Guillemette Jousserand

Publications21
h-index7
Citations304
Highly Influential Citations8
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The pattern and diagnostic criteria of sensory neuronopathy: a case–control study
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
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Acute hemorrhagic leukoencephalopathy associated with influenza A (H1N1) virus
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
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Encéphalite à anticorps anti-récepteur du NMDA : une entité traitable impliquant les lymphocytes B. Deux observations
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
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Brain immunohistopathological study in a patient with anti‐NMDAR encephalitis
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
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A clinical pattern‐based etiological diagnostic strategy for sensory neuronopathies: a French collaborative study
Sensory neuronopathies (SNNs) encompass paraneoplastic, infectious, dysimmune, toxic, inherited, and idiopathic disorders. Recently described diagnostic criteria allow SNN to be differentiated from… Expand
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Musty odour, mental retardation, and spastic paraplegia revealing phenylketonuria in adulthood
Phenylketonuria (PKU) is an inherited autosomal recessive disorder characterized by hyperphenyalaninemia resulting from deficiency of hepatic phenylalanine hydroxylase (PAH), which converts… Expand
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Sensory and motor neuronopathy in a patient with the A382P TDP-43 mutation
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
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Proposition de critères diagnostiques de neuronopathie sensitive
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Hereditary neuropathy with liability to pressure palsy in patients under 30 years old: Neurophysiological data and proposed electrodiagnostic criteria
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
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Novel XK mutation in a McLeod patient diagnosed after heart transplant
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