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Assessment of Side Effects of COVID-19 Vaccination in Child Patients Diagnosed with Type-1 Diabetes Mellitus.
- Published in:
- Firat Tip Dergisi, 2023, v. 28, n. 3, p. 191
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- Publication type:
- Article
Type 1 Diabetes Incidence Trends in a Cohort of Turkish Children and Youth.
- Published in:
- Turkish Archives of Pediatrics, 2023, v. 58, n. 5, p. 539, doi. 10.5152/TurkArchPediatr.2023.23036
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- Publication type:
- Article
Clinical Characteristics and Genetic Analyses of Patients with Idiopathic Hypogonadotropic Hypogonadism.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2023, v. 15, n. 2, p. 160, doi. 10.4274/jcrpe.galenos.2023.2022-10-14
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- Publication type:
- Article
Chronic Disease Management of Children Followed with Type 1 Diabetes Mellitus.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2023, v. 15, n. 2, p. 172, doi. 10.4274/jcrpe.galenos.2023.2022-8-4
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- Publication type:
- Article
Liraglutide Treatment in a Morbidly Obese Adolescent with a MC4R Gene Variant: Side Effects Reduce Success.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2023, v. 15, n. 2, p. 225, doi. 10.4274/jcrpe.galenos.2021.2021.0158
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- Publication type:
- Article
Distal Renal Tubular Acidosis can be the Cause of Hypokalemia in Graves' Disease: A Rare Association.
- Published in:
- Medical Records, 2023, v. 5, n. 2, p. 423, doi. 10.37990/medr.1180665
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- Publication type:
- Article
Ana sınıfında veya ilkokulda okuyan tip 1 diabetes mellitus tanılı çocukların okulda hastalık yönetimi ile ilgili yaşadıkları sorunlar.
- Published in:
- Ege Journal of Medicine, 2023, v. 62, n. 1, p. 61, doi. 10.19161/etd.1262450
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- Publication type:
- Article
Factors Associated with Low Bone Mineral Density at the Time of Diagnosis in Children with Celiac Disease.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2023, v. 15, n. 1, p. 62, doi. 10.4274/jcrpe.galenos.2022.2022-5-18
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- Publication type:
- Article
Presentation, Diagnosis, and Follow-Up Characteristics of 17α-Hydroxylase Deficiency Cases with Exon 1–6 Deletion (Founder Mutation) in the CYP17A1Gene: 20-Year Single-Center Experience.
- Published in:
- 2023
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- Publication type:
- Case Study
Is There a Predictive Factor for an Association with Autoimmune Glandular Disease in Children Diagnosed with Celiac Disease?
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2022, v. 14, n. 4, p. 409, doi. 10.4274/jcrpe.galenos.2022.2022-2-14
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- Publication type:
- Article
A girl diagnosed with familial hypocalciuric hypercalcemia with heterozygous p.Cys575Tyr variation in the CaSR gene.
- Published in:
- 2022
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- Publication type:
- Case Study
Evaluation of endocrine functions before and after enzyme replacement therapy in children with mucopolysaccharidosis.
- Published in:
- Medicine Science, 2022, v. 11, n. 3, p. 1184, doi. 10.5455/medscience.2022.03.053
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- Publication type:
- Article
Change in clinical presentation at admission in children with newly diagnosed type 1 diabetes during the COVID-19 pandemic in the eastern region of Turkey.
- Published in:
- Annals of Medical of Research, 2022, v. 29, n. 7, p. 755, doi. 10.5455/annalsmedres.2022.01.035
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- Publication type:
- Article
46,XY Sex Development Defect due to a Novel Homozygous (Splice Site) c.673_1G>C Variation in the HSD17B3 Gene: Case Report.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2022, v. 14, n. 2, p. 233, doi. 10.4274/jcrpe.galenos.2020.2020.0249
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- Publication type:
- Article
TSHRV656F Activating Variant of the Thyroid Stimulating Hormone Receptor Gene in Neonatal Onset Hyperthyroidism: A Case Review.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2022, v. 14, n. 1, p. 114, doi. 10.4274/jcrpe.galenos.2020.2020.0229
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- Publication type:
- Article
Trend in initial presenting features of type 1 diabetes mellitus over a 24 year period in Turkey: a retrospective analysis of 814 cases.
- Published in:
- Turkish Journal of Pediatrics, 2022, v. 64, n. 1, p. 40, doi. 10.24953/turkjped.2020.3580
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- Publication type:
- Article
Tiroid Nodülü Olan Çocuklarda Laboratuvar, Radyolojik ve Sitopatolojik Değerlendirmelerin Histopatolojik Sonuçlarla İlişkisi.
- Published in:
- Journal of Ankara University Faculty of Medicine / Ankara Üniversitesi Tip Fakültesi Mecmuasi, 2021, v. 74, n. 1, p. 68, doi. 10.4274/atfm.galenos.2020.30922
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- Publication type:
- Article
Pediatric Primary Adrenal Insufficiency: A 21-year Single Center Experience.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 1, p. 88, doi. 10.4274/jcrpe.galenos.2020.2020.0132
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- Publication type:
- Article
Novel Mutations in Obesity-related Genes in Turkish Children with Non-syndromic Early Onset Severe Obesity: A Multicentre Study.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2019, v. 11, n. 4, p. 341, doi. 10.4274/jcrpe.galenos.2019.2019.0021
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- Publication type:
- Article
A Case of Cleidocranial Dysplasia with a Novel Mutation and Growth Velocity Gain with Growth Hormone Treatment.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2019, v. 11, n. 3, p. 301, doi. 10.4274/jcrpe.galenos.2018.2018.0211
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- Publication type:
- Article
Laron syndrome related to homozygous growth hormone receptor c.784>C mutation in a patient with hypoplastic pulmonary arteries.
- Published in:
- Cardiovascular Journal of Africa, 2019, v. 30, n. 2, p. e7, doi. 10.5830/CVJA-2019-002
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- Publication type:
- Article
Prospective Follow-up of Children with Idiopathic Growth Hormone Deficiency After Termination of Growth Hormone Treatment: Is There Really Need for Treatment at Transition to Adulthood?
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2018, v. 10, n. 3, p. 247, doi. 10.4274/jcrpe.0010
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- Publication type:
- Article
Prematür adrenarşli olgularda hematolojik parametrelerin değerlendirilmesi.
- Published in:
- Ortadogu Medical Journal / Ortadogu Tip Dergisi, 2018, v. 10, n. 3, p. 268, doi. 10.21601/ortadogutipdergisi.429250
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- Publication type:
- Article
Delayed Diagnosis of a 17-Hydroxylase/17,20-Lyase Deficient Patient Presenting as a 46,XY Female: A Low Normal Potassium Level Can Be an Alerting Diagnostic Sign.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2017, v. 9, n. 2, p. 163, doi. 10.4274/jcrpe.3839
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- Publication type:
- Article
Response to Anastrozole Treatment in a Case with Peutz-Jeghers Syndrome and a Large Cell Calcifying Sertoli Cell Tumor.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2017, v. 9, n. 2, p. 168, doi. 10.4274/jcrpe.3625
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- Publication type:
- Article
The Association between Premature Adrenarche and Cardiovascular Risk May Be Greater than Expected.
- Published in:
- Hormone Research in Paediatrics, 2017, v. 87, n. 1, p. 7, doi. 10.1159/000452445
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- Publication type:
- Article
Coexistence of Mosaic Uniparental Isodisomy and a KCNJ11 Mutation Presenting as Diffuse Congenital Hyperinsulinism and Hemihypertrophy.
- Published in:
- Hormone Research in Paediatrics, 2016, v. 85, n. 6, p. 421, doi. 10.1159/000446153
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- Publication type:
- Article
Gonadotropin-Releasing Hormone Analogue Treatment in Females with Moderately Early Puberty: No Effect on Final Height.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2016, v. 8, n. 2, p. 211, doi. 10.4274/jcrpe.2356
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- Publication type:
- Article
The Effect of Recombinant Growth Hormone Treatment in Children with Idiopathic Short Stature and Low Insulin-Like Growth Factor-1 Levels.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2015, v. 7, n. 4, p. 301, doi. 10.4274/jcrpe.2111
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- Publication type:
- Article
Tamoxifen Treatment for Pubertal Gynecomastia in a Patient with Partial Androgen Insensitivity Syndrome.
- Published in:
- 2015
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- Publication type:
- Abstract
Tamoxifen Treatment for Pubertal Gynecomastia in a Patient with Partial Androgen Insensitivity Syndrome.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2015, v. 7, p. 76
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- Publication type:
- Article
A Deep Intronic HADH Splicing Mutation (c.636+471G>T) in a Congenital Hyperinsulinemic Hypoglycemia Case: Long Term Clinical Course.
- Published in:
- 2015
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- Publication type:
- Case Study
Three cases of Wolfram syndrome with different clinical aspects.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2015, v. 28, n. 3/4, p. 433, doi. 10.1515/jpem-2014-0139
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- Publication type:
- Article
ROHHAD Syndrome: Reasons for Diagnostic Difficulties in Obesity.
- Published in:
- 2014
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- Publication type:
- Case Study
The evaluation of thyroid carcinoma in childhood and concomitance of autoimmune thyroid disorders.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 901, doi. 10.1515/jpem-2013-0273
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- Publication type:
- Article
The clinical and genetic heterogeneity of mixed gonadal dysgenesis: does "disorders of sexual development (DSD)" classification based on new Chicago consensus cover all sex chromosome DSD?
- Published in:
- 2012
- By:
- Publication type:
- journal article
The clinical and genetic heterogeneity of mixed gonadal dysgenesis: does 'disorders of sexual development (DSD)' classification based on new Chicago consensus cover all sex chromosome DSD?
- Published in:
- European Journal of Pediatrics, 2012, v. 171, n. 10, p. 1497, doi. 10.1007/s00431-012-1754-0
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- Publication type:
- Article