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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

99 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Hearing loss in inherited peripheral neuropathies: Molecular diagnosis by NGS in a French series.
Lerat J, Magdelaine C, Roux AF, Darnaud L, Beauvais-Dzugan H, Naud S, Richard L, Derouault P, Ghorab K, Magy L, Vallat JM, Cintas P, Bieth E, Arne-Bes MC, Goizet C, Espil-Taris C, Journel H, Toutain A, Urtizberea JA, Boespflug-Tanguy O, Laffargue F, Corcia P, Pasquier L, Fradin M, Napuri S, Ciron J, Boulesteix JM, Sturtz F, Lia AS. Lerat J, et al. Mol Genet Genomic Med. 2019 Sep;7(9):e839. doi: 10.1002/mgg3.839. Epub 2019 Aug 8. Mol Genet Genomic Med. 2019. PMID: 31393079 Free PMC article.
Implication of the SH3TC2 gene in Charcot-Marie-Tooth disease associated with deafness and/or scoliosis: Illustration with four new pathogenic variants.
Lerat J, Magdelaine C, Lunati A, Dzugan H, Dejoie C, Rego M, Beze Beyrie P, Bieth E, Calvas P, Cintas P, Delaubrier A, Demurger F, Gilbert-Dussardier B, Goizet C, Journel H, Laffargue F, Magy L, Taithe F, Toutain A, Urtizberea JA, Sturtz F, Lia AS. Lerat J, et al. J Neurol Sci. 2019 Nov 15;406:116376. doi: 10.1016/j.jns.2019.06.027. Epub 2019 Jun 26. J Neurol Sci. 2019. PMID: 31634715
High prevalence of congenital deafness on Reunion Island is due to a founder variant of LHFPL5.
Lerat J, Bonnet C, Cartault F, Loundon N, Jacquemont ML, Darcel F, Rouillon I, Mezouaghi K, Guichet A, Litzler J, Gesny R, Gherbi S, Aissa IB, Digeon FSJ, Garabedian EN, Bonnefont JP, Genin E, Denoyelle F, Jonard L, Marlin S. Lerat J, et al. Clin Genet. 2019 Jan;95(1):177-181. doi: 10.1111/cge.13460. Epub 2018 Nov 4. Clin Genet. 2019. PMID: 30298622
A sudden bilateral hearing loss caused by inner ear hemorrhage.
Meunier A, Clavel P, Aubry K, Lerat J. Meunier A, et al. Among authors: lerat j. Eur Ann Otorhinolaryngol Head Neck Dis. 2020 Jan;137(1):65-67. doi: 10.1016/j.anorl.2019.05.021. Epub 2019 Jun 6. Eur Ann Otorhinolaryngol Head Neck Dis. 2020. PMID: 31178427 Free article.
Guidelines (short version) of the French Society of Otorhinolaryngology (SFORL) on cervical lymphatic malformation in adults and children: Diagnosis.
Lerat J, Bisdorff-Bresson A, Borsic M, Chopinet C, Couloignier V, Fakhry N, Fayoux P, Jegoux F, Larralde A, Leboulanger N, Nicollas R, Letourmy SP; SFORL work group. Lerat J, et al. Eur Ann Otorhinolaryngol Head Neck Dis. 2019 Apr;136(2):109-112. doi: 10.1016/j.anorl.2019.02.005. Epub 2019 Feb 25. Eur Ann Otorhinolaryngol Head Neck Dis. 2019. PMID: 30819600 Free article.
Isolated hypoglossal palsy due to cervical osteophyte.
Patron V, Roudaut PY, Lerat J, Vivent M, Bessède JP, Aubry K. Patron V, et al. Among authors: lerat j. Eur Ann Otorhinolaryngol Head Neck Dis. 2012 Feb;129(1):44-6. doi: 10.1016/j.anorl.2011.01.006. Epub 2011 Apr 22. Eur Ann Otorhinolaryngol Head Neck Dis. 2012. PMID: 21514267 Free article.
99 results