Hereditary gelsolin amyloidosis (HGA): a neglected cause of bilateral progressive or recurrent facial palsy-Reference-Cited by-同舟云学术

Hereditary gelsolin amyloidosis (HGA): a neglected cause of bilateral progressive or recurrent facial palsy

Published:2017-03 Issue:1 Volume:22 Page:59-63
ISSN:1085-9489
Container-title:Journal of the Peripheral Nervous System
language:en
Short-container-title:J Peripher Nerv Syst

Author:

Sagnelli Anna¹,Piscosquito Giuseppe¹,Di Bella Daniela²,Fadda Laura³,Melzi Lisa⁴,Morico Antonio⁵,Ciano Claudia²,Taroni Franco²,Facchetti Dante⁶,Salsano Ettore¹,Pareyson Davide¹

Affiliation:

1. Department of Clinical Neurosciences; IRCCS Foundation, “C. Besta” Neurological Institute; Milan Italy

2. Department of Diagnostic and Applied Technology; IRCCS Foundation, “C. Besta” Neurological Institute; Milan Italy

3. Department of Neurology; University of Cagliari; Cagliari Italy

4. Department of Ophthalmology, Neuro-ophthalmology Unit; Milan Italy

5. Department of Ophthalmology, Corneal Service; IRCCS Istituto Auxologico Italiano; Milan Italy

6. Department of Neurology; ASST Niguarda Hospital; Milan Italy

Publisher

Wiley

Subject

Neurology (clinical),General Neuroscience

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jns.12200/fullpdf

Reference19 articles.

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2. Lattice corneal dystrophy, gelsolin type (Meretoja's syndrome);Carrwik;Acta Ophthalmol,2009

3. Progressive bilateral facial weakness;Carswell;Pract Neurol,2015

4. Gelsolin-derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187;Chapelle;Nat Genet,1992

5. Bilateral facial nerve paralysis in the outpatient setting; the need for follow-up in the face of a serious pathology;Chaucer;Am J Emerg Med,2016

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