Found: 11
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Congenital nystagmus: randomized, controlled, double-masked trial of memantine/gabapentin.
- Published in:
- 2007
- By:
- Publication type:
- journal article
Congenital nystagmus: Randomized, controlled, double‐masked trial of memantine/gabapentin.
- Published in:
- Annals of Neurology, 2007, v. 61, n. 2, p. 130, doi. 10.1002/ana.21065
- By:
- Publication type:
- Article
Autosomal-dominant nystagmus, foveal hypoplasia and presenile cataract associated with a novel PAX6 mutation.
- Published in:
- European Journal of Human Genetics, 2014, v. 22, n. 3, p. 344, doi. 10.1038/ejhg.2013.162
- By:
- Publication type:
- Article
Neuropsychological outcomes of children with Optic Pathway Glioma.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-59896-2
- By:
- Publication type:
- Article
Syphilis presenting as acute multifocal retino-choroiditis.
- Published in:
- 2006
- By:
- Publication type:
- journal article
Syphilis presenting as acute multifocal retino-choroiditis.
- Published in:
- 2006
- By:
- Publication type:
- Case Study
Abnormal retinal development associated with FRMD7 mutations.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 15, p. 4086, doi. 10.1093/hmg/ddu122
- By:
- Publication type:
- Article
Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus.
- Published in:
- Nature Genetics, 2006, v. 38, n. 11, p. 1242, doi. 10.1038/ng1893
- By:
- Publication type:
- Article
The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmus.
- Published in:
- Brain: A Journal of Neurology, 2011, v. 134, n. 3, p. 892, doi. 10.1093/brain/awq373
- By:
- Publication type:
- Article
Phenotypical characteristics of idiopathic infantile nystagmus with and without mutations in FRMD7.
- Published in:
- Brain: A Journal of Neurology, 2008, v. 131, n. 5, p. 1259, doi. 10.1093/brain/awn046
- By:
- Publication type:
- Article
Corrigendum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus.
- Published in:
- 2011
- By:
- Publication type:
- Correction notice