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Diagnosis of hereditary transthyretin amyloidosis in patients with suspected chronic inflammatory demyelinating polyneuropathy unresponsive to intravenous immunoglobulins: results of a retrospective study.

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Title: Diagnosis of hereditary transthyretin amyloidosis in patients with suspected chronic inflammatory demyelinating polyneuropathy unresponsive to intravenous immunoglobulins: results of a retrospective study.
Authors: Péréon, Yann1 (AUTHOR) yann.pereon@univ-nantes.fr, Adams, David2 (AUTHOR), Camdessanché, Jean-Philippe3 (AUTHOR), Chanson, Jean-Baptiste4 (AUTHOR), Cintas, Pascal5 (AUTHOR), Magy, Laurent6 (AUTHOR), Signaté, Aïssatou7 (AUTHOR), Solé, Guilhem8 (AUTHOR), Svahn, Juliette9 (AUTHOR), Tard, Céline10 (AUTHOR), Hababou, Cyrla11 (AUTHOR), Attarian, Shahram12 (AUTHOR)
Source: Orphanet Journal of Rare Diseases. 3/1/2025, Vol. 20 Issue 1, p1-7. 7p.
Database: Academic Search Ultimate
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  Data: Diagnosis of hereditary transthyretin amyloidosis in patients with suspected chronic inflammatory demyelinating polyneuropathy unresponsive to intravenous immunoglobulins: results of a retrospective study.
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  Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 3/1/2025, Vol. 20 Issue 1, p1-7. 7p.
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        Value: 10.1186/s13023-025-03589-4
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              Text: 3/1/2025
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