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2018 1
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2022 3
2023 2
2024 2

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Page 1
Defective α-tectorin may involve tectorial membrane in familial Meniere disease.
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. Roman-Naranjo P, et al. Among authors: eckhard ah. Clin Transl Med. 2022 Jun;12(6):e829. doi: 10.1002/ctm2.829. Clin Transl Med. 2022. PMID: 35653455 Free PMC article. No abstract available.
Menière's Syndrome Associated With Fibrous Dysplasia of the Temporal Bone.
Weiss NM, Breitsprecher TM, Dlugaiczyk J, Kämmerer F, Lukas C, Dazert S, Eckhard AH, Bächinger D. Weiss NM, et al. Among authors: eckhard ah. Otol Neurotol. 2023 Jul 1;44(6):e445-e448. doi: 10.1097/MAO.0000000000003891. Epub 2023 May 9. Otol Neurotol. 2023. PMID: 37167637 Free PMC article. No abstract available.
A novel nonsense variant in the CENPP gene segregates in a Swiss family with autosomal dominant low-frequency sensorineural hearing loss.
Robles-Bolivar P, Bächinger D, Parra-Perez AM, Román-Naranjo P, Escalera-Balsera A, Gallego-Martinez A, Eckhard AH, Lopez-Escamez JA. Robles-Bolivar P, et al. Among authors: eckhard ah. Eur J Hum Genet. 2022 Nov;30(11):1301-1305. doi: 10.1038/s41431-022-01184-w. Epub 2022 Sep 7. Eur J Hum Genet. 2022. PMID: 36071244 Free PMC article.
17 results