J. Antoine

S. Rheims, J. Honnorat, J. Antoine, 2017, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Autoimmune episodic ataxia in patients with anti-CASPR2 antibody-associated encephalitis

F. Ducray, P. Convers, J. Honnorat, 2017, Neurology: Neuroimmunology & Neuroinflammation.

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.

Guidelines on the detection of paraneoplastic anti-neuronal-specific antibodies

J. Honnorat, B. Giometto, J. Delattre, 1995, Neurology.

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

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

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

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

Creutzfeldt‐Jakob disease after extracranial dura mater embolization for a nasopharyngeal angiofibroma

J. Hauw, D. Michel, J. Laplanche, 1997, Neurology.

Pathophysiology and biomarkers in chronic inflammatory demyelinating polyradiculoneuropathies.

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

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

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

A novel CRYAB mutation resulting in multisystemic disease

L. Féasson, J. Antoine, A. Casarín, 2012, Neuromuscular Disorders.

A retrospective study on the efficacy and safety of intraveinous immunoglobulin (Tegeline®) in patients with chronic inflammatory demyelinating polyneuropathy.

G. Edan, J. Pouget, J. Antoine, 2015, Presse medicale.

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.

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

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

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.

Safety of Intravenous Immunoglobulin (Tegeline®), Administered at Home in Patients with Autoimmune Disease: Results of a French Study

J. Antoine, E. Hachulla, J. Azulay, 2018, BioMed Research International.

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

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

Impact of Coronavirus Disease 2019 in a French Cohort of Myasthenia Gravis

D. Annane, L. Kremer, T. Stojkovic, 2021, Neurology.

231st ENMC International Workshop: International Standard for CIDP Registry and Biobank, Naarden, The Netherlands, 12–14 May 2017

P. Bergh, J. Vallat, J. Antoine, 2017, Neuromuscular Disorders.

Carcinoma associated paraneoplastic peripheral neuropathies in patients with and without anti-onconeural antibodies

P. Convers, D. Michel, J. Honnorat, 1999, Journal of neurology, neurosurgery, and psychiatry.

Chronic inflammatory demyelinating polyneuropathy associated with carcinoma.

B. Laurent, P. Convers, D. Michel, 1996, Journal of neurology, neurosurgery, and psychiatry.

Immunological mechanisms in paraneoplastic peripheral neuropathy

J. Antoine, 2000, Clinical reviews in allergy & immunology.

Phrenic Nerve Conduction in Healthy Subjects

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

[Fatal peripheral neuropathy with predominant motor involvement associated with anti-MAG IgM monoclonal gammapathy].

D. Michel, A. Steck, J. Antoine, 1993, Revue neurologique.

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.

Paraneoplastic disorders of the peripheral nervous system.

J. Antoine, J. Camdessanché, J. Camdessanche, 2013, Presse medicale.

Treatment Options in Paraneoplastic Disorders of the Peripheral Nervous System

J. Antoine, J. Camdessanché, J. Camdessanche, 2013, Current Treatment Options in Neurology.

[Paraneoplastic peripheral neuropathies].

J. Antoine, 2001, Revue neurologique.

Limbic encephalitis and immunological perturbations in two patients with thymoma.

D. Michel, J. Honnorat, J. Antoine, 1995, Journal of neurology, neurosurgery, and psychiatry.

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

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

Small-cell lung cancer, paraneoplastic cerebellar degeneration and the Lambert-Eaton myasthenic syndrome.

W. Mason, M. Rosenblum, F. Valldeoriola, 1997, Brain : a journal of neurology.

Evaluation of the application of the European guidelines for the diagnosis and clinical care of amyotrophic lateral sclerosis (ALS) patients in six French ALS centres

G. Lemasson, E. Beghi, G. Logroscino, 2016, European journal of neurology.

Trismus as the first symptom of amyotrophic lateral sclerosis

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

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

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

Clinical Spectrum of Encephalitis Associated With Antibodies Against the α-Amino-3-Hydroxy-5-Methyl-4-Isoxazolepropionic Acid Receptor: Case Series and Review of the Literature.

F. Ducray, J. Honnorat, A. Idbaih, 2015, JAMA neurology.

Antibodies to metabotropic glutamate receptor 5 in the Ophelia syndrome

R. Balice-Gordon, J. Honnorat, C. Bien, 2011, Neurology.

Brain immunohistopathological study in a patient with anti‐NMDAR encephalitis

P. Convers, J. Honnorat, J. Antoine, 2011, European 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.

Characteristics in limbic encephalitis with anti–adenylate kinase 5 autoantibodies

F. Ducray, J. Honnorat, F. Tison, 2017, Neurology.

Paraneoplastic anti‐CV2 antibodies react with peripheral nerve and are associated with a mixed axonal and demyelinating peripheral neuropathy

M. Magistris, J. Honnorat, J. Antoine, 2001, Annals of neurology.

Paraneoplastic demyelinating neuropathy, subacute sensory neuropathy, and anti‐hu antibodies: Clinicopathological study of an autopsy case

P. Convers, D. Michel, J. Honnorat, 1998, Muscle & nerve.

Clinical characterisation of sensory neuropathy with anti-FGFR3 autoantibodies

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

Stratégie diagnostique devant une neuronopathie sensitive

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

Encephalitis with mGluR5 antibodies

N. Tubridy, M. Rosenfeld, J. Antoine, 2018, Neurology.

Sensory neuronopathies, diagnostic criteria and causes

J. Antoine, 2022, Current opinion in neurology.

Peripheral neuropathies associated with antibodies directed to intracellular neural antigens.

J. Antoine, 2014, Revue neurologique.

CSF IgA NMDAR antibodies are potential biomarkers for teratomas in anti-NMDAR encephalitis

F. Ducray, J. Honnorat, O. Pascual, 2015, Neurology: Neuroimmunology & Neuroinflammation.

Paraneoplastic peripheral neuropathies

J. Antoine, J. Camdessanché, J. Camdessanche, 2014, Dysimmune Neuropathies.

Paraneoplastic Peripheral Neuropathy Associated With Anti‐hu Antibodies. A Clinical And Electrophysiological Study Of 20 Patients

P. Convers, D. Michel, J. Honnorat, 2002 .

Paraneoplastic sensory neuropathy, demyelinating features, and response to immunotherapy

J. Antoine, J. Antoine, 1998, Muscle & nerve.

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.

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.

Onco-neural antibodies and tumour type determine survival and neurological symptoms in paraneoplastic neurological syndromes with Hu or CV2/CRMP5 antibodies

J. Honnorat, E. Decullier, D. Ricard, 2008, Journal of Neurology, Neurosurgery, and Psychiatry.

Antiamphiphysin antibodies are associated with various paraneoplastic neurological syndromes and tumors.

P. De Camilli, D. Michel, J. Honnorat, 1999, Archives of neurology.

Pathology of roots, spinal cord and brainstem in syringomyelia-like syndrome of Tangier disease

B. Laurent, P. Convers, D. Michel, 1991, Journal of the Neurological Sciences.

Treatment and outcome of children and adolescents with N-methyl-d-aspartate receptor encephalitis

F. Ducray, J. Honnorat, J. Delattre, 2015, Journal of Neurology.

Cerebrospinal fluid and serum immune complex in acute inflammatory polyneuritis

B. Laurent, D. Michel, J. Antoine, 1986 .

Conformation-stabilizing ELISA and cell-based assays reveal patient subgroups targeting three different epitopes of AGO1 antibodies

J. Antoine, J. Camdessanché, C. Moritz, 2022, Frontiers in Immunology.

Spastic paraplegia due to recessive or dominant mutations in ERLIN2 can convert to ALS

M. Amador, G. Stevanin, J. Antoine, 2019, Neurology: Genetics.

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.

[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.

Acute hemorrhagic leukoencephalopathy associated with influenza A (H1N1) virus

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

[Benign acute cerebral angiopathy. 4 cases].

B. Laurent, D. Michel, M. Trillet, 1985, Revue neurologique.

The Lists of Necropolis Workmen in Theban Graffiti and Ostraca of the 21st Dynasty.

J. Antoine, 2019, Zeitschrift für Ägyptische Sprache und Altertumskunde.

The Geographical and Administrative Landscape of Lower Middle Egypt in Text B of the Wilbour Papyrus

J. Antoine, 2017 .

Biallelic MYORG mutation carriers exhibit primary brain calcification with a distinct phenotype.

L. Defebvre, M. Vidailhet, J. Pariente, 2019, Brain : a journal of neurology.

Seronegative paraneoplastic cerebellar degeneration: the PNS Euronetwork experience

F. Ducray, J. Honnorat, B. Giometto, 2014, European journal of neurology.

[Paraneoplastic neurological syndromes].

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

Paraneoplastic opsomyoclonus, cerebellar ataxia and encephalopathy associated with anti-Purkinje cell antibodies

J. Honnorat, M. Trillet, J. Dalmau, 1997, Journal of Neurology.

Are the “newly discovered” paraneoplastic anti‐collapsin response‐mediator protein 5 antibodies simply anti‐cv2 antibodies?

J. Antoine, M. Belin, J. Honnorat, 2001, Annals of neurology.

Herpes simplex virus type 1 encephalitis associated with acute retinal necrosis syndrome in an immunocompetent patient.

P. Gain, C. Chiquet, J. Antoine, 2002, Acta ophthalmologica Scandinavica.

Reducing the risk of misdiagnosis of indirect ELISA by normalizing serum-specific background noise: The example of detecting anti-FGFR3 autoantibodies.

J. Antoine, J. Camdessanché, C. Moritz, 2019, Journal of immunological methods.

Dural localization of extramedullary hematopoiesis. Report of a case

J. Antoine, J. Camdessanché, R. Mohammedi, 2009, Journal of Neurology.

Autoimmunity in paraneoplastic neurological disorders 1 This meeting was held at Somerville College, Oxford, April 6-7, 1997. 1

J. Honnorat, B. Giometto, A. Vincent, 1998, Journal of Neuroimmunology.

Autoantigenomics: Holistic characterization of autoantigen repertoires for a better understanding of autoimmune diseases.

Stéphane Paul, Christian P Moritz, Oda Stoevesandt, 2019, Autoimmunity reviews.

The pattern and diagnostic criteria of sensory neuronopathy: a case–control study

J. Honnorat, J. Antoine, P. Petiot, 2009, Brain : a journal of neurology.

Anti-N-methyl-d-aspartate receptor encephalitis after Herpes simplex virus-associated encephalitis: an emerging disease with diagnosis and therapeutic challenges

C. Boutet, J. Antoine, F. Lucht, 2017, Infection.

Clinical specificities of adult male patients with NMDA receptor antibodies encephalitis

F. Ducray, J. Honnorat, J. Delattre, 2014, Neurology.

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.

Myasthenia gravis exacerbation or unmasking associated with telithromycin treatment

S. Vukusic, C. Confavreux, J. Antoine, 2006, Neurology.

Clinical features and pathophysiological basis of sensory neuronopathies (ganglionopathies)

A. Steck, J. Antoine, T. Kuntzer, 2004, Muscle & nerve.

[Sneddon syndrome: 9 cases].

F. Barral, B. Laurent, D. Michel, 1994, Revue neurologique.

A clinical pattern‐based etiological diagnostic strategy for sensory neuronopathies: a French collaborative study

J. Pouget, T. Maisonobe, J. Antoine, 2012, Journal of the peripheral nervous system : JPNS.

Impact of a frequent nearsplice SOD1 variant in amyotrophic lateral sclerosis: optimising SOD1 genetic screening for gene therapy opportunities

Y. Marie, V. Meininger, F. Salachas, 2021, Journal of Neurology, Neurosurgery, and Psychiatry.

Ulip/CRMP proteins are recognized by autoantibodies in paraneoplastic neurological syndromes

J. Honnorat, D. Aunis, M. Mattei, 1999, The European journal of neuroscience.

Malignant tumors in autoimmune encephalitis with anti-NMDA receptor antibodies

F. Ducray, J. Honnorat, J. Delattre, 2018, Journal of Neurology.

Neuroleptic intolerance in patients with anti-NMDAR encephalitis

M. Leboyer, F. Ducray, J. Honnorat, 2016, Neurology: Neuroimmunology & Neuroinflammation.

CANOMAD: a neurological monoclonal gammopathy of clinical significance that benefits from B-cell targeted therapies.

T. Maisonobe, A. Echaniz-Laguna, J. Antoine, 2020, Blood.

Brain hemorrhage as a complication of type I cryoglobulinemia vasculopathy

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

Identifying a therapeutic window in acute and subacute inflammatory sensory neuronopathies

J. Lefaucheur, J. Pouget, T. Maisonobe, 2016, Journal of the Neurological Sciences.

Proposition de critères diagnostiques de neuronopathie sensitive

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

Antiganglioside antibodies in paraneoplastic peripheral neuropathies

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

Unusual amyloid polyneuropathy with predominant lurnbosacral nerve roots and plexus involvement

F. Barral, P. Convers, D. Michel, 1991, Neurology.

J. Honnorat, B. Giometto, J. Antoine, 2011, Journal of Neurology.

Clinical spectrum and diagnostic pitfalls of neurologic syndromes with Ri antibodies

F. Ducray, J. Honnorat, J. Antoine, 2020, Neurology: Neuroimmunology & Neuroinflammation.

Landholding and Agriculture in Late Ramesside Theban Documents

J. Antoine, 2015 .

Social position and the organisation of landholding in Ramesside Egypt: an analysis of the Wilbour Papyrus

J. Antoine, 2014 .

Isolated body lateropulsion caused by a lesion of the cerebellar peduncles.

F. Barral, P. Convers, D. Michel, 1996, Journal of neurology, neurosurgery, and psychiatry.

Prognostic Factors and Treatment Efficacy in Spinal Cord Sarcoidosis

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

[Anti-neuronal antibodies and central nervous system diseases: contribution to diagnosis and pathophysiology].

J. Honnorat, J. Antoine, 2000, Revue neurologique.

[Natural history of adult-onset eIF2B-related disorders: a multicentric survey of 24 cases].

F. Mauguière, F. Sedel, S. Vukusic, 2011, Revue neurologique.

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

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

[Diagnostic value of autoantibodies to MAG by ELISA Bühlmann in 117 immune-mediated peripheral neuropathies associated with monoclonal IgM to SGPG/SGLPG].

J. Antoine, P. Gonnaud, P. Petiot, 2006, Annales de biologie clinique.

[Diagnostic value of the anti-IgM SGPG Elisa (Bühlmann laboratories AG) in 147 sera with a monoclonal IgM anti-MAG/SGPG antibody-associated neuropathy].

J. Antoine, P. Gonnaud, P. Petiot, 2007, Annales de biologie clinique.

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.

Safety and efficacy of a 6-month home-based exercise program in patients with facioscapulohumeral muscular dystrophy

B. Wuyam, G. Millet, S. Vergès, 2016, Medicine.

Convergence of patient- and physician-reported outcomes in the French National Registry of Facioscapulohumeral Dystrophy

F. Rivier, C. Béroud, F. Chapon, 2022, Orphanet Journal of Rare Diseases.

A. Gabelle, E. Coudeyre, J. Antoine, 2005, Revue neurologique.

Aicardi–Goutières syndrome: a possible explanation of angiokeratoma of Mibelli

P. Rubegni, J. Antoine, E. Cinotti, 2021, Journal of the European Academy of Dermatology and Venereology : JEADV.

Progressive dementia associated with ataxia or obesity in patients with Tropheryma whipplei encephalitis

Claire Paquet, Didier Raoult, Jean-Christophe Antoine, 2011, BMC infectious diseases.

Brain magnetic resonance imaging findings in cryptogenic stroke patients under 60 years with patent foramen ovale.

F. Schneider, F. Barral, C. Boutet, 2014, European journal of radiology.

Adenovirus vector targeted to dorsal root ganglia as a future tool for the treatment of sensory neuron diseases

J. Antoine, 2009 .

Brain plasticity in the motor network is correlated with disease progression in amyotrophic lateral sclerosis

F. Schneider, I. Faillenot, J. Antoine, 2013, Human brain mapping.

Unclear association between COVID-19 and Guillain-Barré syndrome

G. Gigli, J. Honnorat, J. Antoine, 2021, Brain : a journal of neurology.

[Extrapontine myelinolysis of favorable outcome in a patient with autoimmune polyglandular syndrome].

J. Antoine, J. Camdessanché, M. Koenig, 2005, La Revue de medecine interne.

[Chronic peripheral neuropathies with corticosensitive heredodegenerative aspects: 2 cases].

B. Laurent, D. Michel, J. Antoine, 1989, Revue neurologique.

Delayed onset of a second paraneoplastic neurological syndrome in eight patients

F. Ducray, J. Honnorat, J. Antoine, 2010, Journal of Neurology, Neurosurgery & Psychiatry.

[Myxoma of the left atrium with neurologic manifestations: 8 cases].

F. Barral, D. Michel, P. Gain, 1994, Revue neurologique (Paris).

Musty odour, mental retardation, and spastic paraplegia revealing phenylketonuria in adulthood

J. Antoine, G. Jousserand, J. Camdessanche, 2010, Journal of Neurology.

Exploring the diagnosis delay and ALS functional impairment at diagnosis as relevant criteria for clinical trial enrolment*

F. Viader, D. Hannequin, P. Preux, 2017, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Home care organization impacts patient management and survival in ALS

I. Court-Fortune, F. Costes, J. Antoine, 2017, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Trismus as the fi rst symptom of amyotrophic lateral sclerosis

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

[Sjogren-Larsson syndrome: two cases with delayed diagnosis].

J. Antoine, R. Wanders, C. Has, 2002, Annales de medecine interne.

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

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

Lumbosacral meningoradiculitis associated with Chlamydia pneumoniae infection.

D. Michel, J. Antoine, F. Lucht, 1992, Journal of neurology, neurosurgery, and psychiatry.

CIDP Antibodies Target Junction Proteins and Identify Patient Subgroups

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

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.

Autoimmune encephalitis: paving the way for early diagnosis

J. Antoine, 2016, The Lancet Neurology.

Anti-AGO1 Antibodies Identify a Subset of Autoimmune Sensory Neuronopathy

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

Paraneoplastic neurological syndromes

J. Honnorat, J. Antoine, 2007, Orphanet journal of rare diseases.

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.

Prospective Study of Positional Nystagmus in 100 Consecutive Patients

P. Bertholon, J. Antoine, S. Tringali, 2006, The Annals of otology, rhinology, and laryngology.

The Delay of the Grain Ration and its Social Consequences at Deir El-Medîna in the Twentieth Dynasty: A Statistical Analysis

J. Antoine, 2009 .

A novel CRYAB mutation resulting in multisystemic disease

L. Féasson, J. Antoine, A. Casarín, 2012, Neuromuscular Disorders.