Detalhe da pesquisa
1.
Cochlear dysfunction evidenced by reduction of amplitude of otoacoustic responses in patients with congenital hypothyroidism.
Int J Pediatr Otorhinolaryngol
; 122: 12-17, 2019 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-30928865
2.
Association between BRAF (V600E) mutation and clinicopathological features of papillary thyroid carcinoma: a Brazilian single-centre case series.
Arch Endocrinol Metab
; 63(2): 97-106, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30916170
3.
Mutation screening in the genes PAX-8, NKX2-5, TSH-R, HES-1 in cohort of 63 Brazilian children with thyroid dysgenesis.
Arch Endocrinol Metab
; 62(4): 466-471, 2018 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-30304112
4.
The c.63A>G polymorphism in the NKX2.5 gene is associated with thyroid hypoplasia in children with thyroid dysgenesis.
Arch Endocrinol Metab
; 59(6): 562-7, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26421664
5.
Iodine nutritional status in Brazil: a meta-analysis of all studies performed in the country pinpoints to an insufficient evaluation and heterogeneity.
Arch Endocrinol Metab
; 59(1): 13-22, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25926109
6.
An international survey of screening and management of hypothyroidism during pregnancy in Latin America.
Arq Bras Endocrinol Metabol
; 58(9): 906-11, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25627045
7.
Association between BRAF (V600E) mutation and clinicopathological features of papillary thyroid carcinoma: a Brazilian single-centre case series
Arch. endocrinol. metab. (Online)
; 63(2): 97-106, Mar.-Apr. 2019. tab, graf
Artigo
em Inglês
| LILACS | ID: biblio-1001222
8.
Mutation screening in the genes PAX-8, NKX2-5, TSH-R, HES-1 in cohort of 63 Brazilian children with thyroid dysgenesis
Arch. endocrinol. metab. (Online)
; 62(4): 466-471, July-Aug. 2018. tab, graf
Artigo
em Inglês
| LILACS | ID: biblio-950085
9.
The c.63A>G polymorphism in the NKX2.5 gene is associated with thyroid hypoplasia in children with thyroid dysgenesis
Arch. endocrinol. metab. (Online)
; 59(6): 562-567, Dec. 2015. tab, graf
Artigo
em Inglês
| LILACS | ID: lil-767919
10.
Iodine nutritional status in Brazil: a meta-analysis of all studies performed in the country pinpoints to an insufficient evaluation and heterogeneity
Arch. endocrinol. metab. (Online)
; 59(1): 13-22, 02/2015. tab, graf
Artigo
em Inglês
| LILACS | ID: lil-746444
11.
An international survey of screening and management of hypothyroidism during pregnancy in Latin America / Uma avaliação internacional do rastreio e manejo do hipotireoidismo durante a gestação na América Latina
Arq. bras. endocrinol. metab
; 58(9): 906-911, 12/2014. tab, graf
Artigo
em Inglês
| LILACS | ID: lil-732193
12.
Estudo clínico, genético e molecular de pacientes com Disgenesia Tireoidiana
Salvador; s.n; 2016. 105 p. ilus.
Tese
em Português
| LILACS | ID: biblio-870325
13.
Estudo clínico, genético e molecular de pacientes com Disgenesia Tireoidiana
Tese
em Português
| Arca: Repositório institucional da Fiocruz | ID: arc-14834
14.
Iodine nutritional status in Brazil: a meta-analysis of all studies performed in the country pinpoints to an insufficient evaluation and heterogeneity
Artigo
em Inglês
| Arca: Repositório institucional da Fiocruz | ID: arc-24747
15.
Extreme phenotypic variability of thyroid dysgenesis in six new cases of congenital hypothyroidism due to PAX8 gene loss-of-function mutations
Artigo
em Inglês
| Arca: Repositório institucional da Fiocruz | ID: arc-19036