Detalles de la búsqueda
1.
Sesquiterpene Lactones from Calea pinnatifida: Absolute Configuration and Structural Requirements for Antitumor Activity.
Molecules
; 25(13)2020 Jun 30.
Artículo
Inglés
| MEDLINE | ID: mdl-32630070
2.
Congenital hypothyroidism and thyroid cancer.
Endocr Relat Cancer
; 28(9): R217-R230, 2021 09 01.
Artículo
Inglés
| MEDLINE | ID: mdl-34378152
3.
Association of low sodium-iodide symporter messenger ribonucleic acid expression in malignant thyroid nodules with increased intracellular protein staining.
J Clin Endocrinol Metab
; 93(10): 4141-5, 2008 Oct.
Artículo
Inglés
| MEDLINE | ID: mdl-18628528
4.
Phenotypic variation among four family members with congenital hypothyroidism caused by two distinct thyroglobulin gene mutations.
Thyroid
; 18(7): 783-6, 2008 Jul.
Artículo
Inglés
| MEDLINE | ID: mdl-18631008
5.
HOPX homeobox methylation in differentiated thyroid cancer and its clinical relevance.
Endocr Connect
; 7(12): 1333-1342, 2018 Dec.
Artículo
Inglés
| MEDLINE | ID: mdl-30400039
6.
A novel system of genetic transformation allows multiple integrations of a desired gene in Saccharomyces cerevisiae chromosomes.
J Microbiol Methods
; 67(3): 437-45, 2006 Dec.
Artículo
Inglés
| MEDLINE | ID: mdl-16831478
7.
Human recombinant TSH preceding a therapeutic dose of radioiodine for multinodular goiters has no significant effect in the surge of TSH-receptor and TPO antibodies.
Thyroid
; 15(2): 134-9, 2005 Feb.
Artículo
Inglés
| MEDLINE | ID: mdl-15753672
8.
Thyroperoxidase gene mutations in congenital goitrous hypothyroidism with total and partial iodide organification defect.
Thyroid
; 13(12): 1145-51, 2003 Dec.
Artículo
Inglés
| MEDLINE | ID: mdl-14751036
9.
Hypermethylation of a New Distal Sodium/Iodide Symporter (NIS) enhancer (NDE) is associated with reduced NIS expression in thyroid tumors.
J Clin Endocrinol Metab
; 99(6): E944-52, 2014 Jun.
Artículo
Inglés
| MEDLINE | ID: mdl-24432988
10.
Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defect.
Arq Bras Endocrinol Metabol
; 54(8): 732-7, 2010 Nov.
Artículo
Inglés
| MEDLINE | ID: mdl-21340161
11.
Mutations of the thyroglobulin gene and its relevance to thyroid disorders.
Curr Opin Endocrinol Diabetes Obes
; 16(5): 373-8, 2009 Oct.
Artículo
Inglés
| MEDLINE | ID: mdl-19633549
12.
High prevalence of side effects after recombinant human thyrotropin-stimulated radioiodine treatment with 30 mCi in patients with multinodular goiter and subclinical/clinical hyperthyroidism.
Thyroid
; 19(9): 945-51, 2009 Sep.
Artículo
Inglés
| MEDLINE | ID: mdl-19678745
13.
The prevalence of thyroid dysfunction in elderly cardiology patients with mild excessive iodine intake in the urban area of São Paulo.
Clinics (Sao Paulo)
; 64(2): 135-42, 2009.
Artículo
Inglés
| MEDLINE | ID: mdl-19219319
14.
The p.A2215D thyroglobulin gene mutation leads to deficient synthesis and secretion of the mutated protein and congenital hypothyroidism with wide phenotype variation.
J Clin Endocrinol Metab
; 94(8): 2938-44, 2009 Aug.
Artículo
Inglés
| MEDLINE | ID: mdl-19509106
15.
A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation.
Arq Bras Endocrinol Metabol
; 52(8): 1337-44, 2008 Nov.
Artículo
Inglés
| MEDLINE | ID: mdl-19169491
16.
Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defect / Mutação monoalélica no gene da tireoperoxidase em paciente com hipotireoidismo congênito com defeito total de incorporação de iodeto
Arq. bras. endocrinol. metab
; 54(8): 732-737, Nov. 2010. ilus, tab
Artículo
Inglés
| LILACS | ID: lil-578348
17.
The prevalence of thyroid dysfunction in elderly cardiology patients with mild excessive iodine intake in the urban area of São Paulo
Clinics
; 64(2): 135-142, 2009. graf, tab
Artículo
Inglés
| LILACS | ID: lil-505375
18.
Administration of a single dose of recombinant human thyrotrophin enhances the efficacy of radioiodine treatment of large compressive multinodular goitres.
Clin Endocrinol (Oxf)
; 60(3): 300-8, 2004 Mar.
Artículo
Inglés
| MEDLINE | ID: mdl-15008994
19.
A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation / Análise molecular e acompanhamento a longo prazo de dois irmãos com hipotireoidismo congênito portadores da mutação intrônica IVS30+1G>T no gene da tireoglobulina
Arq. bras. endocrinol. metab
; 52(8): 1337-1344, Nov. 2008. ilus, graf, tab
Artículo
Inglés
| LILACS | ID: lil-503302
20.
Prolonged follow-up of multinodular goitre patients treated with radioiodine preceded or not by human recombinant TSH.
Clin Endocrinol (Oxf)
; 64(4): 474, 2006 Apr.
Artículo
Inglés
| MEDLINE | ID: mdl-16584523