Detalhe da pesquisa
1.
Prolonged Bleeding After Dental Extraction Due to Decreased Serum Level of Von Willebrand Factor Caused by Untreated Profound Hypothyroidism.
J Pediatr Hematol Oncol
; 45(5): e660-e661, 2023 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36706297
2.
Proteinuria in a patient with Graves' disease: Questions.
Pediatr Nephrol
; 34(8): 1379-1381, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30843109
3.
Proteinuria in a patient with Graves' disease: Answers.
Pediatr Nephrol
; 34(8): 1383-1385, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30843111
4.
A Rare Presentation of Homozygous Pathogenic Variant in MC2R Gene with Salt-Wasting Crisis in a Neonate.
Mol Syndromol
; 15(1): 77-82, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38357256
5.
Comprehensive Insights into Pediatric Craniopharyngioma: Endocrine and Metabolic Profiles, Treatment Challenges, and Long-term Outcomes with a Multicenter Approach.
J Clin Res Pediatr Endocrinol
; 2024 Apr 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38664994
6.
Thyroid Nodules in Children and Adolescents: A Single Institution's Experience.
Turk Arch Pediatr
; 58(4): 401-406, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-37317576
7.
Left Ventricular Systolic Dysfunction Related to Adrenal Insufficiency in a Case due to Autoimmune Polyendocrine Syndrome Type 1 with a Novel Variant.
Mol Syndromol
; 14(1): 65-70, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36777707
8.
Temporary Thyroid Dysfunction and Catecholamine Excess Due to Mercury Poisoning in 6 Cases.
Turk Arch Pediatr
; 2023 Oct 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37818842
9.
Assessment of Serum Spexin Levels in Obese Adolescents with Metabolic Syndrome Antecedents: Preliminary Results.
Horm Res Paediatr
; 94(9-10): 343-352, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34839286
10.
Elevated Urinary VEGF-A, Transferrin, and Angiotensinogen Levels in Normoalbuminuric Children and Adolescents with Type 1 Diabetes: Can They Be Early Markers of Diabetic Kidney Disease?
Horm Res Paediatr
; 94(11-12): 426-432, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34915504
11.
Different clinical entities of the same mutation: a case report of three sisters with Wolfram syndrome and efficacy of dipeptidyl peptidase-4 inhibitor therapy.
J Pediatr Endocrinol Metab
; 34(8): 1049-1053, 2021 Aug 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-33882198
12.
Clinical and Genetic Characteristics of Patients with Corticosterone Methyloxidase Deficiency Type 2: Novel Mutations in CYP11B2
J Clin Res Pediatr Endocrinol
; 13(2): 232-238, 2021 06 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32539318
13.
Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome
J Clin Res Pediatr Endocrinol
; 13(3): 308-319, 2021 08 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-33565750
14.
An Unusual Presentation of Carney Complex
J Clin Res Pediatr Endocrinol
; 12(1): 117-121, 2020 03 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-31117334
15.
Two Novel Variants and One Previously Reported Variant in the Insulin Receptor Gene in Two Cases with Severe Insulin Resistance Syndrome.
Mol Syndromol
; 11(2): 90-96, 2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-32655340
16.
Two Childhood Pheochromocytoma Cases due to von Hippel-Lindau Disease, One Associated with Pancreatic Neuroendocrine Tumor: A Very Rare Manifestation
J Clin Res Pediatr Endocrinol
; 10(2): 179-182, 2018 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29022557
17.
Serum vitamin D levels during activation and remission periods of patients with juvenile idiopathic arthritis and familial Mediterranean fever.
Turk J Pediatr
; 58(2): 125-131, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27976551