Detalhe da pesquisa
1.
Differentiated Thyroid Cancer in Children: Prevalence and Predictors in a Large Cohort with Thyroid Nodules Followed Prospectively.
J Pediatr
; 167(1): 199-201, 2015 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-26117640
2.
Congenital goitrous hypothyroidism: mutation analysis in the thyroid peroxidase gene.
Clin Endocrinol (Oxf)
; 76(4): 568-76, 2012 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-21981063
3.
Differentiated thyroid carcinoma: presentation and follow-up in children and adolescents.
J Pediatr Endocrinol Metab
; 24(9-10): 743-8, 2011.
Artigo
Inglês
| MEDLINE | ID: mdl-22145467
4.
Molecular analysis of congenital goitres with hypothyroidism caused by defective thyroglobulin synthesis. Identification of a novel c.7006C>T [p.R2317X] mutation and expression of minigenes containing nonsense mutations in exon 7.
Clin Endocrinol (Oxf)
; 72(1): 112-21, 2010 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-19438905
5.
17alpha-hydroxyprogesterone and cortisol serum levels in neonates and young children: influence of age, gestational age, gender and methodological procedures.
J Pediatr Endocrinol Metab
; 23(1-2): 121-32, 2010.
Artigo
Inglês
| MEDLINE | ID: mdl-20432815
6.
Genotyping of resistance to thyroid hormone in South American population. Identification of seven novel missense mutations in the human thyroid hormone receptor beta gene.
Mol Cell Probes
; 23(3-4): 148-53, 2009.
Artigo
Inglês
| MEDLINE | ID: mdl-19268523
7.
Thyroid disorders of neonates born to mothers with Graves' disease.
J Pediatr Endocrinol Metab
; 22(6): 547-53, 2009 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-19694202
8.
Recurrence of the p.R277X/p.R1511X compound heterozygous mutation in the thyroglobulin gene in unrelated families with congenital goiter and hypothyroidism: haplotype analysis using intragenic thyroglobulin polymorphisms.
J Endocrinol
; 195(1): 167-77, 2007 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-17911408
9.
Pilot Neonatal Screening Program for Central Congenital Hypothyroidism: Evidence of Significant Detection.
Horm Res Paediatr
; 88(3-4): 274-280, 2017.
Artigo
Inglês
| MEDLINE | ID: mdl-28898885
10.
[Transient congenital hypothyroidism due to biallelic defects of DUOX2 gene. Two clinical cases]. / Hipotiroidismo congénito transitorio por defectos bialélicos del gen DUOX2. Dos casos clínicos.
Arch Argent Pediatr
; 115(3): e162-e165, 2017 06 01.
Artigo
Espanhol
| MEDLINE | ID: mdl-28504502
11.
Efficacy of congenital hypothyroidism neonatal screening in preterms less than 32 weeks of gestational age: more evidence.
J Pediatr Endocrinol Metab
; 18(4): 373-7, 2005 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-15844471
12.
Five novel inactivating mutations in the thyroid peroxidase gene responsible for congenital goiter and iodide organification defect.
Hum Mutat
; 22(3): 259, 2003 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-12938097
13.
Congenital secondary hypothyroidism due to a mutation C105Vfs114X thyrotropin-beta mutation: genetic study of five unrelated families from Switzerland and Argentina.
Thyroid
; 13(6): 553-9, 2003 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-12930599
14.
Pediatric Graves' disease: outcome and treatment.
J Pediatr Endocrinol Metab
; 16(9): 1249-55, 2003 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-14714747
15.
Prevalence and etiology of congenital hypothyroidism detected through an argentine neonatal screening program (1997-2010).
Horm Res Paediatr
; 80(3): 185-92, 2013.
Artigo
Inglês
| MEDLINE | ID: mdl-24008435
16.
NoÌdulos tiroideos en pediatriÌa: predictores de malignidad / Pediatric thyroid nodules: predictors of malignancy
Rev. Hosp. Niños B.Aires
; 60(270): 223-229, sept. 2018.
Artigo
Espanhol
| LILACS | ID: biblio-998455
17.
New insights into thyroglobulin gene: molecular analysis of seven novel mutations associated with goiter and hypothyroidism.
Mol Cell Endocrinol
; 365(2): 277-91, 2013 Jan 30.
Artigo
Inglês
| MEDLINE | ID: mdl-23164529
18.
Severe congenital non-autoimmune hyperthyroidism associated to a mutation in the extracellular domain of thyrotropin receptor gene.
Arq Bras Endocrinol Metabol
; 56(8): 513-8, 2012 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-23295291
19.
Variable clinical presentation and outcome in pediatric patients with resistance to thyroid hormone (RTH).
Endocrine
; 41(1): 130-7, 2012 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-21870171
20.
Hipotiroidismo congénito transitorio por defectos bialélicos del genDUOX2. Dos casos clínicos / Transient congenital hypothyroidism due to biallelic defects of DUOX2 gene. Two clinical cases
Arch. argent. pediatr
; 115(3): 162-165, jun. 2017. ilus
Artigo
Espanhol
| LILACS, BINACIS | ID: biblio-887328