Usher Syndrome
Autor Satpal Ahujaen Limba Engleză Hardback – 19 oct 2011
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Specificații
ISBN-13: 9781612092270
ISBN-10: 1612092276
Pagini: 458
Ilustrații: b/w photos & illus
Dimensiuni: 259 x 182 x 33 mm
Greutate: 1.05 kg
Ediția:New.
Editura: Nova Science Publishers Inc
ISBN-10: 1612092276
Pagini: 458
Ilustrații: b/w photos & illus
Dimensiuni: 259 x 182 x 33 mm
Greutate: 1.05 kg
Ediția:New.
Editura: Nova Science Publishers Inc
Cuprins
The Swedish RD Registry- A Source to Identify Families with Retinal Degeneration Suitable for Treatment Trials; Molecular Epidemiology of Usher syndrome; Usher syndrome: 27 Years of Research in Colombia, South America; Protein Networks Related to the Usher syndrome Gain Insights in the Molecular Basis of the Disease; The Usher Interactome Functions in Inner Ear & Retina; Comparative Pathogenesis; Fashioning a Hair Bundle: Role of the Usher Proteins & PCP Pathway in Styling the Sensory Apparatus of the Inner Ear; Regulation of Cochlear Development & Function: A Scenario for Growth Factor Actions; Role of Connexins in Hearing & Sensorineural Hearing Impairment; MicroRNAs in the Inner Ear: Implications for Hearing Loss; MicroRNAs in Retinal Pathophysiology & Therapeutics; Usher Syndrome: Diagnostic Utility of the Asper Biotechs Genotyping Microarray; Clinical Features, Diagnostic Options & Therapeutic Prospects of Retinal Malfunctioning in Usher syndrome; Approaches to the Treatment of Usher syndrome; A Cell Replacement Therapy for Sensory System; Retinal Stem Cell Transplantation; Retinal Full Thickness Transplantation Strategies Towards Clinical Therapy; Retinal Prosthesis; Remediation of Severe or Total Losses of Hearing with Cochlear Implants; Cochlear Implants in Individuals with Usher syndrome; Electronic Implants for Hearing in Usher syndrome; Aminoglycoside Mediated Suppression of Nonsense Mutations as a Potential Therapy for Usher syndrome; Current Therapeutic Strategies for Human Usher syndrome; Gene Therapy for Retinal Degenerations; Pioneers for the Basic Understanding of Usher syndrome.