-
1
-
-
33745318070
-
Update of newborn screening and therapy for congenital hypothyroidism
-
American Academy of Pediatrics, American Thyroid Association, Lawson Wilkins Pediatric Endocrine Society
-
American Academy of Pediatrics, American Thyroid Association, Lawson Wilkins Pediatric Endocrine Society: Update of newborn screening and therapy for congenital hypothyroidism. Pediatrics 2006, 117:2290-2303.
-
(2006)
Pediatrics
, vol.117
, pp. 2290-2303
-
-
-
2
-
-
34548488231
-
Neonatal Screening in Europe; the situation in 2004
-
Loeber JG: Neonatal Screening in Europe; the situation in 2004. J Inherit Metab Dis 2007, 30:430-438.
-
(2007)
J Inherit Metab Dis
, vol.30
, pp. 430-438
-
-
Loeber, J.G.1
-
3
-
-
34249338694
-
Increase in congenital hypothyroidism in New York State and United States
-
Harris K, Pass KA: Increase in congenital hypothyroidism in New York State and United States. Mol Gen Metab 2007, 91:268-277.
-
(2007)
Mol Gen Metab
, vol.91
, pp. 268-277
-
-
Harris, K.1
Pass, K.A.2
-
4
-
-
0027369699
-
Guidelines for neonatal screening programs for congenital hypothyroidism
-
ESPE Working Group on Congenital Hypothyroidism
-
ESPE Working Group on Congenital Hypothyroidism: Guidelines for neonatal screening programs for congenital hypothyroidism. Eur J Pediatr 1993, 152:974-975.
-
(1993)
Eur J Pediatr
, vol.152
, pp. 974-975
-
-
-
5
-
-
0008893892
-
Proposte di linee guida per lo screening dell'ipotiroidismo congenito
-
Antonozzi I, Baserga M, Berti T, Bucci I, et al.: Proposte di linee guida per lo screening dell'ipotiroidismo congenito. Riv Ital Pediatr (IJP) 2000, 26:731-736.
-
(2000)
Riv Ital Pediatr (IJP)
, vol.26
, pp. 731-736
-
-
Antonozzi, I.1
Baserga, M.2
Berti, T.3
Bucci, I.4
-
6
-
-
0027517385
-
The National Register of infants with congenital hypothyroidism detected by neonatal screening
-
Sorcini M, Balestrazzi P, Grandolfo ME, Carta S, Giovannelli G: The National Register of infants with congenital hypothyroidism detected by neonatal screening. J Endocrinol Invest 1993, 16:573-577.
-
(1993)
J Endocrinol Invest
, vol.16
, pp. 573-577
-
-
Sorcini, M.1
Balestrazzi, P.2
Grandolfo, M.E.3
Carta, S.4
Giovannelli, G.5
-
7
-
-
34547790883
-
High risk of congenital hypothyroidism in multiple pregnancies
-
The Study Group for Congenital Hypothyroidism
-
Olivieri A, Medda E, De Angelis S, Valensise H, De Felice M, Fazzini C, Cascino I, Cordeddu V, Sorcini M, Stazi MA, The Study Group for Congenital Hypothyroidism: High risk of congenital hypothyroidism in multiple pregnancies. J Clin Endocrinol Metab 2007, 92:3141-3147.
-
(2007)
J Clin Endocrinol Metab
, vol.92
, pp. 3141-3147
-
-
Olivieri, A.1
Medda, E.2
De Angelis, S.3
Valensise, H.4
De Felice, M.5
Fazzini, C.6
Cascino, I.7
Cordeddu, V.8
Sorcini, M.9
Stazi, M.A.10
-
8
-
-
0037252430
-
Changes in twinning rate: Italy 1950 - 1996
-
Astolfi P, Ulizzi L, Zonta LA: Changes in twinning rate: Italy 1950 - 1996. Hum Reprod 2003, 1:207-211.
-
(2003)
Hum Reprod
, vol.1
, pp. 207-211
-
-
Astolfi, P.1
Ulizzi, L.2
Zonta, L.A.3
-
9
-
-
0030010798
-
What proportion of multiple births are due to ovulation induction? A register-based study in Italy
-
Corchia C, Mastroiacovo P, Lanni R, Mannazzu R, Curro V, Fabris C: What proportion of multiple births are due to ovulation induction? A register-based study in Italy. Am J Pub Health 1996, 86:851-854.
-
(1996)
Am J Pub Health
, vol.86
, pp. 851-854
-
-
Corchia, C.1
Mastroiacovo, P.2
Lanni, R.3
Mannazzu, R.4
Curro, V.5
Fabris, C.6
-
10
-
-
0037626139
-
Trends in multiple births conceived using assisted reproductive technology, United States, 1997-2000
-
Reynolds MA, Schieve LA, Martin JA, Jeng G, Macaluso M: Trends in multiple births conceived using assisted reproductive technology, United States, 1997-2000. Pediatrics 2003, 111:1159-1162.
-
(2003)
Pediatrics
, vol.111
, pp. 1159-1162
-
-
Reynolds, M.A.1
Schieve, L.A.2
Martin, J.A.3
Jeng, G.4
Macaluso, M.5
-
11
-
-
0028073061
-
Incidence of congenital malformations in congenital hypothyroiidsm
-
Cassio A, Tatò L, Colli C, Spolettini E, Costantini E, Cacciari E: Incidence of congenital malformations in congenital hypothyroiidsm. Screening 1994, 3:125-130.
-
(1994)
Screening
, vol.3
, pp. 125-130
-
-
Cassio, A.1
Tatò, L.2
Colli, C.3
Spolettini, E.4
Costantini, E.5
Cacciari, E.6
-
13
-
-
18244368524
-
A population-based study on the frequency of additional congenital malformations in infants with congenital hypothyroidism: Data from the Italian Registry for Congenital Hypothyroidism (1991- 1998)
-
The Study Group for Congenital Hypothyroidism
-
Olivieri A, Stazi MA, Mastroiacovo P, Fazzini C, Medda E, Spagnolo A, De Angelis S, Grandolfo ME, Taruscio D, Cordeddu V, Sorcini M, The Study Group for Congenital Hypothyroidism: A population-based study on the frequency of additional congenital malformations in infants with congenital hypothyroidism: data from the Italian Registry for Congenital Hypothyroidism (1991- 1998). J Clin Endocrinol Metab 2002, 87:557-562.
-
(2002)
J Clin Endocrinol Metab
, vol.87
, pp. 557-562
-
-
Olivieri, A.1
Stazi, M.A.2
Mastroiacovo, P.3
Fazzini, C.4
Medda, E.5
Spagnolo, A.6
De Angelis, S.7
Grandolfo, M.E.8
Taruscio, D.9
Cordeddu, V.10
Sorcini, M.11
-
15
-
-
0032479573
-
Congenital heart disease caused by mutations in the transcription factor NKX2.5
-
Schott JJ, Benson DW, Basson CT, Silberbach GM, Moak JP, Maron BJ, Seidman CE, Seidman JG: Congenital heart disease caused by mutations in the transcription factor NKX2.5. Science 1998, 281:108-111.
-
(1998)
Science
, vol.281
, pp. 108-111
-
-
Schott, J.J.1
Benson, D.W.2
Basson, C.T.3
Silberbach, G.M.4
Moak, J.P.5
Maron, B.J.6
Seidman, C.E.7
Seidman, J.G.8
-
16
-
-
33646034932
-
Missense mutation in the transcription factor NKX2.5: A novel molecular event in the pathogenesis of thyroid dysgenesis
-
Dentice M, Cordeddu V, Rosica A, Ferrara AM, Santarpia L, Salvatore D, et al.: Missense mutation in the transcription factor NKX2.5: a novel molecular event in the pathogenesis of thyroid dysgenesis. J Clin Endocrinol Metab 2006, 91:1428-1433.
-
(2006)
J Clin Endocrinol Metab
, vol.91
, pp. 1428-1433
-
-
Dentice, M.1
Cordeddu, V.2
Rosica, A.3
Ferrara, A.M.4
Santarpia, L.5
Salvatore, D.6
-
17
-
-
27844536962
-
A mouse model demonstrates a multigenic origin of congenital hypothyroidism
-
Amendola E, De Luca P, Macchia PE, Terracciano D, Rosica A, Chiappetta G, et al.: A mouse model demonstrates a multigenic origin of congenital hypothyroidism. Endocrinology 2005, 146:5038-5047.
-
(2005)
Endocrinology
, vol.146
, pp. 5038-5047
-
-
Amendola, E.1
De Luca, P.2
Macchia, P.E.3
Terracciano, D.4
Rosica, A.5
Chiappetta, G.6
-
18
-
-
21644489783
-
Molecular mechanisms of thyroid dysgenesis
-
Polak M, Sura-Trueba S, Chanty A, Szinnai G, Carrè A, Castanet M: Molecular mechanisms of thyroid dysgenesis. Horm Res 2004, 62:14-21.
-
(2004)
Horm Res
, vol.62
, pp. 14-21
-
-
Polak, M.1
Sura-Trueba, S.2
Chanty, A.3
Szinnai, G.4
Carrè, A.5
Castanet, M.6
-
19
-
-
39049092782
-
Biallelic inactivation of the dual oxidase maturation factor 2 (DUOXA2) gene as a novel cause of congenital hypothyroidism
-
Zamproni I, Grasberger H, Cortinovis F, Vigone MC, Chiumello G, Mora S, et al.: Biallelic inactivation of the dual oxidase maturation factor 2 (DUOXA2) gene as a novel cause of congenital hypothyroidism. J Clin Endocrinol Metab 2008, 93:605-610.
-
(2008)
J Clin Endocrinol Metab
, vol.93
, pp. 605-610
-
-
Zamproni, I.1
Grasberger, H.2
Cortinovis, F.3
Vigone, M.C.4
Chiumello, G.5
Mora, S.6
-
20
-
-
57349097244
-
Molecular characterization of iodotyrosine dehalogenase deficiency in patients with hypothyroidism
-
Afink G, Kulik W, Overmars H, de Randamie J, Veenboer T, van Cruchten A, et al.: Molecular characterization of iodotyrosine dehalogenase deficiency in patients with hypothyroidism. J Clin Endocrinol Metab 2008, 93(12):4894-4901
-
(2008)
J Clin Endocrinol Metab
, vol.93
, Issue.12
, pp. 4894-4901
-
-
Afink, G.1
Kulik, W.2
Overmars, H.3
De Randamie, J.4
Veenboer, T.5
Van Cruchten, A.6
-
21
-
-
29644435607
-
Risk factors for congenital hypothyroidism: Results of a population case-control study (1997-2003)
-
Medda E, Olivieri A, Stazi MA, Grandolfo ME, Fazzini C, Baserga M, et al.: Risk factors for congenital hypothyroidism: results of a population case-control study (1997-2003). Eur J Endocrinol 2005, 153:765-773.
-
(2005)
Eur J Endocrinol
, vol.153
, pp. 765-773
-
-
Medda, E.1
Olivieri, A.2
Stazi, M.A.3
Grandolfo, M.E.4
Fazzini, C.5
Baserga, M.6
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