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Results: 1-7 |
Results: 7

Authors: Burstedt, MSL Forsman-Semb, K Golovleva, I Janunger, T Wachtmeister, L Sandgren, O
Citation: Msl. Burstedt et al., Ocular phenotype of Bothnia dystrophy, an autosomal recessive retinitis pigmentosa associated with an R234W mutation in the RLBP1 gene, ARCH OPHTH, 119(2), 2001, pp. 260-267

Authors: Mambule, C Ando, Y Anan, I Holmgren, G Sandgren, O Stigbrandt, T Tashima, K Suhr, OB
Citation: C. Mambule et al., Enhancement of AA-amyloid formation in mice by transthyretin amyloid fragments and polyethylene glycol, BBA-GEN SUB, 1474(3), 2000, pp. 331-336

Authors: Olsen, KE Sletten, K Sandgren, O Olsson, H Myrvold, K Westermark, P
Citation: Ke. Olsen et al., What is the role of giant cells in AL-amyloidosis?, AMYLOID, 6(2), 1999, pp. 89-97

Authors: Ando, Y Ando, E Ohlsson, PI Olofsson, A Sandgren, O Suhr, O Terazaki, H Obayashi, K Lundgren, E Ando, M Negi, A
Citation: Y. Ando et al., Analysis of transthyretin amyloid fibrils from vitreous samples in familial amyloidotic polyneuropathy (Val30Met), AMYLOID, 6(2), 1999, pp. 119-123

Authors: Bakall, B Marknell, T Ingvast, S Koisti, MJ Sandgren, O Li, W Bergen, AAB Andreasson, S Rosenberg, T Petrukhin, K Wadelius, C
Citation: B. Bakall et al., The mutation spectrum of the bestrophin protein - functional implications, HUM GENET, 104(5), 1999, pp. 383-389

Authors: Burstedt, MSI Sandgren, O Holmgren, G Forsman-Semb, K
Citation: Msi. Burstedt et al., Bothnia dystrophy caused by mutations in the cellular retinaldehyde-binding protein gene (RLBP1) on chromosome 15q26, INV OPHTH V, 40(5), 1999, pp. 995-1000

Authors: Stathakis, DG Udar, N Sandgren, O Andreasson, S Bryant, PJ Small, K Forsman-Semb, K
Citation: Dg. Stathakis et al., Genomic organization of human DLG4, the gene encoding postsynaptic density95, J NEUROCHEM, 73(6), 1999, pp. 2250-2265
Risultati: 1-7 |