APA (7th ed.) Citation

Péréon, Y., Adams, D., Camdessanché, J., Chanson, J., Cintas, P., Magy, L., . . . Attarian, S. (2025). Diagnosis of hereditary transthyretin amyloidosis in patients with suspected chronic inflammatory demyelinating polyneuropathy unresponsive to intravenous immunoglobulins: Results of a retrospective study. Orphanet Journal of Rare Diseases, 20(1), 1. https://doi.org/10.1186/s13023-025-03589-4

Chicago Style (17th ed.) Citation

Péréon, Yann, et al. "Diagnosis of Hereditary Transthyretin Amyloidosis in Patients with Suspected Chronic Inflammatory Demyelinating Polyneuropathy Unresponsive to Intravenous Immunoglobulins: Results of a Retrospective Study." Orphanet Journal of Rare Diseases 20, no. 1 (2025): 1. https://doi.org/10.1186/s13023-025-03589-4.

MLA (9th ed.) Citation

Péréon, Yann, et al. "Diagnosis of Hereditary Transthyretin Amyloidosis in Patients with Suspected Chronic Inflammatory Demyelinating Polyneuropathy Unresponsive to Intravenous Immunoglobulins: Results of a Retrospective Study." Orphanet Journal of Rare Diseases, vol. 20, no. 1, 2025, p. 1, https://doi.org/10.1186/s13023-025-03589-4.