Udsalget slutter om
Udvidet returret til d. 31. januar 2025

Physician's Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases - Nenad Blau - Bog

Bag om Physician's Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases

This updated and enlarged second edition 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 clinicians and laboratory personnel alike ¿ reference laboratory data is scattered, and clinical descriptions can be obscure. The new Physician¿s Guide with the additional more than 600 diseases now featured, documents 1200 conditions grouped according to type of disorder, organ system affected (e.g. liver, kidney, etc) or phenotype (e.g. neurological, hepatic, etc). It includes relevant clinical findings and highlights the pathological values for diagnostic metabolites. Guidance on appropriate biochemical genetic testing is also provided and established experimental therapeutic protocols are described, with recommendations on follow-up and monitoring. The authors are acknowledged experts, and the book is a valuable desk reference for all who deal with inherited metabolic diseases. Chapter 73 is available open access under a Creative Commons Attribution 4.0 International License via link.springer.com

Vis mere
  • Sprog:
  • Engelsk
  • ISBN:
  • 9783030677268
  • Indbinding:
  • Hardback
  • Sideantal:
  • 1600
  • Udgivet:
  • 22. februar 2022
  • Udgave:
  • 22002
  • Størrelse:
  • 215x91x285 mm.
  • Vægt:
  • 4800 g.
  • Ukendt - mangler pt..
Forlænget returret til d. 31. januar 2025

Normalpris

  • BLACK FRIDAY
    : :

Medlemspris

Prøv i 30 dage for 45 kr.
Herefter fra 79 kr./md. Ingen binding.

Beskrivelse af Physician's Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases

This updated and enlarged second edition 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 clinicians and laboratory personnel alike ¿ reference laboratory data is scattered, and clinical descriptions can be obscure. The new Physician¿s Guide with the additional more than 600 diseases now featured, documents 1200 conditions grouped according to type of disorder, organ system affected (e.g. liver, kidney, etc) or phenotype (e.g. neurological, hepatic, etc). It includes relevant clinical findings and highlights the pathological values for diagnostic metabolites. Guidance on appropriate biochemical genetic testing is also provided and established experimental therapeutic protocols are described, with recommendations on follow-up and monitoring.
The authors are acknowledged experts, and the book is a valuable desk reference for all who deal with inherited metabolic diseases.
Chapter 73 is available open access under a Creative Commons Attribution 4.0 International License via link.springer.com

Brugerbedømmelser af Physician's Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases



Gør som tusindvis af andre bogelskere

Tilmeld dig nyhedsbrevet og få gode tilbud og inspiration til din næste læsning.