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Items: 1 to 20 of 128

1.

Abnormal visual pathways in normally pigmented cats that are heterozygous for albinism.

Leventhal AG, Vitek DJ, Creel DJ.

Science. 1985 Sep 27;229(4720):1395-7.

PMID:
3929383
2.
3.

Sensitivity deficits consistent with aberrant crossed visual pathways in human albinos.

St John R, Timney B.

Invest Ophthalmol Vis Sci. 1981 Dec;21(6):873-7.

PMID:
7309439
4.

Albinism. Recent advances.

Jay B, Carroll W.

Trans Ophthalmol Soc U K. 1980;100(4):467-71.

PMID:
6797109
5.

Genetic mechanisms determining the central visual pathways of mice.

Guillery RW, Scott GL, Cattanach BM, Deol MS.

Science. 1973 Mar 9;179(4077):1014-6.

PMID:
4687586
6.

Abnormal ipsilateral visual field representation in areas 17 and 18 of hypopigmented cats.

Ault SJ, Leventhal AG, Vitek DJ, Creel DJ.

J Comp Neurol. 1995 Apr 3;354(2):181-92.

PMID:
7782497
7.

Visual evoked potentials in Negro carriers of the gene for tyrosinase positive oculocutaneous albinism.

Castle D, Kromberg J, Kowalsky R, Moosa R, Gillman N, Zwane E, Fritz V.

J Med Genet. 1988 Dec;25(12):835-7.

8.
9.

Albinism, or the NOACH syndrome (the book of Enoch c.v. 1-20).

van Dorp DB.

Clin Genet. 1987 Apr;31(4):228-42.

PMID:
3109790
10.

Extrinsic modulation of retinal ganglion cell projections: analysis of the albino mutation in pigmentation mosaic mice.

Rice DS, Goldowitz D, Williams RW, Hamre K, Johnson PT, Tan SS, Reese BE.

Dev Biol. 1999 Dec 1;216(1):41-56.

11.

Abnormalities of the central visual pathways in Prader-Willi syndrome associated with hypopigmentation.

Creel DJ, Bendel CM, Wiesner GL, Wirtschafter JD, Arthur DC, King RA.

N Engl J Med. 1986 Jun 19;314(25):1606-9.

PMID:
3713758
12.

The recognition and management of albinism.

Abadi R, Pascal E.

Ophthalmic Physiol Opt. 1989 Jan;9(1):3-15. Review.

PMID:
2512527
13.

Autosomal recessive ocular albinism associated with a functionally significant tyrosinase gene polymorphism.

Fukai K, Holmes SA, Lucchese NJ, Siu VM, Weleber RG, Schnur RE, Spritz RA.

Nat Genet. 1995 Jan;9(1):92-5.

PMID:
7704033
14.

Differentiation of heterozygotes in recessive albinism.

Roberts DF, Kromberg JG, Jenkins T.

J Med Genet. 1986 Aug;23(4):323-7.

15.
16.

Albinism and visual pathways.

Dräger UC.

N Engl J Med. 1986 Jun 19;314(25):1636-8. No abstract available.

PMID:
3713761
17.
18.

Abnormal axons in the albino optic tract.

Guibal C, Baker GE.

Invest Ophthalmol Vis Sci. 2009 Dec;50(12):5516-21. doi: 10.1167/iovs.09-3950. Epub 2009 Jul 23.

PMID:
19628745
19.

Abnormal retinotopic organization of the dorsal lateral geniculate nucleus of the tyrosinase-negative albino cat.

Schmolesky MT, Wang Y, Creel DJ, Leventhal AG.

J Comp Neurol. 2000 Nov 13;427(2):209-19.

PMID:
11054689
20.

Visual pathway abnormalities in albinism and infantile nystagmus: VECPs and stereoacuity measurements.

Guo SQ, Reinecke RD, Fendick M, Calhoun JH.

J Pediatr Ophthalmol Strabismus. 1989 Mar-Apr;26(2):97-104.

PMID:
2709284

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