Skip to main content

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

This is a preview of subscription content, access via your institution.

Fig. 1

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

    CAS  Article  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

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Céline Derollez MD.

Ethics declarations

Declarations of interest

The authors declare that they have no conflict of interest.

Ethical approval

This article does not contain any studies with human participants or animals performed by any of the authors.

Additional information

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

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

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

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