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Items: 1 to 20 of 203

1.

Congenital tritanopia without neuroretinal disease.

Smith DP, Cole BL, Isaacs A.

Invest Ophthalmol. 1973 Aug;12(8):608-17. No abstract available.

PMID:
4542649
2.

Further studies supporting the identity of congenital tritanopia and hereditary dominant optic atrophy.

Krill AE, Smith VC, Pokorny J.

Invest Ophthalmol. 1971 Jun;10(6):457-65. No abstract available.

PMID:
5314165
3.

Colour vision, ophthalmological and linkage studies in a pedigree with a tritan defect.

Went LN, Völker-Dieben H, de Vries-de Mol EC.

Mod Probl Ophthalmol. 1974;13(0):272-6. No abstract available.

PMID:
4548144
4.

Comparative colour vision and other ophthalmological studies in three families with dominant inherited juvenile optic atrophy.

Völker-Dieben HJ, Went LN, de Vries-de Mol EC.

Mod Probl Ophthalmol. 1974;13(0):277-81. No abstract available.

PMID:
4548145
5.

Differential diagnosis of congenital tritanopia and dominantly inherited juvenile optic atrophy.

Miyake Y, Yagasaki K, Ichikawa H.

Arch Ophthalmol. 1985 Oct;103(10):1496-501.

PMID:
3876823
6.

Reflections, old and new, concerning acquired defects of color vision.

Linksz A.

Surv Ophthalmol. 1973 Jan-Feb;17(4):229-40. Review. No abstract available.

PMID:
4606997
7.

Colour vision in a pedigree with autosomal dominant optic atrophy.

Ohba N, Imamura PM, Tanino T.

Mod Probl Ophthalmol. 1976;17:315-9. No abstract available.

PMID:
1085884
8.

[Tritanopia and dominantly inherited optic atrophy (author's transl)].

Frey RG.

Klin Monbl Augenheilkd. 1975 Oct;167(4):577-80. German.

PMID:
1082048
9.

Diagnostic criteria in cominantly inherited juvenile optic atrophy. A report of three new families.

Smith DP.

Am J Optom Arch Am Acad Optom. 1972 Mar;49(3):183-200. No abstract available.

PMID:
4502353
10.

A family with optic atrophy and congenital hearing loss.

Amemiya T, Honda A.

Ophthalmic Genet. 1994 Jun;15(2):87-93.

PMID:
7850273
11.

Tritan pedigree without optic-nerve atrophy.

Higgins KE, Brooks DN, Gottschalk G.

Am J Optom Physiol Opt. 1983 Dec;60(12):964-9.

PMID:
6606981
12.

[Congenital achromatopsia].

Pinckers A.

Ann Ocul (Paris). 1972 Jul;205(7):821-34. French. No abstract available.

PMID:
4539461
13.

Hereditary optic atrophy with onset in early childhood.

Brodrick JD.

Br J Ophthalmol. 1974 Sep;58(9):817-22. No abstract available.

14.

Dominant optic atrophy. The clinical profile.

Kline LB, Glaser JS.

Arch Ophthalmol. 1979 Sep;97(9):1680-6.

PMID:
314284
15.

[Juvenile optic atrophy with dominant inheritance].

Werner W, Benedikt O.

Klin Monbl Augenheilkd. 1971 Dec;159(6):798-803. German. No abstract available.

PMID:
5316708
16.

Studies on color vision anomalies in subjects with alcoholism.

Sakuma Y.

Ann Ophthalmol. 1973 Dec;5(12):1277-92. No abstract available.

PMID:
4543804
17.

Dominant congenital deafness and progressive optic nerve atrophy. Occurrence in four generations of a family.

Konigsmark BW, Knox DL, Hussels IE, Moses H.

Arch Ophthalmol. 1974 Feb;91(2):99-103. No abstract available.

PMID:
4544000
18.

[The acute phase of leber's optic nerve atrophy (author's transl)].

Gács Gy, Rácz P, Szilvássy J.

Klin Monbl Augenheilkd. 1975 Sep;167(3):489-95. German.

PMID:
1214431
19.

Four families with the dominant infantile form of optic nerve atrophy.

Kok-van Alphen CC.

Acta Ophthalmol (Copenh). 1970;48(5):905-16. No abstract available.

PMID:
5312507
20.

The AN-59 anomaloscope in the research of acquired colour vision deficiencies.

Mailáth L.

Mod Probl Ophthalmol. 1972;11:34-9. No abstract available.

PMID:
4544966

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