Charles H. Vite - Search Results

Year	Number of Results
2002	4
2003	4
2004	3
2005	3
2006	1
2007	1
2008	4
2009	1
2010	4
2011	5
2012	4
2013	3
2014	7
2015	7
2016	8
2017	3
2018	3
2019	4
2020	6
2021	2
2022	1
2023	4
2024	2

1

Biodistribution of Adeno-Associated Virus Gene Therapy Following Cerebrospinal Fluid-Directed Administration.

Chen X, Lim DA, Lawlor MW, Dimmock D, Vite CH, Lester T, Tavakkoli F, Sadhu C, Prasad S, Gray SJ. Chen X, et al. Among authors: vite ch. Hum Gene Ther. 2023 Feb;34(3-4):94-111. doi: 10.1089/hum.2022.163. Hum Gene Ther. 2023. PMID: 36606687 Review.

2

Efficacy and Safety of a Krabbe Disease Gene Therapy.

Hordeaux J, Jeffrey BA, Jian J, Choudhury GR, Michalson K, Mitchell TW, Buza EL, Chichester J, Dyer C, Bagel J, Vite CH, Bradbury AM, Wilson JM. Hordeaux J, et al. Among authors: vite ch. Hum Gene Ther. 2022 May;33(9-10):499-517. doi: 10.1089/hum.2021.245. Epub 2022 Mar 22. Hum Gene Ther. 2022. PMID: 35333110 Free PMC article.

3

Aging in the canine and feline brain.

Vite CH, Head E. Vite CH, et al. Vet Clin North Am Small Anim Pract. 2014 Nov;44(6):1113-29. doi: 10.1016/j.cvsm.2014.07.008. Epub 2014 Nov 1. Vet Clin North Am Small Anim Pract. 2014. PMID: 25441628 Free PMC article. Review.

4

Insights into the Pathogenesis and Treatment of Krabbe Disease.

Bongarzone ER, Escolar ML, Gray SJ, Kafri T, Vite CH, Sands MS. Bongarzone ER, et al. Pediatr Endocrinol Rev. 2016 Jun;13 Suppl 1:689-96. Pediatr Endocrinol Rev. 2016. PMID: 27491217 Review.

5

Canine and Feline Models of Human Genetic Diseases and Their Contributions to Advancing Clinical Therapies .

Gurda BL, Bradbury AM, Vite CH. Gurda BL, et al. Among authors: vite ch. Yale J Biol Med. 2017 Sep 25;90(3):417-431. eCollection 2017 Sep. Yale J Biol Med. 2017. PMID: 28955181 Free PMC article. Review.

6

Collaborative development of 2-hydroxypropyl-β-cyclodextrin for the treatment of Niemann-Pick type C1 disease.

Ottinger EA, Kao ML, Carrillo-Carrasco N, Yanjanin N, Shankar RK, Janssen M, Brewster M, Scott I, Xu X, Cradock J, Terse P, Dehdashti SJ, Marugan J, Zheng W, Portilla L, Hubbs A, Pavan WJ, Heiss J, Vite CH, Walkley SU, Ory DS, Silber SA, Porter FD, Austin CP, McKew JC. Ottinger EA, et al. Among authors: vite ch. Curr Top Med Chem. 2014;14(3):330-9. doi: 10.2174/1568026613666131127160118. Curr Top Med Chem. 2014. PMID: 24283970 Free PMC article. Review.

7

Myotonia and disorders of altered muscle cell membrane excitability.

Vite CH. Vite CH. Vet Clin North Am Small Anim Pract. 2002 Jan;32(1):169-87, vii. doi: 10.1016/s0195-5616(03)00084-6. Vet Clin North Am Small Anim Pract. 2002. PMID: 11785728 Review.

8

A review of gene therapy in canine and feline models of lysosomal storage disorders.

Bradbury AM, Gurda BL, Casal ML, Ponder KP, Vite CH, Haskins ME. Bradbury AM, et al. Among authors: vite ch. Hum Gene Ther Clin Dev. 2015 Mar;26(1):27-37. doi: 10.1089/humc.2015.002. Epub 2015 Feb 11. Hum Gene Ther Clin Dev. 2015. PMID: 25671613 Free PMC article. Review.

9

Gene therapy for lysosomal storage diseases: the lessons and promise of animal models.

Ellinwood NM, Vite CH, Haskins ME. Ellinwood NM, et al. Among authors: vite ch. J Gene Med. 2004 May;6(5):481-506. doi: 10.1002/jgm.581. J Gene Med. 2004. PMID: 15133760 Review.

10

Large animal models contribute to the development of therapies for central and peripheral nervous system dysfunction in patients with lysosomal storage diseases.

Gurda BL, Vite CH. Gurda BL, et al. Among authors: vite ch. Hum Mol Genet. 2019 Oct 1;28(R1):R119-R131. doi: 10.1093/hmg/ddz127. Hum Mol Genet. 2019. PMID: 31384936 Review.

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