Detalhe da pesquisa
1.
Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance.
Cell
; 140(1): 74-87, 2010 Jan 08.
Artigo
Inglês
| MEDLINE | ID: mdl-20074521
2.
Advancing health equity in pediatric eye care: the role of school-based vision programs, research, advocacy, community engagement, and medical education.
J AAPOS
; 27(2): 70-74, 2023 04.
Artigo
Inglês
| MEDLINE | ID: mdl-36898658
3.
Depression, Anxiety, and Stress in Parents of Patients With Retinoblastoma.
Am J Ophthalmol
; 207: 130-143, 2019 11.
Artigo
Inglês
| MEDLINE | ID: mdl-31163135
4.
Vision Screening Requirements for School-age Children during the COVID-19 Pandemic.
Ophthalmic Epidemiol
; 29(6): 707-709, 2022 12.
Artigo
Inglês
| MEDLINE | ID: mdl-34965190
5.
CFEOM1, the classic familial form of congenital fibrosis of the extraocular muscles, is genetically heterogeneous but does not result from mutations in ARIX.
BMC Genet
; 3: 3, 2002.
Artigo
Inglês
| MEDLINE | ID: mdl-11882252
6.
Strabismus in cerebral palsy: when and why to operate.
Am Orthopt J
; 64: 17-20, 2014.
Artigo
Inglês
| MEDLINE | ID: mdl-25313106
7.
Ocular manifestations of autism in ophthalmology.
Strabismus
; 21(2): 98-102, 2013 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-23713930
8.
Retinoblastoma: the Zimmerman family story.
JAMA Ophthalmol
; 132(5): 519-20, 2014 May.
Artigo
Inglês
| MEDLINE | ID: mdl-24626469
9.
Repeat probing for treatment of persistent nasolacrimal duct obstruction.
J AAPOS
; 13(3): 306-7, 2009 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-19541274