Detalhe da pesquisa
1.
Thyroid function, glycemic control, and diabetic nephropathy in patients with type 2 diabetes over 24 months: prospective observational study.
BMC Endocr Disord
; 23(1): 146, 2023 Jul 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37430240
2.
Isolated ACTH deficiency following immunization with the BNT162b2 SARS-CoV-2 vaccine: a case report.
BMC Endocr Disord
; 22(1): 185, 2022 Jul 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-35854260
3.
Hypopituitarism and cranial nerve involvement mimicking Tolosa-Hunt syndrome as the initially presenting feature of diffuse large B-cell lymphoma: a case report.
BMC Endocr Disord
; 22(1): 65, 2022 Mar 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-35287660
4.
Predictive and sensitive biomarkers for thyroid dysfunctions during treatment with immune-checkpoint inhibitors.
Cancer Sci
; 111(5): 1468-1477, 2020 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-32086984
5.
Autoimmune polyglandular syndrome type 2 and autoimmune hepatitis with thymoma-associated myasthenia gravis: case report.
BMC Endocr Disord
; 20(1): 47, 2020 Apr 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32264857
6.
Expression of unfolded protein response markers in the pheochromocytoma with Waardenburg syndrome: a case report.
BMC Endocr Disord
; 20(1): 90, 2020 Jun 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-32571297
7.
The influence of thyroid autoimmunity on pregnancy outcome in infertile women: a prospective study.
Endocr J
; 67(8): 859-868, 2020 Aug 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-32336697
8.
False-positive staining of thyroglobulin distinguished from mixed medullary and follicular thyroid carcinoma by duplex in situ hybridization.
Endocr J
; 67(10): 1007-1017, 2020 Oct 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-32522910
9.
MSH6/2 and PD-L1 Expressions Are Associated with Tumor Growth and Invasiveness in Silent Pituitary Adenoma Subtypes.
Int J Mol Sci
; 21(8)2020 Apr 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-32325698
10.
Comparative analysis of human leucocyte antigen between idiopathic and anti-PD-1 antibody induced isolated adrenocorticotropic hormone deficiency: A pilot study.
Clin Endocrinol (Oxf)
; 91(6): 786-792, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31468541
11.
Atypical pituitary adenoma with MEN1 somatic mutation associated with abnormalities of DNA mismatch repair genes; MLH1 germline mutation and MSH6 somatic mutation.
Endocr J
; 64(9): 895-906, 2017 Sep 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-28701629
12.
Profiling of Unfolded Protein Response Markers and Effect of IRE1α-specific Inhibitor in Pituitary Neuroendocrine Tumor.
Endocrinology
; 165(4)2024 Feb 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38289718
13.
Effect of SARS-CoV-2 BNT162b2 mRNA vaccine on thyroid autoimmunity: A twelve-month follow-up study.
Front Endocrinol (Lausanne)
; 14: 1058007, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36777341
14.
Autosomal Dominant Hypocalcemia With Atypical Urine Findings Accompanied by Novel CaSR Gene Mutation and VitD Deficiency.
J Endocr Soc
; 5(3): bvaa190, 2021 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33506158
15.
Early detection of euglycemic ketoacidosis during thoracic surgery associated with empagliflozin in a patient with type 2 diabetes: A case report.
J Diabetes Investig
; 12(4): 664-667, 2021 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-32686282
16.
Thyroid storm with delayed hyperbilirubinemia and severe heart failure: indication and contraindication of plasma exchange.
Endocrinol Diabetes Metab Case Rep
; 20202020 Sep 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33434181
17.
Head and Neck Paraganglioma Atypically Carrying a Succinate Dehydrogenase Subunit B Mutation (L157X).
Intern Med
; 59(9): 1167-1171, 2020 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32023584
18.
Nicotinic acetylcholine receptor signaling regulates inositol-requiring enzyme 1α activation to protect ß-cells against terminal unfolded protein response under irremediable endoplasmic reticulum stress.
J Diabetes Investig
; 11(4): 801-813, 2020 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-31925927
19.
Neonatal diabetes caused by the heterozygous Pro1198Leu mutation in the ABCC8 gene in a male infant: 6-year clinical course.
J Diabetes Investig
; 11(2): 502-505, 2020 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-31390154
20.
Identification of a compound heterozygous inactivating ABCC8 gene mutation responsible for young-onset diabetes with exome sequencing.
J Diabetes Investig
; 11(2): 333-336, 2020 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-31479591