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akaturk Akademik ölçüm

Akademisyen profili · DOÇENT

BAHAR ÖZCABI

İSTANBUL ATLAS ÜNİVERSİTESİ

  • Ana Dal Sağlık Bilimleri Temel Alanı
  • Yan Dal Çocuk Endokrinolojisi (Çocuk Sağlığı ve Hastalıkları)
  • TIP FAKÜLTESİ
  • TIP PR.
Makale 30
Proje 0
Kitap 7
Bildiri 21
Patent 1
Sanatsal 1
Scopus (SJR)
Q1
1
Q2
17
Q3
3
Q4
2
WoS (JCR)
Q1
1
Q2
4
Q3
11
Q4
8
TR Index
15 makale

Dizin ve quartile filtreleri

Toplam 30 yayın

Makaleler

  1. 2023 A Rare Case of Monogenic Obesity due to a Novel Variant in the ADCY3 Gene: Challenges in Follow-up and Treatment. Journal of clinical research in pediatric endocrinology DOI 10.4274/jcrpe.galenos.2023.2023-7-2
  2. 2022 Evaluation of the impact of childhood obesity on retrobulbar hemodynamics and retinal microvasculature European Journal of Ophthalmology DOI 10.1177/11206721221086244
  3. 2022 The association between vitamin B12, folate, homocysteine levels, and carotid intima-media thickness in children with obesity: a cross-sectional study JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM DOI 10.1515/jpem-2022-0250
  4. 2022 Factors Affecting Metabolic Bone Disease of Prematurity: Is Hypothyroxinemia included? SiSli Etfal Hastanesi Tip Bulteni / The Medical Bulletin of Sisli Hospital DOI 10.14744/SEMB.2021.99076
  5. 2021 Is Waist-height Ratio Associated with Thyroid Antibody Levels in Children with Obesity? Galenos Yayinevi DOI 10.4274/jcrpe.galenos.2020.2020.0170
  6. 2021 Hypogonadism: Is It Always Hypogonadotropic in an Adolescent With a Cleft Palate? A Surprising Case of Klinefelter Syndrome The Cleft Palate-Craniofacial Journal DOI 10.1177/1055665620967601
  7. 2021 Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism Genetics in Medicine DOI 10.1038/s41436-020-01087-5
  8. 2021 Evaluation of clinical, endocrine and metabolic findings in obese children with and without hepatosteatosis Journal of Pediatric Endocrinology and Metabolism DOI 10.1515/jpem-2021-0034
  9. 2021 Management of Rapidly Progressive Precocious Puberty in a Patient with Mosaic Turner Syndrome Acta Endocrinologica (Bucharest) DOI 10.4183/aeb.2021.101
  10. 2021 Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome Journal of Clinical Research in Pediatric Endocrinology DOI 10.4274/jcrpe.galenos.2021.2020.0228
  11. 2021 Clinical and Genetic Characteristics of Patients with Corticosterone Methyloxidase Deficiency Type 2: Novel Mutations in CYP11B2 Journal of Clinical Research in Pediatric Endocrinology DOI 10.4274/jcrpe.galenos.2020.2019.0216
  12. 2021 Evaluation of Thyroid Nodules in Children and Adolescents: Multicenter Study in Turkey The Journal of Current Pediatrics DOI 10.4274/jcp.2021.43926
  13. 2021 Associations of Respiratory Distress Syndrome Severity and Other Factors With Transient Hypothyroxinemia of Prematurity Cureus DOI 10.7759/cureus.17159
  14. 2021 ŞİŞMAN ÇOCUK VE ERGENLERDE DEPRESYONUN UYKU MİKTARI ve ŞİŞMANLIĞIN DERECESİ İLE İLİŞKİSİ Acta Medica Alanya DOI 10.30565/medalanya.784624
  15. 2020 A Case of Sotos Syndrome Caused by a Novel Variant in the NSD1 Gene: A Proposed Rationale to Treat Accompanying Precocious Puberty Acta Endocrinologica (Bucharest) DOI 10.4183/aeb.2020.245
  16. 2019 Left and right ventricular function by echocardiography, tissue Doppler imaging, carotid intima-media thickness, and asymmetric dimethyl arginine levels in obese adolescents with metabolic syndrome Cardiology in the Young DOI 10.1017/S1047951118002329
  17. 2019 Lipid accumulation product is a predictor of nonalcoholic fatty liver disease in childhood obesity Korean Journal of Pediatrics DOI 10.3345/kjp.2019.00248
  18. 2019 Ergen kızlarda polikistik over sendromu: klinik, endokrin ve metabolik bulgular Zeynep Kamil Tıp Bülteni DOI 10.16948/zktipb.499708
  19. 2018 Incidence of Type 1 Diabetes in Children Aged Below 18 Years During 2013-2015 in Northwest Turkey Journal of Clinical Research in Pediatric Endocrinology DOI 10.4274/jcrpe.0025
  20. 2018 Neonatal Diabetes: Two Cases with Isolated Pancreas Agenesis due to Homozygous PTF1A Enhancer Mutations and One with Developmental Delay, Epilepsy, and Neonatal Diabetes Syndrome due to KCNJ11 Mutation Journal of Clinical Research in Pediatric Endocrinology DOI 10.4274/jcrpe.5162

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