Nystagmus

Current Opinion in Ophthalmology

Volumn 12, Issue 5, 2001, Pages 378-383

  Gottlob, I ^a  

^a UNIVERSITY OF WARWICK   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

4 METHYLPYRAZOLE; AMIODARONE; CARBAMAZEPINE; ETHYLENE GLYCOL; KETAMINE; LITHIUM CARBONATE; MORPHINE; PHENYTOIN;

ALBINISM; AUTOSOMAL RECESSIVE DISORDER; BLINDNESS; CATARACT EXTRACTION; COLOR BLINDNESS; CONTACT LENS; DISEASE CLASSIFICATION; DRUG INTOXICATION; DRUG MEGADOSE; EYE MOVEMENT; HUMAN; INHERITANCE; JOUBERT SYNDROME; NYSTAGMUS; PATHOPHYSIOLOGY; POSTOPERATIVE COMPLICATION; PRIORITY JOURNAL; RETINA DISEASE; REVIEW; SPECTACLES;

HUMANS; NYSTAGMUS, PATHOLOGIC;

EID: 0034796899     PISSN: 10408738     EISSN: None     Source Type: Journal    
DOI: 10.1097/00055735-200110000-00010     Document Type: Review

References (60)

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4. Modeling of congenital nystagmus waveforms produced by saccadic system abnormalities
5. A hypothetical explanation of congenital nystagmus
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7. Waveform characteristics of manifest latent nystagmus
8. Latent, manifest latent and congenital nystagmus
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11. Nystagmus mimicking spasmus nutans as the presenting sign of Biedl syndrome
12. Retinal disease masquerading as spasmus nutans
13. Quanitative eye and head movement recordings of retinal disease mimicking spasmus nutans
14. Results of cataract surgery in young children in east Africa
15. Examination and refractive management of patients with nystagmus
16. Reduction of congenital nystagmus amplitude with auditory biofeedback
17. Clinical rationale for manifest congenital nystagmus surgery
18. Modified Kestenbaum surgery for correction of abnormal head posture in infantile nystagmus: Outcome in 63 patients with graded augmentaton
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20. OFD II, OFDVI, and Joubert syndrome manifestations in 2 sibs
21. Homozygosity mapping in families with Joubert syndrome identifies a locus on chromosome 9q34.4 and evidence for genetic hetergenity
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26. Joubert's syndrome, ocular fibrosis, and normal histidine levels
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28. Coexistence of Gaucher disease type 1 and Joubert syndrome
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30. Ocular manifestations in Proteus syndrome
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33. An uncommon and often overlooked cause of failure to thrive: Diencephalic syndrome
34. Ophthalmic complications of childhood medulloblastoma
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48. Downbeat nystagmus associated with intravenous patient-controlled administration of morphine
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57. Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21
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60. The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein