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Inherited disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. The different clinical types based on symptoms correspond to the presence of a variety of mutations in several different proteins including transthyretin (PREALBUMIN); APOLIPOPROTEIN A-I; and GELSOLIN.
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Genes
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| TTR |
100
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 Individual Studies |
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Homo sapiens
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Mutations/Phenotypic
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Diagnostic pitfalls in sporadic transthyretin familial amyloid polyneuropathy (TTR-FAP).
Authors: V Planté-Bordeneuve, A Ferreira, T Lalu, C Zaros, C Lacroix, D Adams, G Said
Neurology 2007 Aug 14 -
Neurodegeneration in familial amyloid polyneuropathy: from pathology to molecular signaling.
Authors: Mónica Mendes Sousa, Maria João Saraiva
Progress in neurobiology 2003 Dec
Thought leaders and organizations working on research involving familial amyloid polyneuropathy.
- National Center for Research Resources (NCRR)
- Boston University
- FoldRx Pharmaceuticals
- Shinshu University School of Medicine
- Nagoya University Graduate School of Medicine
- Hôpital Bichat
- University of Porto
- Kanazawa University Graduate School of Medical Science
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Safety and Efficacy Study of Fx-1006A in Patients With Familial Amyloidosis
conditions: Familial Amyloid Polyneuropathy
interventions: Fx-1006A
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An Open-Label Extension of Study Fx-005 Evaluating Long-Term Safety and Clinical Outcomes of Fx-1006A in Patients With Transthyretin Amyloid Transthyretin Amyloidosis With Polyneuropathy
conditions: Familial Amyloid Polyneuropathy ; ATTR-PN
interventions: Fx-1006A
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