Which Leber congenital amaurosis patients are eligible for gene therapy trials?

著者: Drack, Arlene V., Johnston, Rebecca, Stone, Edwin M.
出版事項 2009

From the Laboratory to the Clinic: Molecular Genetic Testing in Pediatric Ophthalmology

著者: Drack, Arlene V., Lambert, Scott R., Stone, Edwin M.
出版事項 2010

The clinical evaluation of infantile nystagmus: What to do first and why

著者: Bertsch, Morgan, Floyd, Michael, Kehoe, Taylor, Pfeifer, Wanda, Drack, Arlene V.
出版年 Ophthalmic Genet (2017)

Improved ocular alignment with adjustable sutures in adults undergoing strabismus surgery

著者: Zhang, Monica S., Hutchinson, Amy K., Drack, Arlene V., Cleveland, Julia, Lambert, Scott R.
出版事項 2011

TRIP8b Is Required for Maximal Expression of HCN1 in the Mouse Retina

著者: Pan, Yuan, Bhattarai, Sajag, Modestou, Modestos, Drack, Arlene V., Chetkovich, Dane M., Baker, Sheila A.
出版事項 2014

A novel mutation in ACTG1 can cause either isolated hearing loss or Baraitser-Winter syndrome

著者: Kemerley, Andrew, Sloan-Heggen, Christina M, Pfeifer, Wanda L, Smith, Richard JH, Drack, Arlene V
出版年 Ophthalmic Genet (2016)

Efficacy of topical brinzolamide in children with retinal dystrophies

著者: Scruggs, Brittni A., Chen, Constance V., Pfeifer, Wanda, Wiley, Jill S., Wang, Kai, Drack, Arlene V.
出版年 Ophthalmic Genet (2019)

Prevalence and Characteristics of Abnormal Head Posture in children with Down syndrome – a 20 year retrospective, descriptive review

著者: Dumitrescu, Alina V, Moga, Daniela C, Longmuir, Susannah Q, Olson, Richard J, Drack, Arlene V
出版年 Ophthalmology (2011)

Presentation of TRPM1-Associated Congenital Stationary Night Blindness in Children

著者: Miraldi Utz, Virginia, Pfeifer, Wanda, Longmuir, Susannah Q., Olson, Richard John, Wang, Kai, Drack, Arlene V.
出版年 JAMA Ophthalmol (2018)

Vitritis in Pediatric Genetic Retinal Disorders

著者: Stunkel, Maria, Bhattarai, Sajag, Kemerley, Andrew, Stone, Edwin M., Wang, Kai, Mullins, Robert F., Drack, Arlene V.
出版年 Ophthalmology (2014)

TUDCA Slows Retinal Degeneration in Two Different Mouse Models of Retinitis Pigmentosa and Prevents Obesity in Bardet-Biedl Syndrome Type 1 Mice

著者: Drack, Arlene V., Dumitrescu, Alina V., Bhattarai, Sajag, Gratie, Daniel, Stone, Edwin M., Mullins, Robert, Sheffield, Val C.
出版事項 2012

Ectopic Expression of Human BBS4 Can Rescue Bardet-Biedl Syndrome Phenotypes in Bbs4 Null Mice

著者: Chamling, Xitiz, Seo, Seongjin, Bugge, Kevin, Searby, Charles, Guo, Deng F., Drack, Arlene V., Rahmouni, Kamal, Sheffield, Val C.
出版事項 2013

Accumulation of non-outer segment proteins in the outer segment underlies photoreceptor degeneration in Bardet–Biedl syndrome

著者: Datta, Poppy, Allamargot, Chantal, Hudson, Joseph S., Andersen, Emily K., Bhattarai, Sajag, Drack, Arlene V., Sheffield, Val C., Seo, Seongjin
出版年 Proc Natl Acad Sci U S A (2015)

RNA Interference-Based Therapy for Spinocerebellar Ataxia Type 7 Retinal Degeneration

著者: Ramachandran, Pavitra S., Bhattarai, Sajag, Singh, Pratibha, Boudreau, Ryan L., Thompson, Stewart, LaSpada, Albert R., Drack, Arlene V., Davidson, Beverly L.
出版事項 2014

Complement activation and choriocapillaris loss in early AMD: Implications for pathophysiology and therapy

著者: Whitmore, S.Scott, Sohn, Elliott H., Chirco, Kathleen R., Drack, Arlene V., Stone, Edwin M., Tucker, Budd A., Mullins, Robert F.
出版年 Prog Retin Eye Res (2014)

Subretinal Gene Therapy of Mice With Bardet-Biedl Syndrome Type 1

著者: Seo, Seongjin, Mullins, Robert F., Dumitrescu, Alina V., Bhattarai, Sajag, Gratie, Daniel, Wang, Kai, Stone, Edwin M., Sheffield, Val, Drack, Arlene V.
出版事項 2013

BBS mutations modify phenotypic expression of CEP290-related ciliopathies

著者: Zhang, Yan, Seo, Seongjin, Bhattarai, Sajag, Bugge, Kevin, Searby, Charles C., Zhang, Qihong, Drack, Arlene V., Stone, Edwin M., Sheffield, Val C.
出版事項 2014

Nanophthalmos patient with a THR518MET mutation in MYRF, a case report

著者: Hagedorn, Joshua, Avdic, Armin, Schnieders, Michael J., Roos, Benjamin R., Kwon, Young H., Drack, Arlene V., Boese, Erin A., Fingert, John H.
出版年 BMC Ophthalmol (2020)

Efficacy of phosphodiesterase‐4 inhibitors in juvenile Batten disease (CLN3)

著者: Aldrich, Amy, Bosch, Megan E., Fallet, Rachel, Odvody, Jessica, Burkovetskaya, Maria, Rama Rao, Kakulavarapu V., Cooper, Jonathan D., Drack, Arlene V., Kielian, Tammy
出版年 Ann Neurol (2016)

Assessing Ganglion Cell Layer Topography in Human Albinism Using Optical Coherence Tomography

著者: Woertz, Erica N., Omoba, Bisola S., Dunn, Taylor M., Chiu, Stephanie J., Farsiu, Sina, Strul, Sasha, Summers, C. Gail, Drack, Arlene V., Carroll, Joseph
出版年 Invest Ophthalmol Vis Sci (2020)