Melo R
J Audiol Otol. 2024; 28(4):314-317.
PMID: 38973322
PMC: 11540971.
DOI: 10.7874/jao.2024.00045.
Sinno S, Najem F, Dumas G, Abouchacra K, Mallinson A, Perrin P
Audiol Res. 2022; 12(3):316-326.
PMID: 35735366
PMC: 9219718.
DOI: 10.3390/audiolres12030033.
Chan C, Wang F, Omar H, Tan H
Case Rep Otolaryngol. 2021; 2021:2918859.
PMID: 34373798
PMC: 8349271.
DOI: 10.1155/2021/2918859.
van de Berg R, Widdershoven J, Bisdorff A, Evers S, Wiener-Vacher S, Cushing S
J Vestib Res. 2021; 31(1):1-9.
PMID: 33386837
PMC: 9249292.
DOI: 10.3233/VES-200003.
Antoine M, Zhu X, Dieterich M, Brandt T, Vijayakumar S, McKeehan N
PLoS Biol. 2018; 16(3):e2002988.
PMID: 29534062
PMC: 5849283.
DOI: 10.1371/journal.pbio.2002988.
Predictive Factors for Vestibular Loss in Children With Hearing Loss.
Janky K, Thomas M, High R, Schmid K, Ogun O
Am J Audiol. 2018; 27(1):137-146.
PMID: 29482202
PMC: 6105082.
DOI: 10.1044/2017_AJA-17-0058.
Hearing-impaired young people - a physician's guide .
Easson A, Walter S
Clin Med (Lond). 2017; 17(6):521-524.
PMID: 29196352
PMC: 6297701.
DOI: 10.7861/clinmedicine.17-6-521.
Big Stimulus, Little Ears: Safety in Administering Vestibular-Evoked Myogenic Potentials in Children.
Thomas M, Fitzpatrick D, McCreery R, Janky K
J Am Acad Audiol. 2017; 28(5):395-403.
PMID: 28534730
PMC: 5443117.
DOI: 10.3766/jaaa.15097.
The Severity of Vestibular Dysfunction in Deafness as a Determinant of Comorbid Hyperactivity or Anxiety.
Antoine M, Vijayakumar S, McKeehan N, Jones S, Hebert J
J Neurosci. 2017; 37(20):5144-5154.
PMID: 28438970
PMC: 5444197.
DOI: 10.1523/JNEUROSCI.3545-16.2017.
Assessing residual vestibular function in adults with congenital hearing loss.
Lin B, Young Y
Eur Arch Otorhinolaryngol. 2016; 273(12):4209-4214.
PMID: 27295174
DOI: 10.1007/s00405-016-4137-8.
Genetics of peripheral vestibular dysfunction: lessons from mutant mouse strains.
Jones S, Jones T
J Am Acad Audiol. 2014; 25(3):289-301.
PMID: 25032973
PMC: 4310552.
DOI: 10.3766/jaaa.25.3.8.
A quantitative survey of gravity receptor function in mutant mouse strains.
Jones S, Johnson K, Yu H, Erway L, Alagramam K, Pollak N
J Assoc Res Otolaryngol. 2005; 6(4):297-310.
PMID: 16235133
PMC: 2504620.
DOI: 10.1007/s10162-005-0009-4.
[Retinitis pigmentosa, symmetrical inner ear deafness, typical inverse vascular fistula symptom without fistula and vestibular sensitivity disease; combined hereditary ear and eye diseases].
STENGER H
Arch Ohren Nasen Kehlkopfheilkd. 1956; 170(2):187-98.
PMID: 13382283
Pendred syndrome.
Reardon W, Trembath R
J Med Genet. 1996; 33(12):1037-40.
PMID: 9004139
PMC: 1050818.
DOI: 10.1136/jmg.33.12.1037.
Usher's syndrome, with special reference to heterozygous manifestations.
DE HAAS E, Van Lith G, Rijnders J, Rumke A, Volmer C
Doc Ophthalmol. 1970; 28(1):166-90.
PMID: 5312273
DOI: 10.1007/BF00153876.
[Diagnosis of malformations of the ear and temporal bone].
TERRAHE K
Arch Klin Exp Ohren Nasen Kehlkopfheilkd. 1972; 202(1):85-151.
PMID: 5032730
Inherited diseases of the inner ear in man in the light of studies on the mouse.
Deol M
J Med Genet. 1968; 5(2):137-58.
PMID: 4972661
PMC: 1468516.
DOI: 10.1136/jmg.5.2.137.