camdessanche, 2017, Revue neurologique.

Clinical, Electrophysiological and Genetic Studies of Two Families with Mutations in the GDAP1 Gene

P. Latour, J. Camdessanché, F. Prieur, 2008, Neuropediatrics.

[Review of the current use of rituximab during 4 years in a French university hospital].

P. Cathébras, Q. Reynaud, J. Camdessanché, 2015, La Revue de medecine interne.

In situ evidence of involvement of Schwann cells in ulcerative colitis: autocrine and paracrine signaling by A disintegrin and metalloprotease-17-mediated tumor necrosis factor alpha production.

A. Jarry, J. Antoine, J. Mosnier, 2009, Human pathology.