Publications by authors named "Doris Nekahm-Heis"

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Evaluation of auditory development in infants and toddlers who received cochlear implants under the age of 24 months with the LittlEARS) Auditory Questionnaire.
Birgit May-Mederake, Heike Kuehn, Arno Vogel, Annerose Keilmann, Andrea Bohnert, Doris Nekahm-Heis

Int J Pediatr Otorhinolaryngol· October 2010

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Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene.
Nele Hilgert, Matthew J Huentelman, Ashley Q Thorburn, Erik Fransen, Nele Dieltjens, Doris Nekahm-Heis

Eur J Hum Genet· April 2009

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Universal newborn hearing screening and postnatal hearing loss.
Viktor Weichbold, Doris Nekahm-Heis, Kunigunde Welzl-Mueller

Pediatrics· April 2006

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Ten-year outcome of newborn hearing screening in Austria.
Viktor Weichbold, Doris Nekahm-Heis, Kunigunde Welzl-Mueller

Int J Pediatr Otorhinolaryngol· February 2006

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GJB2 mutations and degree of hearing loss: a multicenter study.
Rikkert L Snoeckx, Patrick L M Huygen, Delphine Feldmann, Sandrine Marlin, Françoise Denoyelle, Doris Nekahm-Heis

Am J Hum Genet· December 2005

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[Evaluation of the Austrian Newborn Hearing Screening Program].
Viktor Weichbold, Doris Nekahm-Heis, Kunigunde Welzl-Müller

Wien Klin Wochenschr· September 2005

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The 342-kb deletion in GJB6 is not present in patients with non-syndromic hearing loss from Austria.
Barbara Günther, Andrea Steiner, Doris Nekahm-Heis, Klaus Albegger, Patrick Zorowka

Hum Mutat· August 2003

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Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations--phenotypic spectrum and frequencies of GJB2 mutations in Austria.
Andreas R Janecke, Almut Hirst-Stadlmann, Barbara Günther, Barbara Utermann, Thomas Müller, Doris Nekahm-Heis

Hum Genet· August 2002

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