Works matching IS 00124486 AND DT 2018 AND VI 137 AND IP 1
Results: 8
Riggs-type dominant congenital stationary night blindness: ERG findings, a new GNAT1 mutation and a systemic association.
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- Documenta Ophthalmologica, 2018, v. 137, n. 1, p. 57, doi. 10.1007/s10633-018-9651-0
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- Publication type:
- Article
Clinical display of mfERG data.
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- Documenta Ophthalmologica, 2018, v. 137, n. 1, p. 63, doi. 10.1007/s10633-018-9650-1
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- Publication type:
- Article
Clinical and genetic findings of a Japanese patient with RP1-related autosomal recessive retinitis pigmentosa.
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- Documenta Ophthalmologica, 2018, v. 137, n. 1, p. 47, doi. 10.1007/s10633-018-9649-7
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- Article
The clinical value of the multi-channel PVEP and PERG in the diagnosis and management of the patient with pituitary adenoma: a case report.
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- 2018
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- Publication type:
- Case Study
Macular staphyloma in patients affected by Joubert syndrome with retinal dystrophy: a new finding detected by SD-OCT.
- Published in:
- Documenta Ophthalmologica, 2018, v. 137, n. 1, p. 25, doi. 10.1007/s10633-018-9646-x
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- Publication type:
- Article
Dark-adapted red flash ERGs in healthy adults.
- Published in:
- Documenta Ophthalmologica, 2018, v. 137, n. 1, p. 1, doi. 10.1007/s10633-018-9642-1
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- Publication type:
- Article
Deferoxamine-induced electronegative ERG responses.
- Published in:
- 2018
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- Publication type:
- Case Study
Congenital grouped albinotic spots of the retinal pigment epithelium in a patient with hemihypertrophy and café au lait spots.
- Published in:
- Documenta Ophthalmologica, 2018, v. 137, n. 1, p. 9, doi. 10.1007/s10633-018-9639-9
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- Publication type:
- Article