Doç. Dr. EMİNE ÇAMTOSUN

Yayın Ağı

Makaleler 56

1. Examining the relationship between family functioning and healthy lifestyle behaviors in children with chronic illness

ÖZARSLAN S., GÜNAY U., Çetin K., Tokmak G., Yavaş R. N., VAROL F. İ., et al.

Journal of Pediatric Nursing , cilt.90, ss.437-445, 2026 (SCI-Expanded, SSCI, Scopus)

2. Small Airway Dysfunction Assessed by Impulse Oscillometry in Children with Congenital Adrenal Hyperplasia: A Preliminary Case–Control Study

YILMAZ E., TOPAL E., DÜNDAR İ., YAMANCAN YILMAZ Z., Koker Ozer N., KAYA E., et al.

Journal of Clinical Medicine , cilt.15, sa.15, 2026 (SCI-Expanded, Scopus)

3. Impulse Oscillometry Reveals Predominantly Mechanical Drivers of Small Airway Dysfunction in Obese Children

YILMAZ E., YAMANCAN YILMAZ Z., DÜNDAR İ., ÇAMTOSUN E., TOPAL E.

Journal of Clinical Medicine , cilt.15, sa.12, 2026 (SCI-Expanded, Scopus)

4. Genotype, Phenotype, and Clinical Characteristics of Maturity-Onset Diabetes of the Young (MODY): Predominance of GCK-MODY.

Kayaş L., Akıncı A., Çamtosun E., Dündar İ., Çiftçi N., Esener Z., et al.

Journal of clinical research in pediatric endocrinology , cilt.17, sa.4, ss.468-476, 2025 (SCI-Expanded, Scopus, TRDizin)

5. The First-Year Outcomes of the Nationwide Neonatal CAH Screening in Türkiye: High Rate of False Positives for 21-Hydroxylase Deficiency and a Higher Detection Rate of Non-Classical Cases.

Güran T., Yürüker E., Anık A., Atar M., Çamtosun E., Eviz E., et al.

Journal of clinical research in pediatric endocrinology , cilt.17, sa.4, ss.488-493, 2025 (SCI-Expanded, Scopus, TRDizin)

6. Trends and clinical features of childhood diabetes subgroups: 28 years of single center experience

DÜNDAR İ., Akıncı A., ÇAMTOSUN E., Yılmaz Z. Y., KAYA E.

Turkish Journal of Pediatrics , cilt.67, sa.5, ss.700-710, 2025 (SCI-Expanded, Scopus, TRDizin)

7. Long-term Impact of Continuous Glucose Monitoring Assistance on Glycemic Control in Children and Adolescents with Type 1 Diabetes Following the 2023 Kahramanmaraş Earthquake.

Tarçın G., Ataş N., Yaşar M., Şahin K. C., Trabzon G., Dündar İ., et al.

Journal of clinical research in pediatric endocrinology , cilt.17, sa.2, ss.161-167, 2025 (SCI-Expanded, Scopus, TRDizin)

8. Treatment and Prevention of Adrenal Crisis and Family Education.

Çamtosun E., Sangün Ö.

Journal of clinical research in pediatric endocrinology , cilt.17, sa.Suppl 1, ss.80-92, 2025 (SCI-Expanded, Scopus, TRDizin)

9. Natural history of ENPP1 deficiency: Nationwide Turkish Cohort Study of autosomal-recessive hypophosphataemic rickets type 2.

Dursun F., Turan İ., Bitkin E. Ç., Bayramoğlu E., Çayır A., Erdeve Ş. S., et al.

Clinical endocrinology , cilt.101, sa.5, ss.475-484, 2024 (SCI-Expanded, Scopus)

10. Comprehensive Insights Into Pediatric Craniopharyngioma: Endocrine and Metabolic Profiles, Treatment Challenges, and Long-term Outcomes from a Multicenter Study.

Şıklar Z., Özsu E., Kızılcan Çetin S., Özen S., Çizmecioğlu-Jones F., Balkı H. G., et al.

Journal of clinical research in pediatric endocrinology , cilt.16, sa.3, ss.288-296, 2024 (SCI-Expanded, Scopus, TRDizin)

11. Adherence to Growth Hormone Treatment in Children During the COVID-19 Pandemic.

ÇETİNKAYA S., ÖNGEL Y. D., TERCAN U., DARCAN Ş., TURAN H., AYDIN M., et al.

Journal of clinical research in pediatric endocrinology , cilt.16, sa.3, ss.256-263, 2024 (SCI-Expanded, Scopus, TRDizin)

12. 17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort.

Siklar Z., Camtosun E., Bolu S., Yildiz M., Akinci A., Bas F., et al.

Endocrine , cilt.85, sa.3, ss.1407-1416, 2024 (SCI-Expanded, Scopus)

13. Evaluation of inflammation with CRP, Pro-BNP, Leptin and Pentraxin-3 levels in children with obesity-related hypertension

KARAKUŞ G., KARAKURT C., ELKIRAN Ö., ÖNCÜL M., TABEL Y., ÇAMTOSUN E., et al.

Azerbaijan Journal of Cardiovascular Surgery , cilt.5, sa.3, ss.64-72, 2024 (Hakemli Dergi)

14. Assessment of Side Effects of COVID-19 Vaccination in Child Patients Diagnosed with Type-1 Diabetes Mellitus

ÇİFTCİ N., ÇAMTOSUN E., DÜNDAR İ., YAĞIN F. H., AKINCI A.

Fırat Tıp Dergisi , cilt.28, ss.191-198, 2023 (TRDizin)

15. Type 1 Diabetes Incidence Trends in a Cohort of Turkish Children and Youth.

Dündar İ., Akıncı A., Çamtosun E., Kayaş L., Çiftçi N., Özçetin E.

Turkish archives of pediatrics , cilt.58, sa.5, ss.539-545, 2023 (ESCI, Scopus, TRDizin)

16. Liraglutide Treatment in a Morbidly Obese Adolescent with a MC4R Gene Variant: Side Effects Reduce Success.

Çamtosun E., Akıncı A., Kayaş L., Çiftçi N., Tekedereli İ.

Journal of clinical research in pediatric endocrinology , cilt.15, sa.2, ss.225-229, 2023 (SCI-Expanded, Scopus, TRDizin)

17. Chronic Disease Management of Children Followed with Type 1 Diabetes Mellitus.

Guven Baysal S., Ciftci N., Dundar İ., Buyukavcı M. A., Yagin F. H., Camtosun E., et al.

Journal of clinical research in pediatric endocrinology , cilt.15, sa.2, ss.172-181, 2023 (SCI-Expanded, Scopus, TRDizin)

18. Clinical Characteristics and Genetic Analyses of Patients with Idiopathic Hypogonadotropic Hypogonadism.

Çiftci N., Akıncı A., Akbulut E., Çamtosun E., Dündar İ., Doğan M., et al.

Journal of clinical research in pediatric endocrinology , cilt.15, sa.2, ss.160-171, 2023 (SCI-Expanded, Scopus, TRDizin)

19. Distal Renal Tubular Acidosis can be the Cause of Hypokalemia in Graves’ Disease: A Rare Association

DÜNDAR İ., AKINCI A., ÇAMTOSUN E., ÇİFTCİ N., KAYAŞ L.

Medical records-international medical journal (Online) , cilt.5, 2023 (TRDizin)

20. Ana sınıfında veya ilkokulda okuyan tip 1 diabetes mellitus tanılı çocukların okulda hastalık yönetimi ile ilgili yaşadıkları sorunlar

Çiftci N., ÇAMTOSUN E., DÜNDAR İ., AKINCI A.

Ege Tıp Dergisi , cilt.62, sa.1, ss.61-67, 2023 (TRDizin)

21. Factors Associated with Low Bone Mineral Density at the Time of Diagnosis in Children with Celiac Disease.

Çamtosun E., Varol F. İ., Güngör Ş., Selimoğlu M. A.

Journal of clinical research in pediatric endocrinology , cilt.15, sa.1, ss.62-68, 2023 (SCI-Expanded, Scopus, TRDizin)

22. 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.

Dundar İ., Akinci A., Camtosun E., Ciftci N., Kayas L.

Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation , cilt.17, sa.1, ss.43-50, 2023 (SCI-Expanded, Scopus)

23. Is There a Predictive Factor for an Association with Autoimmune Glandular Disease in Children Diagnosed with Celiac Disease?

Varol F. İ., Çamtosun E., Selimoğlu M. A., Güngör Ş.

Journal of clinical research in pediatric endocrinology , cilt.14, sa.4, ss.409-414, 2022 (SCI-Expanded, Scopus, TRDizin)

24. Survey to Investigate Adherence to Growth Hormone Treatment in Children: The Impact of COVID-19 Pandemic

EREN E., Cetinkaya S., Ongen Y. D., Tercan U., DARCAN Ş., TURAN H., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.95, sa.SUPPL 2, ss.263, 2022 (SCI-Expanded, Scopus)

25. 46, XY Sex Development Defect due to a Novel Homozygous (splice site) c.673_1G>C Variation in the HSD17B3 Gene: Case Report.

Çiftci N., Kayaş L., Çamtosun E., Akıncı A.

Journal of clinical research in pediatric endocrinology , cilt.14, ss.233-238, 2022 (SCI-Expanded, Scopus, TRDizin)

26. TSHRV656F Activating Variant of the Thyroid Stimulating Hormone Receptor Gene in Neonatal Onset Hyperthyroidism: A Case Review.

Kayaş L., Çamtosun E., Akıncı A., Bircan R.

Journal of clinical research in pediatric endocrinology , cilt.14, ss.114-118, 2022 (SCI-Expanded, Scopus, TRDizin)

27. A girl diagnosed with familial hypocalciuric hypercalcemia with heterozygous p.Cys575Tyr variation in the CaSR gene

DÜNDAR İ., ÇAMTOSUN E., DOĞAN M., KAYAŞ L., ÇİFTCİ N., AKINCI A.

Medicine Science , cilt.11, 2022 (TRDizin)

28. Evaluation of endocrine functions before and after enzyme replacement therapy in children with mucopolysaccharidosis

DÜNDAR İ., ÇİFTCİ N., AKINCI A., ÇAMTOSUN E., KAYAŞ L., SIĞIRCI A., et al.

Medicine Science , cilt.11, ss.1184-1189, 2022 (TRDizin)

29. Trend in initial presenting features of type 1 diabetes mellitus over a 24 year period in Turkey: a retrospective analysis of 814 cases

Dundar İ., AKINCI A., ÇAMTOSUN E., Ciftci N., Kayas L., Nalbantoglu O.

TURKISH JOURNAL OF PEDIATRICS , cilt.64, sa.1, ss.40-48, 2022 (SCI-Expanded, Scopus, TRDizin)

30. 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

DÜNDAR İ., AKINCI A., ÇAMTOSUN E., ÇİFTCİ N., KAYAŞ L.

İnönü Üniversitesi Tıp Fakültesi Dergisi , cilt.29, 2022 (TRDizin)

31. Relationship Between Laboratory, Radiological and Cytopathological Evaluations with Histopathological Results in Children with Thyroid Nodules

ÇAMTOSUN E., AKINCI A., ÇİFTCİ N., GÖKÇE H., KAYAŞ L.

Journal of Ankara University Faculty of Medicine , cilt.74, ss.68-75, 2021 (TRDizin)

32. Pediatric Primary Adrenal Insufficiency: A 21-year Single Center Experience.

Çamtosun E., Dündar İ., Akıncı A., Kayaş L., Çiftçi N.

Journal of clinical research in pediatric endocrinology , cilt.13, sa.1, ss.88-99, 2021 (SCI-Expanded, Scopus, TRDizin)

33. NUTRİSYONEL RAŞİTİZM HALEN BİR SORUN: D VİTAMİNİ PROFİLAKSİSİ PROGRAMINA SIKI SARILMALIYIZ

Çamtosun E., Akıncı A., Çelik N., Dündar İ.

STED / Sürekli Tıp Eğitimi Dergisi , cilt.29, sa.1, ss.54-60, 2020 (TRDizin)

34. Novel Mutations in Obesity-related Genes in Turkish Children with Non-syndromic Early Onset Severe Obesity: A Multicentre Study

Akıncı A., Turkkahraman D., Tekedereli İ., Ozer L., Evren B., Şahin İ., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.11, ss.341-349, 2019 (SCI-Expanded, Scopus, TRDizin)

35. A Case of Cleidocranial Dysplasia with a Novel Mutation and Growth Velocity Gain with Growth Hormone Treatment

Çamtosun E., Akıncı A., Demiral E., Tekedereli İ., Sigirci A.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.11, ss.301-305, 2019 (SCI-Expanded, Scopus, TRDizin)

36. Autosomal recessive cutis laxa: a novel mutation in the FBLN5 gene in a family

TEKEDERELİ İ., Demiral E., GÖKCE İ. K., Esener Z., ÇAMTOSUN E., AKINCI A.

CLINICAL DYSMORPHOLOGY , cilt.28, sa.2, ss.63-65, 2019 (SCI-Expanded, Scopus)

37. Laron syndrome related to homozygous growth hormone receptor c.784 > C mutation in a patient with hypoplastic pulmonary arteries

AKINCI A., KARAKURT C., Hwa V., Dundar İ., ÇAMTOSUN E.

CARDIOVASCULAR JOURNAL OF AFRICA , cilt.30, sa.2, 2019 (SCI-Expanded, Scopus)

38. Prematür adrenarşli olgularda hematolojik parametrelerin değerlendirilmesi

ÇELİK N., ÇAMTOSUN E., Dündar İ.

Ortadoğu Tıp Dergisi , cilt.10, sa.3, ss.268-273, 2018 (TRDizin)

39. 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?

Camtosun E., Siklar Z., Berberoglu M.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.10, sa.3, ss.247-255, 2018 (SCI-Expanded, Scopus, TRDizin)

40. Two Siblins and Three Cousins with Allgrove (4A) Syndrome in a Turkish Family: A Novel Mutation in the 'Aladin' Gene

AKINCI A., Dundar İ., ÇAMTOSUN E., Kayas L.

HORMONE RESEARCH IN PAEDIATRICS , cilt.90, ss.150, 2018 (SCI-Expanded, Scopus)

41. Response to Anastrozole Treatment in a Case with Peutz-Jeghers Syndrome and a Large Cell Calcifying Sertoli Cell Tumor

Yekeduz M. K., Siklar Z., Burgu B., Kuloglu Z., Kocaay P., Camtosun E., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.9, sa.2, ss.168-171, 2017 (SCI-Expanded, Scopus, TRDizin)

42. 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

Camtosun E., Siklar Z., CEYLANER S., Kocaay P., Berberoglu M.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.9, sa.2, ss.163-167, 2017 (SCI-Expanded, Scopus, TRDizin)

43. The Association between Premature Adrenarche and Cardiovascular Risk May Be Greater than Expected

ÇELİK N., ALP H., Camtosun E., ALP E., ÇELİK S., BERK E.

HORMONE RESEARCH IN PAEDIATRICS , cilt.87, sa.1, ss.7-14, 2017 (SCI-Expanded, Scopus)

44. Gonadotropin-Releasing Hormone Analogue Treatment in Females with Moderately Early Puberty: No Effect on Final Height

Savas-Erdeve S., Siklar Z., Hacihamdioglu B., Kocaay P., Camtosun E., Ocal G., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.8, sa.2, ss.211-217, 2016 (SCI-Expanded, Scopus, TRDizin)

45. Coexistence of Mosaic Uniparental Isodisomy and a KCNJ11 Mutation Presenting as Diffuse Congenital Hyperinsulinism and Hemihypertrophy

Kocaay P., Siklar Z., Ellard S., Yagmurlu A., Camtosun E., Erden E., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.85, sa.6, ss.421-425, 2016 (SCI-Expanded, Scopus)

46. The Effect of Recombinant Growth Hormone Treatment in Children with Idiopathic Short Stature and Low Insulin-Like Growth Factor-1 Levels

Siklar Z., Kocaay P., Camtosun E., Isakoca M., Hacihamdioglu B., Erdeve S. S., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.7, sa.4, ss.301-306, 2015 (SCI-Expanded, Scopus, TRDizin)

47. A Deep Intronic HADH Splicing Mutation (c.636+471G > T) in a Congenital Hyperinsulinemic Hypoglycemia Case: Long Term Clinical Course

Camtosun E., Flanagan S. E., Ellard S., Siklar Z., Hussain K., Kocaay P., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.7, sa.2, ss.144-147, 2015 (SCI-Expanded, Scopus, TRDizin)

48. Diagnostic Characteristics and Metabolic Risk Factors of Cases with Polycystic Ovary Syndrome during Adolescence

Siklar Z., Berberoglu M., Camtosun E., Kocaay P.

JOURNAL OF PEDIATRIC AND ADOLESCENT GYNECOLOGY , cilt.28, sa.2, ss.78-83, 2015 (SCI-Expanded, Scopus)

49. Three cases of Wolfram syndrome with different clinical aspects

Camtosun E., Siklar Z., Kocaay P., Ceylaner S., Flanagan S. E., Ellard S., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.28, ss.433-438, 2015 (SCI-Expanded, Scopus)

50. Clinical Review of 95 Patients with 46,XX Disorders of Sex Development Based on the New Chicago Classification

Ocal G., Berberoglu M., Siklar Z., Aycan Z., Hacihamdioglu B., Erdeve S. S., et al.

JOURNAL OF PEDIATRIC AND ADOLESCENT GYNECOLOGY , cilt.28, sa.1, ss.6-11, 2015 (SCI-Expanded, Scopus)

51. ROHHAD Syndrome: Reasons for Diagnostic Difficulties in Obesity

Kocaay P., Siklar Z., Camtosun E., Kendirli T., Berberoglu M.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.6, sa.4, ss.254-257, 2014 (SCI-Expanded, Scopus)

52. The evaluation of thyroid carcinoma in childhood and concomitance of autoimmune thyroid disorders

Hacihamdioglu B., Ocal G., Berberoglu M., Erdeve S. S., Camtosun E., Kocaay P., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.27, ss.901-908, 2014 (SCI-Expanded, Scopus)

53. PREPERITONEAL FAT TISSUE MAY BE ASSOCIATED WITH ARTERIAL STIFFNESS IN OBESE ADOLESCENTS

Hacihamdioglu B., Ocal G., Berberoglu M., Siklar Z., Fitoz S., Tutar E., et al.

ULTRASOUND IN MEDICINE AND BIOLOGY , cilt.40, sa.5, ss.871-876, 2014 (SCI-Expanded, Scopus)

54. A Novel Heterozygous Mutation in Steroidogenic Factor-1 in Pubertal Virilization of a 46,XY Female Adolescent

Siklar Z., Berberoglu M., Ceylaner S., Camtosun E., Kocaay P., Gollu G., et al.

JOURNAL OF PEDIATRIC AND ADOLESCENT GYNECOLOGY , cilt.27, sa.2, ss.98-101, 2014 (SCI-Expanded, Scopus)

55. 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?

Ocal G., Berberoglu M., Siklar Z., Ruhi H. I., Tukun A., Camtosun E., et al.

EUROPEAN JOURNAL OF PEDIATRICS , cilt.171, sa.10, ss.1497-1502, 2012 (SCI-Expanded, Scopus)

56. Tenya (Şerit)

PÜRÇÜKLÜ E., KARA A.

Clinic Pediatri , cilt.3, sa.5, ss.46-53, 2008 (Hakemsiz Dergi)

Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 107

1. Çocukluk Çağı Diyabet Alt gruplarının Eğilimleri ve Klinik Özellikleri:28 yıllık tek merkez deneyimi

ÖNCÜL M., AKINCI A., DÜNDAR İ., ÇAMTOSUN E., YAMANCAN Z.

5. Doğu Pediatri KOngresi, Türkiye, 25 Eylül 2025, (Özet Bildiri)

2. Hiperfosfatemik Ailevi Tümöral Kalsinozis Klinik Tanısıyla Izlenen, Sevelamer, Asetozalamid ve Topikal Sodyum Tiyosülfat Tedavilerine Kısmi Cevap Alınan Olgu.

YAMANCAN Z., ÇAMTOSUN E., DÜNDAR İ., KAYA E.

29. Ulusal Pediyatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Türkiye, 15 - 20 Nisan 2025, (Özet Bildiri)

3. Neonatal Hipoglisemi, Yarık Damak Dudak Anomalisi, Postaksiyel Polidaktili, Çoklu Hipofizer Hormon Eksikligi: Culler Jones Sendromlu (GLI2) Olgu

KAYA E., ÇAMTOSUN E., DÜNDAR İ., YAMANCAN Z., AYKUT A., DURMAZ A.

29. Ulusal Pediyatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Türkiye, 15 - 20 Nisan 2025, (Özet Bildiri)

4. Önce Hipoglisemi Atakları Sonra Otoantikor Negatif Diyabet ile Prezente Olan, KLF11 (MODY-7) Geninde Yeni Bir Varyasyon Saptanan Olgu

YAMANCAN Z., ÇAMTOSUN E., DÜNDAR İ., KAYA E., EKİCİ C., SARAÇ H.

29. Ulusal Pediyatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Türkiye, 15 - 20 Nisan 2025, (Özet Bildiri)

5. 21-hidroksilaz Eksikligine Baglı Klasik Olmayan Konjenital Adrenal Hiperplazi Tanısı Için Standart Doz Synacthen Testinde 30. Dakikada 17-hidroksiprogesteron Ölçümü Gerekli Midir?

ÇİFTCİ N., ÇAMTOSUN E., DÜNDAR İ., UNAL E., ÇELİK N., AKINCI A.

29. Ulusal Pediyatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Türkiye, 15 - 20 Nisan 2025, (Özet Bildiri)

6. TMEM38B Geninde Novel Varyasyon Saptanan Osteogenezis Imperfekta Tip XIV Tanılı Olgunun Pamidronat Tedavisi Ile Sekiz Yıllık Klinik Izlemi.

KAYA E., ÇAMTOSUN E., DÜNDAR İ., YAMANCAN Z., TEKEDERELİ İ.

29. Ulusal Pediyatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Türkiye, 15 - 20 Nisan 2025, (Özet Bildiri)

7. KAH Dışı Primer Adrenal Yetmezlik Serisi-1: Triple A Sendromu

ÇAMTOSUN E.

Çocuk Endokrinolojisi ve Diyabet Derneği Adrenal Çalışma Grubu Semineri, Çevrimiçi, 27 Kasım 2024

8. ENNP1 Geninde Aynı Mutasyona Bağlı İki Farklı Prezentasyon: Hipofosfatemik Raşitizm, Çoklu Arteryel Stenoz Birlikteliği Ve İntrauterin Başlangıçlı Jeneralize Arteryel Kalsifikasyon

ÇAMTOSUN E., YAMANCAN Z., ELKIRAN Ö., ESER M., DÜNDAR İ., ALAGÖZ M.

Çocuk Endokrinolojisi Olgu Sunumları-12 Sempozyumu, Ankara, Türkiye, 2 - 03 Kasım 2024, (Özet Bildiri)

9. Görünürde Mineralokortikoid Fazlalığı Tanısı İle İzlenen Pediyatrik Olguda Hipertansiyonun Kontrolü: İki Yıllık Deneyim

ÇAMTOSUN E., KAYA E., TABEL Y., DÜNDAR İ., YAMANCAN Z.

Çocuk Endokrinolojisi Olgu Sunumları-12 Sempozyumu, Ankara, Türkiye, 2 - 03 Kasım 2024, (Özet Bildiri)

10. Yaz Aylarında Tekrarlayan Ciddi Hiponatremi İle Başvuran Olguda İzole Hiperklorhidroz.

YAMANCAN Z., ÇAMTOSUN E., DÜNDAR İ., KAYA E.

Çocuk Endokrinolojisi Olgu Sunumları-12 Sempozyumu, Ankara, Türkiye, 2 - 03 Kasım 2024, (Özet Bildiri)

11. P3H1 (LEPRE1) Geninde Novel Varyasyon Saptanan Osteogenezis İmperfekta Tip VIII Tanılı Olgunun Pamidronat Tedavisi İle Uzun Dönem İzlemi

KAYA E., ÇAMTOSUN E., DÜNDAR İ., YAMANCAN Z.

Çocuk Endokrinolojisi Olgu Sunumları-12 Sempozyumu, Ankara, Türkiye, 2 - 03 Kasım 2024, (Özet Bildiri)

12. Kronik Hastalığı Olan Çocukların Aile Fonksiyonları İle Sağlıklı Yaşam Davranışları Arasındaki İlişkinin İncelenmesi

Özarslan S., Çetin K., Günay U., Tokmak G., Yavaş N., Elkıran Ö., et al.

2. Uluslararası Hemşirelikte Palyatif Bakım Kongresi, Malatya, Türkiye, 9 - 12 Ekim 2024, (Özet Bildiri)