Works matching IS 00124486 AND DT 2023 AND VI 146 AND IP 3
Results: 8
Retinitis pigmentosa and nanophthalmos in a patient with attenuated Hunter's syndrome.
- Published in:
- 2023
- By:
- Publication type:
- Case Study
Electroretinographic abnormalities in Alport syndrome with a novel COL4A5 truncated variant (p.Try20GlyfsTer19).
- Published in:
- Documenta Ophthalmologica, 2023, v. 146, n. 3, p. 281, doi. 10.1007/s10633-023-09935-w
- By:
- Publication type:
- Article
ISCEV guidelines for calibration and verification of stimuli and recording instruments (2023 update).
- Published in:
- Documenta Ophthalmologica, 2023, v. 146, n. 3, p. 199, doi. 10.1007/s10633-023-09932-z
- By:
- Publication type:
- Article
Early recognition of CLN3 disease facilitated by visual electrophysiology and multimodal imaging.
- Published in:
- Documenta Ophthalmologica, 2023, v. 146, n. 3, p. 241, doi. 10.1007/s10633-023-09930-1
- By:
- Publication type:
- Article
Rod photoreceptor activation and deactivation in early-stage diabetic eye disease.
- Published in:
- Documenta Ophthalmologica, 2023, v. 146, n. 3, p. 229, doi. 10.1007/s10633-023-09925-y
- By:
- Publication type:
- Article
Frequency-domain analysis of transient visual evoked potentials in schizophrenia.
- Published in:
- Documenta Ophthalmologica, 2023, v. 146, n. 3, p. 211, doi. 10.1007/s10633-023-09921-2
- By:
- Publication type:
- Article
Evaluation of correlation between Diopsys® NOVA™ fixed-luminance flicker ERG and Diagnosys® Espion 2™ flicker ERG parameters.
- Published in:
- Documenta Ophthalmologica, 2023, v. 146, n. 3, p. 257, doi. 10.1007/s10633-023-09934-x
- By:
- Publication type:
- Article
Phenotypic variability in PRPH2 as demonstrated by a family with incomplete penetrance of autosomal dominant cone-rod dystrophy.
- Published in:
- Documenta Ophthalmologica, 2023, v. 146, n. 3, p. 267, doi. 10.1007/s10633-022-09916-5
- By:
- Publication type:
- Article