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Hearing in Children with Congenital Cytomegalovirus Infection: Results of a Longitudinal Study

The Journal of pediatrics, 2016-05, Vol.172, p.110-115.e2

2016

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A wide range of protective and predisposing variants in aggrecan influence the susceptibility for otosclerosis

Human genetics, 2022-04, Vol.141 (3-4), p.951-963

2022

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Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment

Genes, 2020-06, Vol.11 (6), p.687

2020

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Risk Factors for Natural Hearing Evolution in Newborns With Congenital Cytomegalovirus Infection

JAMA otolaryngology-- head & neck surgery, 2024-01, Vol.150 (1), p.30

2024

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Risk Factors for Hearing Loss at Birth in Newborns With Congenital Cytomegalovirus Infection

JAMA otolaryngology-- head & neck surgery, 2023-02, Vol.149 (2), p.122

2023

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Congenital CMV-Associated Hearing Loss: Can Brain Imaging Predict Hearing Outcome?

Ear and hearing, 2021-03, Vol.42 (2), p.373-380

2021

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Insufficient evidence for a role of SERPINF1 in otosclerosis

Molecular genetics and genomics : MGG, 2019-08, Vol.294 (4), p.1001-1006

2019

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Congenital cytomegalovirus infection registry in flanders: opportunities and pitfalls

Acta clinica belgica (English ed. Online), 2021-06, Vol.76 (3), p.169-176

2021

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Outcome of cochlear implantation at different ages from 0 to 6 years

Otology & neurotology, 2002-11, Vol.23 (6), p.885-890

2002

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Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment

Nature genetics, 1998-05, Vol.19 (1), p.60-62

1998

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A Second Gene for Otosclerosis, OTSC2, Maps to Chromosome 7q34-36

American journal of human genetics, 2001-02, Vol.68 (2), p.495-500

2001

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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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Transmeatal Procurement of Allograft Tympano-Ossicular Systems: Preliminary Report (Alternative to the intracranial bone plug technique by Schuknecht)

The journal of international advanced otology, 2012-05, Vol.8 (2), p.154

2012

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Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations

Human genetics, 2002-05, Vol.110 (5), p.389-394

2002

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Middle and inner ear malformations in velocardiofacial syndrome

American journal of medical genetics. Part A, 2004-12, Vol.131A (2), p.225-226

2004

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The Use of Malleus Allografts in Ossiculoplasty

The Laryngoscope, 2002-10, Vol.112 (10), p.1782-1784

2002

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A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24

American journal of human genetics, 1997-05, Vol.60 (5), p.1168-1173

1997

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A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2)

Journal of medical genetics, 1998-02, Vol.35 (2), p.151-152

1998

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Linkage Analysis of Progressive Hearing Loss in Five Extended Families Maps the DFNA2 Gene to a 1.25-Mb Region on Chromosome 1p

Genomics (San Diego, Calif.), 1997-04, Vol.41 (1), p.70-74

1997

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Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment

Human genetics, 2000-07, Vol.107 (1), p.7-11

2000

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Clinical presentation of DFNA8-DFNA12

Advances in oto-rhino-laryngology, 2002, Vol.61, p.60-65

2002

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A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing loss

The American journal of otology (New York, N.Y.), 1998-11, Vol.19 (6), p.718

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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Middle and inner ear malformations in velocardiofacial syndrome

American journal of medical genetics. Part A, 2004, Vol.131 (2), p.225-226

2004

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74-week follow-up of safety of infliximab in patients with refractory rheumatoid arthritis

Arthritis research & therapy, 2010-01, Vol.12 (3), p.R121-R121, Article R121

2010

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Ear, Auditive Nerve, Cochleovestibular Tract, Facial Nerve: Diseases, Semeiology
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Otorhinolaryngology. Stomatology
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Hearing in Children with Congenital Cytomegalovirus Infection: Results of a Longitudinal Study

A wide range of protective and predisposing variants in aggrecan influence the susceptibility for otosclerosis

Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment

Risk Factors for Natural Hearing Evolution in Newborns With Congenital Cytomegalovirus Infection

Risk Factors for Hearing Loss at Birth in Newborns With Congenital Cytomegalovirus Infection

Congenital CMV-Associated Hearing Loss: Can Brain Imaging Predict Hearing Outcome?

Insufficient evidence for a role of SERPINF1 in otosclerosis

Congenital cytomegalovirus infection registry in flanders: opportunities and pitfalls

Outcome of cochlear implantation at different ages from 0 to 6 years

Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment

A Second Gene for Otosclerosis, OTSC2, Maps to Chromosome 7q34-36

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

Transmeatal Procurement of Allograft Tympano-Ossicular Systems: Preliminary Report (Alternative to the intracranial bone plug technique by Schuknecht)

Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations

Middle and inner ear malformations in velocardiofacial syndrome

The Use of Malleus Allografts in Ossiculoplasty

A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24

A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2)

Linkage Analysis of Progressive Hearing Loss in Five Extended Families Maps the DFNA2 Gene to a 1.25-Mb Region on Chromosome 1p

Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment

Clinical presentation of DFNA8-DFNA12

A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing loss

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

Middle and inner ear malformations in velocardiofacial syndrome

74-week follow-up of safety of infliximab in patients with refractory rheumatoid arthritis

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