| review article | Q7318358 |
| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1046847468 |
| P356 | DOI | 10.1038/SJ.EYE.6702851 |
| P8608 | Fatcat ID | release_s75miui6kjdifjybgvhp5er2wq |
| P698 | PubMed publication ID | 17914430 |
| P5875 | ResearchGate publication ID | 5931428 |
| P2093 | author name string | Taylor D | |
| P2860 | cites work | Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse | Q24323305 |
| Coloboma, congenital heart disease, and choanal atresia with multiple anomalies: CHARGE association | Q28262038 | ||
| A history of the optic nerve and its diseases. | Q30344193 | ||
| The achiasmia spectrum: congenitally reduced chiasmal decussation | Q30478817 | ||
| Reversible carotid artery narrowing in morning glory disc anomaly | Q33222961 | ||
| Localising patterns of optic nerve hypoplasia--retina to occipital lobe | Q33646173 | ||
| The eye in the CHARGE association | Q33648152 | ||
| Spectrum of optic nerve hypoplasia | Q33650521 | ||
| The tilted disc | Q33650527 | ||
| Coloboma of optic nerve with overlay of peripapillary retina | Q33650724 | ||
| The clinical and morphologic spectrum of optic nerve hypoplasia | Q33728741 | ||
| Homonymous hemioptic hypoplasia. Fundoscopic features in standard and red-free illumination in three patients with congenital hemiplegia | Q33972897 | ||
| Optic disc duplication or coloboma? | Q35592820 | ||
| Infantile infection and diabetes insipidus in children with optic nerve hypoplasia | Q35593728 | ||
| Duplication of the optic disc: true or pseudo? A coloboma or not a coloboma? | Q35767852 | ||
| Non-decussating retinal-fugal fibre syndrome. An inborn achiasmatic malformation associated with visuotopic misrouting, visual evoked potential ipsilateral asymmetry and nystagmus | Q71579983 | ||
| Retinal Arteriovenous Communications in the Morning Glory Disc Anomaly | Q72007704 | ||
| Atypical retinochoroidal coloboma in patients with dysplastic optic discs and transsphenoidal encephalocele | Q72231707 | ||
| Morning Glory syndrome. MR imaging | Q73042951 | ||
| Visual function and brain organization in non-decussating retinal-fugal fibre syndrome | Q73365186 | ||
| Periventricular leukomalacia: an intracranial cause of pseudoglaucomatous cupping | Q73735519 | ||
| Optic disc shape, corneal astigmatism, and amblyopia | Q73886729 | ||
| Capillary haemangiomas in association with morning glory disc anomaly | Q77591627 | ||
| Colobomatous microphthalmia and orbital neuroglial cyst: case report | Q77811419 | ||
| Early diagnosis of the papillorenal syndrome by optic disc morphology | Q81181921 | ||
| Anterior coloboma with macrophthalmos and cyst: MR findings | Q81453238 | ||
| Intraocular surgery for optic nerve disorders | Q35944004 | ||
| Ocular and systemic manifestations of PHACES (Posterior fossa malformations, Hemangiomas, Arterial anomalies, Cardiac defects and coarctation of the Aorta, Eye abnormalities, and Sternal abnormalities or ventral developmental defects) syndrome | Q36101723 | ||
| Multicystic dysplastic kidney and variable phenotype in a family with a novel deletion mutation of PAX2. | Q36210080 | ||
| Do we really understand the difference between optic nerve hypoplasia and atrophy? | Q36293110 | ||
| Septo-optic dysplasia complex: a heterogeneous malformation syndrome. | Q36352647 | ||
| Risk factors for amblyopia in children with capillary hemangiomas of the eyelids and orbit | Q36524684 | ||
| Visual impairment in Swedish children. I. Register and prevalence data | Q36867455 | ||
| Superior segmental optic hypoplasia. A sign of maternal diabetes | Q39004295 | ||
| Large cups in normal-sized optic discs: a variant of optic nerve hypoplasia in children with periventricular leukomalacia | Q39454671 | ||
| Optic nerve morphology may reveal adverse events during prenatal and perinatal life--digital image analysis | Q39521609 | ||
| Population prevalence of tilted optic disks and the relationship of this sign to refractive error | Q39601548 | ||
| The morning glory disc anomaly: contractile movement, classification, and embryogenesis | Q39685241 | ||
| UNUSUAL COLOBOMA OF THE OPTIC NERVE ENTRANCE. | Q39840952 | ||
| Sudden death in septo-optic dysplasia. Report of 5 cases | Q40659517 | ||
| Visual impairment in Swedish children. III. Diagnoses | Q41732238 | ||
| See-saw nystagmus and congenital nystagmus identified in the non-decussating retinal-fugal fiber syndrome | Q43796940 | ||
| Contractile optic disc coloboma | Q44508996 | ||
| Retinal detachment caused by a slitlike break within the excavated disc in morning glory syndrome | Q45010619 | ||
| Joubert syndrome: long-term follow-up | Q45097334 | ||
| Thunderstorm asthma due to grass pollen | Q45250721 | ||
| The value of visual evoked potentials in the evaluation of periorbital hemangiomas. | Q46640237 | ||
| Peripapillary staphyloma: clinical features and visual outcome in 19 cases | Q46748081 | ||
| Optic nerve size evaluated by magnetic resonance imaging in children with optic nerve hypoplasia, multiple pituitary hormone deficiency, isolated growth hormone deficiency, and idiopathic short stature | Q47404234 | ||
| Severe visual impairment and blindness in children in the UK. | Q47415547 | ||
| Normal maturation of the neonatal and infant brain: MR imaging at 1.5 T. | Q48134897 | ||
| A unique achiasmatic anomaly detected in non-albinos with misrouted retinal-fugal projections | Q48167193 | ||
| Ocular malformations, moyamoya disease, and midline cranial defects: a distinct syndrome | Q48256603 | ||
| Optic nerve hypoplasia. Clinical significance of associated central nervous system abnormalities on magnetic resonance imaging | Q48362143 | ||
| Pediatric homonymous hemianopia. | Q48482395 | ||
| Bilateral aplasia of the optic nerves, chiasm, and tracts in an otherwise healthy infant | Q48558382 | ||
| Optic nerve axons: life and death before birth | Q48564085 | ||
| Aplasia of the optic chiasm and tracts with unifocal polymicrogyria in an otherwise healthy infant. | Q48586976 | ||
| Visual impairment in Swedish children. II. Etiological factors. | Q50949940 | ||
| Morning glory syndrome and basal encephalocele. | Q51637588 | ||
| Acuity, ophthalmoscopy, and visually evoked potentials in the prediction of visual outcome in infants with bilateral optic nerve hypoplasia | Q52017098 | ||
| Visual-evoked potential evidence of chiasmal hypoplasia. | Q52172457 | ||
| Clinical feature analysis of congenital optic nerve abnormalities. | Q53595379 | ||
| Optic nerve hypoplasia: Risk factors and epidemiology. | Q54183813 | ||
| Papillorenal ("renal coloboma") syndrome. | Q54372333 | ||
| Morning Glory Syndrome: Unusual Congenital Optic Disk Anomaly | Q56759823 | ||
| Geographical Distribution of Optic Nerve Hypoplasia and Septo-optic Dysplasia in Northwest England | Q62750190 | ||
| Blindness Due to Optic-nerve Atrophy and Hypoplasia in Children: an Epidemiological Study (1944-1974) | Q67012532 | ||
| Congenital optic tract syndrome | Q67938478 | ||
| Hereditary microphthalmia with colobomatous cyst | Q68190306 | ||
| Functional amblyopia associated with abnormalities of the optic nerve | Q71347719 | ||
| P433 | issue | 10 | |
| P304 | page(s) | 1271-1284 | |
| P577 | publication date | 2007-10-01 | |
| P1433 | published in | Eye | Q10278937 |
| P1476 | title | Developmental abnormalities of the optic nerve and chiasm | |
| P478 | volume | 21 |
| Q41060821 | A Rare Case of Symptomatic Double Optic Disc Pit without Maculopathy. |
| Q64945781 | Abnormalities of the Optic Nerve in Down Syndrome and Associations With Visual Acuity. |
| Q37778487 | Eye Development |
| Q35897704 | High-Resolution Imaging of the Optic Nerve and Retina in Optic Nerve Hypoplasia |
| Q33873832 | Incidental finding of bilateral altitudinal visual field defects |
| Q43294414 | Light-adapted electroretinograms in optic nerve hypoplasia. |
| Q35166672 | Nonsyndromic bilateral and unilateral optic nerve aplasia: first familial occurrence and potential implication of CYP26A1 and CYP26C1 genes. |
| Q47198074 | Optic Nerve Measurement on MRI in the Pediatric Population: Normative Values and Correlations. |
| Q98771723 | RINT1 Loss Impairs Retinogenesis Through TRP53-Mediated Apoptosis |
| Q42359930 | Retinal complications associated with congenital optic disc anomalies determined by swept source optical coherence tomography. |
| Q39018594 | VEP analysis methods in children with optic nerve hypoplasia: relationship to visual acuity and optic disc diameter |
| Q48650661 | VEP characteristics in children with achiasmia, in comparison to albino and healthy children |
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