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Inner Ear Development and Hearing Loss
Retail Price: $209.00
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$188.10
Editors: Saima Riazuddin, Zubair Ahmed (Division of Pediatric Otolaryngology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH)
Book Description:
This book is a user-friendly book directed at practicing general otolaryngologists, developmental biologist, geneticists and researcher focused on understanding the inner ear structure and biology. This book is both comprehensive, easy to follow and each chapter is short, informative and self-contained. It will provide an overview of four main topics related to inner ear development, hearing loss and clinical remedies, genetics of deafness in the post genomic era. The overall objective of this book is to bring together noted otolaryngologists and scientists from the perspective of complementary disciplines for a review of the current state of knowledge and available clinical therapies, genetics testing practices in various populations and molecular components of inner ear and their function in sound perception. (Imprint: Nova Biomedical)

Please click on a chapter below to purchase separately

Chapter 1 - The birth of a mechanosensor: development of vertebrate hair cells (pp. 1-24)
Authors / Editors: (Tomoko Kita, Stephen Freeman, Raj K. Ladher, Laboratory for Sensory Development, RIKEN Center for Developmental Biology, Kobe, Japan)

Chapter 2 - Tight junctions-Barriers against hair cell toxicity and hearing loss (pp. 25-46)
Authors / Editors: (Gowri D. Nayak, Zubair M. Ahmed, Saima Riazuddin, Laboratory of Molecular Genetics, Divisions of Pediatric Otolaryngology Head & Neck Surgery and Ophthalmology, Cincinnati Children’s Hospital Research Foundation, Cincinnati, OH, USA)
***Open Access Chapter. Free Download Available***

Chapter 3 - Usher and Bardet-Biedl syndrome proteins: New pieces in the planar cell polarity puzzle (pp. 47-66)
Authors / Editors: (Arnaud Giese, Saima Riazuddin, Zubair M. Ahmed, Divisions of Pediatric Ophthalmology and Otolaryngology Head & Neck Surgery, Cincinnati Children’s Hospital Research Foundation, Cincinnati, OH, USA)
***Open Access Chapter. Free Download Available***

Chapter 4 - Autoimmune inner ear disease (AIED) (pp. 67-76)
Authors / Editors: (Roberto Bovo, Chiara Faccioli, ENT department, University Hospital of Padua, Italy)

Chapter 5 - Labyrinthine aplasia, microtia, and microdontia (LAMM) syndrome and FGF3 mutations (pp. 77-86)
Authors / Editors: (Kumarie Latchman, Mustafa Tekin, Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL, USA)

Chapter 6 - Social implications of cochlear implantation in children (pp. 87-100)
Authors / Editors: (Matthew Provenzano, Daniel I. Choo, Division of Pediatric Otolaryngology Head & Neck Surgery, Cincinnati Children’s Hospital Research Foundation, Cincinnati, OH, USA)

Chapter 7 - Hereditary deafness and cochlear implantation (pp. 101-126)
Authors / Editors: (Viet Pham, Rebecca Cook, Dayton Young, Tomoko Makishima, Department of Otolaryngology, University of Texas Medical Branch, Galveston, Texas, USA)

Chapter 8 - Deafness gene discovery in the genomic era (pp. 127-142)
Authors / Editors: (Tal Elkan-Miller, Karen B. Avraham, Department of Human Molecular Genetics and Biochemistry, Sackler Faculty of Medicine and Sagol School of Neuroscience, Tel Aviv University, Tel Aviv, Israel)

Chapter 9 - Nonsyndromic hearing impairment: The utility of families for the identification of hearing impairment genes, variants and phenotypes (pp. 143-158)
Authors / Editors: (Regie Lyn P. Santos-Cortez, Suzanne M. Leal, Center for Statistical Genetics, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA)

Chapter 10 - Interpretation of variants of uncertain clinical significance (VUCS): the paradigm of Usher syndrome (pp. 159-174)
Authors / Editors: (David Baux, Christel Vache, Susan Malcolm, Mireille Claustres, Anne-Francoise Roux, Laboratoire de génétique moléculaire, CHU Montpellier, Montpellier, France. Clinical and Molecular Genetics, Institute of Child Health, University College London, UK, INSERM, U827, Montpellier, France. University Montpellier I, Montpellier, France)

Chapter 11 - Molecular genetic studies on the GJB2 gene in the Korean population (pp. 175-182)
Authors / Editors: (Soo-Young Choi, Kyu Yup Lee, Un-Kyung Kim, Department of Biology, College of Natural Sciences, Kyungpook National University, Daegu, Korea, Department of Otolaryngology, College of Medicine, Kyungpook National University, Daegu, Korea)

Chapter 12 - Hereditary hearing loss and its management in the Japanese population (pp. 183-188)
Authors / Editors: (Koji Nishimura, Shin-ichiro Kitajiri, Department of Otolaryngology, Head and Neck Surgery, Graduate School of Medicine, Kyoto University, Japan)

   Series:
      Human Anatomy and Physiology
   Binding: Hardcover
   Pub. Date: 2013- January
   Pages: 102, 7 x 10 (NBC - C)
   ISBN: 978-1-62417-011-9
   Status: AV
  
Status Code Description
AN Announcing
FM Formatting
PP Page Proofs
FP Final Production
EP Editorial Production
PR At Prepress
AP At Press
AV Available
  
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Inner Ear Development and Hearing Loss