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Gottlob

Showing results (291-300 of 322) with videos related to

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Neuron|August 14, 2012
Plasticity and stability of the visual system in human achiasmaMichael 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 DefectsJong 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 specializationHelen 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 StudySohaib R Rufai, Mervyn G Thomas, Oliver R Marmoy, et al.
Brain Communications|March 13, 2026
<i>CACNB3</i> defects are associated with infantile idiopathic nystagmusChristoph Jüschke, Kira Linsel, Marta Owczarek-Lipska, et al.
Eye (London, England)|January 2, 2022
Electrophysiological and fundoscopic detection of intracranial hypertension in craniosynostosisSohaib 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 nystagmusAnja K Mayer, Muhammad Mahajnah, Mervyn G Thomas, et al.
Scientific Reports|July 10, 2025
Identifying biomarkers for papilledema and pseudopapilledemaRishi 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 nystagmusMervyn G Thomas, Moira Crosier, Susan Lindsay, et al.
Nature Materials|March 21, 2017
Functional electronic inversion layers at ferroelectric domain wallsJ A Mundy, J Schaab, Y Kumagai, et al.
Pageof 33

Showing results (291-300 of 322) with videos related to

Sort By:
Pageof 33
Neuron|August 14, 2012
Plasticity and stability of the visual system in human achiasmaMichael 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 DefectsJong 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 specializationHelen 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 StudySohaib R Rufai, Mervyn G Thomas, Oliver R Marmoy, et al.
Brain Communications|March 13, 2026
<i>CACNB3</i> defects are associated with infantile idiopathic nystagmusChristoph Jüschke, Kira Linsel, Marta Owczarek-Lipska, et al.
Eye (London, England)|January 2, 2022
Electrophysiological and fundoscopic detection of intracranial hypertension in craniosynostosisSohaib 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 nystagmusAnja K Mayer, Muhammad Mahajnah, Mervyn G Thomas, et al.
Scientific Reports|July 10, 2025
Identifying biomarkers for papilledema and pseudopapilledemaRishi 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 nystagmusMervyn G Thomas, Moira Crosier, Susan Lindsay, et al.
Nature Materials|March 21, 2017
Functional electronic inversion layers at ferroelectric domain wallsJ A Mundy, J Schaab, Y Kumagai, et al.
Pageof 33