Abnormalities of ocular motility in myotonic dystrophy

[From gene to disease; non-syndromic, autosomal dominant, low-frequency sensorineural hearing loss (DFNA6/14)].

Nederlands tijdschrift voor geneeskunde·2003

Hereditary cochleovestibular dysfunction due to a COCH gene mutation (DFNA9): a follow-up study of a family.

Clinical otolaryngology and allied sciences·2002

Fluctuant, progressive hearing loss associated with Menière like vertigo in three patients with the Pendred syndrome.

International journal of pediatric otorhinolaryngology·2001

Progressive fluctuant hearing loss, enlarged vestibular aqueduct, and cochlear hypoplasia in branchio-oto-renal syndrome.

Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology·2001

The DFNA10 phenotype.

The Annals of otology, rhinology, and laryngology·2001