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ÇUKUROVA ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ

  • Ana Dal Sağlık Bilimleri Temel Alanı
  • Yan Dal Çocuk Metabolizma Hastalıkları (Çocuk Sağlığı ve Hastalıkları)

Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.

  • Makale 86
  • Proje 0
  • Kitap 0
  • Bildiri 0
  • Patent 0
  • Sanatsal 0
Scopus (SJR) Q1 18 Q2 28 Q3 22 Q4 4
WoS (JCR) Q1 7 Q2 22 Q3 23 Q4 24
TR Index 30 makale

Alan+yıl+tür normalize OpenAlex yüzdelik — Clarivate ESI / SciVal değildir.

Üst %1 makale 0
Üst %10 makale 4
Ort. yüzdelik 52.1%
Üst %1 payı 0.0%
Üst %10 payı 5.5%

Makaleler

YÖKSİS ve OpenAlex kaynak ayrımıyla makaleler; quartile ve TR Index ile daraltabilirsiniz.

Dizin filtreleri

Toplam 86 yayın

Scopus (SJR)
Q1 18 Q2 28 Q3 22 Q4 4
WoS (JCR)
Q1 7 Q2 22 Q3 23 Q4 24
TR Index
30 makale

Makale listesi

  1. 2025 First evaluation of fibroblast growth factor 21 levels in patients diagnosed with glycogen storage diseases with liver involvement Journal of Pediatric Endocrinology and Metabolism DOI 10.1515/jpem-2025-0255 YÖKSİS SJR Q3 JCR Q3 OpenAlex 25.3%
  2. 2025 Genotype–Phenotype Correlations and Shifting Diagnosis Age in Turkish Mucopolysaccharidosis Type II Patients: A Multicenter Retrospective Study Diagnostics DOI 10.3390/diagnostics15212773 YÖKSİS SJR Q2 JCR Q1 OpenAlex 30.9%
  3. 2025 Bi-allelic variants in MRPL49 cause variable clinical presentations, including sensorineural hearing loss, leukodystrophy, and ovarian insufficiency The American Journal of Human Genetics DOI 10.1016/j.ajhg.2025.02.005 YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 92.2%
  4. 2025 A novel homozygous missense DNAJC3 variant in syndromic juvenile-onset diabetes Journal of Pediatric Endocrinology and Metabolism DOI 10.1515/jpem-2025-0072 YÖKSİS SJR Q3 JCR Q3 OpenAlex 74.8%
  5. 2025 A comprehensive integrated disease management program for phenylketonuria (IDMP-PKU) from Türkiye: rationale, design and patient characteristics Orphanet Journal of Rare Diseases DOI 10.1186/s13023-025-03702-7 YÖKSİS SJR Q1 JCR Q2 OpenAlex 87.2%
  6. 2025 Neurological involvement in 51 cystinosis patients: A single-center experience European Journal of Paediatric Neurology DOI 10.1016/j.ejpn.2025.05.011 YÖKSİS SJR Q1 JCR Q1 OpenAlex 80.8%
  7. 2025 Clinical features and rare complications in 132 patients with hepatic glycogenosis Orphanet Journal of Rare Diseases DOI 10.1186/s13023-025-03783-4 YÖKSİS SJR Q1 JCR Q2 OpenAlex 24.6%
  8. 2025 Feeding Models in Classical Phenylketonuria: Do They Make a Difference in Infant Sleep? Nutrients DOI 10.3390/nu17183022 YÖKSİS SJR Q1 JCR Q1 OpenAlex 23.1%
  9. 2025 Audiovestibular Findings in Gaucher Disease Types I and III: Evidence of Vestibular Involvement in GD1 Journal of Inherited Metabolic Disease DOI 10.1002/jimd.70046 YÖKSİS SJR Q1 JCR Q2 OpenAlex 65.9%
  10. 2025 Nutritional management in MNGIE disease: A case report CLINICAL SCIENCE OF NUTRITION DOI 10.62210/ClinSciNutr.2025.104 YÖKSİS TR Index OpenAlex 70.7%
  11. 2025 İnfantil başlangıçlı Pompe hastalığı olan 44 Türk hastada klinik ve moleküler bulgular Cukurova Medical Journal DOI 10.17826/cumj.1710811 YÖKSİS TR Index JCR Q4 OpenAlex 25.4%
  12. 2025 Sistinozis Hastalarında İskelet Sağlığının Değerlendirilmesi: Çukurova Üniversitesi Deneyimi Ankara Eğitim ve Araştırma Hastanesi Tıp Dergisi DOI 10.20492/aeahtd.1615823 YÖKSİS TR Index OpenAlex 27.1%
  13. 2025 5-Oxoprolinase deficiency and epilepsy: report of four cases with new clinical findings and clinical diversity even in the same family Molecular Syndromology DOI 10.1159/000545609 YÖKSİS SJR Q3 JCR Q4 OpenAlex 7.4%
  14. 2025 Long-Term Outcomes of Chenodeoxycholic Acid Therapy for Cerebrotendinous Xanthomatosis: A Nationwide Study on Prognostic Factors and Treatment Response JOURNAL OF INHERITED METABOLIC DISEASE DOI 10.1002/jimd.70069 YÖKSİS SJR Q1 JCR Q2 OpenAlex üst %10 OpenAlex 95.8%
  15. 2025 Expert opinion on clinical presentation, diagnosis and treatment of infantile onset pompe disease: a delphi study in Türkiye Turkish Journal of Medical Sciences DOI 10.55730/1300-0144.6005 YÖKSİS TR Index SJR Q3 JCR Q2 OpenAlex 15.4%
  16. 2024 Pediatric Cardiomyopathies from the Landscape of Inherited Metabolic Disorders in Southeastern Turkey Iranian Journal of Pediatrics DOI 10.5812/ijp-141783 YÖKSİS SJR Q3 JCR Q4 OpenAlex 0.3%
  17. 2024 Early diagnostic clues of mucolipidosis type II: Significance of radiological findings. American journal of medical genetics. Part A DOI 10.1002/ajmg.a.63545 YÖKSİS SJR Q2 JCR Q3 OpenAlex 72.2%
  18. 2023 Actions speak louder than words: Home visits and its effect on dietary adherence in patients with phenylketonuria Journal of Paediatrics and Child Health DOI 10.1111/jpc.16488 YÖKSİS SJR Q2 JCR Q2 OpenAlex 47.5%
  19. 2023 Perspectives of adult patients with lysosomal storage diseases on the transition from pediatric to adult healthcare in Turkey Archives de Pediatrie DOI 10.1016/j.arcped.2023.04.006 YÖKSİS SJR Q2 JCR Q3 OpenAlex 62.6%
  20. 2023 Expanding the phenotypic landscape of Gaucher disease type 3c with a novel entity - Transient neonatal cholestasis European Journal of Medical Genetics DOI 10.1016/j.ejmg.2023.104764 YÖKSİS SJR Q2 JCR Q4 OpenAlex 70.5%

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