logo

EbookBell.com

Most ebook files are in PDF format, so you can easily read them using various software such as Foxit Reader or directly on the Google Chrome browser.
Some ebook files are released by publishers in other formats such as .awz, .mobi, .epub, .fb2, etc. You may need to install specific software to read these formats on mobile/PC, such as Calibre.

Please read the tutorial at this link:  https://ebookbell.com/faq 


We offer FREE conversion to the popular formats you request; however, this may take some time. Therefore, right after payment, please email us, and we will try to provide the service as quickly as possible.


For some exceptional file formats or broken links (if any), please refrain from opening any disputes. Instead, email us first, and we will try to assist within a maximum of 6 hours.

EbookBell Team

Physicians Guide To The Diagnosis Treatment And Followup Of Inherited Metabolic Diseases 1st Edition Nenad Blau

  • SKU: BELL-4664436
Physicians Guide To The Diagnosis Treatment And Followup Of Inherited Metabolic Diseases 1st Edition Nenad Blau
$ 31.00 $ 45.00 (-31%)

5.0

28 reviews

Physicians Guide To The Diagnosis Treatment And Followup Of Inherited Metabolic Diseases 1st Edition Nenad Blau instant download after payment.

Publisher: Springer-Verlag Berlin Heidelberg
File Extension: PDF
File size: 16.03 MB
Pages: 867
Author: Nenad Blau, Marinus Duran, K Michael Gibson, Carlo Dionisi Vici (eds.)
ISBN: 9783642403361, 9783642403378, 3642403360, 3642403379
Language: English
Year: 2014
Edition: 1

Product desciption

Physicians Guide To The Diagnosis Treatment And Followup Of Inherited Metabolic Diseases 1st Edition Nenad Blau by Nenad Blau, Marinus Duran, K Michael Gibson, Carlo Dionisi Vici (eds.) 9783642403361, 9783642403378, 3642403360, 3642403379 instant download after payment.

This book, combining and updating two previous editions, is a unique source of information on the diagnosis, treatment, and follow-up of metabolic diseases. The clinical and laboratory data characteristic of rare metabolic conditions can be bewildering for both clinicians and laboratory personnel. Reference laboratory data are scattered, and clinical descriptions may be obscure. The Physician’s Guide documents the features of more than five hundred conditions, grouped according to type of disorder, organ system affected (e.g. liver, kidney, etc) or phenotype (e.g. neurological, hepatic, etc). Relevant clinical findings are provided and pathological values for diagnostic metabolites highlighted. Guidance on appropriate biochemical genetic testing is provided. Established experimental therapeutic protocols are described, with recommendations on follow-up and monitoring. The authors are acknowledged experts, and the book will be a valuable desk reference for all who deal with inherited metabolic diseases.

Related Products