Detalhe da pesquisa
1.
Effectiveness of Two Different Methods for Pain Reduction During Insulin Injection in Children With Type 1 Diabetes: Buzzy and ShotBlocker.
Worldviews Evid Based Nurs
; 15(6): 464-470, 2018 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-30307692
2.
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
3.
Further Evidence for RFWD3 Gene Causing Fanconi Anemia Complementation Group W: Detailed Clinical Report of the Second Case in the Literature.
Mol Syndromol
; 14(6): 509-515, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-38058754
4.
Comparison of anxiety, stress, and social support levels of female patients with type 1 diabetes and mothers whose children have type 1 diabetes.
J Diabetes Metab Disord
; 22(1): 333-340, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-37255808
5.
Relation of serum irisin levels to obesity and non-alcoholic fatty liver disease.
Turk J Pediatr
; 64(2): 246-254, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35611413
6.
A case of familial recurrent 17q12 microdeletion syndrome presenting with severe diabetic ketoacidosis.
Turk J Pediatr
; 64(3): 558-565, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35899569
7.
Increased Severe Cases and New-Onset Type 1 Diabetes Among Children Presenting With Diabetic Ketoacidosis During First Year of COVID-19 Pandemic in Turkey.
Front Pediatr
; 10: 926013, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35844756
8.
The association of lipid metabolism and non-alcoholic fatty liver disease in children with obesity.
Turk Pediatri Ars
; 55(3): 263-269, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33061754
9.
Revisiting Classical 3ß-hydroxysteroid Dehydrogenase 2 Deficiency: Lessons from 31 Pediatric Cases.
J Clin Endocrinol Metab
; 105(3)2020 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31950145
10.
Nationwide Turkish Cohort Study of Hypophosphatemic Rickets
J Clin Res Pediatr Endocrinol
; 12(2): 150-159, 2020 06 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31514490
11.
Quality-of-life Evaluation of Healthy Siblings of Children with Chronic Illness
Balkan Med J
; 37(1): 34-42, 2019 12 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-31647208
12.
The Frequency of Metabolic Syndrome and Serum Osteopontin Levels in Survivors of Childhood Acute Lymphoblastic Leukemia.
J Adolesc Young Adult Oncol
; 7(4): 480-487, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29641359
13.
Analysis of the GCK gene in 79 MODY type 2 patients: A multicenter Turkish study, mutation profile and description of twenty novel mutations.
Gene
; 641: 186-189, 2018 Jan 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-29056535
14.
Two Frameshift Mutations in MKRN3 in Turkish Patients with Familial Central Precocious Puberty.
Horm Res Paediatr
; 87(6): 405-411, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-27798941
15.
A case of Donohue syndrome "Leprechaunism" with a novel mutation in the insulin receptor gene.
Turk Pediatri Ars
; 52(4): 226-230, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-29483803
16.
A novel mutation in a case of pseudohypoparathyroidism type Ia.
Turk J Pediatr
; 58(1): 101-105, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27922245
17.
Blood lead levels of maternal-cord pairs, children and adults who live in a central urban area in Turkey.
Turk J Pediatr
; 47(2): 125-31, 2005.
Artigo
em Inglês
| MEDLINE | ID: mdl-16052851
18.
Biallelic RFX6 mutations can cause childhood as well as neonatal onset diabetes mellitus.
Eur J Hum Genet
; 23(12): 1744-8, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26264437
19.
Five novel mutations in the SCNN1A gene causing autosomal recessive pseudohypoaldosteronism type 1.
Eur J Endocrinol
; 168(5): 707-15, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23416952
20.
Serum visfatin levels, adiposity and glucose metabolism in obese adolescents.
J Clin Res Pediatr Endocrinol
; 4(2): 76-81, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22672864