Authors:
Eksandh, L
Ekstrom, U
Abrahamson, M
Bauer, B
Andreasson, S
Citation: L. Eksandh et al., Different clinical expressions in two families with Stargardt's macular dystrophy (STGD1), ACT OPHTH S, 79(5), 2001, pp. 524-530
Citation: J. Larsson et S. Andreasson, Photopic 30 Hz flicker ERG as a predictor for rubeosis in central retinal vein occlusion, BR J OPHTH, 85(6), 2001, pp. 683-685
Authors:
Wissinger, B
Gamer, D
Jagle, H
Giorda, R
Marx, T
Mayer, S
Tippmann, S
Broghammer, M
Jurklies, B
Rosenberg, T
Jacobson, SG
Sener, EC
Tatlipinar, S
Hoyng, CB
Castellan, C
Bitoun, P
Andreasson, S
Rudolph, G
Kellner, U
Lorenz, B
Wolff, G
Verellen-Dumoulin, C
Schwartz, M
Cremers, FPM
Apfelstedt-ylla, E
Zrenner, E
Salati, R
Sharpe, LT
Kohl, S
Citation: B. Wissinger et al., CNGA3 mutations in hereditary cone photoreceptor disorders, AM J HU GEN, 69(4), 2001, pp. 722-737
Citation: J. Larsson et al., The 30-Hz flicker cone ERG for monitoring the early course of central retinal vein occlusion, ACT OPHTH S, 78(2), 2000, pp. 187-190
Authors:
Jensen, E
Sandstrom, K
Andreasson, S
Nilsson, K
Berggren, H
Larsson, LE
Citation: E. Jensen et al., Increased levels of S-100 protein after cardiac surgery with cardiopulmonary bypass and general surgery in children, PAEDIATR AN, 10(3), 2000, pp. 297-302
Citation: H. Hansagi et al., Parental divorce: psychosocial well-being, mental health and mortality during youth and young adulthood - A longitudinal study of Swedish conscripts, EUR J PUB H, 10(2), 2000, pp. 86-92
Authors:
Pusch, CM
Zeitz, C
Brandau, O
Pesch, K
Achatz, H
Feil, S
Scharfe, C
Maurer, J
Jacobi, FK
Pinckers, A
Andreasson, S
Hardcastle, A
Wissinger, B
Berger, W
Meindl, A
Citation: Cm. Pusch et al., The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein, NAT GENET, 26(3), 2000, pp. 324-327
Citation: S. Andreasson et al., Implementation and dissemination of methods for prevention of alcohol problems in primary health care: A feasibility study, ALC ALCOHOL, 35(5), 2000, pp. 525-530
Authors:
Eksandh, LC
Ponjavic, V
Ayyagari, R
Bingham, EL
Hiriyanna, KT
Andreasson, S
Ehinger, B
Sieving, PA
Citation: Lc. Eksandh et al., Phenotypic expression of juvenile X-linked retinoschisis in Swedish families with different mutations in the XLRS1 gene, ARCH OPHTH, 118(8), 2000, pp. 1098-1104
Authors:
Sandstrom, K
Nilsson, K
Andreasson, S
Larsson, LE
Citation: K. Sandstrom et al., Jugular bulb temperature compared with noninvasive temperatures and cerebral arteriovenous oxygen saturation differences during open heart surgery, PAEDIATR AN, 9(2), 1999, pp. 123-128
Authors:
Sandstrom, K
Nilsson, K
Andreasson, S
Larsson, LE
Citation: K. Sandstrom et al., Open heart surgery; pump prime effects and cerebral arteriovenous differences in glucose, lactate and ketones, PAEDIATR AN, 9(1), 1999, pp. 53-59
Authors:
Hiriyanna, KT
Bingham, EL
Yashar, BM
Ayyagari, R
Fishman, G
Small, KW
Weinberg, DV
Weleber, RG
Lewis, RA
Andreasson, S
Richards, JE
Sieving, PA
Citation: Kt. Hiriyanna et al., Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence change, HUM MUTAT, 14(5), 1999, pp. 423-427
Authors:
Arnell, H
Mantyjarvi, M
Tuppurainen, K
Andreasson, S
Dahl, N
Citation: H. Arnell et al., Stargardt disease: Linkage to the ABCR gene region on 1p21-p22 in Scandinavian families, ACT OPHTH S, 76(6), 1998, pp. 649-652