Dr. Öğr. Üyesi YAĞMUR ÜNSAL

Yayın Ağı

Makaleler 13

1. Calcineurin inhibitor-related hyperkalemia is caused by hyporeninemic hypoaldosteronism and fludrocortisone is an effective treatment: Report of a case series and review of the literature

ÜNSAL Y., BALTU D., GÜLHAN B., OKUR F. V., ÖZALTIN F., DÜZOVA A., et al.

PEDIATRIC TRANSPLANTATION , cilt.28, sa.4, 2024 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

2. Early weight gain after diagnosis may have an impact on remission status in children with new-onset type 1 diabetes mellitus

Emet D. C., Karavar H. N., GÖZMEN O., Agyar A. A., ÜNSAL Y., Canturk M., et al.

Journal of Diabetes , cilt.15, sa.12, ss.1011-1019, 2023 (SCI-Expanded, Scopus)

3. Evaluation of Clinical Characteristics and Growth Hormone Response in a Rare Skeletal Dysplasia: Pycnodysostosis

ÜNSAL Y., ATAR S.

CUREUS , 2023 (ESCI)

4. Challenges During the Coronavirus Disease 2019 Pandemic: Diabetes Control and Psychosocial Issues in Children with Type 1 Diabetes Mellitus and Their Mothers

Emet D. C., Yeşil A. M., Çelik B., Şencan B., ÜNSAL Y., Gönç N., et al.

Turkish Archives of Pediatrics , cilt.58, sa.4, ss.418-424, 2023 (Scopus, TRDizin)

5. Case Report: Severe McCune–Albright syndrome presenting with neonatal Cushing syndrome: navigating through clinical obstacles

ÜNSAL Y., GÖZMEN O., USER İ. R., Hızarcıoglu H., GÜLHAN B., EKİNCİ S., et al.

Frontiers in Endocrinology , cilt.14, 2023 (SCI-Expanded, Scopus)

6. Organic acidemias in the neonatal period: 30 years of experience in a referral center for inborn errors of metabolism

ÜNSAL Y., YURDAKÖK M., YİĞİT Ş., ÇELİK H. T., DURSUN A., SİVRİ H. S., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.35, sa.11, ss.1345-1356, 2022 (SCI-Expanded, Scopus)

7. Psychosocial Impact of the COVID-19 Pandemic on Children with Congenital Adrenal Hyperplasia and Their Families

Çelik N. B., Ünsal Y., Emet D. C., Yeşil A. M., Şencan B., GÖNÇ E. N., et al.

Turkish Archives of Pediatrics , cilt.57, sa.6, ss.621-629, 2022 (Scopus, TRDizin)

8. Apparent mineralocorticoid excess: A diagnosis beyond classical causes of severe hypertension in a child

GÜLHAN B., ÜNSAL Y., BALTU D., ÇELİK ERTAŞ N. B., Ozdemir G., Utine E., et al.

BLOOD PRESSURE MONITORING , cilt.27, sa.3, ss.208-211, 2022 (SCI-Expanded, Scopus)

9. Is conventional treatment still the first choice in pediatric patients with PHEX mutations in an era of monoclonal FGF-23 antibody?

Alikasifoglu A., Unsal Y., Gonc N., Ozon A., Kandemir N., Alikasifoglu M.

HORMONE RESEARCH IN PAEDIATRICS , cilt.94, sa.SUPPL 1, ss.210-211, 2021 (SCI-Expanded, Scopus)

10. Neonatal McCune Albright Syndrome Presenting with Diabetes Mellitus

ÜNSAL Y., Gonc N., USER İ. R., HIZARCIOĞLU GÜLŞEN H., GÜLHAN B., EKİNCİ S., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.94, sa.SUPPL 1, ss.349-350, 2021 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

11. Fludrocortisone is the salvage treatment in cases with calcineurin inhibitor related hyperkalemia

Unsal Y., Baltu D., Gulhan B., Okur F. V., Duzova A., Ozon A., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.94, sa.SUPPL 1, ss.193-194, 2021 (SCI-Expanded, Scopus)

12. Long-term effect of conventional phosphate and calcitriol treatment on metabolic recovery and catch-up growth in children with PHEX mutation

ALİKAŞİFOĞLU A., ÜNSAL Y., GÖNÇ E. N., ÖZÖN Z. A., KANDEMİR N., ALİKAŞİFOĞLU M.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.34, sa.12, ss.1573-1584, 2021 (SCI-Expanded, Scopus)

13. Spondyloocular syndrome: Presentation of two siblings diagnosed with the rare disease and the results of Pamidronate Therapy

VURALLI KARAOĞLAN D., ŞİMŞEK KİPER P. Ö., Utine E., ÜNSAL Y., ALİKAŞİFOĞLU A., KANDEMİR N.

HORMONE RESEARCH IN PAEDIATRICS , cilt.91, ss.387, 2019 (SCI-Expanded, Scopus)

Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 3

1. Spondyloocular syndrome: Presentation of two siblings diagnosed with the rare disease and the results of Pamidronate Therapy

VURALLI KARAOĞLAN D., ŞİMŞEK KİPER P. Ö., UTİNE G. E., ÜNSAL Y., ALİKAŞİFOĞLU A., KANDEMİR N.

The 58th Annual ESPE Meeting, VİYANA, Avusturya, 19 - 21 Eylül 2019, cilt.91, ss.387, (Özet Bildiri)

2. Unusual Presentation of Autoimmune Polyglandular Syndrome Type 1 (Aps1)

VURALLI KARAOĞLAN D., TAN Ç., ÇAĞDAŞ AYVAZ D. N., TEZCAN F. İ., DEMİR H., HIZARCIOĞLU GÜLŞEN H., et al.

58th Annual ESPE, Viyana, Avusturya, 19 - 21 Eylül 2019, cilt.91, ss.245-246, (Tam Metin Bildiri)

3. Glutarik Asidemi Tip 2 Dismorfolojik İpuçları Veren Metabolik Bir Hastalık

AKGÜN DOĞAN Ö., ÜNSAL Y., ŞİMŞEK KİPER P. Ö., ÜTİNE G. E., DURSUN A., TALİM B., et al.

3. Nörometabolik Dismorfoloji Sempozyumu, Türkiye, 10 - 12 Mart 2016, (Tam Metin Bildiri)

Metrikler

Yayın

Yayın (WoS)

Yayın (Scopus)

Atıf (WoS)

H-İndeks (WoS)

Atıf (Scopus)

H-İndeks (Scopus)

BM Sürdürülebilir Kalkınma Amaçları

Yayınlar & Eserler