Ehinger B - Search Results

1

Full-field electroretinograms in patients with central areolar choroidal dystrophy.

Ponjavic V, Andréasson S, Ehinger B. Ponjavic V, et al. Among authors: ehinger b. Acta Ophthalmol (Copenh). 1994 Oct;72(5):537-44. doi: 10.1111/j.1755-3768.1994.tb07176.x. Acta Ophthalmol (Copenh). 1994. PMID: 7887150

2

Standardized full-field electroretinography in rabbits.

Gjörloff K, Andréasson S, Ehinger B. Gjörloff K, et al. Among authors: ehinger b. Doc Ophthalmol. 2004 Sep;109(2):163-8. doi: 10.1007/s10633-004-3924-5. Doc Ophthalmol. 2004. PMID: 15881262

3

Full-field ERG in patients with Batten/Spielmeyer-Vogt disease caused by mutations in the CLN3 gene.

Eksandh LB, Ponjavic VB, Munroe PB, Eiberg HE, Uvebrant PE, Ehinger BE, Mole SE, Andréasson S. Eksandh LB, et al. Among authors: ehinger be. Ophthalmic Genet. 2000 Jun;21(2):69-77. Ophthalmic Genet. 2000. PMID: 10916181

4

Full-field electroretinograms during general anesthesia in normal children compared to examination with topical anesthesia.

Andréasson S, Tornqvist K, Ehinger B. Andréasson S, et al. Among authors: ehinger b. Acta Ophthalmol (Copenh). 1993 Aug;71(4):491-5. doi: 10.1111/j.1755-3768.1993.tb04624.x. Acta Ophthalmol (Copenh). 1993. PMID: 8249580

5

Autosomal dominant retinitis pigmentosa with a rhodopsin mutation (Arg-135-Trp). Disease phenotype in a Swedish family.

Ponjavic V, Abrahamson M, Andréasson S, Ehinger B, Fex G. Ponjavic V, et al. Among authors: ehinger b. Acta Ophthalmol Scand. 1997 Apr;75(2):218-23. doi: 10.1111/j.1600-0420.1997.tb00129.x. Acta Ophthalmol Scand. 1997. PMID: 9197578 Free article.

6

Phenotypic expression of autosomal dominant retinitis pigmentosa in a Swedish family expressing a Phe-211-Leu variant of peripherin/RDS.

Ekström U, Ponjavic V, Abrahamson M, Nilsson-Ehle P, Andrëasson S, Stenström I, Ehinger B. Ekström U, et al. Among authors: ehinger b. Ophthalmic Genet. 1998 Mar;19(1):27-37. doi: 10.1076/opge.19.1.27.2179. Ophthalmic Genet. 1998. PMID: 9587927

7

Clinical expression of X-linked retinitis pigmentosa in a Swedish family with the RP2 genotype.

Ponjavic V, Andréasson S, Abrahamson M, Ehinger B, Gieser L, Fujita R, Swaroop A. Ponjavic V, et al. Among authors: ehinger b. Ophthalmic Genet. 1998 Dec;19(4):187-96. doi: 10.1076/opge.19.4.187.2305. Ophthalmic Genet. 1998. PMID: 9895243

8

Phenotypic expression of juvenile X-linked retinoschisis in Swedish families with different mutations in the XLRS1 gene.

Eksandh LC, Ponjavic V, Ayyagari R, Bingham EL, Hiriyanna KT, Andréasson S, Ehinger B, Sieving PA. Eksandh LC, et al. Among authors: ehinger b. Arch Ophthalmol. 2000 Aug;118(8):1098-104. doi: 10.1001/archopht.118.8.1098. Arch Ophthalmol. 2000. PMID: 10922205

9

Serum transferrin in patients with retinitis pigmentosa.

Andréasson S, Stibler H, Ehinger B. Andréasson S, et al. Among authors: ehinger b. Acta Ophthalmol (Copenh). 1992 Aug;70(4):525-7. doi: 10.1111/j.1755-3768.1992.tb02125.x. Acta Ophthalmol (Copenh). 1992. PMID: 1414300

10

Full-field electroretinograms in patients with the carbohydrate-deficient glycoprotein syndrome.

Andréasson S, Blennow G, Ehinger B, Strömland K. Andréasson S, et al. Among authors: ehinger b. Am J Ophthalmol. 1991 Jul 15;112(1):83-6. doi: 10.1016/s0002-9394(14)76218-x. Am J Ophthalmol. 1991. PMID: 1715674

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