Publications
2023
- Bächinger D, Filidoro N, Naville M, Juchler N, Kurtcuoglu V, Nadol JB Jr, Schuknecht B, Kleinjung T, Veraguth D, Eckhard AH. Radiological feature heterogeneity supports etiological diversity among patient groups in Meniere’s disease. Sci Rep. 2023 Jun 26;13(1):10303.
- Weiss NM, Breitsprecher TM, Dlugaiczyk J, Kämmerer F, Lukas C, Dazert S, Eckhard AH, Bächinger D. Menière’s Syndrome Associated With Fibrous Dysplasia of the Temporal Bone. Otol Neurotol. 2023 Jul 1;44(6):e445-e448.
2022
- Robles-Bolivar P, Bächinger D, Parra-Perez AM, Román-Naranjo P, Escalera-Balsera A, Gallego-Martinez A, Eckhard AH, Lopez-Escamez JA. A novel nonsense variant in the CENPP gene segregates in a Swiss family with autosomal dominant low-frequency sensorineural hearing loss. Eur J Hum Genet. 2022 Nov;30(11):1301-1305.
- Roman-Naranjo P, Parra-Perez AM, Escalera-Balsera A, Soto-Varela A, Gallego-Martinez A, Aran I, Perez-Fernandez N, Bächinger D, Eckhard AH, Gonzalez-Aguado R, Frejo L, Lopez-Escamez JA. Defective α-tectorin may involve tectorial membrane in familial Meniere disease. Clin Transl Med. 2022 Jun;12(6):e829.
- Brada MD, Rushing EJ, Bächinger D, Zoller L, Burger IA, Hüllner MW, Moch H, Huber A, Eckhard AH, Rupp NJ. Immunohistochemical Expression Pattern of Theragnostic Targets SSTR2 and PSMA in Endolymphatic Sac Tumors: A Single Institution Case Series. Head Neck Pathol. 2022 Dec;16(4):1012-1018.
2021
- Roman-Naranjo P, Moleon MDC, Aran I, Escalera-Balsera A, Soto-Varela A, Bächinger D, Gomez-Fiñana M, Eckhard AH, Lopez-Escamez JA. Rare coding variants involving MYO7A and other genes encoding stereocilia link proteins in familial meniere disease. Hear Res. 2021 Sep 15;409:108329.
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