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D Nekahm

Research Profile

Chemicals & Drugs

Disorders

Geographic Areas

Austria

Concepts & Ideas

Physiology

Procedures

Objects

Intensive Care Units, Neonatal

Phenomena

Polymorphism, Single-Stranded Conformational

Genes & Molecular Sequences

Dominant Genes

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Co-author Network

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Publications

TOP 3
D Nekahm; Viktor Weichbold; Kunigunde Welzl-Mueller; Almut Hirst-Stadlmann
Improvement in early detection of congenital hearing impairment due to universal newborn hearing screening.
Andreas R Janecke; D Nekahm; Jürgen Löffler; Almut Hirst-Stadlmann; Thomas Müller; Gerd Utermann
De novo mutation of the connexin 26 gene associated with dominant non-syndromic sensorineural hearing loss.
Jürgen Löffler; D Nekahm; Almut Hirst-Stadlmann; Barbara Günther; HJ Menzel; Gerd Utermann; Andreas R Janecke
Sensorineural hearing loss and the incidence of Cx26 mutations in Austria.

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All Publications

2001: D Nekahm; Viktor Weichbold; Kunigunde Welzl-Mueller; Almut Hirst-Stadlmann
Improvement in early detection of congenital hearing impairment due to universal newborn hearing screening.
International journal of pediatric otorhinolaryngology 2001;59(1):23-8.
2001: Andreas R Janecke; D Nekahm; Jürgen Löffler; Almut Hirst-Stadlmann; Thomas Müller; Gerd Utermann
De novo mutation of the connexin 26 gene associated with dominant non-syndromic sensorineural hearing loss.
Human genetics 2001;108(3):269-70.
2001: Jürgen Löffler; D Nekahm; Almut Hirst-Stadlmann; Barbara Günther; HJ Menzel; Gerd Utermann; Andreas R Janecke
Sensorineural hearing loss and the incidence of Cx26 mutations in Austria.
European journal of human genetics : EJHG 2001;9(3):226-30.
2001: D Nekahm; Viktor Weichbold; Kunigunde Welzl-Müller
Epidemiology of permanent childhood hearing impairment in the Tyrol, 1980-94.
Scandinavian audiology 2001;30(3):197-202.
1997: Kunigunde Welzl-Müller; K Böheim; K Stephan; H Schlögel; A Stadlmann; D Nekahm
[Optimizing hearing screening by transient evoked otoacoustic emissions in newborn infants].
HNO 1997;45(4):227-32.

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