Neurometabolic Hereditary Diseases of Adults

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 regard...

Full description

Bibliographic Details
Corporate Author: SpringerLink (Online service)
Other Authors: Burlina, Alessandro P. (Editor, http://id.loc.gov/vocabulary/relators/edt)
Format: Electronic eBook
Language:English
Published: Cham : Springer International Publishing : Imprint: Springer, 2018.
Edition:1st ed. 2018.
Subjects:
Online Access:Full Text via HEAL-Link
LEADER 02908nam a2200481 4500
001 978-3-319-76148-0
003 DE-He213
005 20191024232019.0
007 cr nn 008mamaa
008 180604s2018 gw | s |||| 0|eng d
020 |a 9783319761480  |9 978-3-319-76148-0 
024 7 |a 10.1007/978-3-319-76148-0  |2 doi 
040 |d GrThAP 
050 4 |a RC346-429.2 
072 7 |a MJN  |2 bicssc 
072 7 |a MED056000  |2 bisacsh 
072 7 |a MKJ  |2 thema 
082 0 4 |a 616.8  |2 23 
245 1 0 |a Neurometabolic Hereditary Diseases of Adults  |h [electronic resource] /  |c edited by Alessandro P. Burlina. 
250 |a 1st ed. 2018. 
264 1 |a Cham :  |b Springer International Publishing :  |b Imprint: Springer,  |c 2018. 
300 |a XIV, 181 p. 29 illus., 16 illus. in color.  |b online resource. 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
347 |a text file  |b PDF  |2 rda 
505 0 |a Principles of human genetics and Mendelian inheritance -- Newborn screening and high risk screening population for neurological inherited metabolic diseases -- Neuroimaging of inherited diseases of adulthood -- Fabry Disease -- Pompe Disease -- Niemann-Pick Disease Type C -- Wilson's Disease -- Homocystinuria. . 
520 |a 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. 
650 0 |a Neurology . 
650 0 |a Metabolic diseases. 
650 0 |a Neuroradiology. 
650 1 4 |a Neurology.  |0 http://scigraph.springernature.com/things/product-market-codes/H36001 
650 2 4 |a Metabolic Diseases.  |0 http://scigraph.springernature.com/things/product-market-codes/H33118 
650 2 4 |a Neuroradiology.  |0 http://scigraph.springernature.com/things/product-market-codes/H2903X 
700 1 |a Burlina, Alessandro P.  |e editor.  |4 edt  |4 http://id.loc.gov/vocabulary/relators/edt 
710 2 |a SpringerLink (Online service) 
773 0 |t Springer eBooks 
776 0 8 |i Printed edition:  |z 9783319761466 
776 0 8 |i Printed edition:  |z 9783319761473 
776 0 8 |i Printed edition:  |z 9783030094140 
856 4 0 |u https://doi.org/10.1007/978-3-319-76148-0  |z Full Text via HEAL-Link 
912 |a ZDB-2-SME 
950 |a Medicine (Springer-11650)