about
Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance.Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesisMutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus.The challenges of amblyopia treatmentCongenital fibrosis syndrome associated with central nervous system abnormalitiesCombined pharmacologic and surgical approach to acquired nystagmus due to multiple sclerosisReading in schizophrenic subjects and their nonsymptomatic first-degree relativesIs handheld optical coherence tomography reliable in infants and young children with and without nystagmus?The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmusHeterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1).Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3).The prevalence of nystagmus: the Leicestershire nystagmus survey.The pharmacological treatment of nystagmus: a review.High-Resolution Imaging of the Optic Nerve and Retina in Optic Nerve Hypoplasia.The Effects of Feedback on Adherence to Treatment: A Systematic Review and Meta-analysis of RCTs.Physiology and pathology of eye-head coordination.Gender- and Ethnicity-Related Differences in Optic Nerve Head Topography in Healthy Indian and Caucasian Participants.Autosomal-dominant nystagmus, foveal hypoplasia and presenile cataract associated with a novel PAX6 mutation.What we know about the generation of nystagmus and other ocular oscillations: are we closer to identifying therapeutic targets?Optical coherence tomography studies provides new insights into diagnosis and prognosis of infantile nystagmus: a review.OKN asymmetry in human subjects: a literature review.Risk factors and genetics in common comitant strabismus: a systematic review of the literature.Aetiology of infantile nystagmus.Nystagmus in childhood.The Role of FRMD7 in Idiopathic Infantile Nystagmus.Vision and multiple sclerosis.Pediatric Optical Coherence Tomography in Clinical Practice-Recent Progress.Normal macular structure measured with optical coherence tomography across ethnicity.Living with nystagmus: a qualitative study.Clinical and oculomotor characteristics of albinism compared to FRMD7 associated infantile nystagmus.Hand-held optical coherence tomography imaging in children with anterior segment dysgenesisPlasticity and stability of the visual system in human achiasma.Albinism: a model of adaptation of the brain in congenital visual disorders.Structural grading of foveal hypoplasia using spectral-domain optical coherence tomography a predictor of visual acuity?A comparative demographicand socioeconomic study of spasmus nutans and infantile nystagmus.Reading performance in infantile nystagmus.Acute adduction deficit in a 7-week-old infant.Comparison between grating acuity measured by visual tracking and preferential looking in infants.Age-related changes in head and eye coordination.The effect of colored overlays on reading performance in infantile nystagmus.
P50
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P50
name
Irene Gottlob
@en
Irene Gottlob
@nl
type
label
Irene Gottlob
@en
Irene Gottlob
@nl
prefLabel
Irene Gottlob
@en
Irene Gottlob
@nl