Silva E - Search Results

1

Possible rare congenital dysinnervation disorder: congenital ptosis associated with adduction.

Mendes S, Beselga D, Campos S, Neves A, Campos J, Carvalho S, Silva E, Castro Sousa JP. Mendes S, et al. Among authors: silva e. Strabismus. 2015;23(1):33-5. doi: 10.3109/09273972.2014.999797. Epub 2015 Jan 12. Strabismus. 2015. PMID: 25581513

2

Quantitative phenotyping of chromatic dysfunction in best macular dystrophy.

Campos SH, Forjaz V, Kozak LR, Silva E, Castelo-Branco M. Campos SH, et al. Among authors: silva e. Arch Ophthalmol. 2005 Jul;123(7):944-9. doi: 10.1001/archopht.123.7.944. Arch Ophthalmol. 2005. PMID: 16009836

3

Novel de novo FOXC1 nonsense mutation in an Axenfeld-Rieger syndrome patient.

Carmona S, da Luz Freitas M, Froufe H, Simões MJ, Sampaio MJ, Silva ED, Egas C. Carmona S, et al. Am J Med Genet A. 2017 Jun;173(6):1607-1610. doi: 10.1002/ajmg.a.38234. Epub 2017 Apr 21. Am J Med Genet A. 2017. PMID: 28432732 No abstract available.

4

Cross-cultural validation of a taste test with paper strips.

Ribeiro JC, Chaves M, Chaves C, Lemos L, Silva ED, Paiva A, Hummel T. Ribeiro JC, et al. Eur Arch Otorhinolaryngol. 2016 Oct;273(10):3407-11. doi: 10.1007/s00405-016-4037-y. Epub 2016 Apr 12. Eur Arch Otorhinolaryngol. 2016. PMID: 27071772

5

Cultural Adaptation of the Portuguese Version of the "Sniffin' Sticks" Smell Test: Reliability, Validity, and Normative Data.

Ribeiro JC, Simões J, Silva F, Silva ED, Hummel C, Hummel T, Paiva A. Ribeiro JC, et al. PLoS One. 2016 Feb 10;11(2):e0148937. doi: 10.1371/journal.pone.0148937. eCollection 2016. PLoS One. 2016. PMID: 26863023 Free PMC article.

6

SVEP1 as a Genetic Modifier of TEK-Related Primary Congenital Glaucoma.

Young TL, Whisenhunt KN, Jin J, LaMartina SM, Martin SM, Souma T, Limviphuvadh V, Suri F, Souzeau E, Zhang X, Dan Y, Anagnos E, Carmona S, Jody NM, Stangel N, Higuchi EC, Huang SJ, Siggs OM, Simões MJ, Lawson BM, Martin JS, Elahi E, Narooie-Nejad M, Motlagh BF, Quaggin SE, Potter HD, Silva ED, Craig JE, Egas C, Maroofian R, Maurer-Stroh S, Bradfield YS, Tompson SW. Young TL, et al. Among authors: silva ed. Invest Ophthalmol Vis Sci. 2020 Oct 1;61(12):6. doi: 10.1167/iovs.61.12.6. Invest Ophthalmol Vis Sci. 2020. PMID: 33027505 Free PMC article.

7

Accelerated age-related olfactory decline among type 1 Usher patients.

Ribeiro JC, Oliveiros B, Pereira P, António N, Hummel T, Paiva A, Silva ED. Ribeiro JC, et al. Sci Rep. 2016 Jun 22;6:28309. doi: 10.1038/srep28309. Sci Rep. 2016. PMID: 27329700 Free PMC article. Clinical Trial.

8

Genetically induced impairment of retinal ganglion cells at the axonal level is linked to extrastriate cortical plasticity.

Mateus C, d'Almeida OC, Reis A, Silva E, Castelo-Branco M. Mateus C, et al. Among authors: silva e. Brain Struct Funct. 2016 Apr;221(3):1767-80. doi: 10.1007/s00429-015-1002-2. Epub 2015 Feb 14. Brain Struct Funct. 2016. PMID: 25680704

9

Risk of multiple sclerosis after optic neuritis in patients with normal baseline brain MRI.

Marques IB, Matias F, Silva ED, Cunha L, Sousa L. Marques IB, et al. J Clin Neurosci. 2014 Apr;21(4):583-6. doi: 10.1016/j.jocn.2013.06.013. Epub 2013 Aug 23. J Clin Neurosci. 2014. PMID: 24231563 Free article.

10

Decreased activity of piriform cortex and orbitofrontal hyperactivation in Usher Syndrome, a human disorder of ciliary dysfunction.

Ferreira S, Duarte IC, Paula A, Pereira AC, Ribeiro JC, Quental H, Reis A, Silva ED, Castelo-Branco M. Ferreira S, et al. Brain Imaging Behav. 2022 Jun;16(3):1176-1185. doi: 10.1007/s11682-021-00594-6. Epub 2021 Nov 30. Brain Imaging Behav. 2022. PMID: 34850367 Free PMC article.

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