Detalhe da pesquisa
1.
Similar age-dependent levothyroxine requirements of schoolchildren with congenital or acquired hypothyroidism.
Eur J Pediatr
; 175(6): 869-72, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26856857
2.
Severe aldosterone synthase deficiency in a nine-day old Lebanese boy: the importance of functional studies to establish pathogenicity of seemingly benign variants in CYP11B2.
Horm Res Paediatr
; 2024 Feb 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38316111
3.
A search for variables predicting cortisol response to low-dose corticotropin stimulation following supraphysiological doses of glucocorticoids.
J Pediatr
; 163(2): 484-8, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23414662
4.
Thyroid function from birth to adolescence in Prader-Willi syndrome.
J Pediatr
; 163(3): 800-5, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23623517
5.
Whole-Exome Sequencing in Congenital Hypothyroidism Due to Thyroid Dysgenesis.
Thyroid
; 32(5): 486-495, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35272499
6.
Are guidelines for glucocorticoid coverage in adrenal insufficiency currently followed?
J Pediatr
; 158(3): 492-498.e1, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21035819
7.
Severe Congenital Hypothyroidism Due to a Novel Deep Intronic Mutation in the TSH Receptor Gene Causing Intron Retention.
J Endocr Soc
; 5(3): bvaa183, 2021 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33506157
8.
Non-immune goiter and hypothyroidism in a 19-week fetus: a plea for conservative treatment.
J Pediatr
; 156(6): 1026-1029, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20304420
9.
Lethal respiratory failure and mild primary hypothyroidism in a term girl with a de novo heterozygous mutation in the TITF1/NKX2.1 gene.
J Clin Endocrinol Metab
; 94(1): 197-203, 2009 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-18957494
10.
A novel presentation of diffuse lung disease caused by congenital hypothyroidism.
J Pediatr
; 155(4): 593-5, 2009 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-19773006
11.
Pediatric thyroidectomy: Favorable outcomes can be achieved by a multidisciplinary team of pediatric providers.
J Pediatr Surg
; 54(3): 527-530, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-30054058
12.
Wide Spectrum of DUOX2 Deficiency: From Life-Threatening Compressive Goiter in Infancy to Lifelong Euthyroidism.
Thyroid
; 29(7): 1018-1022, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31030636
13.
Pseudodominant inheritance of goitrous congenital hypothyroidism caused by TPO mutations: molecular and in silico studies.
J Clin Endocrinol Metab
; 93(2): 627-33, 2008 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18029453
14.
Prophylactic thyroidectomies in MEN2 syndrome: Management and outcomes.
J Pediatr Surg
; 53(2): 283-285, 2018 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-29336779
15.
Isolated autosomal dominant growth hormone deficiency: stimulating mutant GH-1 gene expression drives GH-1 splice-site selection, cell proliferation, and apoptosis.
Endocrinology
; 148(1): 45-53, 2007 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-17038549
16.
Random variability in congenital hypothyroidism from thyroid dysgenesis over 16 years in Québec.
J Clin Endocrinol Metab
; 92(8): 3158-61, 2007 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-17504897
17.
Possible non-Mendelian mechanisms of thyroid dysgenesis.
Endocr Dev
; 10: 29-42, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17684388
18.
From Bioinactive ACTH to ACTH Antagonist: The Clinical Perspective.
Front Endocrinol (Lausanne)
; 8: 17, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28228747
19.
Continuous Subcutaneous Insulin Infusion in Children: A Pilot Study Validating a Protocol to Avoid Hypoglycemia at Initiation.
Front Endocrinol (Lausanne)
; 8: 84, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28484424
20.
Disorders of thyroid morphogenesis.
Best Pract Res Clin Endocrinol Metab
; 31(2): 143-159, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28648504