Tuberous Sclerosis Complex - Genes, Clinical Features and Therapeutics
Reduzierte Artikel in dieser Kategorie
12,79 €
| Verlag | Wiley-VCH |
| Auflage | 2010 |
| Seiten | 410 |
| Format | 17,9 x 24,4 x 2,5 cm |
| Gewicht | 932 g |
| Artikeltyp | Englisches Buch |
| ISBN-10 | 3527322019 |
| EAN | 9783527322015 |
| Bestell-Nr | 52732201A |
Diese einzige derzeit erhältliche Monographie zur tuberösen Sklerose (Bourneville-Pringle-Syndrom), einer nicht seltenen genetischen Erkrankung, befasst sich mit allen Fragen der molekulargenetischen Veränderungen (insbesondere im Hinblick auf die Signaltransduktion), der Diagnose und geeigneter Therapieansätze. Diskutiert wird aus dem Blickwinkel des Forschers, des Klinikers und auch des interessierten Patienten.
The only comprehensive overview of the molecular basis and clinical features of the genetic disorder tuberous sclerosis, which affects approximately 50,000 people in the US alone. Special focus is placed on novel insights into the signal transduction pathways affected by the disease as well as genotype phenotype correlations, while existing and potential therapies are also discussed in depth. The editors are leading experts in research and treatment of the disease as well as the Vice President of the Tuberous Sclerosis Alliance, the only voluntary health organization for TSC in the US.
Rezension:
"This is an amazing collection of all the latest information on this not uncommon neurocutaneous disorders ... All in all this is an amazing collection of current information on Tuberous Sclerosis and is relatively well priced for such an expensively illustrated text. It makes an excellent source for recent information and is of interest to most people in the world of Pediatric Neurology." (Canadian Journal of Neurological Sciences, 1 January 2012)
