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Elizabeth C Engle

Showing results (51-60 of 125) with videos related to

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Ophthalmic Genetics|September 27, 2002
Familial unilateral Brown syndromeAlessandro Iannaccone, Nathalie McIntosh, Maria Laura Ciccarelli, et al.
Brain : a Journal of Neurology|July 4, 2006
Neurological features of congenital fibrosis of the extraocular muscles type 2 with mutations in PHOX2AThomas M Bosley, Darren T Oystreck, Richard L Robertson, et al.
The Journal of Clinical Endocrinology and Metabolism|January 7, 2015
Expanding the phenotypic spectrum and variability of endocrine abnormalities associated with TUBB3 E410K syndromeRavikumar Balasubramanian, Sheena Chew, Sarah E MacKinnon, et al.
Ophthalmology|May 20, 2026
Prevalence of Strabismus and Decreased Stereopsis in Parents of Children with StrabismusSarah MacKinnon, Rachael Zacks, Brenda Barry, et al.
JAMA Ophthalmology|February 15, 2024
Presence of Copy Number Variants Associated With Esotropia in Patients With ExotropiaMayra Martinez Sanchez, Wai-Man Chan, Sarah E MacKinnon, et al.
Human Genetics|June 20, 2002
Congenital fibrosis of the vertically acting extraocular muscles maps to the FEOM3 locusDavid A Mackey, Wai-Man Chan, Christopher Chan, et al.
Investigative Ophthalmology & Visual Science|July 1, 2011
Expansion of the CHN1 strabismus phenotypeNoriko Miyake, Joseph L Demer, Sherin Shaaban, et al.
JAMA Ophthalmology|October 5, 2013
RYR1 mutations as a cause of ophthalmoplegia, facial weakness, and malignant hyperthermiaSherin Shaaban, Leigh Ramos-Platt, Floyd H Gilles, et al.
Ophthalmology|May 3, 2011
Structural grading of foveal hypoplasia using spectral-domain optical coherence tomography a predictor of visual acuity?Mervyn G Thomas, Anil Kumar, Sarim Mohammad, et al.
European Journal of Human Genetics : EJHG|August 15, 2013
Autosomal-dominant nystagmus, foveal hypoplasia and presenile cataract associated with a novel PAX6 mutationShery Thomas, Mervyn G Thomas, Caroline Andrews, et al.
Pageof 13

Showing results (51-60 of 125) with videos related to

Sort By:
Pageof 13
Ophthalmic Genetics|September 27, 2002
Familial unilateral Brown syndromeAlessandro Iannaccone, Nathalie McIntosh, Maria Laura Ciccarelli, et al.
Brain : a Journal of Neurology|July 4, 2006
Neurological features of congenital fibrosis of the extraocular muscles type 2 with mutations in PHOX2AThomas M Bosley, Darren T Oystreck, Richard L Robertson, et al.
The Journal of Clinical Endocrinology and Metabolism|January 7, 2015
Expanding the phenotypic spectrum and variability of endocrine abnormalities associated with TUBB3 E410K syndromeRavikumar Balasubramanian, Sheena Chew, Sarah E MacKinnon, et al.
Ophthalmology|May 20, 2026
Prevalence of Strabismus and Decreased Stereopsis in Parents of Children with StrabismusSarah MacKinnon, Rachael Zacks, Brenda Barry, et al.
JAMA Ophthalmology|February 15, 2024
Presence of Copy Number Variants Associated With Esotropia in Patients With ExotropiaMayra Martinez Sanchez, Wai-Man Chan, Sarah E MacKinnon, et al.
Human Genetics|June 20, 2002
Congenital fibrosis of the vertically acting extraocular muscles maps to the FEOM3 locusDavid A Mackey, Wai-Man Chan, Christopher Chan, et al.
Investigative Ophthalmology & Visual Science|July 1, 2011
Expansion of the CHN1 strabismus phenotypeNoriko Miyake, Joseph L Demer, Sherin Shaaban, et al.
JAMA Ophthalmology|October 5, 2013
RYR1 mutations as a cause of ophthalmoplegia, facial weakness, and malignant hyperthermiaSherin Shaaban, Leigh Ramos-Platt, Floyd H Gilles, et al.
Ophthalmology|May 3, 2011
Structural grading of foveal hypoplasia using spectral-domain optical coherence tomography a predictor of visual acuity?Mervyn G Thomas, Anil Kumar, Sarim Mohammad, et al.
European Journal of Human Genetics : EJHG|August 15, 2013
Autosomal-dominant nystagmus, foveal hypoplasia and presenile cataract associated with a novel PAX6 mutationShery Thomas, Mervyn G Thomas, Caroline Andrews, et al.
Pageof 13