Publications by authors named "Klemens Frei"

28Publications

Spectrum of Novel Hereditary Hemorrhagic Telangiectasia Variants in an Austrian Patient Cohort.

Clin Exp Otorhinolaryngol 2019 Nov 22;12(4):405-411. Epub 2019 Jun 22.

Center for Anatomy and Cell Biology, Department for Cell and Developmental Biology, Medical University of Vienna, Vienna, Austria.

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http://dx.doi.org/10.21053/ceo.2019.00304DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6787484PMC
November 2019

Whole-exome sequencing to identify the cause of congenital sensorineural hearing loss in carriers of a heterozygous GJB2 mutation.

Eur Arch Otorhinolaryngol 2017 Oct 18;274(10):3619-3625. Epub 2017 Aug 18.

Department for Cell and Developmental Biology, Center for Anatomy and Cell Biology, Medical University of Vienna, Vienna, Austria.

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http://dx.doi.org/10.1007/s00405-017-4699-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5591807PMC
October 2017

Epistaxis grading in Osler's disease: comparison of comprehensive scores with detailed bleeding diaries.

Int Forum Allergy Rhinol 2017 03 2;7(3):293-299. Epub 2016 Nov 2.

Department of Otorhinolaryngology, Medical University of Vienna, Vienna, Austria.

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http://dx.doi.org/10.1002/alr.21867DOI Listing
March 2017

A Novel Mutation in SLC26A4 Causes Nonsyndromic Autosomal Recessive Hearing Impairment.

Otol Neurotol 2017 02;38(2):173-179

*Department of Otorhinolaryngology, Head and Neck Surgery †Center of Anatomy and Cell Biology, Department for Cell and Developmental Biology ‡Department of Otorhinolaryngology, Head and Neck Surgery, Medical University of Graz, Graz §High Field MR Center, Department of Biomedical Imaging and Image Guided Therapy, Medical University of Vienna, Vienna, Austria.

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http://dx.doi.org/10.1097/MAO.0000000000001286DOI Listing
February 2017

Effect of postoperative use of diclofenac on pharyngocutaneous fistula development after primary total laryngopharyngectomy: Results of a single-center retrospective study.

Head Neck 2016 04 15;38 Suppl 1:E1515-20. Epub 2015 Dec 15.

Department of Otolaryngology - Head and Neck Surgery, Medical University of Vienna, Vienna, Austria.

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http://dx.doi.org/10.1002/hed.24271DOI Listing
April 2016

Delayed auditory pathway maturation and prematurity.

Wien Klin Wochenschr 2015 Jun 20;127(11-12):440-4. Epub 2014 Nov 20.

Department of Otorhinolaryngology-Head and Neck Surgery, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria,

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http://dx.doi.org/10.1007/s00508-014-0653-yDOI Listing
June 2015

The promoter mutation c.-259C>T (-3438C>T) is not a common cause of non-syndromic hearing impairment in Austria.

Eur Arch Otorhinolaryngol 2015 Jan 2;272(1):229-32. Epub 2014 Aug 2.

Department of Otorhinolaryngology-Head and Neck Surgery, Medical University of Vienna, AKH 8J, Waehringer Guertel 18-20, 1090, Vienna, Austria.

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http://dx.doi.org/10.1007/s00405-014-3223-zDOI Listing
January 2015

A novel missense NDP mutation [p.(Cys93Arg)] with a manifesting carrier in an austrian family with Norrie disease.

Audiol Neurootol 2014 30;19(3):203-9. Epub 2014 Apr 30.

Department of Otorhinolaryngology, Medical University of Vienna, Vienna, Austria.

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http://dx.doi.org/10.1159/000358866DOI Listing
March 2015

Despite a lack of otoacoustic emission, word recognition is not seriously influenced in a TECTA DFNA8/12 family.

Int J Pediatr Otorhinolaryngol 2014 May 26;78(5):837-42. Epub 2014 Feb 26.

Department of Otorhinolaryngology, Medical University of Vienna, Vienna, Austria. Electronic address:

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http://dx.doi.org/10.1016/j.ijporl.2014.02.025DOI Listing
May 2014

Occurrence of coagulation factor deficiency in post-tonsillectomy hemorrhage.

Wien Klin Wochenschr 2011 Apr 11;123(7-8):241-4. Epub 2011 Apr 11.

Department of Otorhinolaryngology, Head and Neck Surgery, Medical University of Vienna, Austria.

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http://dx.doi.org/10.1007/s00508-011-1560-0DOI Listing
April 2011

A FGF3 mutation associated with differential inner ear malformation, microtia, and microdontia.

Laryngoscope 2010 Feb;120(2):359-64

Department of Otorhinolaryngology, Division of Molecular Pharmacokinetics and Imaging, Biochemical Genetics and National Neonatal Screening Laboratories, Vienna, Austria.

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http://dx.doi.org/10.1002/lary.20689DOI Listing
February 2010

Characterization of NKIP: a novel, Na+/K+-ATPase interacting protein mediates neural differentiation and apoptosis.

Exp Cell Res 2008 Feb 24;314(3):463-77. Epub 2007 Nov 24.

Department of Clinical Pharmacology, Section of Experimental Oncology/Molecular Pharmacology, Medical University of Vienna, Vienna, Austria.

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http://dx.doi.org/10.1016/j.yexcr.2007.11.013DOI Listing
February 2008

Relevance of the A1555G mutation in the 12S rRNA gene for hearing impairment in Austria.

Otol Neurotol 2007 Oct;28(7):884-6

Department of Otorhinolaryngology, Medical University of Vienna, Austria.

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October 2007

Relevance of the A1555G Mutation in the 12S rRNA Gene for Hearing Impairment in Austria.

Otol Neurotol 2007 Oct;28(7):884-886

*Department of Otorhinolaryngology; †Center of Anatomy and Cell Biology, Department of Chromatin and Developmental Dynamics, Medical University of Vienna; and ‡Department of Otorhinolaryngology, Krankenhaus der Barmherzigen Brüder, Vienna, Austria.

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http://dx.doi.org/10.1097/MAO.0b013e3181461b26DOI Listing
October 2007

Vasoactive intestinal peptide gene alterations in patients with idiopathic pulmonary arterial hypertension.

Eur J Hum Genet 2007 Jan 27;15(1):18-22. Epub 2006 Sep 27.

Medical University of Vienna, Department of Internal Medicine I, Division Institute of Cancer Research, Borschkegasse 8a, Vienna A-1090, Austria.

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http://www.nature.com/articles/5201711
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http://dx.doi.org/10.1038/sj.ejhg.5201711DOI Listing
January 2007

Van Der Woude syndrome: variable penetrance of a novel mutation (p.Arg 84Gly) of the IRF6 gene in a Turkish family.

Int J Mol Med 2005 Feb;15(2):247-51

University Hospital of Cranio-Maxillofacial and Oral Surgery, Medical University of Vienna, A-1090 Vienna, Austria.

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February 2005

Screening for monogenetic del(GJB6-D13S1830) and digenic del(GJB6-D13S1830)/GJB2 patterns of inheritance in deaf individuals from Eastern Austria.

Hear Res 2004 Oct;196(1-2):115-8

Department of Otorhinolaryngology, Medical University of Vienna, AKH-8J, Waehringer Gürtel 18-20, Vienna A-1090, Austria.

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http://dx.doi.org/10.1016/j.heares.2004.07.001DOI Listing
October 2004

Lack of association between Connexin 31 (GJB3) alterations and sensorineural deafness in Austria.

Hear Res 2004 Aug;194(1-2):81-6

Department of Otorhinolaryngology, University Hospital of Vienna, University of Vienna, AKH-8J Waehringer, Gürtel 18-20, Vienna A-1090, Austria.

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http://dx.doi.org/10.1016/j.heares.2004.03.007DOI Listing
August 2004

A novel connexin 26 mutation associated with autosomal recessive sensorineural deafness.

Audiol Neurootol 2004 Jan-Feb;9(1):47-50

Department of Otorhinolaryngology, Krankenhaus der Barmherzigen Brüder, Vienna, Austria.

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http://dx.doi.org/10.1159/000074186DOI Listing
February 2004

The antioxidant activity of caroverine.

Biochem Pharmacol 2003 Jan;65(1):59-65

Institute of Pharmacology and Toxicology, University of Veterinary Medicine Vienna, Veterinaerplatz 1, A-1210 Vienna, Austria.

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http://dx.doi.org/10.1016/s0006-2952(02)01452-1DOI Listing
January 2003

Connexin 26 mutations in cases of sensorineural deafness in eastern Austria.

Eur J Hum Genet 2002 Jul;10(7):427-32

Department of Otorhinolaryngology, AKH-8J, Währinger Gürtel 18-20, Vienna, Austria, A-1090.

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http://dx.doi.org/10.1038/sj.ejhg.5200826DOI Listing
July 2002