Kenna MA - Search Results

1

Gene Transfer with AAV9-PHP.B Rescues Hearing in a Mouse Model of Usher Syndrome 3A and Transduces Hair Cells in a Non-human Primate.

György B, Meijer EJ, Ivanchenko MV, Tenneson K, Emond F, Hanlon KS, Indzhykulian AA, Volak A, Karavitaki KD, Tamvakologos PI, Vezina M, Berezovskii VK, Born RT, O'Brien M, Lafond JF, Arsenijevic Y, Kenna MA, Maguire CA, Corey DP. György B, et al. Among authors: kenna ma. Mol Ther Methods Clin Dev. 2018 Nov 20;13:1-13. doi: 10.1016/j.omtm.2018.11.003. eCollection 2019 Jun 14. Mol Ther Methods Clin Dev. 2018. PMID: 30581889 Free PMC article.

2

Preclinical testing of AAV9-PHP.B for transgene expression in the non-human primate cochlea.

Ivanchenko MV, Hanlon KS, Devine MK, Tenneson K, Emond F, Lafond JF, Kenna MA, Corey DP, Maguire CA. Ivanchenko MV, et al. Among authors: kenna ma. Hear Res. 2020 Sep 1;394:107930. doi: 10.1016/j.heares.2020.107930. Epub 2020 Feb 26. Hear Res. 2020. PMID: 32145977 Free PMC article.

3

PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing loss.

Redfield SE, De-la-Torre P, Zamani M, Wang H, Khan H, Morris T, Shariati G, Karimi M, Kenna MA, Seo GH, Xu H, Lu W, Naz S, Galehdari H, Indzhykulian AA, Shearer AE, Vona B. Redfield SE, et al. Among authors: kenna ma. Hum Genet. 2024 Mar;143(3):311-329. doi: 10.1007/s00439-024-02649-2. Epub 2024 Mar 9. Hum Genet. 2024. PMID: 38459354 Free PMC article.

4

Hiding in plain sight: genetic deaf-blindness is not always Usher syndrome.

Medina G, Perry J, Oza A, Kenna M. Medina G, et al. Cold Spring Harb Mol Case Stud. 2021 Aug 2;7(4):a006088. doi: 10.1101/mcs.a006088. Print 2021 Aug. Cold Spring Harb Mol Case Stud. 2021. PMID: 34021019 Free PMC article.

5

Peripheral Vestibular Dysfunction Is a Common Occurrence in Children With Non-syndromic and Syndromic Genetic Hearing Loss.

Wang A, Shearer AE, Zhou GW, Kenna M, Poe D, Licameli GR, Brodsky JR. Wang A, et al. Front Neurol. 2021 Oct 21;12:714543. doi: 10.3389/fneur.2021.714543. eCollection 2021. Front Neurol. 2021. PMID: 34744965 Free PMC article.

6

Neonatal hearing screening.

Kenna MA. Kenna MA. Pediatr Clin North Am. 2003 Apr;50(2):301-13. doi: 10.1016/s0031-3955(03)00023-3. Pediatr Clin North Am. 2003. PMID: 12809324

7

Medical management of childhood hearing loss.

Kenna MA. Kenna MA. Pediatr Ann. 2004 Dec;33(12):822-32. doi: 10.3928/0090-4481-20041201-08. Pediatr Ann. 2004. PMID: 15615309 Review.

8

Dark-adapted threshold and electroretinogram for diagnosis of Usher syndrome.

Ambrosio L, Hansen RM, Moskowitz A, Oza A, Barrett D, Manganella J, Medina G, Kawai K, Fulton AB, Kenna M. Ambrosio L, et al. Doc Ophthalmol. 2021 Aug;143(1):39-51. doi: 10.1007/s10633-021-09818-y. Epub 2021 Jan 28. Doc Ophthalmol. 2021. PMID: 33511521

9

Effectiveness of sequencing connexin 26 (GJB2) in cases of familial or sporadic childhood deafness referred for molecular diagnostic testing.

Wu BL, Lindeman N, Lip V, Adams A, Amato RS, Cox G, Irons M, Kenna M, Korf B, Raisen J, Platt O. Wu BL, et al. Genet Med. 2002 Jul-Aug;4(4):279-88. doi: 10.1097/00125817-200207000-00006. Genet Med. 2002. PMID: 12172394 Free article.

10

Postoperative Hearing Loss in a Patient With Crouzon Syndrome: A Case Report.

Butler CG, Kenna MA, Nargozian CD. Butler CG, et al. Among authors: kenna ma. A A Pract. 2018 Jun 1;10(11):310-311. doi: 10.1213/XAA.0000000000000694. A A Pract. 2018. PMID: 29634565

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