Libros importados hasta 50% OFF + Envío Gratis a todo USA  Ver más

menu

0
  • argentina
  • chile
  • colombia
  • españa
  • méxico
  • perú
  • estados unidos
  • internacional
portada Mitochondrial Mechanisms of Degeneration and Repair in Parkinson's Disease (in English)
Type
Physical Book
Publisher
Language
Inglés
Pages
275
Format
Paperback
Dimensions
23.4 x 15.6 x 1.5 cm
Weight
0.41 kg.
ISBN13
9783319825076

Mitochondrial Mechanisms of Degeneration and Repair in Parkinson's Disease (in English)

Buhlman, Lori M. (Author) · Springer · Paperback

Mitochondrial Mechanisms of Degeneration and Repair in Parkinson's Disease (in English) - Buhlman, Lori M.

Physical Book

$ 189.46

$ 199.99

You save: $ 10.53

5% discount
  • Condition: New
It will be shipped from our warehouse between Tuesday, July 30 and Wednesday, July 31.
You will receive it anywhere in United States between 1 and 3 business days after shipment.

Synopsis "Mitochondrial Mechanisms of Degeneration and Repair in Parkinson's Disease (in English)"

This volume brings together various theories of how aberrations in mitochondrial function and morphology contribute to neurodegeneration in idiopathic and familial forms of Parkinson's disease. Moreover, it comprehensively reviews the current search for therapies, and proposes how molecules are involved in specific functions as attractive therapeutic targets. It is expected to facilitate critical thought and discussion about the fundamental aspects of neurodegeneration in Parkinson's disease and foster the development of therapeutic strategies among researchers and graduate students. Theories of idiopathic Parkinson's etiology support roles for chronic inflammation and exposure to heavy metals or pesticides. Interestingly, as this project proposes, a case can be made that abnormalities in mitochondrial morphology and function are at the core of each of these theories. In fact, the most common approach to the generation of animal and cell-culture models of idiopathic Parkinson's disease involves exposure to mitochondrial toxins. Even more compelling is the fact that most familial patients harbor genetic mutations that cause disruptions in normal mitochondrial morphology and function. While there remains to be no effective treatment for Parkinson's disease, efforts to postpone, prevent and "cure" onset mitochondrial aberrations and neurodegeneration associated with Parkinson's disease in various models are encouraging. While only about ten percent of Parkinson's patients inherit disease-causing mutations, discovering common mechanisms by which familial forms of Parkinson's disease manifest will likely shed light on the pathophysiology of the more common idiopathic form and provide insight to the general process of neurodegeneration, thus revealing therapeutic targets that will become more and more accessible as technology improves.

Customers reviews

More customer reviews
  • 0% (0)
  • 0% (0)
  • 0% (0)
  • 0% (0)
  • 0% (0)

Frequently Asked Questions about the Book

All books in our catalog are Original.
The book is written in English.
The binding of this edition is Paperback.

Questions and Answers about the Book

Do you have a question about the book? Login to be able to add your own question.

Opinions about Bookdelivery

More customer reviews