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Feasibility of simultaneous PET/MR imaging in the head and upper neck area

European radiology, 2011-07, Vol.21 (7), p.1439-1446

2011

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Computer-aided endovascular aortic repair using fully automated two- and three-dimensional fusion imaging

Journal of vascular surgery, 2016-12, Vol.64 (6), p.1587-1594.e1

2016

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Occupational Noise, Smoking, and a High Body Mass Index are Risk Factors for Age-related Hearing Impairment and Moderate Alcohol Consumption is Protective: A European Population-based Multicenter Study

Journal of the Association for Research in Otolaryngology, 2008-09, Vol.9 (3), p.264-276

2008

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Frataxin Activates Mitochondrial Energy Conversion and Oxidative Phosphorylation

Proceedings of the National Academy of Sciences - PNAS, 2000-10, Vol.97 (22), p.12239-12243

2000

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Differential expression of otoferlin in brain, vestibular system, immature and mature cochlea of the rat

The European journal of neuroscience, 2006-12, Vol.24 (12), p.3372-3380

2006

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Deficient forward transduction and enhanced reverse transduction in the alpha tectorin C1509G human hearing loss mutation

Disease models & mechanisms, 2010-03, Vol.3 (3-4), p.209-223

2010

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Nonmuscle Myosin Heavy-Chain Gene MYH14 Is Expressed in Cochlea and Mutated in Patients Affected by Autosomal Dominant Hearing Impairment (DFNA4)

American journal of human genetics, 2004-04, Vol.74 (4), p.770-776

2004

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Parathyroid hormone leads to the lysosomal degradation of the renal type II Na/Pi cotransporter

Proceedings of the National Academy of Sciences - PNAS, 1998-02, Vol.95 (4), p.1909-1914

1998

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Aggressiveness in cholesterol granuloma of the temporal bone may be determined by the vigor of its blood source

Otology & neurotology, 2007-02, Vol.28 (2), p.232

2007

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Mice lacking Dfna5 show a diverging number of cochlear fourth row outer hair cells

Neurobiology of disease, 2005-08, Vol.19 (3), p.386-399

2005

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The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells

Histochemistry and cell biology, 2003-03, Vol.119 (3), p.247-256

2003

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Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patients

Human mutation, 2002-03, Vol.19 (3), p.308-309

2002

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High frequency of ENG and ALK1/ACVRL1 mutations in German HHT patients

Human mutation, 2005-06, Vol.25 (6), p.595-595

2005

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Cationic liposome mediated transgene expression in the guinea pig cochlea

Hearing research, 1999-02, Vol.128 (1), p.61-69

1999

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Glossary for Hereditary Hearing Impairment

Ear and hearing, 2003-08, Vol.24 (4), p.260-265

2003

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A 4bp-Insertion in the eya-Homologous Region (eyaHR) of EYA4 Causes Hearing Impairment in a Hungarian Family Linked to DFNA10

Molecular medicine (Cambridge, Mass.), 2002-10, Vol.8 (10), p.607-611

2002

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Ozzy, a Jag1 vestibular mouse mutant, displays characteristics of Alagille syndrome

Neurobiology of disease, 2006-10, Vol.24 (1), p.28-40

2006

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Comprehensive molecular analysis of 61 Egyptian families with hereditary nonsyndromic hearing loss

Clinical genetics, 2020-07, Vol.98 (1), p.32-42

2020

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Otoferlin interacts with myosin VI: implications for maintenance of the basolateral synaptic structure of the inner hair cell

Human molecular genetics, 2009-08, Vol.18 (15), p.2779-2790

2009

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Tinnitus sensitization: Sensory and psychophysiological aspects of a new pathway of acquired centralization of chronic tinnitus

Otology & neurotology, 2006-12, Vol.27 (8), p.1054

2006

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The otoferlin interactome in neurosensory hair cells: Significance for synaptic vesicle release and trans-Golgi network (Review)

International journal of molecular medicine, 2011-09, Vol.28 (3), p.311-314

2011

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Autonomous functions of murine thyroid hormone receptor TRα and TRβ in cochlear hair cells

Molecular and cellular endocrinology, 2014-01, Vol.382 (1), p.26-37

2014

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Feasibility of simultaneous PET/MR imaging in the head and upper neck area

Familial aggregation of pure tone hearing thresholds in an aging European population

Computer-aided endovascular aortic repair using fully automated two- and three-dimensional fusion imaging

GRM7 variants confer susceptibility to age-related hearing impairment

Occupational Noise, Smoking, and a High Body Mass Index are Risk Factors for Age-related Hearing Impairment and Moderate Alcohol Consumption is Protective: A European Population-based Multicenter Study

Frataxin Activates Mitochondrial Energy Conversion and Oxidative Phosphorylation

Differential expression of otoferlin in brain, vestibular system, immature and mature cochlea of the rat

Deficient forward transduction and enhanced reverse transduction in the alpha tectorin C1509G human hearing loss mutation

Nonmuscle Myosin Heavy-Chain Gene MYH14 Is Expressed in Cochlea and Mutated in Patients Affected by Autosomal Dominant Hearing Impairment (DFNA4)

Parathyroid hormone leads to the lysosomal degradation of the renal type II Na/Pi cotransporter

Aggressiveness in cholesterol granuloma of the temporal bone may be determined by the vigor of its blood source

Mice lacking Dfna5 show a diverging number of cochlear fourth row outer hair cells

The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells

Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patients

High frequency of ENG and ALK1/ACVRL1 mutations in German HHT patients

Cationic liposome mediated transgene expression in the guinea pig cochlea

Glossary for Hereditary Hearing Impairment

A 4bp-Insertion in the eya-Homologous Region (eyaHR) of EYA4 Causes Hearing Impairment in a Hungarian Family Linked to DFNA10

Ozzy, a Jag1 vestibular mouse mutant, displays characteristics of Alagille syndrome

Comprehensive molecular analysis of 61 Egyptian families with hereditary nonsyndromic hearing loss

Otoferlin interacts with myosin VI: implications for maintenance of the basolateral synaptic structure of the inner hair cell

Tinnitus sensitization: Sensory and psychophysiological aspects of a new pathway of acquired centralization of chronic tinnitus

Next‐generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read‐through, and PEX26 mutated in Heimler syndrome

The otoferlin interactome in neurosensory hair cells: Significance for synaptic vesicle release and trans-Golgi network (Review)

Autonomous functions of murine thyroid hormone receptor TRα and TRβ in cochlear hair cells

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