Detalhe da pesquisa
1.
Clinical features, diagnosis and treatment outcomes of Cushing's disease in children: A multicenter study.
Clin Endocrinol (Oxf)
; 100(1): 19-28, 2024 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37814958
2.
Clinical Characteristics of Children with Combined Pituitary Hormone Deficiency and the Effects of Growth Hormone Treatment.
Klin Padiatr
; 2023 Dec 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38049102
3.
Systematic genetic testing for recessively inherited monogenic diabetes: a cross-sectional study in paediatric diabetes clinics.
Diabetologia
; 65(2): 336-342, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34686905
4.
Oxytocin receptor gene polymorphism and low serum oxytocin level are associated with hyperphagia and obesity in adolescents.
Int J Obes (Lond)
; 45(9): 2064-2073, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34091593
5.
Early and late diagnoses of 17ß-Hydroxysteroid dehydrogenase type-3 deficiency in two unrelated patients.
Andrologia
; 53(6): e14017, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-33586216
6.
Does fludrocortisone treatment cause hypomagnesemia in children with primary adrenal insufficiency?
Turk J Med Sci
; 51(1): 231-237, 2021 02 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-33155789
7.
The relationship of carotid intima-media thickness with anthropometric and metabolic parameters in patients with classic congenital adrenal hyperplasia
Turk J Med Sci
; 51(4): 1738-1746, 2021 08 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-33486914
8.
Comparison of the effectiveness of simple carbohydrates on hypoglycemic episodes in children and adolescents with type 1 diabetes mellitus: A randomized study in a diabetes camp.
Pediatr Diabetes
; 21(7): 1249-1255, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32662200
9.
NOVEL VDR MUTATIONS IN PATIENTS WITH VITAMIN D-DEPENDENT RICKETS TYPE 2A: A MILD DISEASE PHENOTYPE CAUSED BY A NOVEL CANONICAL SPLICE-SITE MUTATION.
Endocr Pract
; 26(1): 72-81, 2020 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-31557081
10.
Can ocular changes be detected early in children and adolescents with type 1 diabetes mellitus without retinopathy by using optical biometry and optical coherence tomography?
Int Ophthalmol
; 40(10): 2503-2514, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-32488589
11.
Impaired systolic and diastolic left ventricular function in children and adolescents with congenital adrenal hyperplasia receiving corticosteroid therapy.
Cardiol Young
; 29(3): 319-324, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-30675832
12.
Brain injury markers: S100 calcium-binding protein B, neuron-specific enolase and glial fibrillary acidic protein in children with diabetic ketoacidosis.
Pediatr Diabetes
; 19(5): 1000-1006, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29484801
13.
Internet addiction, sleep and health-related life quality among obese individuals: a comparison study of the growing problems in adolescent health.
Eat Weight Disord
; 21(4): 709-717, 2016 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-27757931
14.
Is Patch Testing with Food Additives Useful in Children with Atopic Eczema?
Pediatr Dermatol
; 32(5): 684-9, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25873103
15.
Isolated hyperthyrotropinemia in childhood obesity and its relation with metabolic parameters.
J Endocrinol Invest
; 37(9): 799-804, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24920280
16.
The relation of serum nesfatin-1 level with metabolic and clinical parameters in obese and healthy children.
Pediatr Diabetes
; 14(3): 189-95, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23346951
17.
Clinical and diagnostic characteristics of hyperprolactinemia in childhood and adolescence.
J Pediatr Endocrinol Metab
; 26(1-2): 1-11, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23327784
18.
Resting Electroencephalography Differences Between Eyes-Closed and Eyes-Open Conditions in Children with Subclinical Hypothyroidism.
Turk Arch Pediatr
; 58(1): 34-41, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36598209
19.
Atypical STAT5B deficiency, severe short stature and mild immunodeficiency associated with a novel homozygous STAT5B Variant.
Mol Cell Endocrinol
; 559: 111799, 2023 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36265659
20.
POU6F2 mutation in humans with pubertal failure alters GnRH transcript expression.
Front Endocrinol (Lausanne)
; 14: 1203542, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37600690