Neurometabolic hereditary diseases of adults /: Alessandro P. Burlina, editor.

Burlina, Alessandro P.

doi:10.1007/978-3-319-76148-0

Neurometabolic hereditary diseases of adults / Alessandro P. Burlina, editor.

Burlina, Alessandro P.

2018

RC627.8

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Title

Neurometabolic hereditary diseases of adults / Alessandro P. Burlina, editor.

ISBN

9783319761480 (electronic book)
331976148X (electronic book)
9783319761466

DOI

https://doi.org/10.1007/978-3-319-76148-0

Published

Cham : Springer, 2018.

Language

English

Description

1 online resource

Item Number

10.1007/978-3-319-76148-0 doi

Call Number

RC627.8

Dewey Decimal Classification

616.39042

Summary

This practical book describes only neurometabolic hereditary diseases which have a specific treatment and encourages the general neurologist to think of the most common neurometabolic hereditary diseases, which he might have seen and never considered in the differential diagnosis. Information regarding how to deal with diseases with special therapy is provided (i.e. enzymatic replacement therapy in Fabry disease and Pompe disease), as is information on diseases which are not easily recognized (i.e. Niemann-Pick disease type C), and diseases with clinical features mimicking other common neurodegenrative diseases (i.e. Wilson's disease). Neurometabolic Hereditary Diseases is written with a clinical focus for adult neurologists working in general hospitals.

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Access limited to authorized users.

Digital File Characteristics

text file PDF

Source of Description

Online resource; title from PDF title page (viewed June 12, 2018)

Added Author

Burlina, Alessandro P.

Available in Other Form

Print version: 9783319761466

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