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Do the Anti-Müllerian Hormone Levels of Adolescents with Polycystic Ovary Syndrome, Those Who Are at Risk for Developing Polycystic Ovary Syndrome, and Those Who Exhibit Isolated Oligomenorrhea Differ from Those of Adolescents with Normal Menstrual Cycles?
- Published in:
- Hormone Research in Paediatrics, 2016, v. 85, n. 6, p. 406, doi. 10.1159/000446111
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- Publication type:
- Article
Co-Existence of Thyroid Nodule and Thyroid Cancer in Children and Adolescents with Hashimoto Thyroiditis: A Single-Center Study.
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- Hormone Research in Paediatrics, 2016, v. 85, n. 3, p. 181, doi. 10.1159/000443143
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- Article
A major health problem facing immigrant children: nutritional rickets.
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- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 2, p. 223, doi. 10.1515/jpem-2021-0420
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- Publication type:
- Article
Experience of intravenous calcium treatment and long-term responses to treatment in a patient with hereditary vitamin D-resistant rickets resulting from a novel mutation.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 6, p. 647, doi. 10.1515/jpem-2018-0399
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- Publication type:
- Article
Effects of 1-year growth hormone replacement therapy on thyroid volume and function of the children and adolescents with idiopathic growth hormone deficiency.
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- Journal of Pediatric Endocrinology & Metabolism, 2017, v. 30, n. 11, p. 1187, doi. 10.1515/jpem-2017-0210
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- Publication type:
- Article
AMH levels in girls with various pubertal problems.
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- Journal of Pediatric Endocrinology & Metabolism, 2017, v. 30, n. 3, p. 333, doi. 10.1515/jpem-2016-0217
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- Article
Treatment experience and long-term follow-up data in two severe neonatal hyperparathyroidism cases.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 9, p. 1103, doi. 10.1515/jpem-2015-0261
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- Publication type:
- Article
Risk factors affecting the development of nephrocalcinosis, the most common complication of hypophosphatemic rickets.
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- Journal of Pediatric Endocrinology & Metabolism, 2015, v. 28, n. 11/12, p. 1333, doi. 10.1515/jpem-2014-0447
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- Publication type:
- Article
Rett syndrome and precocious puberty association.
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- Journal of Pediatric Endocrinology & Metabolism, 2015, v. 28, n. 9/10, p. 1197, doi. 10.1515/jpem-2015-0139
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- Publication type:
- Article
17βHSD-3 enzyme deficiency due to novel mutations in the HSD17B3 gene diagnosed in a neonate.
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- Journal of Pediatric Endocrinology & Metabolism, 2015, v. 28, n. 7/8, p. 957, doi. 10.1515/jpem-2014-0354
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- Publication type:
- Article
17α-Hydroylase/17,20-lyase deficiency related to P.Y27*(c.81C>A) mutation in CYP17A1 gene.
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- Journal of Pediatric Endocrinology & Metabolism, 2015, v. 28, n. 7/8, p. 919, doi. 10.1515/jpem-2014-0444
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- Publication type:
- Article
The use of pamidronate for acute vitamin D intoxication, clinical experience with three cases.
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- Journal of Pediatric Endocrinology & Metabolism, 2015, v. 28, n. 5/6, p. 709, doi. 10.1515/jpem-2014-0279
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- Publication type:
- Article
Status of Central Precocious Puberty Cases at the Onset of Coronavirus Disease 2019 Pandemic: A Single-Center Experience.
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- Turkish Archives of Pediatrics, 2022, v. 57, n. 3, p. 349, doi. 10.5152/TurkArchPediatr.2022.2101313
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- Publication type:
- Article
A case of prohormone convertase deficiency diagnosed with type 2 diabetes.
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- Turkish Archives of Pediatrics, 2021, v. 56, n. 1, p. 81, doi. 10.14744/TurkPediatriArs.2020.36459
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- Publication type:
- Article
Perinatal outcomes of high-dose vitamin D administration in the last trimester.
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- Turkish Journal of Obstetrics & Gynecology, 2021, v. 18, n. 2, p. 159, doi. 10.4274/tjod.galenos.2021.90023
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- Publication type:
- Article
Bifid Kosta Anomalisi: Vaka Sunumu.
- Published in:
- 2010
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- Publication type:
- Case Study
Evaluation of final heights in patients with congenital adrenal hyperplasia.
- Published in:
- Pamukkale Medical Journal, 2024, v. 17, n. 2, p. 265, doi. 10.31362/patd.1366476
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- Publication type:
- Article
Referans Bir Çocuk Hastanesine Zehirlenme ID Yakınması ile Başvuran Çocuk Hastaların Analizi.
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- Journal of Dr. Behcet Uz Children's Hospital, 2020, v. 10, n. 3, p. 299, doi. 10.5222/buchd.2020.49765
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- Publication type:
- Article
Early Ophthalmic Artery Blood Flow Parameter Changes in Patients with Type 1 Diabetes Mellitus.
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- Beyoglu Eye Journal, 2020, v. 5, n. 1, p. 17, doi. 10.14744/bej.2020.15238
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- Publication type:
- Article
Early visual field changes in patients with type 1 diabetes mellitus.
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- European Journal of Ophthalmology, 2020, v. 30, n. 6, p. 1467, doi. 10.1177/1120672119872896
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- Publication type:
- Article
Comparison of anterior segment parameters in juvenile diabetes mellitus and healthy eyes.
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- European Journal of Ophthalmology, 2016, v. 26, n. 6, p. 618, doi. 10.5301/ejo.5000764
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- Publication type:
- Article
The Diagnostic Value of Free Androgen Index in Obese Adolescent Females with Idiopathic Hirsutism and Polycystic Ovary Syndrome.
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- Journal of Academic Research in Medicine, 2021, v. 11, n. 1, p. 81, doi. 10.4274/jarem.galenos.2021.22932
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- Publication type:
- Article
The evaluation of transient hypothyroidism in patients diagnosed with congenital hypothyroidism.
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- Turkish Journal of Medical Sciences, 2015, v. 45, n. 4, p. 745, doi. 10.3906/sag-1404-109
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- Publication type:
- Article
Pubertal Dönemde Aktif Rikets; D Vitamini Eksikliği, Yetersiz Kalsiyum Alımı ya da Her İkisi?
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- Journal of Pediatric Disease / Türkiye Çocuk Hastalıkları Dergisi, 2017, v. 11, n. 3, p. 209, doi. 10.12956/tjpd.2015.183
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- Publication type:
- Article
Evaluation of Patients Diagnosed with Nutritional Rickets: A Single Center Study.
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- Journal of Pediatric Disease / Türkiye Çocuk Hastalıkları Dergisi, 2017, v. 11, n. 1, p. 46, doi. 10.12956/tjpd.2016.240
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- Publication type:
- Article
Prematüre Pubarş Olgularının Değerlendirilmesi: Tek Merkez Deneyimi.
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- Journal of Pediatric Disease / Türkiye Çocuk Hastalıkları Dergisi, 2017, v. 11, n. 1, p. 34, doi. 10.12956/tjpd.2016.249
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- Publication type:
- Article
Vitamin D Deficiency/Insufficiency in Children and Adolescents with Chronic Disease.
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- Journal of Pediatric Disease / Türkiye Çocuk Hastalıkları Dergisi, 2016, v. 10, n. 4, p. 259, doi. 10.12956/tjpd.2016.204
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- Publication type:
- Article
Decreased vitamin D levels in children and adolescents with Celiac disease: A nationwide cross-sectional study.
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- Gulhane Medical Journal, 2022, v. 64, n. 3, p. 268, doi. 10.4274/gulhane.galenos.2022.38039
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- Publication type:
- Article
Congenital long-QT syndrome in type 1 diabetes: a unique association.
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- Turkish Journal of Pediatrics, 2019, v. 61, n. 5, p. 791, doi. 10.24953/turkjped.2019.05.022
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- Article
Low hemoglobin A1c levels in a patient with diabetic ketoacidosis: Fulminant type 1 diabetes mellitus.
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- 2018
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- Publication type:
- Case Study
Gonadoblastoma in a patient with 46, XY complete gonadal dysgenesis.
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- Turkish Journal of Pediatrics, 2017, v. 58, n. 5, p. 538
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- Publication type:
- Article
Complete androgen insensitivity syndrome associated with bilateral sertoli cell adenomas and unilateral paratesticular leiomyoma: A case report.
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- Turkish Journal of Pediatrics, 2016, v. 58, n. 6, p. 654, doi. 10.24953/turkjped.2016.06.012
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- Publication type:
- Article
A case with atrophic autoimmune thyroiditis-related hypothyroidism causing multisystem involvement in early childhood.
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- Turkish Journal of Pediatrics, 2016, v. 58, n. 4, p. 446, doi. 10.24953/turkjped.2016.04.019
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- Article
The first childhood case with coexisting Hashimoto thyroiditis, vitiligo and autoimmune hepatitis.
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- Turkish Journal of Pediatrics, 2016, v. 58, n. 4, p. 432, doi. 10.24953/turkjped.2016.04.016
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- Article
Santral Puberte Prekoks Tanılı Kızlarda GNRH Analog Tedavisinin Antropometrik Ölçüm Değerlerine etkisi: Bir Yıllık Takip Sonuçları.
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- Osmangazi Journal of Medicine / Osmangazi Tip Dergisi, 2024, v. 46, n. 4, p. 538, doi. 10.20515/otd.1383498
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- Publication type:
- Article
Clinical and Laboratory Characteristics of MODY Cases, Genetic Mutation Spectrum and Phenotype-genotype Relationship.
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- Journal of Clinical Research in Pediatric Endocrinology, 2024, v. 16, n. 3, p. 297, doi. 10.4274/jcrpe.galenos.2024.2023-10-16
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- Publication type:
- Article
Long-term Clinical Follow-up of Patients with Familial Hypomagnesemia with Secondary Hypocalcemia.
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- Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 3, p. 300, doi. 10.4274/jcrpe.galenos.2021.2020.0192
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- Article
Antimüllerian Hormone Levels of Infants with Premature Thelarche.
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- Journal of Clinical Research in Pediatric Endocrinology, 2019, v. 11, n. 3, p. 287, doi. 10.4274/jcrpe.galenos.2019.2018.0293
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- Publication type:
- Article
Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty.
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- Journal of Clinical Research in Pediatric Endocrinology, 2018, v. 10, n. 3, p. 223, doi. 10.4274/jcrpe.5506
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- Publication type:
- Article
A Patient with Proopiomelanocortin Deficiency: An Increasingly Important Diagnosis to Make.
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- Journal of Clinical Research in Pediatric Endocrinology, 2018, v. 10, n. 1, p. 68, doi. 10.4274/jcrpe.4638
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- Publication type:
- Article
A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene.
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- Journal of Clinical Research in Pediatric Endocrinology, 2017, v. 9, n. 1, p. 91, doi. 10.4274/jcrpe.3238
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- Publication type:
- Article