-
1
-
-
0022617826
-
Prediction and therapy of intrauterine and late onset neonatal hyperthyrodism
-
Zakarija M, McKenzie JM, Hoffman WH: Prediction and therapy of intrauterine and late onset neonatal hyperthyrodism. J Clin Endocrinol Metab 1986;62:368-371.
-
(1986)
J Clin Endocrinol Metab
, vol.62
, pp. 368-371
-
-
Zakarija, M.1
McKenzie, J.M.2
Hoffman, W.H.3
-
2
-
-
0029973239
-
A neomutation of the thyroid-stimulating hormone receptor in a severe neonatal hyperthyroidism
-
Roux N, Polak M, Couet J, Leger J, Czernichow P, Milgrom E, Misrahi M: A neomutation of the thyroid-stimulating hormone receptor in a severe neonatal hyperthyroidism. J Clin Endocrinol 1996;81:2023-2026.
-
(1996)
J Clin Endocrinol
, vol.81
, pp. 2023-2026
-
-
Roux, N.1
Polak, M.2
Couet, J.3
Leger, J.4
Czernichow, P.5
Milgrom, E.6
Misrahi, M.7
-
3
-
-
0028891649
-
Brief report: Congenital hyperthyroidism caused by a mutation in the thyrotropin-receptor gene
-
Kopp P, Van Sande J, Parma J, Duprez L, Gerber H, Joss E, Jameson JL, Dumont JE, Vassart G: Brief Report: Congenital hyperthyroidism caused by a mutation in the thyrotropin-receptor gene. N Engl J Med 1995;332:150-154.
-
(1995)
N Engl J Med
, vol.332
, pp. 150-154
-
-
Kopp, P.1
Van Sande, J.2
Parma, J.3
Duprez, L.4
Gerber, H.5
Joss, E.6
Jameson, J.L.7
Dumont, J.E.8
Vassart, G.9
-
4
-
-
0028240982
-
Germline mutations in the thyrotropin receptor gene cause non-autoimmune autosomal dominant hyperthyroidism
-
Duprez L, Parma J, van Sande J, Allgeier A, Leclere J, Schwartz C, Delisle MJ, Decoulx M, Orgiazzi J, Dumont J, Vassart G: Germline mutations in the thyrotropin receptor gene cause non-autoimmune autosomal dominant hyperthyroidism. Nature Genetics 1994;7: 396-401.
-
(1994)
Nature Genetics
, vol.7
, pp. 396-401
-
-
Duprez, L.1
Parma, J.2
Van Sande, J.3
Allgeier, A.4
Leclere, J.5
Schwartz, C.6
Delisle, M.J.7
Decoulx, M.8
Orgiazzi, J.9
Dumont, J.10
Vassart, G.11
-
5
-
-
0030715694
-
Sporadic congenital hyperthyroidism due to a spontanous germline mutation in the thyrotropin receptor gene
-
Holzapfel HP, Wonerow P, Petrykowski W, Henschen M, Scherbaum WA, Paschke R: Sporadic congenital hyperthyroidism due to a spontanous germline mutation in the thyrotropin receptor gene. J Clin Endocrinol Metab 1997;82:3879-3884.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 3879-3884
-
-
Holzapfel, H.P.1
Wonerow, P.2
Petrykowski, W.3
Henschen, M.4
Scherbaum, W.A.5
Paschke, R.6
-
6
-
-
0030830146
-
Congenital hyperthyroidism caused by a solitary toxic adenoma harboring a novel somatic mutation (Serine281 Isoleucine) in the extracellular domain of the thyrotropin receptor
-
Kopp P, Muirhead S, Jourdain N, Gu WX, Jameson JL, Rodd C: Congenital hyperthyroidism caused by a solitary toxic adenoma harboring a novel somatic mutation (Serine281 Isoleucine) in the extracellular domain of the thyrotropin receptor. J Clin Invest 1997;100:1634-1639.
-
(1997)
J Clin Invest
, vol.100
, pp. 1634-1639
-
-
Kopp, P.1
Muirhead, S.2
Jourdain, N.3
Gu, W.X.4
Jameson, J.L.5
Rodd, C.6
-
7
-
-
0030003969
-
TSH receptor and disease
-
Tonacchera M, van Sande J, Parma J, Duprez L, Cetani F, Costagliola S, Dumont JE, Vassart G: TSH receptor and disease. Clin Endocrinol 1996;44:621-633.
-
(1996)
Clin Endocrinol
, vol.44
, pp. 621-633
-
-
Tonacchera, M.1
Van Sande, J.2
Parma, J.3
Duprez, L.4
Cetani, F.5
Costagliola, S.6
Dumont, J.E.7
Vassart, G.8
-
8
-
-
9044240477
-
Functional characteristics of three new germline mutations of the thyrotropin receptor gene causing autosomal dominant toxic thyroid hyperplasia
-
Tonacchera M, van Sande J, Cetani F, Swillens S, Schwartz C, Winiszewski P, Portmann L, Dumont JE, Vassart G, Parma J: Functional characteristics of three new germline mutations of the thyrotropin receptor gene causing autosomal dominant toxic thyroid hyperplasia. J Clin Endocrinol Metab 1996;81:547-554.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 547-554
-
-
Tonacchera, M.1
Van Sande, J.2
Cetani, F.3
Swillens, S.4
Schwartz, C.5
Winiszewski, P.6
Portmann, L.7
Dumont, J.E.8
Vassart, G.9
Parma, J.10
-
9
-
-
0023097627
-
A sequence in M13 phage detects hypervariable minisatellites in human and animal DNA
-
Vassart G, Georges M, Monsieur R, Brocas H, Lequarre AS, Christophe D: A sequence in M13 phage detects hypervariable minisatellites in human and animal DNA. Science 1987;235: 683-684.
-
(1987)
Science
, vol.235
, pp. 683-684
-
-
Vassart, G.1
Georges, M.2
Monsieur, R.3
Brocas, H.4
Lequarre, A.S.5
Christophe, D.6
-
10
-
-
0027413478
-
Detection of thyroid-stimulating antibody using Chinese hamster ovary cells transfected with cloned human thyrotropin receptor
-
Vitti P, Elisei R, Tonacchera L, Chiovato L, Mancusi F: Detection of thyroid-stimulating antibody using Chinese hamster ovary cells transfected with cloned human thyrotropin receptor. J Clin Endocrinol Metab 1993;76:499-503.
-
(1993)
J Clin Endocrinol Metab
, vol.76
, pp. 499-503
-
-
Vitti, P.1
Elisei, R.2
Tonacchera, L.3
Chiovato, L.4
Mancusi, F.5
-
12
-
-
0026743033
-
The thyrotropin receptor and the regulation of thyrocyte function and growth
-
Vassart G, Dumont JE: The thyrotropin receptor and the regulation of thyrocyte function and growth. Endocr Rev 1992;13:596-611.
-
(1992)
Endocr Rev
, vol.13
, pp. 596-611
-
-
Vassart, G.1
Dumont, J.E.2
-
13
-
-
0030016080
-
Autoimmunity and thyroid growth: Where do we stand?
-
Drexhage HA: Autoimmunity and thyroid growth: Where do we stand? Eur J Endocrinol 1996;135:39-45.
-
(1996)
Eur J Endocrinol
, vol.135
, pp. 39-45
-
-
Drexhage, H.A.1
-
14
-
-
8544221172
-
Diversity and prevalence of somatic mutations in the thyrotropin receptor and Gs alfa genes as a cause of toxic thyroid adenomas
-
Parma J, Duprez L, Van Sande J, Hermans J, Rocmans P, Van Vliet G, Constagliola S, Rodien P, Dumont JE, Vassart G: Diversity and prevalence of somatic mutations in the thyrotropin receptor and Gs alfa genes as a cause of toxic thyroid adenomas. J Clin Endocrinol Metab 1997;82:2695-2701.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 2695-2701
-
-
Parma, J.1
Duprez, L.2
Van Sande, J.3
Hermans, J.4
Rocmans, P.5
Van Vliet, G.6
Constagliola, S.7
Rodien, P.8
Dumont, J.E.9
Vassart, G.10
-
15
-
-
0019967009
-
Familial hyperthyroidism without evidence of autoimmunity
-
Thomas J, Lecklere J, Hartemann P, Duhille J, Orgiazzi J, Petersen M, Janot C, Guedemnet JG: Familial hyperthyroidism without evidence of autoimmunity. Acta Endocrinol 1982; 100:512-518.
-
(1982)
Acta Endocrinol
, vol.100
, pp. 512-518
-
-
Thomas, J.1
Lecklere, J.2
Hartemann, P.3
Duhille, J.4
Orgiazzi, J.5
Petersen, M.6
Janot, C.7
Guedemnet, J.G.8
-
16
-
-
0027303726
-
Graves ophthalmopathy and the TSH receptor
-
Franklyn JA: Graves ophthalmopathy and the TSH receptor. Lancet 1993;342:318-319.
-
(1993)
Lancet
, vol.342
, pp. 318-319
-
-
Franklyn, J.A.1
-
17
-
-
0030981965
-
TSH receptor transcripts and TSH receptor-like immunoreactivity in orbital and pretibial fibroblasts of patients with Graves' ophthalmopathy and pretibial myxedema
-
Stadlmayr W, Spitzweg C, Bichlmair AM, Heufelder AE: TSH receptor transcripts and TSH receptor-like immunoreactivity in orbital and pretibial fibroblasts of patients with Graves' ophthalmopathy and pretibial myxedema. Thyroid 1997;7:3-12.
-
(1997)
Thyroid
, vol.7
, pp. 3-12
-
-
Stadlmayr, W.1
Spitzweg, C.2
Bichlmair, A.M.3
Heufelder, A.E.4
-
18
-
-
0003788413
-
-
New York, Churchill-Livingstone
-
De Groot LJ, Larsen PRN, Hennemann G: The Thyroid and Its Disorders, ed 6. New York, Churchill-Livingstone, 1996.
-
(1996)
The Thyroid and Its Disorders, Ed 6
-
-
De Groot, L.J.1
Larsen, P.R.N.2
Hennemann, G.3
-
19
-
-
0028928244
-
Iodine-131 therapy of hyperthyroidism in pediatric patients
-
Clark JD, Gelfand MJ, Elgazzar AH: Iodine-131 therapy of hyperthyroidism in pediatric patients. J Nucl Med 1995;36:442-445.
-
(1995)
J Nucl Med
, vol.36
, pp. 442-445
-
-
Clark, J.D.1
Gelfand, M.J.2
Elgazzar, A.H.3
-
20
-
-
0028228869
-
Incidence of juvenile thyrotoxicoses in Denmark 1982-88
-
Lavard L, Ranløv I, Perrild H, Andersen O, Jacobsen BB: Incidence of juvenile thyrotoxicoses in Denmark 1982-88. Eur J Endocrinol 1994;130:565-568.
-
(1994)
Eur J Endocrinol
, vol.130
, pp. 565-568
-
-
Lavard, L.1
Ranløv, I.2
Perrild, H.3
Andersen, O.4
Jacobsen, B.B.5
-
23
-
-
0028000178
-
Diagnosis and treatment of thyrotoxicosis in childhood
-
Perrild H, Gruters-Kieslich A, Feldt-Rasmussen U, Grant D, Martino E, Kayser L, DeLange F: Diagnosis and treatment of thyrotoxicosis in childhood. Eur J Endocrinol 1994;131:467-473.
-
(1994)
Eur J Endocrinol
, vol.131
, pp. 467-473
-
-
Perrild, H.1
Gruters-Kieslich, A.2
Feldt-Rasmussen, U.3
Grant, D.4
Martino, E.5
Kayser, L.6
DeLange, F.7
-
24
-
-
0023227143
-
Hyperthyroidism in children treated with long-term medical therapy: Twenty-five percent remission every two years
-
Lippe B, Landaw EM, Kaplan SA: Hyperthyroidism in children treated with long-term medical therapy: Twenty-five percent remission every two years. J Clin Endocrinol. 1987; 64:1241-1245.
-
(1987)
J Clin Endocrinol.
, vol.64
, pp. 1241-1245
-
-
Lippe, B.1
Landaw, E.M.2
Kaplan, S.A.3
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