Almut Hirst-Stadlmann

Sensorineural hearing loss and the incidence of Cx26 mutations in Austria

Judith Löffler, Doris Nekahm, Almut Hirst-Stadlmann et al. · European Journal of Human Genetics · 2001 · 84 citations · Full text

Sensorineural Hearing Loss, Cx26 Mutations, Audiology +5

Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations – phenotypic spectrum and frequencies of GJB2 mutations in Austria

Andreas Janecke, Almut Hirst-Stadlmann, Barbara Günther et al. · Human Genetics · 2002 · 74 citations

Genetic Disorder, Genetics, Audiology +10

De novo mutation of the connexin 26 gene associated with dominant non-syndromic sensorineural hearing loss

Andreas Janecke, Doris Nekahm, Judith Löffler et al. · Human Genetics · 2001 · 35 citations

Developmental Biology, Genetics, Audiology +6

Improvement in early detection of congenital hearing impairment due to universal newborn hearing screening

Doris Nekahm, Viktor Weichbold, Kunigunde Welzl-Mueller et al. · International Journal of Pediatric Otorhinolaryngology · 2001 · 15 citations

Early Diagnosis, Hearing Intervention, Pediatric Otolaryngology +12