Detalhe da pesquisa
1.
Natural history of ENPP1 deficiency: Nationwide Turkish Cohort Study of autosomal-recessive hypophosphataemic rickets type 2.
Clin Endocrinol (Oxf)
; 2024 Feb 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38324408
2.
Adherence to Growth Hormone Treatment in Children During COVID-19 Pandemic
J Clin Res Pediatr Endocrinol
; 2024 03 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38488049
3.
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
4.
Presentation, Diagnosis, and Follow-Up Characteristics of 17α-Hydroxylase Deficiency Cases with Exon 1-6 Deletion (Founder Mutation) in the CYP17A1Gene: 20-Year Single-Center Experience.
Sex Dev
; 17(1): 43-50, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36652930
5.
Factors Associated with Low Bone Mineral Density at the Time of Diagnosis in Children with Celiac Disease
J Clin Res Pediatr Endocrinol
; 15(1): 62-68, 2023 02 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-36264034
6.
Liraglutide Treatment in a Morbidly Obese Adolescent with a MC4R Gene Variant: Side Effects Reduce Success
J Clin Res Pediatr Endocrinol
; 15(2): 225-229, 2023 05 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-34584129
7.
Type 1 Diabetes Incidence Trends in a Cohort of Turkish Children and Youth.
Turk Arch Pediatr
; 58(5): 539-545, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37670553
8.
Clinical Characteristics and Genetic Analyses of Patients with Idiopathic Hypogonadotropic Hypogonadism
J Clin Res Pediatr Endocrinol
; 15(2): 160-171, 2023 05 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-36700485
9.
Chronic Disease Management of Children Followed with Type 1 Diabetes Mellitus
J Clin Res Pediatr Endocrinol
; 15(2): 172-181, 2023 05 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-36700484
10.
The clinical and genetic heterogeneity of mixed gonadal dysgenesis: does "disorders of sexual development (DSD)" classification based on new Chicago consensus cover all sex chromosome DSD?
Eur J Pediatr
; 171(10): 1497-502, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22644991
11.
TSHRV656F Activating Variant of the Thyroid Stimulating Hormone Receptor Gene in Neonatal Onset Hyperthyroidism: A Case Review
J Clin Res Pediatr Endocrinol
; 14(1): 114-118, 2022 03 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33443352
12.
46,XY Sex Development Defect due to a Novel Homozygous (Splice Site) c.673_1G>C Variation in the HSD17B3 Gene: Case Report
J Clin Res Pediatr Endocrinol
; 14(2): 233-238, 2022 06 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33389920
13.
Is There a Predictive Factor for an Association with Autoimmune Glandular Disease in Children Diagnosed with Celiac Disease?
J Clin Res Pediatr Endocrinol
; 14(4): 409-414, 2022 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35770950
14.
Trend in initial presenting features of type 1 diabetes mellitus over a 24 year period in Turkey: a retrospective analysis of 814 cases.
Turk J Pediatr
; 64(1): 40-48, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35286029
15.
Pediatric Primary Adrenal Insufficiency: A 21-year Single Center Experience
J Clin Res Pediatr Endocrinol
; 13(1): 88-99, 2021 02 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-32938577
16.
Laron syndrome related to homozygous growth hormone receptor c.784>C mutation in a patient with hypoplastic pulmonary arteries.
Cardiovasc J Afr
; 30(2): e7-e8, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30720842
17.
A Case of Cleidocranial Dysplasia with a Novel Mutation and Growth Velocity Gain with Growth Hormone Treatment
J Clin Res Pediatr Endocrinol
; 11(3): 301-305, 2019 09 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30468148
18.
Autosomal recessive cutis laxa: a novel mutation in the FBLN5 gene in a family.
Clin Dysmorphol
; 28(2): 63-65, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-30640789
19.
Novel Mutations in Obesity-related Genes in Turkish Children with Non-syndromic Early Onset Severe Obesity: A Multicentre Study
J Clin Res Pediatr Endocrinol
; 11(4): 341-349, 2019 11 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-30991789
20.
Prospective Follow-up of Children with Idiopathic Growth Hormone Deficiency After Termination of Growth Hormone Treatment: Is There Really Need for Treatment at Transition to Adulthood?
J Clin Res Pediatr Endocrinol
; 10(3): 247-255, 2018 07 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-29553045