Authors: Pannain, S Feldman, M Eiholzer, U Weiss, RE Scherberg, NH Refetoff, S

Citation: S. Pannain et al., Familial dysalbuminemic hyperthyroxinemia in a Swiss family caused by a mutant albumin (R218P) shows an apparent discrepancy between serum concentration and affinity for thyroxine, J CLIN END, 85(8), 2000, pp. 2786-2792

Authors: Reutrakul, S Sadow, PM Pannain, S Pohlenz, J Carvalho, GA Macchia, PE Weiss, RE Refetoff, S

Citation: S. Reutrakul et al., Search for abnormalities of nuclear corepressors, coactivators, and a coregulator in families with resistance to thyroid hormone without mutations inthyroid hormone receptor beta or alpha genes, J CLIN END, 85(10), 2000, pp. 3609-3617

Authors: Tiosano, D Pannain, S Vassart, G Parma, J Gershoni-Baruch, R Mandel, H Lotan, R Zaharan, Y Pery, M Weiss, RE Refetoff, S Hochberg, Z

Citation: D. Tiosano et al., The hypothyroidism in an inbred kindred with congenital thyroid hormone and glucocorticoid deficiency is due to a mutation producing a truncated thyrotropin receptor, THYROID, 9(9), 1999, pp. 887-894

Authors: Pannain, S Weiss, RE Jackson, CE Dian, D Beck, JC Sheffield, VC Cox, N Refetoff, S

Citation: S. Pannain et al., Two different mutations in the thyroid peroxidase gene of a large inbred Amish kindred: Power and limits of homozygosity mapping, J CLIN END, 84(3), 1999, pp. 1061-1071

Authors: Pohlenz, J Weiss, RE Macchia, PE Pannain, S Lau, IT Ho, H Refetoff, S

Citation: J. Pohlenz et al., Five new families with resistance to thyroid hormone not caused by mutations in the thyroid hormone receptor beta gene, J CLIN END, 84(11), 1999, pp. 3919-3928