Finnish Type Amyloidosis
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-319-66816-1_1743-1
Reference9 articles.
1. de Souza PVS, Bortholin T, Naylor FGM, Dias RB, Pinto WBVR, Oliveira ASB (2017) Familial progressive bilateral facial paralysis in Finnish type hereditary amyloidosis. Pract Neurol 17:408–409. https://doi.org/10.1136/practneurol-2017-001690
2. Feldt J, Schicht M, Garreis F, Welss J, Schneider UW, Paulsen F (2019) Structure, regulation and related diseases of the actin-binding protein gelsolin. Expert Rev Mol Med 20:e7. https://doi.org/10.1017/erm.2018.7
3. Kiuru S (1992) Familial amyloidosis of the Finnish type (FAF). A clinical study of 30 patients. Acta Neurol Scand 86:346–353. https://doi.org/10.1111/j.1600-0404.1992.tb05099.x
4. Kiuru S (1998) Gelsolin-related familial amyloidosis, Finnish type (FAF), and its variants found worldwide. Amyloid 5:55–66. https://doi.org/10.3109/13506129809007291
5. Kiuru S, Matikainen E, Kupari M, Haltia M, Palo J (1994) Autonomic nervous system and cardiac involvement in familial amyloidosis, Finnish type (FAF). J Neurol Sci 126:40–48. https://doi.org/10.1016/0022-510x(94)90092-2
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