Work

Hereditary transthyretin amyloidosis: a model of medical progress for a fatal disease

Year: 2019

Type: review

Source: Nature Reviews Neurology

DOI: 10.1038/s41582-019-0210-4

Authors: David Adams, Haruki Koike, Michel Slama, Teresa Coelho

Institutions: Université Paris-Sud, Inserm, Assistance Publique – Hôpitaux de Paris, Bicêtre Hospital, Maladies et hormones du système nerveux, Nagoya University, Centre Hospitalier Universitaire Amiens-Picardie, Hôpital Bichat-Claude-Bernard, Mécanismes physiopathologiques et conséquences des calcifications cardiovasculaires, Université de Picardie Jules Verne, Centro Hospitalar do Porto

Language: English

Topic: Amyloidosis: Diagnosis, Treatment, Outcomes

Subfield: Internal Medicine

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: Japan Society for the Promotion of Science

Award: Deciphering the mechanism of neuropathy and development of novel therapies in familial amyloid polyneuropathy

OpenAlex ID: W2952789707

FWCI: 10.58

Cites: 196

Cited by: 476

Related to: 10