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Diagnosis of severe cognitive disorder: the family history as a key issue

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References

  1. Schmitz M, Dittmar K, Llorens F, Gelpi E, Ferrer I, Schulz-Schaeffer WJ, Zerr I (2017) Hereditary human prion diseases: an update. Mol Neurobiol 54:4138–4149

    Article  CAS  Google Scholar 

  2. Geschwind MD, Murray K. Differential diagnosis with other rapid progressive dementias in human prion diseases. In: Handbook of Clinical Neurology. Elsevier; 2018. p. 371–397

  3. Minikel EV, Vallabh SM, Lek M, Estrada K, Samocha KE, Sathirapongsasuti JF, et al. Quantifying prion disease penetrance using large population control cohorts. Science Translational Medicine. 20 janv 2016;8(322):322ra9-322ra9

  4. WHO | Global surveillance, diagnosis and therapy of human transmissible spongiform encephalopathies: report of a WHO consultation. Geneva, Switzerland, 9–11 February 1998. WHO n.d.

  5. Gandini A, Bolognesi ML. Chapter twenty - Therapeutic approaches to prion diseases. In: Legname G, Vanni S, editors. Progress in Molecular Biology and Translational Science, vol. 150, Academic Press; 2017, p. 433–53

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Authors and Affiliations

  1. Department of Neurology, Univ.Lille, INSERM U1171 Degenerative and Vascular Cognitive Disorders, F-59000, Lille, France

    Céline Derollez MD, Florence Pasquier MD PhD & Stéphanie Bombois MD

  2. Unité d’expertise cognitivo-comportementale, Hôpital Roger Salengro, CHRU de Lille, Rue Émile-Laine, 59037, Lille, France

    Céline Derollez MD

  3. Pitié-Salpêtrière Hospital, Cellule nationale de référence des MCJ, AP-HP, Paris, France

    Stéphane Haik

  4. INSERM U1127, Institut du Cerveau et de la Moelle épinière, CNRS UMR7225, Sorbonne Universités, UPMC Université Paris VI UMR, S1127, 75013, Paris, France

    Stéphane Haik

  5. INSERM U 1253 Brain and Imaging, Department of Neurology and Clinical Neurophysiology, Hôpital Bretonneau, 2 bis boulevard Tonnellé, 37044, Tours Cedex, France

    Bertrand De Toffol MD PhD

Authors
  1. Céline Derollez MD
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  2. Stéphane Haik
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  3. Florence Pasquier MD PhD
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  4. Bertrand De Toffol MD PhD
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  5. Stéphanie Bombois MD
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Correspondence to Céline Derollez MD.

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Derollez, C., Haik, S., Pasquier, F. et al. Diagnosis of severe cognitive disorder: the family history as a key issue. Neurol Sci 41, 1945–1947 (2020). https://doi.org/10.1007/s10072-019-04226-2

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  • DOI: https://doi.org/10.1007/s10072-019-04226-2

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