Detalhe da pesquisa
1.
Prism adaptation test before strabismus surgery in patients with decompensated esophoria and decompensated microesotropia.
Int Ophthalmol
; 42(7): 2195-2204, 2022 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-35038124
2.
Biallelic mutations in L-dopachrome tautomerase (DCT) cause infantile nystagmus and oculocutaneous albinism.
Hum Genet
; 140(8): 1157-1168, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-33959807
3.
Tendon elongation with bovine pericardium in strabismus surgery-indications beyond Graves' orbitopathy.
Graefes Arch Clin Exp Ophthalmol
; 259(1): 145-155, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-32949299
4.
Differential Diagnosis of Acquired Esotropia in the Elderly. / Differenzialdiagnose der erworbenen Esotropie im Alter.
Klin Monbl Augenheilkd
; 237(9): 1107-1116, 2020 Sep.
Artigo
em Inglês, Alemão
| MEDLINE | ID: mdl-32818999
5.
A TUBB6 mutation is associated with autosomal dominant non-progressive congenital facial palsy, bilateral ptosis and velopharyngeal dysfunction.
Hum Mol Genet
; 26(20): 4055-4066, 2017 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29016863
6.
[Efficacy of Vertical Muscle Transpositions with and without Simultaneous Rectus Muscle Recession for Unilateral Sixth Nerve Palsy]. / Effekt von Muskeltranspositionen nach dem Hummelsheim-Prinzip mit und ohne zeitgleiche Rücklagerung des M. rectus internus.
Klin Monbl Augenheilkd
; 235(10): 1096-1104, 2018 Oct.
Artigo
em Alemão
| MEDLINE | ID: mdl-29156469
7.
Mutation of POC1B in a severe syndromic retinal ciliopathy.
Hum Mutat
; 35(10): 1153-62, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25044745
8.
Kestenbaum procedure with combined muscle resection and tucking for nystagmus-related head turn.
Graefes Arch Clin Exp Ophthalmol
; 251(12): 2803-9, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23835757
9.
Visual complaints in pregnancy: (pre)eclampsia as a chameleon.
GMS Ophthalmol Cases
; 12: Doc21, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36569356
10.
Horizontal gaze palsy with progressive scoliosis: three novel ROBO3 mutations and descriptions of the phenotypes of four patients.
Mol Vis
; 17: 1978-86, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21850172
11.
Analysis of the CHN1 gene in patients with various types of congenital ocular motility disorders.
Graefes Arch Clin Exp Ophthalmol
; 248(9): 1351-7, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20535495
12.
Ophthalmological manifestations of Parry-Romberg syndrome.
Surv Ophthalmol
; 61(6): 693-701, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27045226
13.
Macular translocation with 360 degrees retinotomy for exudative age-related macular degeneration.
Arch Ophthalmol
; 120(4): 451-9, 2002 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-11934318
14.
Ocular neuromyotonia: a case report.
Strabismus
; 10(2): 119-24, 2002 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-12221490
15.
Sinuorbital complications after intranasal cocaine abuse.
Strabismus
; 12(4): 205-9, 2004 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-15545138
16.
SDOCT thickness measurements of various retinal layers in patients with autosomal dominant optic atrophy due to OPA1 mutations.
Biomed Res Int
; 2013: 121398, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24024178
17.
A novel large in-frame deletion within the CACNA1F gene associates with a cone-rod dystrophy 3-like phenotype.
PLoS One
; 8(10): e76414, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24124559
18.
A cost-effectiveness model of screening strategies for amblyopia and risk factors and its application in a german setting.
Optom Vis Sci
; 80(3): 259-69, 2003 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-12637838