Detalhe da pesquisa
1.
The psychosocial outcomes of advanced hybrid closed-loop system in children and adolescents with type 1 diabetes.
Eur J Pediatr
; 183(7): 3095-3103, 2024 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-38661816
2.
Clinical features of generalized lipodystrophy in Turkey: A cohort analysis.
Diabetes Obes Metab
; 25(7): 1950-1963, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36946378
3.
Loss of thymidine phosphorylase activity disrupts adipocyte differentiation and induces insulin-resistant lipoatrophic diabetes.
BMC Med
; 20(1): 95, 2022 03 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35341481
4.
Local complications of insulin administration sites and effect on diabetes management.
J Clin Nurs
; 31(17-18): 2530-2538, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34622517
5.
A rare cause of syndromic short stature: 3M syndrome in three families.
Am J Med Genet A
; 185(2): 461-468, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33258289
6.
Melanocortin 4 receptor (MC4R) gene variants in children and adolescents having familial early-onset obesity: genetic and clinical characteristics.
Eur J Pediatr
; 179(9): 1445-1452, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-32185475
7.
Renal complications of lipodystrophy: A closer look at the natural history of kidney disease.
Clin Endocrinol (Oxf)
; 89(1): 65-75, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29722904
8.
Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome.
Am J Med Genet A
; 170A(4): 942-8, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26788866
9.
Difficulties experienced by caregivers of patients diagnosed with osteogenesisimperfecta (OI): example of a hospital.
J Pak Med Assoc
; 65(7): 764-70, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26160088
10.
Current Diagnostic Approaches in the Genetic Diagnosis of Disorders of Sex Development.
J Clin Res Pediatr Endocrinol
; 2024 Apr 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38683034
11.
Does minimed 780GTM insulin pump system affect energy and nutrient intake?: long-term follow-up study.
Eur J Clin Nutr
; 2024 Mar 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-38459160
12.
Molecular Genetic Diagnosis with Targeted Next Generation Sequencing in a Cohort of Turkish Osteogenesis Imperfecta Patients and Their Genotype-phenotype Correlation.
J Clin Res Pediatr Endocrinol
; 2024 Jun 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38828893
13.
Impact of lipodystrophy on health-related quality of life: the QuaLip study.
Orphanet J Rare Dis
; 19(1): 10, 2024 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38183080
14.
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
15.
Three patients resembling Teebi-Shaltout syndrome.
Am J Med Genet A
; 161A(10): 2570-5, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23918592
16.
Are low maternal estriol levels a predictor for pro-opiomelanocortin (POMC) deficiency caused by POMC mutation during pregnancy?
Prenat Diagn
; 33(13): 1297-8, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24027193
17.
Frequency and risk factors of endocrine complications in Turkish children and adolescents with sickle cell anemia.
Turk J Haematol
; 30(1): 25-31, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24385749
18.
ABCC8-related maturity-onset diabetes of the young: switching from insulin to sulphonylurea therapy: how long do we need for a good metabolic control?
J Pediatr Endocrinol Metab
; 36(6): 592-597, 2023 Jun 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-37071846
19.
A case-control study of early-stage radiological markers of endothelial dysfunction and cardiovascular findings in patients with osteogenesis imperfecta: genotype-phenotype correlations.
J Pediatr Endocrinol Metab
; 36(12): 1161-1168, 2023 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37859607
20.
A Rare Case of Monogenic Obesity due to a Novel Variant in the ADCY3 Gene: Challenges in Follow-up and Treatment.
J Clin Res Pediatr Endocrinol
; 2023 Oct 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-37855273