Global burden of childhood hearing impairment and disease control priorities for developing countries von Olusanya, Bolajoko O, Dr, Newton, Valerie E, Prof

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Paediatric Audiological Medicine von Newton, Valerie E

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Improving communication with patients with a hearing impairment von Newton, Valerie E, Shah, Seema Rupani

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Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population von XIAO MEI OUYANG, YAN, Denise, BROWN, Steve D. M, BALKANY, Thomas, XUE ZHONG LIU, LI LIN DU, FIELDING HEJTMANCIK, J, JACOBSON, Samuel G, NANCE, Walter E, LI, An Ren, ANGELI, Simon, KAISER, Muriel, NEWTON, Valerie

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Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene von Tassabehji, Mayada, Read, Andrew P, Newton, Valerie E, Harris, Rodney, Balling, Rudi, Gruss, Peter, Strachan, Tom

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Global and regional hearing impairment prevalence: an analysis of 42 studies in 29 countries von Stevens, Gretchen, Flaxman, Seth, Brunskill, Emma, Mascarenhas, Maya, Mathers, Colin D, Finucane, Mariel

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Connexin-26 mutations in sporadic non-syndromal sensorineural deafness von Lench, Nicholas, Houseman, Mark, Newton, Valerie, Camp, Guy Van, Mueller, Robert

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Preventing ototoxicity and its effects von Newton, Valerie E, Fernando, Charmy, Sirimanna, Tony

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Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2 von Tassabehji, May, Read, Andrew P, Newton, Valerie E, Patton, Michael, Gruss, Peter, Harris, Rodney, Strachan, Tom

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Mutations in the Myosin VIIA Gene Cause a Wide Phenotypic Spectrum, Including Atypical Usher Syndrome von Liu, Xue-Zhong, Hope, Carolyn, Walsh, James, Newton, Valerie, Ke, Xiao Mei, Liang, Chuan Yu, Xu, Li Ron, Zhou, Jiu Mu, Trump, Dorothy, Steel, Karen P., Bundey, Sarah, Brown, Steve D.M.

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Clinical Features of the Waardenburg Syndromes von Newton, V.E.

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Waardenburg syndrome von Read, A P, Newton, V E

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Evaluation of the use of a questionnaire to detect hearing loss in Kenyan pre-school children von Newton, Valerie E., Macharia, Isaac, Mugwe, Peter, Ototo, Benson, Kan, S.W.

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Paediatric audiological medicine, second edition von Newton, Valerie E

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Identification of a new mutation of the myosin VII head region in Usher syndrome type 1 von Liu, Xue-zhong, Newton, Valerie E., Steel, Karen P., Brown, Steve D. M.

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The effects of improving hearing in dementia von Allen, N. Harry, Burns, Alistair, Newton, Valerie, Hickson, Frances, Ramsden, Richard, Rogers, Jenny, Butler, Sue, Thistlewaite, Gillian, Morris, Julie

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Symptomatic congenital cytomegalovirus infection after maternal recurrent infection von MORRIS, DAVID J, SIMS, DOUG, CHISWICK, MALCOLM, DAS, VIJAY K, NEWTON, VALERIE E

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Waardenburg syndrome type II: Phenotypic findings and diagnostic criteria von Liu, Xue-Zhong, Newton, Valerie E., Read, Andrew P.

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Paediatric audiological medicine von Newton, Valerie E

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Audiological Assessment and Management in the Era of Precision Medicine von Munro, Kevin J., Newton, Valerie E., Moore, David R.

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