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Montelukast Kullanımı Sonrası İntihar Düşüncesi ve Davranışı Gösteren Olgu.
- Published in:
- Journal of Pediatric Disease / Türkiye Çocuk Hastalıkları Dergisi, 2014, v. 8, n. 4, p. 212, doi. 10.12956/tjpd.2014.69
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- Publication type:
- Article
The Results of 16 Years of Iodization: Assessment of Iodine Deficiency Among School-age Children in Antalya, Turkey.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2020, v. 12, n. 3, p. 256, doi. 10.4274/jcrpe.galenos.2020.2019.0168
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- Publication type:
- Article
Remarkable Increase in the Prevalence of Overweight and Obesity Among School Age Children in Antalya, Turkey, Between 2003 and 2015.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2019, v. 11, n. 1, p. 76, doi. 10.4274/jcrpe.galenos.2018.2018.0108
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- Publication type:
- Article
Basal Serum Neurokinin B Levels in Differentiating Idiopathic Central Precocious Puberty from Premature Thelarche.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2017, v. 9, n. 2, p. 101, doi. 10.4274/jcrpe.3817
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- Publication type:
- Article
Clinical and Molecular Genetic Analysis in Three Children with Wolfram Syndrome: A Novel WFS1 Mutation (c.2534T>A).
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2017, v. 9, n. 1, p. 80, doi. 10.4274/jcrpe.2894
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- Publication type:
- Article
Pyridoxine-Responsive Seizures in Infantile Hypophosphatasia and a Novel Homozygous Mutation in ALPL Gene.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2016, v. 8, n. 3, p. 360, doi. 10.4274/jcrpe.2798
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- Publication type:
- Article
The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A Nationwide Multicenter Study.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2016, v. 8, n. 3, p. 305, doi. 10.4274/jcrpe.3013
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- Publication type:
- Article
An Infantile Hypophosphatasia Patient with a Homozygous Mutation in the ALPS Gene.
- Published in:
- 2015
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- Publication type:
- Abstract
An Infantile Hypophosphatasia Patient with a Homozygous Mutation in the ALPS Gene.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2015, v. 7, p. 79
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- Publication type:
- Article
LC-MS/MS analysis of plasma polyunsaturated fatty acids in patients with homozygous sickle cell disease.
- Published in:
- Clinical & Experimental Medicine, 2015, v. 15, n. 3, p. 397, doi. 10.1007/s10238-014-0293-6
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- Publication type:
- Article
Tibial nerve axonal excitability in type 1 diabetes mellitus.
- Published in:
- 2019
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- Publication type:
- journal article
The molecular basis and genotype–phenotype correlations of congenital adrenal hyperplasia (CAH) in Anatolian population.
- Published in:
- Molecular Biology Reports, 2019, v. 46, n. 4, p. 3677, doi. 10.1007/s11033-019-04809-4
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- Publication type:
- Article
17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort.
- Published in:
- Endocrine (1355008X), 2024, v. 85, n. 3, p. 1407, doi. 10.1007/s12020-024-03962-6
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- Publication type:
- Article
Obezite tanılı çocuk ve ergenlerde psikopatoloji, yaşam kalitesi ve ebeveyn tutumlarının değerlendirilmesi.
- Published in:
- Journal of Dr. Behcet Uz Children's Hospital, 2018, v. 8, n. 1, p. 51, doi. 10.5222/buchd.2018.051
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- Publication type:
- Article
Tibial Sinir Aksonal Uyarılabilirlik Değerlendirmesinin Tip 1 Diyabetik Polinöropati Tanısına Katkısı.
- Published in:
- Journal of Neurological Sciences, 2016, v. 33, p. 14
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- Publication type:
- Article