-
1
-
-
0033924475
-
Risk factors for congenital hypothyroidism: An investigation of infant's birth weight, ethnicity, and gender in California, 1990-1998
-
Waller DK, Anderson JL, Lorey F, Cunningham GC. Risk factors for congenital hypothyroidism: an investigation of infant's birth weight, ethnicity, and gender in California, 1990-1998. Teratology. 2000;62:36-41
-
(2000)
Teratology
, vol.62
, pp. 36-41
-
-
Waller, D.K.1
Anderson, J.L.2
Lorey, F.3
Cunningham, G.C.4
-
2
-
-
0034776299
-
Thyroid dysgenesis caused by PAX8 mutation: The hypermutability with CpG dinucleotides at codon 31
-
Komatsu M, Takahashi T, Takahashi I, Nakamura M, Takahashi I, Takada G. Thyroid dysgenesis caused by PAX8 mutation: the hypermutability with CpG dinucleotides at codon 31. J Pediatr. 2001;139:597-599
-
(2001)
J Pediatr
, vol.139
, pp. 597-599
-
-
Komatsu, M.1
Takahashi, T.2
Takahashi, I.3
Nakamura, M.4
Takahashi, I.5
Takada, G.6
-
3
-
-
0026968920
-
Comparison of epidemiological data on congenital hypothyroidism in Europe with those of other parts in the world
-
Toublanc JE. Comparison of epidemiological data on congenital hypothyroidism in Europe with those of other parts in the world. Horm Res. 1992;38:230-235
-
(1992)
Horm Res
, vol.38
, pp. 230-235
-
-
Toublanc, J.E.1
-
4
-
-
0027618636
-
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;91:1203-1209
-
(1993)
Pediatrics
, vol.91
, pp. 1203-1209
-
-
-
5
-
-
84964131415
-
Benefits and risks of thyroid scintigraphy in congenital primary hypothyroidism
-
Jasko IA, dos Remedios LV, Schoen EJ. Benefits and risks of thyroid scintigraphy in congenital primary hypothyroidism. J Nucl Med Technol. 1984;12:167-169
-
(1984)
J Nucl Med Technol
, vol.12
, pp. 167-169
-
-
Jasko, I.A.1
Dos Remedios, L.V.2
Schoen, E.J.3
-
6
-
-
0023224402
-
Heterogeneity of congenital primary hypothyroidism: The importance of thyroid scintigraphy
-
Schoen EJ, dos Remedios LV, Backstrom M. Heterogeneity of congenital primary hypothyroidism: the importance of thyroid scintigraphy. J Perinat Med. 1987;15:137-142
-
(1987)
J Perinat Med
, vol.15
, pp. 137-142
-
-
Schoen, E.J.1
Dos Remedios, L.V.2
Backstrom, M.3
-
7
-
-
0034455808
-
The hypothalamic-pituitary-thyroid negative feedback control axis in children with treated congenital hypothyroidism
-
Fisher DA, Schoen EJ, La Franchi S, et al. The hypothalamic-pituitary- thyroid negative feedback control axis in children with treated congenital hypothyroidism. J Clin Endocrinol Metab. 2000;85:2722-2727
-
(2000)
J Clin Endocrinol Metab
, vol.85
, pp. 2722-2727
-
-
Fisher, D.A.1
Schoen, E.J.2
La Franchi, S.3
-
8
-
-
0028888593
-
Brief report: Resistance to thyrotropin caused by mutations in the thyrotropin-receptor gene
-
Sunthornthepvarakul T, Gottschalk ME, Hayashi Y, Refetoff S. Brief report: resistance to thyrotropin caused by mutations in the thyrotropin-receptor gene. N Engl J Med. 1995;332:155-160
-
(1995)
N Engl J Med
, vol.332
, pp. 155-160
-
-
Sunthornthepvarakul, T.1
Gottschalk, M.E.2
Hayashi, Y.3
Refetoff, S.4
-
9
-
-
0030901754
-
Congenital hypothyroidism caused by mutations in the thyrotropin-receptor gene
-
Biebermann H, Gruters A, Schoneberg T, Gudermann T. Congenital hypothyroidism caused by mutations in the thyrotropin-receptor gene. N Engl J Med. 1997;336:1390-1391
-
(1997)
N Engl J Med
, vol.336
, pp. 1390-1391
-
-
Biebermann, H.1
Gruters, A.2
Schoneberg, T.3
Gudermann, T.4
-
10
-
-
0030839127
-
Absence of mutations in the gene encoding thyroid transcription factor-1 (TTF-1) in patients with thyroid dysgenesis
-
Perna MG, Civitareale D, De Filippis V, Sacco M, Cisternino C, Tassi V. Absence of mutations in the gene encoding thyroid transcription factor-1 (TTF-1) in patients with thyroid dysgenesis. Thyroid. 1997;7:377-381
-
(1997)
Thyroid
, vol.7
, pp. 377-381
-
-
Perna, M.G.1
Civitareale, D.2
De Filippis, V.3
Sacco, M.4
Cisternino, C.5
Tassi, V.6
-
11
-
-
17344374131
-
PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis
-
Macchia PE, Lapi P, Krude H, et al. PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis. Nat Genet. 1998;19:83-86
-
(1998)
Nat Genet
, vol.19
, pp. 83-86
-
-
Macchia, P.E.1
Lapi, P.2
Krude, H.3
-
12
-
-
0037063119
-
Inactivating mutations in the gene for thyroid oxidase 2 (THOX2) and congenital hypothyroidism
-
Moreno JC, Bikker H, Kempers MJ, et al. Inactivating mutations in the gene for thyroid oxidase 2 (THOX2) and congenital hypothyroidism. N Engl J Med. 2002;347:95-102
-
(2002)
N Engl J Med
, vol.347
, pp. 95-102
-
-
Moreno, J.C.1
Bikker, H.2
Kempers, M.J.3
-
13
-
-
0031777309
-
Follicular cells of the thyroid gland require Pax8 gene function
-
Mansouri A, Chowdhury K, Gruss P. Follicular cells of the thyroid gland require Pax8 gene function. Nat Genet. 1998;19:87-90
-
(1998)
Nat Genet
, vol.19
, pp. 87-90
-
-
Mansouri, A.1
Chowdhury, K.2
Gruss, P.3
-
14
-
-
0032030895
-
Hox group 3 paralogs regulate the development and migration of the thymus, thyroid, and parathyroid glands
-
Manley NR, Capecchi MR. Hox group 3 paralogs regulate the development and migration of the thymus, thyroid, and parathyroid glands. Dev Biol. 1998;195:1-15
-
(1998)
Dev Biol
, vol.195
, pp. 1-15
-
-
Manley, N.R.1
Capecchi, M.R.2
-
15
-
-
0036371225
-
AmphiFoxE4, an amphioxus winged helix/forkhead gene encoding a protein closely related to vertebrate thyroid transcription factor-2: Expression during pharyngeal development
-
Yu JK, Holland LZ, Jamrich M, Blitz IL, Hollan ND. AmphiFoxE4, an amphioxus winged helix/forkhead gene encoding a protein closely related to vertebrate thyroid transcription factor-2: expression during pharyngeal development. Evol Dev. 2002;4:9-15
-
(2002)
Evol Dev
, vol.4
, pp. 9-15
-
-
Yu, J.K.1
Holland, L.Z.2
Jamrich, M.3
Blitz, I.L.4
Hollan, N.D.5
-
16
-
-
0033306083
-
A search for the possible molecular mechanisms of thyroid dysgenesis: Sex ratios and associated malformations
-
Devos H, Rodd C, Gagne N, Laframboise R, Van Vliet G. A search for the possible molecular mechanisms of thyroid dysgenesis: sex ratios and associated malformations. J Clin Endocrinol Metab. 1999;84:2502-2506
-
(1999)
J Clin Endocrinol Metab
, vol.84
, pp. 2502-2506
-
-
Devos, H.1
Rodd, C.2
Gagne, N.3
Laframboise, R.4
Van Vliet, G.5
-
17
-
-
0026904349
-
Birth prevalence of primary congenital hypothyroidism by sex and ethnicity
-
Lorey FW, Cunningham GC. Birth prevalence of primary congenital hypothyroidism by sex and ethnicity. Hum Biol. 1992;64:531-538
-
(1992)
Hum Biol
, vol.64
, pp. 531-538
-
-
Lorey, F.W.1
Cunningham, G.C.2
-
18
-
-
28844498053
-
-
National Market Research Department. Oakland, CA: Kaiser Permanente
-
Kaiser Permanente. National Market Research Department. Golden Gate Service Area Databook, May 2003. Oakland, CA: Kaiser Permanente; 2003
-
(2003)
Golden Gate Service Area Databook, May 2003
-
-
-
19
-
-
28844492621
-
-
National Market Research Department. Oakland, CA: Kaiser Permanente
-
Kaiser Permanente. National Market Research Department. North East Bay Service Area Databook, May 2003. Oakland, CA: Kaiser Permanente; 2003
-
(2003)
North East Bay Service Area Databook, May 2003
-
-
-
20
-
-
0035673475
-
Newborn screening for congenital hypothyroidism, Victoria, Australia, 1977-1997. Part 1: The screening programme, demography, baseline perinatal data and diagnostic classification
-
Connelly JF, Coakley JC, Gold H, et al. Newborn screening for congenital hypothyroidism, Victoria, Australia, 1977-1997. Part 1: the screening programme, demography, baseline perinatal data and diagnostic classification. J Pediatr Endocrinol Metab. 2001;14:1597-1610
-
(2001)
J Pediatr Endocrinol Metab
, vol.14
, pp. 1597-1610
-
-
Connelly, J.F.1
Coakley, J.C.2
Gold, H.3
-
21
-
-
0020000852
-
123I thyroidal uptake and scintigraphy
-
Heyman S, Crigler JF Jr, Treves S. Congenital hypothyroidism: 123I thyroidal uptake and scintigraphy. J Pediatr. 1982;101:571-574
-
(1982)
J Pediatr
, vol.101
, pp. 571-574
-
-
Heyman, S.1
Crigler Jr., J.F.2
Treves, S.3
-
22
-
-
0023956326
-
Thyroid scanning, ultrasound, and serum thyroglobulin in determining the origin of congenital hypothyroidism
-
Muir A, Daneman D, Daneman A, Ehrlich R. Thyroid scanning, ultrasound, and serum thyroglobulin in determining the origin of congenital hypothyroidism. Am J Dis Child. 1988;142:214-216
-
(1988)
Am J Dis Child
, vol.142
, pp. 214-216
-
-
Muir, A.1
Daneman, D.2
Daneman, A.3
Ehrlich, R.4
-
23
-
-
0022459846
-
Technetium 99m pertechnetate thyroid scintigraphy: Congenital hypothyroid screening
-
Wells RG, Sty JR, Duck SC. Technetium 99m pertechnetate thyroid scintigraphy: congenital hypothyroid screening. Pediatr Radiol. 1986;16:368-373
-
(1986)
Pediatr Radiol
, vol.16
, pp. 368-373
-
-
Wells, R.G.1
Sty, J.R.2
Duck, S.C.3
-
24
-
-
0019606906
-
Radiologic considerations of intensive care in the premature infant. Annual oration in honor of William Henry Neil, MD, 1924-1972
-
Singleton EB. Radiologic considerations of intensive care in the premature infant. Annual oration in honor of William Henry Neil, MD, 1924-1972. Radiology. 1981;140:291-300
-
(1981)
Radiology
, vol.140
, pp. 291-300
-
-
Singleton, E.B.1
-
25
-
-
28844468515
-
-
Washington, DC: US Department of Transportation, Federal Aviation Administration
-
Federal Aviation Administration. Advisory circular: radiation exposure of air carrier crewmembers. Washington, DC: US Department of Transportation, Federal Aviation Administration; 1990. Available at: http://ntl.bts.gov/DOCS/ Ac12052.html. Accessed October 15, 2004
-
(1990)
Advisory Circular: Radiation Exposure of Air Carrier Crewmembers
-
-
|