@article{843382,
      recid = {843382},
      author = {Burlina, Alessandro P.},
      title = {Neurometabolic hereditary diseases of adults /},
      pages = {1 online resource},
      abstract = {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.},
      url = {http://library.usi.edu/record/843382},
      doi = {https://doi.org/10.1007/978-3-319-76148-0},
}