Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("TOPSAKAL, Vedat")

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 8 of 8

  • Page / 1
Export

Selection :

  • and

Surgical Results and Technical Refinements in Translabyrinthine Excision of Vestibular Schwannomas: The Gruppo Otologico ExperienceAMMAR, Mehdi Ben; PICCIRILLO, Enrico; TOPSAKAL, Vedat et al.Neurosurgery. 2012, Vol 70, Num 6, pp 1481-1491, issn 0148-396X, 11 p.Article

A splice-site mutation and overexpression of MY06 cause a similar phenotype in two families with autosomal dominant hearing lossHILGERT, Nele; TOPSAKAL, Vedat; VAN DINTHER, Joost et al.European journal of human genetics. 2008, Vol 16, Num 5, pp 593-602, issn 1018-4813, 10 p.Article

The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairmentVAN LAER, Lut; VAN EYKEN, Els; BAUR, Manuela et al.Human molecular genetics (Print). 2008, Vol 17, Num 2, pp 159-169, issn 0964-6906, 11 p.Article

Heritability of audiometric shape parameters and familial aggregation of presbycusis in an elderly Flemish populationDEMEESTER, Kelly; VAN WIERINGEN, Astrid; HENDRICKX, Jan-Jaap et al.Hearing research. 2010, Vol 265, Num 1-2, pp 1-10, issn 0378-5955, 10 p.Article

Genome-wide SNP-Based Linkage Scan Identifies a Locus on 8q24 for an Age-Related Hearing Impairment TraitHUYGHE, Jeroen R; VAN LAER, Lut; MAZZOLI, Manuela et al.American journal of human genetics. 2008, Vol 83, Num 3, pp 401-407, issn 0002-9297, 7 p.Article

Three Cases of Hearing Loss Related to Mumps During a Nationwide Outbreak in The Netherlands, 2009-2013FANOY, Ewout B; WOLTERS, Bert A; TOPSAKAL, Vedat et al.The Pediatric infectious disease journal. 2014, Vol 33, Num 8, pp 889-890, issn 0891-3668, 2 p.Article

Hearing Disability Measured by the Speech, Spatial, and Qualities of Hearing Scale in Clinically Normal-Hearing and Hearing-Impaired Middle-Aged Persons, and Disability Screening by Means of a Reduced SSQ (the SSQ5)DEMEESTER, Kelly; TOPSAKAL, Vedat; HENDRICKX, Jan-Jaap et al.Ear and hearing. 2012, Vol 33, Num 5, pp 615-626, issn 0196-0202, 12 p.Article

Genotype-Phenotype Correlation for DFNA22: Characterization of Non-Syndromic, Autosomal Dominant, Progressive Sensorineural Hearing Loss due to MY06 MutationsTOPSAKAL, Vedat; HILGERT, Nele; VAN DINTHER, Joost et al.Audiology & neuro-otology. 2010, Vol 15, Num 4, pp 211-220, issn 1420-3030, 10 p.Article

  • Page / 1