Zobrazeno 1 - 8
of 8
pro vyhledávání: '"N H, Scherberg"'
Publikováno v:
The Journal of clinical endocrinology and metabolism. 85(8)
Familial dysalbuminemic hyperthyroxinemia (FDH), is the most common cause of inherited increase in serum total T4 (TT4) in the Caucasian population. It is caused by a mutation (R218H) in the human serum albumin (HSA) gene, resulting in 10-fold higher
Autor:
T, Sunthornthepvarakul, S, Likitmaskul, S, Ngowngarmratana, K, Angsusingha, S, Kitvitayasak, N H, Scherberg, S, Refetoff
Publikováno v:
The Journal of clinical endocrinology and metabolism. 83(5)
We report the abnormal albumin in members of a Thai family that presented with high serum total T3 but not T4 when measured by radioimmunoassay. In contrast, total T3 values were very low when measured by ELISA and chemiluminescence. The subjects hav
Publikováno v:
JAMA. 264(17)
Generalized resistance to thyroid hormone (GRTH) is an inherited disease that is usually suspected when elevated serum thyroid hormone levels are associated with nonsuppressed thyrotropin. Often these test results are obtained because of short statur
Publikováno v:
Endocrinologia experimentalis. 24(1-2)
Protein formation in the anterior pituitary was investigated in vitro in thyroidectomized (TX) and/or adrenalectomited (AX) rats treated with a single dose of 100 micrograms/100 g of 3,5,3'-triiodothyronine (T3) and/or with a single dose of 10 microg
Publikováno v:
Journal of Biological Chemistry. 253:1773-1779
Publikováno v:
The Journal of biological chemistry. 253(6)
Autor:
N H, Scherberg, S, Refetoff
Publikováno v:
Methods in cell biology. 10
Autor:
N H, Scherberg, S, Refetoff
Publikováno v:
The Journal of biological chemistry. 249(7)