[Osteogenesis imperfecta tarda and stapes surgery]

Same author

Short-term results from seventy-six patients receiving a bone-anchored hearing implant installed with a novel minimally invasive surgery technique.

Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery·2016

Same author

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

Nederlands tijdschrift voor geneeskunde·2003

Same author

Velo-cardio-facial syndrome: guidelines for diagnosis, treatment and follow-up of ent manifestations.

Acta oto-rhino-laryngologica Belgica·2003

Same author

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

Clinical otolaryngology and allied sciences·2002

Same author

Vibrant semi-implantable hearing device with digital sound processing: effective gain and speech perception.

Archives of otolaryngology--head & neck surgery·2001

Same author

Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.

Human molecular genetics·2001

Related Experiment Videos

[Osteogenesis imperfecta tarda and stapes surgery]

Related Concept Videos

Short-term results from seventy-six patients receiving a bone-anchored hearing implant installed with a novel minimally invasive surgery technique.

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

Velo-cardio-facial syndrome: guidelines for diagnosis, treatment and follow-up of ent manifestations.

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

Vibrant semi-implantable hearing device with digital sound processing: effective gain and speech perception.

Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.

Related Experiment Videos

[Osteogenesis imperfecta tarda and stapes surgery]

Related Concept Videos

Short-term results from seventy-six patients receiving a bone-anchored hearing implant installed with a novel minimally invasive surgery technique.

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

Velo-cardio-facial syndrome: guidelines for diagnosis, treatment and follow-up of ent manifestations.

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

Vibrant semi-implantable hearing device with digital sound processing: effective gain and speech perception.

Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.

Related Experiment Videos

[Osteogenesis imperfecta tarda and stapes surgery]

Related Concept Videos

Related Articles

Short-term results from seventy-six patients receiving a bone-anchored hearing implant installed with a novel minimally invasive surgery technique.

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

Velo-cardio-facial syndrome: guidelines for diagnosis, treatment and follow-up of ent manifestations.

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

Vibrant semi-implantable hearing device with digital sound processing: effective gain and speech perception.

Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.

Related Experiment Videos

[Osteogenesis imperfecta tarda and stapes surgery]

Related Concept Videos

Related Articles

Short-term results from seventy-six patients receiving a bone-anchored hearing implant installed with a novel minimally invasive surgery technique.

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

Velo-cardio-facial syndrome: guidelines for diagnosis, treatment and follow-up of ent manifestations.

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

Vibrant semi-implantable hearing device with digital sound processing: effective gain and speech perception.

Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.