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Genetics of Deafness
Guest Editors: Edi Lúcia Sartorato, Karen Friderici, and Ignacio Del Castillo- Genetics of Deafness, Edi Lúcia Sartorato, Karen Friderici, and Ignacio Del Castillo
Volume 2012 (2012), Article ID 562848, 1 page - Mitochondrial Sensorineural Hearing Loss: A Retrospective Study and a Description of Cochlear Implantation in a MELAS Patient, Mauro Scarpelli, Francesca Zappini, Massimiliano Filosto, Anna Russignan, Paola Tonin, and Giuliano Tomelleri
Volume 2012 (2012), Article ID 287432, 5 pages - The Molecular Biology of Vestibular Schwannomas and Its Association with Hearing Loss: A Review, Erika Celis-Aguilar, Luis Lassaletta, Miguel Torres-Martín, F. Yuri Rodrigues, Manuel Nistal, Javier S. Castresana, Javier Gavilan, and Juan A. Rey
Volume 2012 (2012), Article ID 856157, 10 pages - Hearing Loss in Osteogenesis Imperfecta: Characteristics and Treatment Considerations, Joseph P. Pillion, David Vernick, and Jay Shapiro
Volume 2011 (2011), Article ID 983942, 6 pages - Clinical Application of Screening for GJB2 Mutations before Cochlear Implantation in a Heterogeneous Population with High Rate of Autosomal Recessive Nonsyndromic Hearing Loss, Masoud Motasaddi Zarandy, Mersedeh Rohanizadegan, Hojjat Salmasian, Nooshin Nikzad, Niloofar Bazazzadegan, and Mahdi Malekpour
Volume 2011 (2011), Article ID 787026, 6 pages - Autosomal Recessive Nonsyndromic Hearing Impairment due to a Novel Deletion in the RDX Gene, Kwanghyuk Lee, Mohammad Amin ud Din, Muhammad Ansar, Regie Lyn P. Santos-Cortez, Wasim Ahmad, and Suzanne M. Leal
Volume 2011 (2011), Article ID 294675, 5 pages - The Sound of Silence: Mouse Models for Hearing Loss, Sumantra Chatterjee and Thomas Lufkin
Volume 2011 (2011), Article ID 416450, 9 pages - Assessing Noncoding Sequence Variants of GJB2 for Hearing Loss Association, T. D. Matos, H. Simões-Teixeira, H. Caria, R. Cascão, H. Rosa, A. O'Neill, Ó. Dias, M. E. Andrea, D. P. Kelsell, and G. Fialho
Volume 2011 (2011), Article ID 827469, 8 pages - Molecular Investigation of Pediatric Portuguese Patients with Sensorineural Hearing Loss, Célia Nogueira, Miguel Coutinho, Cristina Pereira, Alessandra Tessa, Filippo M. Santorelli, and Laura Vilarinho
Volume 2011 (2011), Article ID 587602, 5 pages - A Novel ESRRB Deletion Is a Rare Cause of Autosomal Recessive Nonsyndromic Hearing Impairment among Pakistani Families, Kwanghyuk Lee, Saadullah Khan, Muhammad Ansar, Regie Lyn P. Santos-Cortez, Wasim Ahmad, and Suzanne M. Leal
Volume 2011 (2011), Article ID 368915, 4 pages