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Trial protocol: a clustered, randomised, longitudinal, type 2 translational trial of alcohol consumption and alcohol-related harm among adolescents in Australia.
Rowland B, Abraham C, Carter R, Abimanyi-Ochom J, Kelly AB, Kremer P, Williams JW, Smith R, Hall JK, Wagner D, Renner H, Hosseini T, Osborn A, Mohebbi M, Toumbourou JW. Rowland B, et al. Among authors: osborn a. BMC Public Health. 2018 Apr 27;18(1):559. doi: 10.1186/s12889-018-5452-3. BMC Public Health. 2018. PMID: 29703187 Free PMC article. Clinical Trial.
Social marketing and community mobilisation to reduce underage alcohol consumption in Australia: A cluster randomised community trial.
Rowland BC, Williams J, Smith R, Hall JK, Osborn A, Kremer P, Kelly AB, Leslie E, Patton G, Mohebbi M, Toumbourou JW. Rowland BC, et al. Among authors: osborn a. Prev Med. 2018 Aug;113:132-139. doi: 10.1016/j.ypmed.2018.02.032. Epub 2018 Mar 3. Prev Med. 2018. PMID: 29505806 Clinical Trial.
BACKGROUND AND AIMS: In many countries adolescent alcohol use is a major health problem. To supplement national policies, it is important to trial community interventions as a potential strategy to prevent adolescent alcohol use. ...TRIAL REGISTRATION: ACTRN12612000 …
BACKGROUND AND AIMS: In many countries adolescent alcohol use is a major health problem. To supplement national policies, it is impor …
Prevalence and nature of connexin 26 mutations in children with non-syndromic deafness.
Dahl HH, Saunders K, Kelly TM, Osborn AH, Wilcox S, Cone-Wesson B, Wunderlich JL, Du Sart D, Kamarinos M, Gardner RJ, Dennehy S, Williamson R, Vallance N, Mutton P. Dahl HH, et al. Among authors: osborn ah. Med J Aust. 2001 Aug 20;175(4):191-4. doi: 10.5694/j.1326-5377.2001.tb143093.x. Med J Aust. 2001. PMID: 11587277
Connexin26 deafness in several interconnected families.
Wilcox SA, Osborn AH, Allen-Powell DR, Maw MA, Dahl HH, Gardner RJ. Wilcox SA, et al. Among authors: osborn ah. J Med Genet. 1999 May;36(5):383-5. J Med Genet. 1999. PMID: 10353784 Free PMC article.
High frequency hearing loss correlated with mutations in the GJB2 gene.
Wilcox SA, Saunders K, Osborn AH, Arnold A, Wunderlich J, Kelly T, Collins V, Wilcox LJ, McKinlay Gardner RJ, Kamarinos M, Cone-Wesson B, Williamson R, Dahl HH. Wilcox SA, et al. Among authors: osborn ah. Hum Genet. 2000 Apr;106(4):399-405. doi: 10.1007/s004390000273. Hum Genet. 2000. PMID: 10830906
Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing loss.
Houseman MJ, Ellis LA, Pagnamenta A, Di WL, Rickard S, Osborn AH, Dahl HH, Taylor GR, Bitner-Glindzicz M, Reardon W, Mueller RF, Kelsell DP. Houseman MJ, et al. Among authors: osborn ah. J Med Genet. 2001 Jan;38(1):20-5. doi: 10.1136/jmg.38.1.20. J Med Genet. 2001. PMID: 11134236 Free PMC article.
Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene.
Denoyelle F, Weil D, Maw MA, Wilcox SA, Lench NJ, Allen-Powell DR, Osborn AH, Dahl HH, Middleton A, Houseman MJ, Dodé C, Marlin S, Boulila-ElGaïed A, Grati M, Ayadi H, BenArab S, Bitoun P, Lina-Granade G, Godet J, Mustapha M, Loiselet J, El-Zir E, Aubois A, Joannard A, Levilliers J, Garabédian EN, Mueller RF, Gardner RJ, Petit C, et al. Denoyelle F, et al. Among authors: osborn ah. Hum Mol Genet. 1997 Nov;6(12):2173-7. doi: 10.1093/hmg/6.12.2173. Hum Mol Genet. 1997. PMID: 9336442
330 results