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Types of Inheritance and Genes Associated with Familial Meniere Disease.
Parra-Perez AM, Lopez-Escamez JA. Parra-Perez AM, et al. J Assoc Res Otolaryngol. 2023 Jun;24(3):269-279. doi: 10.1007/s10162-023-00896-0. Epub 2023 Apr 6. J Assoc Res Otolaryngol. 2023. PMID: 37022572 Free PMC article. Review.
Meniere disease (MD) is a rare disorder of the inner ear defined by sensorineural hearing loss (SNHL) associated with episodes of vertigo and tinnitus. The phenotype is variable, and it may be associated with other comorbidities such as migraine, respiratory allergi …
Meniere disease (MD) is a rare disorder of the inner ear defined by sensorineural hearing loss (SNHL) associated with episodes …
Genetics of hearing and deafness.
Angeli S, Lin X, Liu XZ. Angeli S, et al. Anat Rec (Hoboken). 2012 Nov;295(11):1812-29. doi: 10.1002/ar.22579. Epub 2012 Oct 8. Anat Rec (Hoboken). 2012. PMID: 23044516 Free PMC article. Review.
Most of the cases of genetic deafness recognized today are monogenic disorders that can be broadly classified by the mode of inheritance (i.e., autosomal dominant, autosomal recessive, X-linked, and mitochondrial inheritance) and by the presence of associated …
Most of the cases of genetic deafness recognized today are monogenic disorders that can be broadly classified by the mode of inheritance (i. …
[Genetics of congenital deafness].
Faundes V, Pardo RA, Castillo Taucher S. Faundes V, et al. Med Clin (Barc). 2012 Oct 20;139(10):446-51. doi: 10.1016/j.medcli.2012.02.014. Epub 2012 Apr 24. Med Clin (Barc). 2012. PMID: 22538062 Review. Spanish.
Congenital deafness is defined as the hearing loss which is present at birth and, consequently, before speech development. It is the most prevalent sensor neural disorder in developed countries, and its incidence is estimated between 1-3 children per 1,000 newborns, …
Congenital deafness is defined as the hearing loss which is present at birth and, consequently, before speech development. It …
Introduction to genetics for otorhinolaryngology nurses.
Malone KJ, Cook SS. Malone KJ, et al. ORL Head Neck Nurs. 2006 Spring;24(2):8-18. ORL Head Neck Nurs. 2006. PMID: 16696290 Review.
This article presents information about basic inheritance patterns (autosomal dominant and recessive, X-linked, and mitochondrial) and compares single-gene disorders to complex or mutifactorial diseases. Cleft lip and palate disorders (Robin sequence and Van der Wou …
This article presents information about basic inheritance patterns (autosomal dominant and recessive, X-linked, and mitochondr …