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1.
Natural history of ENPP1 deficiency: Nationwide Turkish Cohort Study of autosomal-recessive hypophosphataemic rickets type 2.
Clin Endocrinol (Oxf)
; 2024 Feb 07.
Article
in English
| MEDLINE | ID: mdl-38324408
2.
Could Fetuin-A Be a Biomarker for Autism Spectrum Disorder and Cognitive Developmental Delay?
Biochemistry (Mosc)
; 87(6): 559-565, 2022 Jun.
Article
in English
| MEDLINE | ID: mdl-35790414
3.
Clinical, biochemical, and echocardiographic evaluation of neonates with vitamin D deficiency due to maternal vitamin D deficiency.
Cardiol Young
; 32(1): 88-93, 2022 Jan.
Article
in English
| MEDLINE | ID: mdl-33941295
4.
WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome.
Am J Hum Genet
; 102(1): 27-43, 2018 01 04.
Article
in English
| MEDLINE | ID: mdl-29276006
5.
Vici syndrome in siblings born to consanguineous parents.
Am J Med Genet A
; 170A(1): 220-5, 2016 Jan.
Article
in English
| MEDLINE | ID: mdl-26395118
6.
Endothelial dysfunction biomarker, endothelial cell-specific molecule-1, and pediatric metabolic syndrome.
Pediatr Int
; 58(11): 1124-1129, 2016 Nov.
Article
in English
| MEDLINE | ID: mdl-27011259
7.
The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey.
J Hum Genet
; 60(1): 1-9, 2015 Jan.
Article
in English
| MEDLINE | ID: mdl-25296579
8.
An examination of the mutual effects of valproic acid, carbamazepine, and phenobarbital on 25-hydroxyvitamin D levels and thyroid function tests.
Neuropediatrics
; 45(1): 16-21, 2014 Feb.
Article
in English
| MEDLINE | ID: mdl-23888467
9.
Serum vitamin D levels in children with recurrent otitis media.
Eur Arch Otorhinolaryngol
; 271(4): 689-93, 2014 Apr.
Article
in English
| MEDLINE | ID: mdl-23543299
10.
Vitamin D levels in children diagnosed with acute otitis media.
J Pak Med Assoc
; 64(11): 1274-7, 2014 Nov.
Article
in English
| MEDLINE | ID: mdl-25831645
11.
Assessment of Executive Function Skills in Children with Isolated Growth Hormone Deficiency: A Cross-sectional Study
J Clin Res Pediatr Endocrinol
; 16(2): 177-184, 2024 05 31.
Article
in English
| MEDLINE | ID: mdl-38275147
12.
Severe Early-Onset Obesity and Diabetic Ketoacidosis due to a Novel Homozygous c.169C>T p.Arg57* Variant in CEP19 Gene.
Mol Syndromol
; 15(2): 104-113, 2024 Mar.
Article
in English
| MEDLINE | ID: mdl-38585545
13.
Clinical and Laboratory Characteristics of MODY (Maturity Onset Diabetes of Young) Cases, Genetic Mutation Spectrum and Phenotype-genotype Relationship.
J Clin Res Pediatr Endocrinol
; 2024 Apr 26.
Article
in English
| MEDLINE | ID: mdl-38665000
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.
Article
in English
| MEDLINE | ID: mdl-36194344
15.
Genetic Forms of Calciopenic Rickets.
Eurasian J Med
; 54(Suppl1): 159-163, 2022 Dec.
Article
in English
| MEDLINE | ID: mdl-36655461
16.
A Genetic Approach in the Evaluation of Short Stature.
Eurasian J Med
; 54(Suppl1): 179-186, 2022 Dec.
Article
in English
| MEDLINE | ID: mdl-36655465
17.
Relationship between the TAS2R38 and TAS1R2 polymorphisms and the dental status in obese children.
Dent Med Probl
; 59(2): 233-240, 2022.
Article
in English
| MEDLINE | ID: mdl-35510485
18.
High Fetuin-A Levels in Children with Celiac Disease.
Eurasian J Med
; 54(2): 186-190, 2022 Jun.
Article
in English
| MEDLINE | ID: mdl-35703528
19.
A rare cause of primary amenorrhea: LHCGR gene mutations.
Eur J Obstet Gynecol Reprod Biol
; 272: 193-197, 2022 May.
Article
in English
| MEDLINE | ID: mdl-35366614
20.
Is Serum Progranulin Level a Biomarker in Autism and Cognitive Development Disorders?
Eurasian J Med
; 54(1): 50-53, 2022 Feb.
Article
in English
| MEDLINE | ID: mdl-35307629