AAAAAA
Results:
1-7
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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
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