-
1
-
-
0030994365
-
Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin causing profound hypoplasia of the thyroid gland
-
ABRAMOWICS MJ, DUPREZ L, PARMA J, VASSART G, HEINRICHS C: Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin causing profound hypoplasia of the thyroid gland. J Clin Invest 99, 3018-3024, 1997
-
(1997)
J Clin Invest
, vol.99
, pp. 3018-3024
-
-
Abramowics, M.J.1
Duprez, L.2
Parma, J.3
Vassart, G.4
Heinrichs, C.5
-
2
-
-
0025934765
-
Pseudomalabsorption of levothyroxine
-
AIN KB, REFETOFF S, FEIN HG, WEINTRAUB BD: Pseudomalabsorption of levothyroxine. JAMA 266, 2118-2120, 1991
-
(1991)
JAMA
, vol.266
, pp. 2118-2120
-
-
Ain, K.B.1
Refetoff, S.2
Fein, H.G.3
Weintraub, B.D.4
-
3
-
-
0030983833
-
Mutations of the human thyrotropin receptor gene causng thyroid hypoplasisa and persistant congenutal hypothyroidism
-
BIEBERMAN H, SCHONEBERG T, KRUDE H, SCHUKTZ G, GUDERMAN T, GRUTERS A: Mutations of the human thyrotropin receptor gene causng thyroid hypoplasisa and persistant congenutal hypothyroidism. J Clin Endocrinol Metab 82, 3471-3480, 1997
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 3471-3480
-
-
Bieberman, H.1
Schoneberg, T.2
Krude, H.3
Schuktz, G.4
Guderman, T.5
Gruters, A.6
-
4
-
-
0030989828
-
Two novel mutations in the thyrotropin (TSH) receptor gene in a child with resistance to TSH
-
CLIFTON-BLIGH RG, GREGORY JW, LUDGATE M et al.: Two novel mutations in the thyrotropin (TSH) receptor gene in a child with resistance to TSH. J Clin Endocrinol Metab 82, 1094-1100, 1997
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 1094-1100
-
-
Clifton-Bligh, R.G.1
Gregory, J.W.2
Ludgate, M.3
-
5
-
-
10544240361
-
Four families with loss of function mutations of the thyrotropin receptor
-
DE Roux N, MISRAHI M, BRAUNER Pet al.: Four families with loss of function mutations of the thyrotropin receptor. J Clin Endocrinol Metab 81, 4229-4235, 1996
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 4229-4235
-
-
De Roux, N.1
Misrahi, M.2
Brauner, P.3
-
6
-
-
0031755047
-
Apparent congenital athyreosis contrasting with normal plasma thyroglobulin levels and associated with inactivating mutations in the thyrotropin receptor gene: Are athyreosis and ectopic thyroid distinct entities?
-
GAGNE N, PARMA J, DEAL C, VASSART G, VAN VLIET G: Apparent congenital athyreosis contrasting with normal plasma thyroglobulin levels and associated with inactivating mutations in the thyrotropin receptor gene: are athyreosis and ectopic thyroid distinct entities? J Clin Endocrinol Metab 83, 1771-1775, 1998
-
(1998)
J Clin Endocrinol Metab
, vol.83
, pp. 1771-1775
-
-
Gagne, N.1
Parma, J.2
Deal, C.3
Vassart, G.4
Van Vliet, G.5
-
7
-
-
0034137331
-
Pseudomalabsorption of levothyroxine: A case reports
-
OGAWA D, OTSUKA F, MIMURA Y, UENO A, HASHIMOTO H, KISHIDA M, OGURA T, MAKINO H: Pseudomalabsorption of levothyroxine: a case reports. Endocrine J 47, 45-50, 2000
-
(2000)
Endocrine J
, vol.47
, pp. 45-50
-
-
Ogawa, D.1
Otsuka, F.2
Mimura, Y.3
Ueno, A.4
Hashimoto, H.5
Kishida, M.6
Ogura, T.7
Makino, H.8
-
8
-
-
0014425946
-
Congenital hypothyroidism with impaired thyroid response to thyrotropin
-
STANBURY JB, ROCMANS F, BUHLER UK, OCHI Y: Congenital hypothyroidism with impaired thyroid response to thyrotropin. N Eng J Med 21, 1132-1136, 1968
-
(1968)
N Eng J Med
, vol.21
, pp. 1132-1136
-
-
Stanbury, J.B.1
Rocmans, F.2
Buhler, U.K.3
Ochi, Y.4
-
9
-
-
0028888593
-
Resistance to thyrotropin caused by mutations in the thyrotropin-receptor gene
-
SUNTHORNTHEPVARAKUL T, GOTTSCHALK ME, HAYASHI Y, REFETOFF S: resistance to thyrotropin caused by mutations in the thyrotropin-receptor gene. N Eng J Med 332, 156-160, 1995
-
(1995)
N Eng J Med
, vol.332
, pp. 156-160
-
-
Sunthornthepvarakul, T.1
Gottschalk, M.E.2
Hayashi, Y.3
Refetoff, S.4
-
10
-
-
0034454929
-
Congenital hypothyroidism with impaired thyroid response to thyrotropin (TSH) and absent circulating thyroglobulin: Evidence for a new inactivating mutation of the TSh receptor gene
-
TONACCHERA M, AGRETI P, PINCHERA A, ROSELLINI V, PERRI A, COLLECCHI P, VITTI P, CHIOVATO L: Congenital hypothyroidism with impaired thyroid response to thyrotropin (TSH) and absent circulating thyroglobulin: Evidence for a new inactivating mutation of the TSh receptor gene. J Clin Endocrinol Metab 85, 1001-1008, 2000
-
(2000)
J Clin Endocrinol Metab
, vol.85
, pp. 1001-1008
-
-
Tonacchera, M.1
Agreti, P.2
Pinchera, A.3
Rosellini, V.4
Perri, A.5
Collecchi, P.6
Vitti, P.7
Chiovato, L.8
|