Items where contributor is "Gürtler, Nicolas A.L."
2010Reinert, Julia and Honegger, Flurin and Gürtler, Nicolas. (2010) High homogeneity in auditory outcome of pediatric CI-patients with mutations in Gap-Junction-Protein Beta2. International journal of pediatric otorhinolaryngology, Vol. 74, H. 7. pp. 791-795. Candreia, Claudia and Schmuziger, Nicolas and Gürtler, Nicolas. (2010) Molecular analysis of aquaporin genes 1 to 4 in patients with Menière's disease. Kosmos Studienbücher. pp. 787-792. 2009Pantel, G. and Probst, R. and Podvinec, M. and Gürtler, N.. (2009) Hearing loss and fluctuating hearing levels in X-linked hypophosphataemic osteomalacia. The Journal of Laryngology & Otology, Vol. 123. pp. 136-140. 2008Gürtler, Nicolas and Egenter, Carole and Bösch, Nemya and Plasilova, Martina. (2008) Mutation analysis of the Cx26, Cx30, and Cx31 genes in autosomal recessive nonsyndromic hearing impairment. Acta oto-laryngologica, Vol. 128, no. 10. pp. 1056-1062. Kraft, Marcel and Laeng, Hubert and Schmuziger, Nicolas and Arnoux, André and Gürtler, Nicolas. (2008) Comparison of ultrasound-guided core-needle biopsy and fine-needle aspiration in the assessment of head and neck lesions. Head & neck, Vol. 30, H. 11. pp. 1457-1463. |
