-
1
-
-
0032811842
-
Congenital hypothyroidism: Etiologies, diagnosis, and management
-
LaFranchi S. Congenital hypothyroidism: etiologies, diagnosis, and management. Thyroid 1999;9:735-40.
-
(1999)
Thyroid
, vol.9
, pp. 735-740
-
-
LaFranchi, S.1
-
2
-
-
0032622056
-
Thyroid function in mothers of hypothyroid newborns
-
Dussault JH, Fisher DA. Thyroid function in mothers of hypothyroid newborns. Obstet Gynecol 1999;93:15-20.
-
(1999)
Obstet Gynecol
, vol.93
, pp. 15-20
-
-
Dussault, J.H.1
Fisher, D.A.2
-
3
-
-
0029863763
-
Incidence of transient congenital hypothyroidism due to maternal thyrotropin receptor-blocking antibodies in over one million babies
-
Brown RS, Bellisario RL, Botero D, Fournier L, Abrams CA, Cowger ML, et al. Incidence of transient congenital hypothyroidism due to maternal thyrotropin receptor-blocking antibodies in over one million babies. J Clin Endocrinol Metab 1996;81:1147-51.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 1147-1151
-
-
Brown, R.S.1
Bellisario, R.L.2
Botero, D.3
Fournier, L.4
Abrams, C.A.5
Cowger, M.L.6
-
4
-
-
0030711064
-
Topical iodine-containing antiseptics and subclinical hypothyroidism in preterm infants
-
Linder N, Davidovitch N, Reichman B, Kuint J, Lubin D, Meyerovitch J, et al. Topical iodine-containing antiseptics and subclinical hypothyroidism in preterm infants. J Pediatr 1997;131:434-9.
-
(1997)
J Pediatr
, vol.131
, pp. 434-439
-
-
Linder, N.1
Davidovitch, N.2
Reichman, B.3
Kuint, J.4
Lubin, D.5
Meyerovitch, J.6
-
5
-
-
0018390505
-
Screening for congenital hypothyroidism: Results of screening one million North American infants
-
Fisher DA, Dussault JH, Foley TP Jr, Klein AH, LaFranchi S, Larsen PR, et al. Screening for congenital hypothyroidism: results of screening one million North American infants. J Pediatr 1979;94:700-5.
-
(1979)
J Pediatr
, vol.94
, pp. 700-705
-
-
Fisher, D.A.1
Dussault, J.H.2
Foley Jr., T.P.3
Klein, A.H.4
LaFranchi, S.5
Larsen, P.R.6
-
6
-
-
0033036689
-
Neonatal hypothyroidism: Treatment and outcome
-
Van Vliet G. Neonatal hypothyroidism: treatment and outcome. Thyroid 1999;9:79-84.
-
(1999)
Thyroid
, vol.9
, pp. 79-84
-
-
Van Vliet, G.1
-
7
-
-
0035210805
-
Association Francaise pour le Depistage et la Prevetion des Handicaps de l'Enfant
-
Leger J, Larroque B, Norton J. Association Francaise pour le Depistage et la Prevetion des Handicaps de l'Enfant. Influence of severity of congenital hypothyroidism and adequacy of treatment on school achievement in young adolescents: a population-based cohort study. Acta Paediatr 2001; 90:1249-56.
-
(2001)
Acta Paediatr
, vol.90
, pp. 1249-1256
-
-
Leger, J.1
Larroque, B.2
Norton, J.3
-
8
-
-
17744381340
-
Autosomal dominant transmission of congenital thyroid hypoplasia due to loss-of-function mutation of PAX8
-
Vilain C, Rydlewski C, Duprez L, Heinrichs C, Abramowicz M, Malvaux P, et al. Autosomal dominant transmission of congenital thyroid hypoplasia due to loss-of-function mutation of PAX8. J Clin Endocrinol Metab 2001;86:234-8.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 234-238
-
-
Vilain, C.1
Rydlewski, C.2
Duprez, L.3
Heinrichs, C.4
Abramowicz, M.5
Malvaux, P.6
-
9
-
-
0035050820
-
Maternal isodisomy for chromosome 2p causing severe congenital hypothyroidism
-
Bakker B, Bikker H, Hennekam RC, Lommen EJ, Schipper MG, Vulsma T, et al. Maternal isodisomy for chromosome 2p causing severe congenital hypothyroidism. J Clin Endocrinol Metab 2001;86:1164-8.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 1164-1168
-
-
Bakker, B.1
Bikker, H.2
Hennekam, R.C.3
Lommen, E.J.4
Schipper, M.G.5
Vulsma, T.6
-
10
-
-
0031763451
-
High prevalence of T354P sodium/iodide symporter gene mutation in Japanese patients with iodide transport defect who have heterogeneous clinical pictures
-
Kosugi S, Sato Y, Matsuda A, Ohyama Y, Fujieda K, Inomata H, et al. High prevalence of T354P sodium/iodide symporter gene mutation in Japanese patients with iodide transport defect who have heterogeneous clinical pictures. J Clin Endocrinol Metab 1998;83:4123-9.
-
(1998)
J Clin Endocrinol Metab
, vol.83
, pp. 4123-4129
-
-
Kosugi, S.1
Sato, Y.2
Matsuda, A.3
Ohyama, Y.4
Fujieda, K.5
Inomata, H.6
-
11
-
-
0035673475
-
Newborn screening for congenital hypothyroidism, Victoria, Australia, 1977-1997, I: The screening programme, demography, baseline perinatal data and diagnostic classification
-
Connelly JF, Coakley JC, Gold H, Francis I, Mathur KS, Rickards AL, et al. Newborn screening for congenital hypothyroidism, Victoria, Australia, 1977-1997, I: the screening programme, demography, baseline perinatal data and diagnostic classification. J Pediatr Endocrinol Metab 2001;14: 1597-610.
-
(2001)
J Pediatr Endocrinol Metab
, vol.14
, pp. 1597-1610
-
-
Connelly, J.F.1
Coakley, J.C.2
Gold, H.3
Francis, I.4
Mathur, K.S.5
Rickards, A.L.6
-
12
-
-
0029039137
-
Identification of five novel inactivating mutations in the human thyroid peroxidase gene by denaturing gradient gel electrophoresis
-
Bikker H, Vulsma T, Baas F, de Vijlder JJ. Identification of five novel inactivating mutations in the human thyroid peroxidase gene by denaturing gradient gel electrophoresis. Hum Mutat 1995;6:9-16.
-
(1995)
Hum Mutat
, vol.6
, pp. 9-16
-
-
Bikker, H.1
Vulsma, T.2
Baas, F.3
De Vijlder, J.J.4
-
13
-
-
0025892017
-
Diagnostic dilemmas. Results of screening tests for congenital hypothyroidism
-
Willi SM, Moshang T Jr. Diagnostic dilemmas. Results of screening tests for congenital hypothyroidism. Pediatr Clin North Am 1991;38:555-66.
-
(1991)
Pediatr Clin North Am
, vol.38
, pp. 555-566
-
-
Willi, S.M.1
Moshang Jr., T.2
-
14
-
-
0036361026
-
The continuing importance of thyroid scintigraphy in the era of high-resolution ultrasound
-
review
-
Meller J, Becker W. The continuing importance of thyroid scintigraphy in the era of high-resolution ultrasound. [review]. Eur J Nucl Med Mol Imaging 2002;29(Suppl 2):S425-38.
-
(2002)
Eur J Nucl Med Mol Imaging
, vol.29
, Issue.2 SUPPL.
-
-
Meller, J.1
Becker, W.2
-
15
-
-
0031025824
-
Molecular analysis of mutated thyroid peroxidase detected in patients with total iodide organification defects
-
Bikker H, Baas F, de Vijlder JJ. Molecular analysis of mutated thyroid peroxidase detected in patients with total iodide organification defects. J Clin Endocrinol Metab 1997;82:649-53.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 649-653
-
-
Bikker, H.1
Baas, F.2
De Vijlder, J.J.3
-
16
-
-
0030060625
-
Outcome of severe congenital hypothyroidism: Closing the developmental gap with early high dose levothyroxine treatment
-
Dubuis JM, Glorieux J, Richer F, Deal CL, Dussault JH, Van Vliet G. Outcome of severe congenital hypothyroidism: closing the developmental gap with early high dose levothyroxine treatment. J Clin Endocrinol Metab 1996;81:222-7.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 222-227
-
-
Dubuis, J.M.1
Glorieux, J.2
Richer, F.3
Deal, C.L.4
Dussault, J.H.5
Van Vliet, G.6
-
17
-
-
0036146483
-
Effect of different starting doses of levothyroxine on growth and intellectual outcome at four years of age in congenital hypothyroidism
-
Salerno M, Militerni R, Bravaccio C, Micillo M, Capalbo D, Di MS, et al. Effect of different starting doses of levothyroxine on growth and intellectual outcome at four years of age in congenital hypothyroidism. Thyroid 2002; 12:45-52.
-
(2002)
Thyroid
, vol.12
, pp. 45-52
-
-
Salerno, M.1
Militerni, R.2
Bravaccio, C.3
Micillo, M.4
Capalbo, D.5
Di, M.S.6
-
18
-
-
0027205113
-
Newborn screening for congenital hypothyroidism: Recommended guidelines
-
American Academy of Pediatrics AAP Section on Endocrinology and Committee on Genetics, and American Thyroid Association Committee on Public Health. Newborn screening for congenital hypothyroidism: recommended guidelines. Pediatrics 1993;91:1203-9.
-
(1993)
Pediatrics
, vol.91
, pp. 1203-1209
-
-
-
19
-
-
0036022448
-
Clinical utility of thyroid ultrasonography in the diagnosis of congenital hypothyroidism
-
Ohnishi H, Inomata H, Watanabe T, Wataki K, Sato H, Sanayama K, et al. Clinical utility of thyroid ultrasonography in the diagnosis of congenital hypothyroidism. Endocr J 2002;49:293-7.
-
(2002)
Endocr J
, vol.49
, pp. 293-297
-
-
Ohnishi, H.1
Inomata, H.2
Watanabe, T.3
Wataki, K.4
Sato, H.5
Sanayama, K.6
-
20
-
-
0022469774
-
Transient neonatal "athyreosis" resulting from thyrotropin-binding inhibitory immunoglobulins
-
Connors MH, Styne DM. Transient neonatal 'athyreosis" resulting from thyrotropin-binding inhibitory immunoglobulins. Pediatrics 1986; 78:287-90.
-
(1986)
Pediatrics
, vol.78
, pp. 287-290
-
-
Connors, M.H.1
Styne, D.M.2
|