£217.89

CRC Press Gaucher Disease

Name: Gaucher Disease
Brand: CRC Press
Price: 217.89 GBP
Availability: InStock

Public Health

This is the most expensive it has ever been. Walk away.

£218 today · previous high £218 · all-time low £169

NEW HERE?

Amazon shows you one price. We show you all of them.

Tosheroon watches Amazon prices so you don't have to. Every product on Amazon has a price history — we make it visible. Set the price you'd actually pay, and we'll email you the second it gets there. No app, no account, one email.

WHAT'S ON THIS PAGE

↓ Price chart
when this has been cheap or pricey

↓ Forecast
where the price is heading next

↓ Statistics
all-time high & low, recent range

↑ Price alert
name your number, we'll email you

Price History & Forecast

Grey patches = out of stock. Cheaper = lower on the chart. Hover for exact prices.

Last 591 days • 591 data points (No recent data available)

Historical

Generating forecast...

Price Distribution

Price distribution over 591 days • 6 price levels

Days at Price

Current Price

Price Analysis

Most common price: £201 (252 days, 42.6%)

Price range: £169 - £218

Price levels: 6 different prices over 591 days

Description

In September of 2007 Gaucher Disease received a commendation in the Haematology category of the 2007 British Medical Association Medical Book Competition! Although rare in the general population, Gaucher disease is the most prevalent of the lysosomal storage disorders, making research into this particular orphan disorder an invaluable prototype for the diagnosis, research, and treatment of others. Like many rare conditions, Gaucher disease has benefited from the explosion of medical research in the last decade, the amount of new information on this disease is staggering and the rate of new discoveries has left previous books on the subject unable to provide useful, up-to-date information. The most current, fully comprehensive reference to date, Gaucher Disease provides valuable information for academic and industry scientists, and clinicians. Outlining the latest research on the biochemical mechanisms and pathology of lysosomal storage disorders, this book covers diverse topics including animal models, crystallography, imaging and radionuclide evaluation. It not only addresses the developmental basis for current treatments like the now widely available enzyme replacement therapy, but also includes chapters introducing new therapies on the horizon. With contributions from world-renowned experts in substrate reduction therapy, pharmaceutical chaperone therapy, hematopoietic stem cell transplantation and gene therapy, as well as chapters on a second generation of enzyme replacement therapy, this book explores the full spectrum of possibilities offered by the most recent advances in medicine. Some of the most interesting aspects of the book include the discussions on patient management, those touching on the ethics of research, and the societal aspects of treating rare diseases with expensive therapy.

Product Specifications

Brand: CRC Press
Format: hardcover
ASIN: 0849338166
Category: Books > Subjects > Health, Family & Lifestyle > Medical & Healthcare Practitioners > General Medical Issues > Public Health
Domain: Amazon UK
Release Date: 07 July 2006
Listed Since: 13 February 2007

Barcode

No barcode data available

CRC Press Gaucher Disease

This is the most expensive it has ever been. Walk away.

Price History & Forecast

Price Distribution

Price Analysis

Description

Product Specifications

Barcode

Similar Products You Might Like

The Chromosome 22q11.2 Deletion Syndrome: A Multidisciplinary Approach to Diagnosis and Treatment

Velo-Cardio-Facial Syndrome: Diagnosis and Evaluation v. 1 (Genetic Syndromes and Communication Disorders)

Neurochemistry of Metabolic Diseases: Lysosomal Storage Diseases, Phenylketonuria, and Canavan Disease

Lysosomal Storage Disorders: A Practical Guide

Genomics of Rare Diseases: Understanding Disease Genetics Using Genomic Approaches (Translational and Applied Genomics)

Röntgendiagnostik der Skeleterkrankungen Teil 3 / Diseases of the Skeletal System (Roentgen Diagnosis) Part 3: 5 / 3 (Handbuch der medizinischen Radiologie Encyclopedia of Medical Radiology, 5 / 3)

Gangliosides: Methods and Protocols: 1804 (Methods in Molecular Biology, 1804)

Molecular Mechanisms of Ataxia Telangiectasia (Medical Intelligence Unit (Unnumbered))

Molecular Pathology: A Primer for Laboratory Scientists

ICMR-NIIH Practical Guide to Laboratory Immunohematology

Neurometabolic Hereditary Diseases of Adults

Molecular Mechanisms of Cockayne Syndrome (Medical Intelligence Unit (Unnumbered))

Neuronal Tissue-Nonspecific Alkaline Phosphatase (TNAP): 76 (Subcellular Biochemistry, 76)

Developmental Neuropathology

Gene Correction: Methods and Protocols: 1114 (Methods in Molecular Biology, 1114)

Management of Genetic Syndromes

Advances in Medicine & Biology: Volume 62 (Advances in Medicine and Biology)

Advances in Cancer Research: 83: Volume 83

PRADER WILLI SYNDROME (Congenital Disorders - Laboratory and Clinical Research: Genetics - Research and Issues)

Complete Directory for Pediatric Disorders, 2017/18: Print Purchase Includes 1 Year Free Online Access (Complete Directory of Pediatric Disorders)

Lysosomal Storage Diseases: Pathobiology & Therapeutic Consideration

Humana ATM Kinase: Methods and Protocols 1599 Book

Der intrazelluläre Proteintransport bei Erkrankungen im Kindesalter

Génétique médicale: De la biologie à la pratique clinique