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Prevalence and causes of hearing impairment in Africa

Tropical medicine & international health, 2016-02, Vol.21 (2), p.158-165

2016

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A congenital mucocele of the anterior dorsal tongue

International journal of pediatric otorhinolaryngology, 2014-07, Vol.78 (7), p.1179-1181

2014

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Mutations in the KCNQ4 Gene Are Responsible for Autosomal Dominant Deafness in Four DFNA2 Families

Human molecular genetics, 1999-07, Vol.8 (7), p.1321-1328

1999

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A novel locus for autosomal dominant non-syndromic hearing loss, DFNA31, maps to chromosome 6p21.3

Journal of medical genetics, 2004-01, Vol.41 (1), p.11-13

2004

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Dysphagia is present but mild in myotonic dystrophy type 2

Neuromuscular disorders : NMD, 2009-03, Vol.19 (3), p.196-198

2009

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D.P.4.02 Dysphagia in Myotonic Dystrophy type 2

Neuromuscular disorders : NMD, 2008-10, Vol.18 (9), p.796-797

2008

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Deafness linked to DFNA2: one locus but how many genes?

Nature genetics, 1999-03, Vol.21 (3), p.263-263

1999

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A Dutch family with progressive sensorineural hearing impairment linked to the DFNA2 region

European archives of oto-rhino-laryngology, 2000, Vol.257 (2), p.62-67

2000

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Proximal symphalangism and congenital conductive hearing loss: otologic aspects

The American journal of otology (New York, N.Y.), 1999-05, Vol.20 (3), p.344

1999

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Diagnostic image (367). A man with foetor ex ore

Nederlands tijdschrift voor geneeskunde, 2008-04, Vol.152 (14), p.803

2008

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Hearing loss in the Saethre-Chotzen syndrome

Journal of laryngology and otology, 1996-10, Vol.110 (10), p.952-957

1996

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A highly mobile laryngeal tumour: inspiratory stridor and coughing attacks

Anaesthesia, 2002-01, Vol.57 (1), p.92

2002

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A new type of maxillofacial dysostosis, inherited as an X-linked or autosomal recessive trait

Genetic counseling, 1997, Vol.8 (4), p.285

1997

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Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region

American journal of medical genetics, 2000-07, Vol.93 (3), p.184-187

2000

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Congenital conductive hearing loss in the lacrimoauriculodentodigital syndrome

Archives of otolaryngology--head & neck surgery, 1997-01, Vol.123 (1), p.97-99

1997

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Early-onset sensorineural hearing loss and late-onset neurologic complaints caused by a mitochondrial mutation at position 7472

Archives of otolaryngology--head & neck surgery, 1998-08, Vol.124 (8), p.886

1998

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A highly mobile laryngeal tumour: inspiratory stridor and coughing attacks

Anaesthesia, 2002-01, Vol.57 (1), p.82-101

2002

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Nonsyndromic Autosomal Dominant Progressive Sensorineural Hearing Loss: Audiologic Analysis of a Pedigree Linked to DFNA2

The Laryngoscope, 1998-01, Vol.108 (1), p.74-80

1998

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A Dutch family with progressive autosomal dominant non-syndromic sensorineural hearing impairment linked to DFNA13

Clinical otolaryngology and allied sciences, 2001-08, Vol.26 (4), p.310-316

2001

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A dutch family with progressive autosomal dominant non-syndromic sensorineural hearing impairment linked to DFNA13

Clinical otolaryngology, 2001-08, Vol.26 (4), p.310

2001

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Mitochondrial inherited hearing loss

Clinical otolaryngology and allied sciences, 1998-02, Vol.23 (1), p.3-8

1998

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Mitochondrial inherited hearing loss

Clinical otolaryngology, 1998-02, Vol.23 (1), p.3

1998

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Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene

European journal of human genetics : EJHG, 1999-01, Vol.7 (1), p.45-51

1999

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Non-syndromic dominant sensorineural hearing loss: from a few phenotypes to many genotypes

International journal of pediatric otorhinolaryngology, 1997-01, Vol.38 (3), p.237-245

1997

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Speech recognition scores related to age and degree of hearing impairment in DFNA2/KCNQ4 and DFNA9/COCH

Archives of otolaryngology--head & neck surgery, 2001-09, Vol.127 (9), p.1045

2001

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Prevalence and causes of hearing impairment in Africa

A congenital mucocele of the anterior dorsal tongue

Mutations in the KCNQ4 Gene Are Responsible for Autosomal Dominant Deafness in Four DFNA2 Families

A novel locus for autosomal dominant non-syndromic hearing loss, DFNA31, maps to chromosome 6p21.3

Dysphagia is present but mild in myotonic dystrophy type 2

D.P.4.02 Dysphagia in Myotonic Dystrophy type 2

Deafness linked to DFNA2: one locus but how many genes?

A Dutch family with progressive sensorineural hearing impairment linked to the DFNA2 region

Proximal symphalangism and congenital conductive hearing loss: otologic aspects

Diagnostic image (367). A man with foetor ex ore

Hearing loss in the Saethre-Chotzen syndrome

A highly mobile laryngeal tumour: inspiratory stridor and coughing attacks

A new type of maxillofacial dysostosis, inherited as an X-linked or autosomal recessive trait

Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region

Congenital conductive hearing loss in the lacrimoauriculodentodigital syndrome

Early-onset sensorineural hearing loss and late-onset neurologic complaints caused by a mitochondrial mutation at position 7472

A highly mobile laryngeal tumour: inspiratory stridor and coughing attacks

Nonsyndromic Autosomal Dominant Progressive Sensorineural Hearing Loss: Audiologic Analysis of a Pedigree Linked to DFNA2

A Dutch family with progressive autosomal dominant non-syndromic sensorineural hearing impairment linked to DFNA13

A dutch family with progressive autosomal dominant non-syndromic sensorineural hearing impairment linked to DFNA13

Mitochondrial inherited hearing loss

Mitochondrial inherited hearing loss

Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene

Non-syndromic dominant sensorineural hearing loss: from a few phenotypes to many genotypes

Speech recognition scores related to age and degree of hearing impairment in DFNA2/KCNQ4 and DFNA9/COCH

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