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Emine Çamtosun

Observed names: Camtosun, Emine, Emine Camtosun, Emine ÇAMTOSUN, ÇAMTOSUN, EMİNE
Institution: Inonu University
Observed institutions: Ankara University, Inonu University, Sağlık Bilimleri Üniversitesi, Intergen (Turkey), İstanbul Başakşehir Çam ve Sakura Şehir Hastanesi, Turgut Özal University
ORCID: 0000-0002-8144-4409
Observed ORCID: 0000-0002-8144-4409
OpenAlex ID: A5024520248
Novel Mutations in Obesity-related Genes in Turkish Children with Non-syndromic Early Onset Severe Obesity: A Multicentre Study
2019 · Ayşehan Akıncı, Doğa Türkkahraman, et al. · Journal of Clinical Research in Pediatric Endocrinology · 37
ROHHAD Syndrome: Reasons for Diagnostic Difficulties in Obesity
2014 · Pınar Kocaay, Zeynep Şıklar, et al. · Journal of Clinical Research in Pediatric Endocrinology · 29
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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?
2012 · Gönül Öcal, Merih Berberoğlu, et al. · European Journal of Pediatrics · 29
Gonadotropin-Releasing Hormone Analogue Treatment in Females with Moderately Early Puberty: No Effect on Final Height
2016 · Şenay Savaş-Erdeve, Zeynep Şıklar, et al. · Journal of Clinical Research in Pediatric Endocrinology · 24
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Diagnostic Characteristics and Metabolic Risk Factors of Cases with Polycystic Ovary Syndrome during Adolescence
2014 · Zeynep Sıklar, Merih Berberoğlu, et al. · Journal of Pediatric and Adolescent Gynecology · 24
A Novel Heterozygous Mutation in Steroidogenic Factor-1 in Pubertal Virilization of a 46,XY Female Adolescent
2013 · Zeynep Sıklar, Merih Berberoğlu, et al. · Journal of Pediatric and Adolescent Gynecology · 22
17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort
2024 · Zeynep Siklar, Emine Camtosun, et al. · Endocrine · 21
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Clinical Review of 95 Patients with 46,XX Disorders of Sex Development Based on the New Chicago Classification
2014 · Gönül Öcal, Merih Berberoğlu, et al. · Journal of Pediatric and Adolescent Gynecology · 21
Pediatric Primary Adrenal Insufficiency: A 21-year Single Center Experience
2020 · Emine Çamtosun, İsmail Dündar, et al. · Journal of Clinical Research in Pediatric Endocrinology · 19
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The Association between Premature Adrenarche and Cardiovascular Risk May Be Greater than Expected
2016 · Nurullah Çelik, Hayrullah Alp, et al. · Hormone Research in Paediatrics · 19
A Deep Intronic HADH Splicing Mutation (c.636+471G>T) in a Congenital Hyperinsulinemic Hypoglycemia Case: Long Term Clinical Course
2015 · Emine Çamtosun, Sarah E. Flanagan, et al. · Journal of Clinical Research in Pediatric Endocrinology · 16
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Preperitoneal Fat Tissue May Be Associated with Arterial Stiffness in Obese Adolescents
2014 · Bülent Hacıhamdioğlu, Gönül Öçal, et al. · Ultrasound in Medicine & Biology · 16
Type 1 Diabetes Incidence Trends in a Cohort of Turkish Children and Youth
2023 · Ismail Dundar, Aysehan Akinci, et al. · Turkish Archives of Pediatrics · 11
A Case of Cleidocranial Dysplasia with a Novel Mutation and Growth Velocity Gain with Growth Hormone Treatment
2018 · Emine Çamtosun, Ayşehan Akıncı, et al. · Journal of Clinical Research in Pediatric Endocrinology · 10
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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
2016 · Emine Çamtosun, Zeynep Şıklar, et al. · Journal of Clinical Research in Pediatric Endocrinology · 10
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The Effect of Recombinant Growth Hormone Treatment in Children with Idiopathic Short Stature and Low Insulin-Like Growth Factor-1 Levels
2015 · Zeynep Şıklar, Pınar Kocaay, et al. · Journal of Clinical Research in Pediatric Endocrinology · 10
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Comprehensive Insights into Pediatric Craniopharyngioma: Endocrine and Metabolic Profiles, Treatment Challenges, and Long-term Outcomes with a Multicenter Approach
2024 · Zeynep Şıklar, Elif Özsu, et al. · Journal of Clinical Research in Pediatric Endocrinology · 9
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Chronic Disease Management of Children Followed with Type 1 Diabetes Mellitus
2023 · Şenay Güven Baysal, Nurdan Çiftci, et al. · Journal of Clinical Research in Pediatric Endocrinology · 9
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Clinical Characteristics and Genetic Analyses of Patients with Idiopathic Hypogonadotropic Hypogonadism
2023 · Nurdan Çiftci, Ayşehan Akıncı, et al. · Journal of Clinical Research in Pediatric Endocrinology · 9
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Liraglutide Treatment in a Morbidly Obese Adolescent with a MC4R Gene Variant: Side Effects Reduce Success
2021 · Emine Çamtosun, Ayşehan Akıncı, et al. · Journal of Clinical Research in Pediatric Endocrinology · 9
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Coexistence of Mosaic Uniparental Isodisomy and a KCNJ11 Mutation Presenting as Diffuse Congenital Hyperinsulinism and Hemihypertrophy
2016 · Pınar Kocaay, Zeynep Şiklar, et al. · Hormone Research in Paediatrics · 9
Autosomal recessive cutis laxa: a novel mutation in the FBLN5 gene in a family
2019 · Ibrahim Tekedereli, Emine Demiral, et al. · Clinical Dysmorphology · 8
The evaluation of thyroid carcinoma in childhood and concomitance of autoimmune thyroid disorders
2014 · Bülent Hacıhamdioğlu, Gönül Öçal, et al. · Journal of Pediatric Endocrinology and Metabolism · 8
TSHRV656F Activating Variant of the Thyroid Stimulating Hormone Receptor Gene in Neonatal Onset Hyperthyroidism: A Case Review
2021 · Leman Kayaş, Emine Çamtosun, et al. · Journal of Clinical Research in Pediatric Endocrinology · 7
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Three cases of Wolfram syndrome with different clinical aspects
2014 · Emine Çamtosun, Zeynep Şıklar, et al. · Journal of Pediatric Endocrinology and Metabolism · 7
Works count: 68
Citation count: 445
H-index: 12
I10-index: 16
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