Central nervous system involvement in two siblings affected by hereditary transthyretin amyloidosis 30 years after liver transplantation: a model for gene-silencing therapies

Author:

Di Paolantonio A1ORCID,Romano A1,Guglielmino V12,Vitali F12,Sciarrone MA12,Bisogni G3,Verdolotti T4,Maceroni M1,Minnella AM15,Luigetti M12

Affiliation:

1. Università Cattolica del Sacro Cuore, Rome, Italy

2. Fondazione Policlinico Universitario A. Gemelli IRCCS, UOC Neurologia, Rome, Italy

3. Centro Clinico NEMO Adulti, Rome, Italy

4. Fondazione Policlinico Universitario A. Gemelli IRCCS, UOC Radiologia e Neuroradiologia, Rome, Italy

5. Fondazione Policlinico Universitario A. Gemelli IRCCS, UOC Oftalmologia, Rome, Italy

Funder

no funding

Publisher

Informa UK Limited

Subject

Neurology (clinical),Neurology,General Medicine

Reference25 articles.

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

2. Renal Involvement in Hereditary Transthyretin Amyloidosis: An Italian Single-Centre Experience

3. Localization of human prealbumin in choroid plexus epithelium.

4. Pfeffer BA, Becerra SP, Borst DE, et al. Expression of transthyretin and retinol binding protein mRnas and secretion of transthyretin by cultured monkey retinal pigment epithelium. Mol Vis. 2004;10:8.

5. Transthyretin: a multifaceted protein

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