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Histological assessment of titanium and polypropylene fiber mesh implantation with and without fibrin tissue glue

Journal of biomedical materials research. Part A, 2007-02, Vol.80A (2), p.372-380

2007

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Psychological counselling in patients with a peripheral facial palsy: initial experience from an expert centre

Journal of plastic, reconstructive & aesthetic surgery, 2022-05, Vol.75 (5), p.1639-1643

2022

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In vivo experiments with tracheostoma tissue connector prototypes

Journal of biomedical materials research. Part A, 2007-07, Vol.82A (1), p.62-72

2007

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Outcomes of endoscopic cricopharyngeal myotomy with CO2 laser surgery: A retrospective study of 47 patients: Outcomes of endoscopic cricopharyngeal myotomy with CO2 laser surgery

Head & neck, 2016-07, Vol.38 (7), p.1022-1027

2016

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Dosimetric Analysis of Radioimmunotherapy with 186Re-Labeled Bivatuzumab in Patients with Head and Neck Cancer

The Journal of nuclear medicine (1978), 2003-10, Vol.44 (10), p.1690-1699

2003

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Hearing Loss in the Treacher-Collins Syndrome

Advances in oto-rhino-laryngology, 2002, Vol.61, p.209-215

2002

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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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18F-FLT PET Does Not Discriminate Between Reactive and Metastatic Lymph Nodes in Primary Head and Neck Cancer Patients

The Journal of nuclear medicine (1978), 2007-05, Vol.48 (5), p.726-735

2007

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Effect of routine follow‐up after treatment for laryngeal cancer on life expectancy and mortality

Cancer, 2007-01, Vol.109 (2), p.239-247

2007

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Identification of three novel mutations in human EYA1 protein associated with branchio-oto-renal syndrome

Human mutation, 1998, Vol.11 (6), p.443-449

1998

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Quality of integrated care for patients with nonsmall cell lung cancer

Cancer, 2007-10, Vol.110 (8), p.1782-1790

2007

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Phase I Therapy Study with 186Re-labeled Humanized Monoclonal Antibody BIWA 4 (Bivatuzumab) in Patients with Head and Neck Squamous Cell Carcinoma

Clinical cancer research, 2003-09, Vol.9 (10), p.3961s

2003

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Prognostic index for patients with parotid carcinoma

Cancer, 2003-03, Vol.97 (6), p.1453-1463

2003

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Autosomal dominant branchio-oto-renal syndrome—localization of a disease gene to chromosome 8q by linkage in a Dutch family

Human molecular genetics, 1992-10, Vol.1 (7), p.491-495

1992

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Treating age-related hearing loss: hearing aids are not very popular

Nederlands tijdschrift voor geneeskunde, 2013, Vol.157 (17), p.A5007

2013

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DFNA2/KCNQ4 and its manifestations

Advances in oto-rhino-laryngology, 2002, Vol.61, p.41-46

2002

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A child with an oesophageal foreign body for 1.5 years

Nederlands tijdschrift voor geneeskunde, 2010, Vol.154, p.A1482

2010

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Descending necrotizing mediastinitis: the need for early diagnosis and aggressive treatment

Nederlands tijdschrift voor geneeskunde, 2009, Vol.153, p.B364

2009

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The Treacher Collins syndrome. A clinical, radiological, and genetic linkage study on two pedigrees

Archives of otolaryngology--head & neck surgery, 1995-05, Vol.121 (5), p.509

1995

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Pharmacokinetics and Immunological Aspects of a Phase Ib Study with Intratumoral Administration of Recombinant Human Interleukin-12 in Patients with Head and Neck Squamous Cell Carcinoma

Clinical cancer research, 2003-08, Vol.9 (8), p.2950

2003

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Refining the region of branchio-oto-renal syndrome and defining the flanking markers on chromosome 8q by genetic mapping

American journal of human genetics, 1994-12, Vol.55 (6), p.1188-1194

1994

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Hearing levels in the Cornelia de Lange syndrome. A report of seven cases

International journal of pediatric otorhinolaryngology, 1989-09, Vol.18 (1), p.31-37

1989

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Autosomal-dominant branchio-otic (BO) syndrome is not allelic to the branchio-oto-renal (BOR) Gene at 8q13

American journal of medical genetics, 1998-04, Vol.76 (5), p.395-401

1998

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Inherited nonsyndromic hearing loss. An audiovestibular study in a large family with autosomal dominant progressive hearing loss related to DFNA2

Archives of otolaryngology--head & neck surgery, 1997-06, Vol.123 (6), p.573

1997

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CHRONIQUE GÉOGRAPHIQUE

Annales de géographie, 1945-01, Vol.53/54 (293), p.67-77

1945

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Audiometry, Pure-Tone
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Histological assessment of titanium and polypropylene fiber mesh implantation with and without fibrin tissue glue

Psychological counselling in patients with a peripheral facial palsy: initial experience from an expert centre

In vivo experiments with tracheostoma tissue connector prototypes

Outcomes of endoscopic cricopharyngeal myotomy with CO2 laser surgery: A retrospective study of 47 patients: Outcomes of endoscopic cricopharyngeal myotomy with CO2 laser surgery

Dosimetric Analysis of Radioimmunotherapy with 186Re-Labeled Bivatuzumab in Patients with Head and Neck Cancer

Hearing Loss in the Treacher-Collins Syndrome

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

18F-FLT PET Does Not Discriminate Between Reactive and Metastatic Lymph Nodes in Primary Head and Neck Cancer Patients

Effect of routine follow‐up after treatment for laryngeal cancer on life expectancy and mortality

Identification of three novel mutations in human EYA1 protein associated with branchio-oto-renal syndrome

Quality of integrated care for patients with nonsmall cell lung cancer

Phase I Therapy Study with 186Re-labeled Humanized Monoclonal Antibody BIWA 4 (Bivatuzumab) in Patients with Head and Neck Squamous Cell Carcinoma

Prognostic index for patients with parotid carcinoma

Autosomal dominant branchio-oto-renal syndrome—localization of a disease gene to chromosome 8q by linkage in a Dutch family

Treating age-related hearing loss: hearing aids are not very popular

DFNA2/KCNQ4 and its manifestations

A child with an oesophageal foreign body for 1.5 years

Descending necrotizing mediastinitis: the need for early diagnosis and aggressive treatment

The Treacher Collins syndrome. A clinical, radiological, and genetic linkage study on two pedigrees

Pharmacokinetics and Immunological Aspects of a Phase Ib Study with Intratumoral Administration of Recombinant Human Interleukin-12 in Patients with Head and Neck Squamous Cell Carcinoma

Refining the region of branchio-oto-renal syndrome and defining the flanking markers on chromosome 8q by genetic mapping

Hearing levels in the Cornelia de Lange syndrome. A report of seven cases

Autosomal-dominant branchio-otic (BO) syndrome is not allelic to the branchio-oto-renal (BOR) Gene at 8q13

Inherited nonsyndromic hearing loss. An audiovestibular study in a large family with autosomal dominant progressive hearing loss related to DFNA2

CHRONIQUE GÉOGRAPHIQUE

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