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Auditory Processing Disorder Targets Phonetics, Not Phonology.
Hestvik A, Morlet T, Nagao K, Han C. Hestvik A, et al. Among authors: morlet t. Proc Annu Boston Univ Conf Lang Dev. 2023;2023(1):356-365. Proc Annu Boston Univ Conf Lang Dev. 2023. PMID: 37560553 Free PMC article. No abstract available.
Clinical management guidelines for Friedreich ataxia: best practice in rare diseases.
Corben LA, Collins V, Milne S, Farmer J, Musheno A, Lynch D, Subramony S, Pandolfo M, Schulz JB, Lin K, Delatycki MB; Clinical Management Guidelines Writing Group. Corben LA, et al. Orphanet J Rare Dis. 2022 Nov 12;17(1):415. doi: 10.1186/s13023-022-02568-3. Orphanet J Rare Dis. 2022. PMID: 36371255 Free PMC article.
Mutations in LOXHD1 gene can cause auditory neuropathy spectrum disorder.
Morlet T, Robbins KM, Stabley D, Holbrook J; University of Washington Center for Mendelian Genomics; Sol-Church K, O'Reilly RC. Morlet T, et al. Otolaryngol Case Rep. 2021 Nov;21:100367. doi: 10.1016/j.xocr.2021.100367. Epub 2021 Oct 9. Otolaryngol Case Rep. 2021. PMID: 35875410 Free PMC article.
Cochlear implantation in a patient with mucopolysaccharidosis IVA.
Nagao K, Walter C, Parkes WJ, Teixido M, Theroux MC, Szymkowski S, Morlet T, Tomatsu S. Nagao K, et al. Among authors: morlet t. SAGE Open Med Case Rep. 2019 Aug 30;7:2050313X19873791. doi: 10.1177/2050313X19873791. eCollection 2019. SAGE Open Med Case Rep. 2019. PMID: 31516706 Free PMC article.
Recessive GM3 synthase deficiency: Natural history, biochemistry, and therapeutic frontier.
Bowser LE, Young M, Wenger OK, Ammous Z, Brigatti KW, Carson VJ, Moser T, Deline J, Aoki K, Morlet T, Scott EM, Puffenberger EG, Robinson DL, Hendrickson C, Salvin J, Gottlieb S, Heaps AD, Tiemeyer M, Strauss KA. Bowser LE, et al. Among authors: morlet t. Mol Genet Metab. 2019 Apr;126(4):475-488. doi: 10.1016/j.ymgme.2019.01.013. Epub 2019 Jan 21. Mol Genet Metab. 2019. PMID: 30691927
64 results