Assessment of patients with hereditary transthyretin amyloidosis – understanding the impact of management and disease progression-Reference-Cited by-同舟云学术

Assessment of patients with hereditary transthyretin amyloidosis – understanding the impact of management and disease progression

Published:2019-07-03 Issue:3 Volume:26 Page:103-111
ISSN:1350-6129
Container-title:Amyloid
language:en
Short-container-title:Amyloid

Author:

Conceição Isabel¹,Coelho Teresa²,Rapezzi Claudio³,Parman Yeşim⁴,Obici Laura⁵,Galán Lucía⁶,Rousseau Antoine⁷

Affiliation:

1. CHLN-Hospital Santa Maria, IMM, Unversidade de Lisboa, Lisbon, Portugal;

2. Unidade Corino de Andrade, Hospital de Santo António, Centro Hospitalar Universitário do Porto, Porto, Portugal;

3. Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy;

4. Neurology Department, Neuromuscular Unit, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey;

5. IRCCS Fondazione Policlinico San Matteo, Amyloidosis Research and Treatment Center, Pavia, Italy;

6. Department of Neurology, Hospital Clinico San Carlos IdiSSC, Madrid, Spain;

7. Department of Ophthalmology, Bicêtre Hospital Université Paris-Sud, Le Kremlin-Bicêtre, France APHP, DHU Sight Restore, French Reference centre for H-ATTR (NNERF), French Reference Network for Rare Ophthalmic Diseases (OPHTARA), Le Kremlin-Bicêtre, France

Publisher

Informa UK Limited

Subject

Internal Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/13506129.2019.1627312

Reference49 articles.

1. The molecular biology and clinical features of amyloid neuropathy

2. Guideline of transthyretin-related hereditary amyloidosis for clinicians

3. “Red‐flag” symptom clusters in transthyretin familial amyloid polyneuropathy

4. Atteintes oculaires des neuropathies amyloïdes héréditaires liées à la transthyrétine

5. Diagnosis and management of transthyretin familial amyloid polyneuropathy in Japan: red-flag symptom clusters and treatment algorithm

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