Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2006 1
2012 2
2023 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

4 results

Results by year

Filters applied: . Clear all
Your search was processed without automatic term mapping because it retrieved zero results.
Page 1
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. ...Familial MD shows different types of inheritance, including autosomal dominant and compound recessive
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. ...More than 400 syndromes accompanied of deafness have been described, which represent about 30% of cases of congenital hearing loss
Congenital deafness is defined as the hearing loss which is present at birth and, consequently, before speech development. ... …
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 …