Titlebook: Rare Diseases; Integrative PPPM App Meral ?zgü? Book 2015 Springer Science+Business Media Dordrecht 2015 Invivo disease models.Personalized

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書目名稱Rare Diseases影響因子(影響力)




書目名稱Rare Diseases影響因子(影響力)學(xué)科排名




書目名稱Rare Diseases網(wǎng)絡(luò)公開度




書目名稱Rare Diseases網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Rare Diseases被引頻次




書目名稱Rare Diseases被引頻次學(xué)科排名




書目名稱Rare Diseases年度引用




書目名稱Rare Diseases年度引用學(xué)科排名




書目名稱Rare Diseases讀者反饋




書目名稱Rare Diseases讀者反饋學(xué)科排名

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熱心

filial

Adeno-Associated Virus Gene Therapy and Its Application to the Prevention and Personalised Treatmenis applied to rare diseases, the first section of this chapter aims to illustrate how gene therapy aligns to the principles of PPPM whereas the second part of the chapter intends to provide an in depth review of the developments in the AAV field that underpin the use of these viruses as gene therapy delivery systems.

似少年

National Plans on Rare Diseases,specific features and approaches. It critically assesses the national achievements in this field, drawing conclusions to further strengthen the process of planning, implementing and evaluating RD national policies..A national plan for RD can be defined as an official strategic public health document

laxative

,Biobanking for Rare Diseases – Impact on Personalised Medicine,ee the rights of stakeholders. Due to their medical and scientific expertise, they offer collections of human biological resources that meet with research project requirements. Because of their secure storage capacities, biobanks are front-line actors in collection management by enabling their devel

detach

invade

Personalized Medicine for Hereditary Deafness,s. While the clinical phenotype, deafness, is shared and similar across different individuals, the substantial genetic heterogeneity makes the genetic etiology in individual cases rare. Identification of genetic causes has been central to a growing body of knowledge related to diagnostic tools, gene

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