Implications of molecular diagnostics in endocrine diseases caused by defects in hormone synthesis or action;Molekylærdiagnostikk av endokrine sykdommer
Genotyping is a valuable diagnostic complement to neonatal screening for congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency
Nordenstrom A, Thilen A, Hagenfeldt L et al. Genotyping is a valuable diagnostic complement to neonatal screening for congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency. J Clin Endocrinol Metab 1999; 84: 1505-9.
The role of bilateral adrenalectomy in the treatment of congenital adrenal hyperplasia
Van Wyk JJ, Ritzen EM. The role of bilateral adrenalectomy in the treatment of congenital adrenal hyperplasia. J Clin Endocrinol Metab 2003; 88: 2993-8.
Thyreoideahormonresistens. Klinisk, biokjemisk og genetisk utredning av en familie
Erichsen KE, Berg JP, Torjesen PA et al. Thyreoideahormonresistens. Klinisk, biokjemisk og genetisk utredning av en familie. Tidsskr Nor Lægeforen 1998; 118: 525-9.
Retarded bone growth in thyroid hormone resistance. A clinical study of a large family with a novel thyroid hormone receptor mutation
Kvistad PH, Lovas K, Boman H, Myking OL. Retarded bone growth in thyroid hormone resistance. A clinical study of a large family with a novel thyroid hormone receptor mutation. Eur J Endocrinol 2004; 150: 425-30.
Parathyroid adenoma in a subject with familial hypocalciuric hypercalcemia: Coincidence or causality?
Burski K, Torjussen B, Paulsen AQ et al. Parathyroid adenoma in a subject with familial hypocalciuric hypercalcemia: coincidence or causality? J Clin Endocrinol Metab 2002; 87: 1015-6.