Andréasson S - Search Results

1

Phenotype variations within a choroideremia family lacking the entire CHM gene.

Ponjavic V, Abrahamson M, Andréasson S, Van Bokhoven H, Cremers FP, Ehinger B, Fex G. Ponjavic V, et al. Among authors: andreasson s. Ophthalmic Genet. 1995 Dec;16(4):143-50. doi: 10.3109/13816819509057855. Ophthalmic Genet. 1995. PMID: 8749050

2

Serum transferrin in patients with retinitis pigmentosa.

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

3

[Current diagnostic and therapeutic possibilities in tapetoretinal degeneration].

Andréasson S, Ehinger B. Andréasson S, et al. Nord Med. 1992;107(12):311-2. Nord Med. 1992. PMID: 1465345 Swedish.

4

A six-generation family with autosomal dominant retinitis pigmentosa and a rhodopsin gene mutation (arginine-135-leucine).

Andréasson S, Ehinger B, Abrahamson M, Fex G. Andréasson S, et al. Ophthalmic Paediatr Genet. 1992 Sep;13(3):145-53. doi: 10.3109/13816819209046483. Ophthalmic Paediatr Genet. 1992. PMID: 1484692

5

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

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

6

Electroretinographic diagnosis in families with X-linked retinitis pigmentosa.

Andréasson SO, Ehinger B. Andréasson SO, et al. Acta Ophthalmol (Copenh). 1990 Apr;68(2):139-44. doi: 10.1111/j.1755-3768.1990.tb01894.x. Acta Ophthalmol (Copenh). 1990. PMID: 2356700

7

A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.

Tranebjaerg L, Schwartz C, Eriksen H, Andreasson S, Ponjavic V, Dahl A, Stevenson RE, May M, Arena F, Barker D, et al. Tranebjaerg L, et al. Among authors: andreasson s. J Med Genet. 1995 Apr;32(4):257-63. doi: 10.1136/jmg.32.4.257. J Med Genet. 1995. PMID: 7643352 Free PMC article.

8

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

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

9

Mutation spectrum in the CHM gene of Danish and Swedish choroideremia patients.

van Bokhoven H, Schwartz M, Andréasson S, van den Hurk JA, Bogerd L, Jay M, Rüther K, Jay B, Pawlowitzki IH, Sankila EM, et al. van Bokhoven H, et al. Among authors: andreasson s. Hum Mol Genet. 1994 Jul;3(7):1047-51. doi: 10.1093/hmg/3.7.1047. Hum Mol Genet. 1994. PMID: 7981671

10

[Vitamin A in retinitis pigmentosa. An effective treatment, for the first time].

Andréasson S, Ehinger B, Nilsson SE, Skoog KO. Andréasson S, et al. Lakartidningen. 1993 Sep 22;90(38):3181. Lakartidningen. 1993. PMID: 8231469 Swedish. No abstract available.

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