01906nam 2200421 450 991013815450332120231130182233.0953-51-6497-X(CKB)3230000000075527(NjHacI)993230000000075527(oapen)https://directory.doabooks.org/handle/20.500.12854/65160(EXLCZ)99323000000007552720221010d2011 uy 0engur|||||||||||txtrdacontentcrdamediacrrdacarrierAmyloidosis mechanisms and prospects for therapy /edited by Svetlana SarantsevaIntechOpen2011Rijeka, Croatia :InTech,[2011]©20111 online resource (228 pages)953-307-253-9 Amyloidoses are a heterogeneous group of diverse etiology diseases. They are characterized by an endogenous production of abnormal proteins called amyloid proteins, which are not hydrosoluble, form depots in various organs and tissue of animals and humans and cause dysfunctions. Despite many decades of research, the origin of the pathogenesis and the molecular determinants involved in amyloid diseases has remained elusive. At present, there is not an effective treatment to prevent protein misfolding in these amyloid diseases. The aim of this book is to present an overview of different aspects of amyloidoses from basic mechanisms and diagnosis to latest advancements in treatment.AmyloidosisAmyloidosisInfectious & contagious diseasesAmyloidosis.616.3995Sarantseva Svetlanaedt1439615Sarantseva SvetlanaNjHacINjHaclBOOK9910138154503321Amyloidosis3601912UNINA