181 related articles for article (PubMed ID: 23326768)
41. 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; Burroni M; Cacciari E; Calaciura F; Cassio A; Chiovato L; Costa P; Leonardi D; Martucci M; Moschini L; Pagliardini S; Parlato G; Pignero A; Pinchera A; Sala D; Sava L; Stoppioni V; Tancredi F; Valentini F; Vigneri R; Sorcini M
Eur J Endocrinol; 2005 Dec; 153(6):765-73. PubMed ID: 16322381
[TBL] [Abstract][Full Text] [Related]
42. Additional phenotypic abnormalities with presence of cysts within the empty thyroid area in patients with congenital hypothyroidism with thyroid dysgenesis.
Marinovic D; Garel C; Czernichow P; Léger J
J Clin Endocrinol Metab; 2003 Mar; 88(3):1212-6. PubMed ID: 12629108
[TBL] [Abstract][Full Text] [Related]
43. [Epidemiology of congenital hypothyroidism in France: recent data].
Léger J
Biol Aujourdhui; 2019; 213(1-2):1-5. PubMed ID: 31274097
[TBL] [Abstract][Full Text] [Related]
44. Screening for mutations in transcription factors in a Czech cohort of 170 patients with congenital and early-onset hypothyroidism: identification of a novel PAX8 mutation in dominantly inherited early-onset non-autoimmune hypothyroidism.
Al Taji E; Biebermann H; Límanová Z; Hníková O; Zikmund J; Dame C; Grüters A; Lebl J; Krude H
Eur J Endocrinol; 2007 May; 156(5):521-9. PubMed ID: 17468187
[TBL] [Abstract][Full Text] [Related]
45. Thyroid scintigraphy in three-year-old children with congenital hypothyroidism in correlation with neonatal TSH.
Aminzadeh M
Endokrynol Pol; 2019; 70(1):43-48. PubMed ID: 30450534
[TBL] [Abstract][Full Text] [Related]
46. The etiologies and incidences of congenital hypothyroidism before and after neonatal TSH screening program implementation: a study in southern Thailand.
Jaruratanasirikul S; Piriyaphan J; Saengkaew T; Janjindamai W; Sriplung H
J Pediatr Endocrinol Metab; 2018 Jun; 31(6):609-617. PubMed ID: 29750647
[TBL] [Abstract][Full Text] [Related]
47. Permanent vs Transient Congenital Hypothyroidism: Assessment of Predictive Variables.
Oron T; Lazar L; Ben-Yishai S; Tenenbaum A; Yackobovitch-Gavan M; Meyerovitch J; Phillip M; Lebenthal Y
J Clin Endocrinol Metab; 2018 Dec; 103(12):4428-4436. PubMed ID: 30272179
[TBL] [Abstract][Full Text] [Related]
48. Increased Prevalence of TG and TPO Mutations in Sudanese Children With Congenital Hypothyroidism.
Bruellman RJ; Watanabe Y; Ebrhim RS; Creech MK; Abdullah MA; Dumitrescu AM; Refetoff S; Weiss RE
J Clin Endocrinol Metab; 2020 May; 105(5):1564-72. PubMed ID: 31867598
[TBL] [Abstract][Full Text] [Related]
49. [Congenital forms of hypothyroidism: study of risk factors and preventive interventions].
Olivieri A; Fazzini C; Grandolfo ME; Medda E; Stazi MA; D'Archivio M; De Angelis S; Sorcini M
Ann Ist Super Sanita; 1999; 35(2):273-82. PubMed ID: 10645661
[TBL] [Abstract][Full Text] [Related]
50. Evolution of congenital hypothyroidism in a cohort of preterm born children.
Scavone M; Giancotti L; Anastasio E; Pensabene L; Sestito S; Concolino D
Pediatr Neonatol; 2020 Dec; 61(6):629-636. PubMed ID: 32771362
[TBL] [Abstract][Full Text] [Related]
51. EPIDEMIOLOGIC CHARACTERISTICS AND RISK FACTORS FOR CONGENITAL HYPOTHYROIDISM FROM 2009 TO 2018 IN XIAMEN, CHINA.
Chen J; Lin S; Zeng G; Wang W; Lin Z; Xu C; He Y; Shi J; Zhou X; Niu C; Che L
Endocr Pract; 2020 Jun; 26(6):585-594. PubMed ID: 31968198
[No Abstract] [Full Text] [Related]
52. Thyroglobulin gene mutations and other genetic defects associated with congenital hypothyroidism.
Vono-Toniolo J; Kopp P
Arq Bras Endocrinol Metabol; 2004 Feb; 48(1):70-82. PubMed ID: 15611820
[TBL] [Abstract][Full Text] [Related]
53. Clinical genetics of defects in thyroid hormone synthesis.
Kwak MJ
Ann Pediatr Endocrinol Metab; 2018 Dec; 23(4):169-175. PubMed ID: 30599477
[TBL] [Abstract][Full Text] [Related]
54. Athyreosis, dysgenesis, and dyshormonogenesis in congenital hypothyroidism.
Topaloglu AK
Pediatr Endocrinol Rev; 2006 Aug; 3 Suppl 3():498-502. PubMed ID: 17551472
[TBL] [Abstract][Full Text] [Related]
55. DUOXS defects: Genotype-phenotype correlations.
Fugazzola L; Muzza M; Weber G; Beck-Peccoz P; Persani L
Ann Endocrinol (Paris); 2011 Apr; 72(2):82-6. PubMed ID: 21511237
[TBL] [Abstract][Full Text] [Related]
56. Prevalence and predictive factors of transient and permanent congenital hypothyroidism in Fars province, Iran.
Habib A; Shojazadeh A; Molayemat M; Habib A; Jeddi M; Arabsolghar R; Nahas M; Rahimi N; Ardekani FM
BMC Pediatr; 2021 Jun; 21(1):264. PubMed ID: 34090374
[TBL] [Abstract][Full Text] [Related]
57. Alterations of neonatal thyroid function.
Grüters A; Krude H; Biebermann H; Liesenkötter KP; Schöneberg T; Gudermann T
Acta Paediatr Suppl; 1999 Feb; 88(428):17-22. PubMed ID: 10102047
[TBL] [Abstract][Full Text] [Related]
58. Sonographic assessment of congenitally hypothyroid children in Iran.
Hoseini M; Hekmatnia A; Hashemipour M; Basiratnia R; Omidifar N; Rezazade A; Koohi R
Endokrynol Pol; 2010; 61(6):665-70. PubMed ID: 21104640
[TBL] [Abstract][Full Text] [Related]
59. A high prevalence of consanguineous and severe congenital hypothyroidism in an Iranian population.
Ordookhani A; Mirmiran P; Moharamzadeh M; Hedayati M; Azizi F
J Pediatr Endocrinol Metab; 2004 Sep; 17(9):1201-9. PubMed ID: 15506679
[TBL] [Abstract][Full Text] [Related]
60. Heterogeneous phenotype in children affected by non-autoimmune hypothyroidism: an update.
Vigone MC; Di Frenna M; Weber G
J Endocrinol Invest; 2015 Aug; 38(8):835-40. PubMed ID: 25916430
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]