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Ugeskrift for Laeger|December 17, 1990
[Optic nerve atrophy with particular attention to perinatal damage]J R Petersen, T Rosenberg, K K IbsenOphthalmic Genetics|December 1, 1996
Novel rhodopsin mutation (M216R) in a Danish family with autosomal dominant retinitis pigmentosaM Haim, K Grundmann, A Gal, et al.Brain, Behavior, and Immunity|June 1, 1988
Prolonged effect of psychological disturbance on macrophage chemiluminescence in the squirrel monkeyC L Coe, L T Rosenberg, S LevineThe International Journal of Neuroscience|June 1, 1988
Effect of maternal separation on the complement system and antibody responses in infant primatesC L Coe, L T Rosenberg, S LevinePacing and Clinical Electrophysiology : PACE|November 1, 1980
Exit block in myxedema, treated effectively by thyroid hormone therapyZ Schlesinger, T Rosenberg, D Stryjer, et al.Ophthalmic Genetics|October 16, 1999
Genotype-phenotype correlation in X-linked retinitis pigmentosa 2 (RP2)T Rosenberg, U Schwahn, S Feil, et al.Clinical Genetics|October 1, 1988
Marner's cataract (CAM) assigned to chromosome 16: linkage to haptoglobinH Eiberg, E Marner, T Rosenberg, et al.Biochemical and Biophysical Research Communications|March 15, 1991
Mutation detection in Leber's hereditary optic neuropathy by PCR with allele-specific primingS Nørby, P Lestienne, I Nelson, et al.Israel Journal of Medical Sciences|September 1, 1990
Prevalence of thyroid disorders among the elderly in IsraelI Berlowitz, Y Ramot, T Rosenberg, et al.Acta Ophthalmologica Scandinavica|February 1, 1996
Dominant optic atrophy mapped to chromosome 3q region. II. Clinical and epidemiological aspectsB Kjer, H Eiberg, P Kjer, et al.Pageof 30