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Elizabeth C Engle

Showing results (31-40 of 125) with videos related to

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Investigative Ophthalmology & Visual Science|April 16, 2010
Evidence of an asymmetrical endophenotype in congenital fibrosis of extraocular muscles type 3 resulting from TUBB3 mutationsJoseph L Demer, Robert A Clark, Max A Tischfield, et al.
Investigative Ophthalmology & Visual Science|January 2, 2007
Magnetic resonance imaging evidence for widespread orbital dysinnervation in dominant Duane's retraction syndrome linked to the DURS2 locusJoseph L Demer, Robert A Clark, Key-Hwan Lim, et al.
Journal of Visualized Experiments : Jove|August 6, 2019
Ex Vivo Oculomotor Slice Culture from Embryonic GFP-Expressing Mice for Time-Lapse Imaging of Oculomotor Nerve OutgrowthMary C Whitman, Jessica L Bell, Elaine H Nguyen, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|June 23, 2009
Clinical features associated with an I126M alpha2-chimaerin mutation in a family with autosomal-dominant Duane retraction syndromeClaudia E Murillo-Correa, Veronica Kon-Jara, Elizabeth C Engle, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 11, 2011
Two novel CHN1 mutations in 2 families with Duane retraction syndromeWai-Man Chan, Noriko Miyake, Lily Zhu-Tam, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|May 6, 2008
Magnetic resonance imaging of the endophenotype of a novel familial Möbius-like syndromeSean Dumars, Caroline Andrews, Wai-Man Chan, et al.
Gene Expression Patterns : GEP|April 3, 2012
Spatiotemporal expression pattern of KIF21A during normal embryonic development and in congenital fibrosis of the extraocular muscles type 1 (CFEOM1)Jigar Desai, Marie Pia Rogines Velo, Koki Yamada, et al.
Journal of Visualized Experiments : Jove|December 3, 2019
Isolation and Culture of Oculomotor, Trochlear, and Spinal Motor Neurons from Prenatal Islmn:GFP Transgenic MiceRyosuke Fujiki, Joun Y Lee, Julie A Jurgens, et al.
American Journal of Medical Genetics. Part A|March 11, 2006
HOXA1 mutations are not a common cause of Duane anomalyMax A Tischfield, Wai-Man Chan, Jann-Frederik Grunert, et al.
American Journal of Medical Genetics. Part A|December 25, 2009
CHN1 mutations are not a common cause of sporadic Duane's retraction syndromeNoriko Miyake, Caroline Andrews, Wen Fan, et al.
Pageof 13

Showing results (31-40 of 125) with videos related to

Sort By:
Pageof 13
Investigative Ophthalmology & Visual Science|April 16, 2010
Evidence of an asymmetrical endophenotype in congenital fibrosis of extraocular muscles type 3 resulting from TUBB3 mutationsJoseph L Demer, Robert A Clark, Max A Tischfield, et al.
Investigative Ophthalmology & Visual Science|January 2, 2007
Magnetic resonance imaging evidence for widespread orbital dysinnervation in dominant Duane's retraction syndrome linked to the DURS2 locusJoseph L Demer, Robert A Clark, Key-Hwan Lim, et al.
Journal of Visualized Experiments : Jove|August 6, 2019
Ex Vivo Oculomotor Slice Culture from Embryonic GFP-Expressing Mice for Time-Lapse Imaging of Oculomotor Nerve OutgrowthMary C Whitman, Jessica L Bell, Elaine H Nguyen, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|June 23, 2009
Clinical features associated with an I126M alpha2-chimaerin mutation in a family with autosomal-dominant Duane retraction syndromeClaudia E Murillo-Correa, Veronica Kon-Jara, Elizabeth C Engle, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 11, 2011
Two novel CHN1 mutations in 2 families with Duane retraction syndromeWai-Man Chan, Noriko Miyake, Lily Zhu-Tam, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|May 6, 2008
Magnetic resonance imaging of the endophenotype of a novel familial Möbius-like syndromeSean Dumars, Caroline Andrews, Wai-Man Chan, et al.
Gene Expression Patterns : GEP|April 3, 2012
Spatiotemporal expression pattern of KIF21A during normal embryonic development and in congenital fibrosis of the extraocular muscles type 1 (CFEOM1)Jigar Desai, Marie Pia Rogines Velo, Koki Yamada, et al.
Journal of Visualized Experiments : Jove|December 3, 2019
Isolation and Culture of Oculomotor, Trochlear, and Spinal Motor Neurons from Prenatal Islmn:GFP Transgenic MiceRyosuke Fujiki, Joun Y Lee, Julie A Jurgens, et al.
American Journal of Medical Genetics. Part A|March 11, 2006
HOXA1 mutations are not a common cause of Duane anomalyMax A Tischfield, Wai-Man Chan, Jann-Frederik Grunert, et al.
American Journal of Medical Genetics. Part A|December 25, 2009
CHN1 mutations are not a common cause of sporadic Duane's retraction syndromeNoriko Miyake, Caroline Andrews, Wen Fan, et al.
Pageof 13