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- Publications
- Influence
The pattern and diagnostic criteria of sensory neuronopathy: a case–control study
- J. Camdessanché, G. Jousserand, +4 authors J. Antoine
- Medicine
- Brain : a journal of neurology
- 8 June 2009
Acquired sensory neuronopathies encompass a group of paraneoplastic, dysimmune, toxic or idiopathic disorders characterized by degeneration of peripheral sensory neurons in dorsal root ganglia. As… Expand
Acute hemorrhagic leukoencephalopathy associated with influenza A (H1N1) virus
- F. Cissé, J. Antoine, S. Pillet, G. Jousserand, M. Reynaud-Salard, J. Camdessanché
- Medicine
- Journal of Neurology
- 1 March 2011
Since the declaration of the novel influenza A (H1N1) pandemic by the World Health Organization in June 2009, several neurologic complications have been reported including encephalitis,… Expand
Encéphalite à anticorps anti-récepteur du NMDA : une entité traitable impliquant les lymphocytes B. Deux observations
- A. Richard-Mornas, G. Jousserand, J.-P. Camdessanché, Fabien Forest, S. Paul, J. Antoine
- Medicine
- 2012
Resume Introduction L’encephalite a anticorps anti-recepteur N-methyl- d -aspartate (NMDA) du glutamate (Ac anti-NMDA-r) est de description recente. Nous rapportons deux observations illustrant sa… Expand
Brain immunohistopathological study in a patient with anti‐NMDAR encephalitis
- J. Camdessanché, N. Streichenberger, +5 authors J. Antoine
- Medicine
- European journal of neurology
- 1 June 2011
Background and purpose: Anti‐N‐methyl‐d‐asparate (NMDA) receptor encephalitis is thought to be antibody‐mediated. To perform an immunohistopathological study of the inflammatory reaction in a brain… Expand
A clinical pattern‐based etiological diagnostic strategy for sensory neuronopathies: a French collaborative study
- J. Camdessanché, G. Jousserand, +7 authors J. Antoine
- Medicine
- Journal of the peripheral nervous system : JPNS
- 1 September 2012
Sensory neuronopathies (SNNs) encompass paraneoplastic, infectious, dysimmune, toxic, inherited, and idiopathic disorders. Recently described diagnostic criteria allow SNN to be differentiated from… Expand
Musty odour, mental retardation, and spastic paraplegia revealing phenylketonuria in adulthood
- G. Jousserand, J. Antoine, J. Camdessanché
- Medicine
- Journal of Neurology
- 1 February 2010
Phenylketonuria (PKU) is an inherited autosomal recessive disorder characterized by hyperphenyalaninemia resulting from deficiency of hepatic phenylalanine hydroxylase (PAH), which converts… Expand
Sensory and motor neuronopathy in a patient with the A382P TDP-43 mutation
- J. Camdessanché, V. Belzil, +4 authors J. Antoine
- Biology, Medicine
- Orphanet journal of rare diseases
- 5 February 2011
Patients with TARDBP mutations have so far been classified as ALS, sometimes with frontal lobe dysfunction. A 66-year-old patient progressively developed a severe sensory disorder, followed by a… Expand
Proposition de critères diagnostiques de neuronopathie sensitive
- J.-P. Camdessanché, G. Jousserand, +4 authors J. Antoine
- Medicine
- 2009
Hereditary neuropathy with liability to pressure palsy in patients under 30 years old: Neurophysiological data and proposed electrodiagnostic criteria
- Florence Robert-Varvat, G. Jousserand, +13 authors J. Camdessanché
- Medicine
- Muscle & nerve
- 1 February 2018
Introduction: In young patients with mononeuropathy who lack family history and precipitating factors, hereditary neuropathy with liability to pressure palsy (HNPP) may be a possibility. Our… Expand
Novel XK mutation in a McLeod patient diagnosed after heart transplant
- C. Laurencin, L. Sebbag, G. Jousserand, Marie Demontès, S. Thobois
- Medicine
- Clinical Neurology and Neurosurgery
- 1 March 2018