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Neuron
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August 14, 2012
Plasticity and stability of the visual system in human achiasma
Michael B Hoffmann, Falko R Kaule, Netta Levin, et al.
American Journal of Human Genetics
|
May 17, 2016
Loss of MAFB Function in Humans and Mice Causes Duane Syndrome, Aberrant Extraocular Muscle Innervation, and Inner-Ear Defects
Jong G Park, Max A Tischfield, Alicia A Nugent, et al.
Human Molecular Genetics
|
August 4, 2020
SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization
Helen J Kuht, Jinu Han, Gail D E Maconachie, et al.
American Journal of Ophthalmology
|
August 29, 2024
Optic Nerve Head Morphological Variation in Craniosynostosis: A Cohort Study
Sohaib R Rufai, Mervyn G Thomas, Oliver R Marmoy, et al.
Brain Communications
|
March 13, 2026
<i>CACNB3</i> defects are associated with infantile idiopathic nystagmus
Christoph Jüschke, Kira Linsel, Marta Owczarek-Lipska, et al.
Eye (London, England)
|
January 2, 2022
Electrophysiological and fundoscopic detection of intracranial hypertension in craniosynostosis
Sohaib R Rufai, Oliver R Marmoy, Dorothy A Thompson, et al.
Brain : a Journal of Neurology
|
April 23, 2019
Homozygous stop mutation in AHR causes autosomal recessive foveal hypoplasia and infantile nystagmus
Anja K Mayer, Muhammad Mahajnah, Mervyn G Thomas, et al.
Scientific Reports
|
July 10, 2025
Identifying biomarkers for papilledema and pseudopapilledema
Rishi Sekhri, Helen J Kuht, Zhanhan Tu, et al.
Brain : a Journal of Neurology
|
February 10, 2011
The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmus
Mervyn G Thomas, Moira Crosier, Susan Lindsay, et al.
Nature Materials
|
March 21, 2017
Functional electronic inversion layers at ferroelectric domain walls
J A Mundy, J Schaab, Y Kumagai, et al.
Page
of 33
Search research articles
Search
Showing results (291-300 of 322) with videos related to
Sort By:
Page
of 33
Neuron
|
August 14, 2012
Plasticity and stability of the visual system in human achiasma
Michael B Hoffmann, Falko R Kaule, Netta Levin, et al.
American Journal of Human Genetics
|
May 17, 2016
Loss of MAFB Function in Humans and Mice Causes Duane Syndrome, Aberrant Extraocular Muscle Innervation, and Inner-Ear Defects
Jong G Park, Max A Tischfield, Alicia A Nugent, et al.
Human Molecular Genetics
|
August 4, 2020
SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization
Helen J Kuht, Jinu Han, Gail D E Maconachie, et al.
American Journal of Ophthalmology
|
August 29, 2024
Optic Nerve Head Morphological Variation in Craniosynostosis: A Cohort Study
Sohaib R Rufai, Mervyn G Thomas, Oliver R Marmoy, et al.
Brain Communications
|
March 13, 2026
<i>CACNB3</i> defects are associated with infantile idiopathic nystagmus
Christoph Jüschke, Kira Linsel, Marta Owczarek-Lipska, et al.
Eye (London, England)
|
January 2, 2022
Electrophysiological and fundoscopic detection of intracranial hypertension in craniosynostosis
Sohaib R Rufai, Oliver R Marmoy, Dorothy A Thompson, et al.
Brain : a Journal of Neurology
|
April 23, 2019
Homozygous stop mutation in AHR causes autosomal recessive foveal hypoplasia and infantile nystagmus
Anja K Mayer, Muhammad Mahajnah, Mervyn G Thomas, et al.
Scientific Reports
|
July 10, 2025
Identifying biomarkers for papilledema and pseudopapilledema
Rishi Sekhri, Helen J Kuht, Zhanhan Tu, et al.
Brain : a Journal of Neurology
|
February 10, 2011
The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmus
Mervyn G Thomas, Moira Crosier, Susan Lindsay, et al.
Nature Materials
|
March 21, 2017
Functional electronic inversion layers at ferroelectric domain walls
J A Mundy, J Schaab, Y Kumagai, et al.
Page
of 33