Detalhe da pesquisa
1.
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
2.
Early puberty paradox: an investigation of anxiety levels of mothers and children, children's quality of life, and psychiatric diagnoses.
Eur J Pediatr
; 182(8): 3775-3783, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37335399
3.
Neonatal classic galactosemia-diagnosis, clinical profile and molecular characteristics in unscreened Turkish population.
J Trop Pediatr
; 68(6)2022 10 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36375035
4.
Neonatal diabetes due to homozygous INS gene promoter mutations: Highly variable phenotype, remission and early relapse during the first 3 years of life.
Pediatr Diabetes
; 21(7): 1169-1175, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32656923
5.
Short-term results of continuous venovenous haemodiafiltration versus peritoneal dialysis in 40 neonates with inborn errors of metabolism.
Eur J Pediatr
; 178(6): 829-836, 2019 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-30895385
6.
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
7.
Severe renal failure and hyperammonemia in a newborn with propionic acidemia: effects of treatment on the clinical course.
Ren Fail
; 36(3): 451-2, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24329397
8.
Transient nephrogenic diabetes insipidus caused by fetal exposure to haloperidol.
Ren Fail
; 36(6): 951-2, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24673433
9.
A very rare presentation of mitochondrial elongation factor Tu deficiency-TUFM mutation and literature review.
J Pediatr Endocrinol Metab
; 2024 Apr 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38630895
10.
Evaluation of patients diagnosed with congenital hypothyroidism by newborn screening between 2011-2019 in Diyarbakir, Turkey.
Medicine (Baltimore)
; 102(51): e36778, 2023 Dec 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38134076
11.
Evaluation and management of neonatal onset hyperinsulinemic hypoglycemia: a single neonatal center experience.
J Matern Fetal Neonatal Med
; 36(2): 2272014, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37860935
12.
Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year
J Clin Res Pediatr Endocrinol
; 15(3): 329-333, 2023 08 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-35735786
13.
Glutaric aciduria and L-2-hydroxyglutaric aciduria: Clinical and molecular findings of 35 patients from Turkey.
Mol Genet Metab Rep
; 36: 100979, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37275239
14.
The clinical and laboratory features of patients with triple A syndrome: a single-center experience in Turkey.
Endocrine
; 79(2): 376-383, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36194344
15.
Evaluation of patients diagnosed with phenylketonuria and biotinidase deficiency by the newborn screening program: a ten-year retrospective study.
Turk J Pediatr
; 64(6): 985-992, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36583880
16.
Revisiting the Annual Incidence of Type 1 Diabetes Mellitus in Children from the Southeastern Anatolian Region of Turkey: A Regional Report
J Clin Res Pediatr Endocrinol
; 14(2): 172-178, 2022 06 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35014245
17.
The effects of the covid-19 pandemic on puberty: a cross-sectional, multicenter study from Turkey.
Ital J Pediatr
; 48(1): 144, 2022 Aug 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-35964090
18.
Catch-up Growth and Discontinuation of Fludrocortisone Treatment in Aldosterone Synthase Deficiency.
J Clin Endocrinol Metab
; 107(1): e106-e117, 2022 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34415991
19.
Recommendations for Clinical Decision-making in Children with Type 1 Diabetes and Celiac Disease: Type 1 Diabetes and Celiac Disease Joint Working Group Report
J Clin Res Pediatr Endocrinol
; 14(1): 1-9, 2022 03 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34538045
20.
A homozygous recurring mutation in WISP3 causing progressive pseudorheumatoid arthropathy.
J Pediatr Endocrinol Metab
; 24(1-2): 105-8, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21528827