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HALİSE NESLİHAN ÖNENLİ MUNGAN

PROFESÖR

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 137
  • Proje 0
  • Kitap 0
  • Bildiri 0
  • Patent 0
  • Sanatsal 0
Scopus (SJR) Q1 28 Q2 35 Q3 34 Q4 4
WoS (JCR) Q1 16 Q2 23 Q3 27 Q4 39
TR Index 39 makale

Makaleler

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

Dizin filtreleri

Toplam 137 yayın

Scopus (SJR)
Q1 28 Q2 35 Q3 34 Q4 4
WoS (JCR)
Q1 16 Q2 23 Q3 27 Q4 39
TR Index
39 makale

Makale listesi

  1. 2025 The effect of triheptanoin treatment on clinical and laboratory outcomes in patients with long-chain fatty acid oxidation disorder European Journal of Pediatrics DOI 10.1007/s00431-025-06216-3 YÖKSİS SJR Q1 JCR Q1
  2. 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
  3. 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
  4. 2025 Hepatic Phenotype in NBAS‐Associated Disease: Clinical Course, Prognostic Factors and Outcome in 230 Patients Liver International DOI 10.1111/liv.70146 YÖKSİS SJR Q1 JCR Q1
  5. 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
  6. 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
  7. 2025 Feeding Models in Classical Phenylketonuria: Do They Make a Difference in Infant Sleep? Nutrients DOI 10.3390/nu17183022 YÖKSİS SJR Q1 JCR Q1
  8. 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
  9. 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
  10. 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
  11. 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
  12. 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
  13. 2025 Nutritional management in MNGIE disease: A case report CLINICAL SCIENCE OF NUTRITION DOI 10.62210/ClinSciNutr.2025.104 YÖKSİS TR Index
  14. 2025 Clinical and molecular findings in 44 Turkish patients with infantile-onset Pompe disease Cukurova Medical Journal DOI 10.17826/cumj.1710811 YÖKSİS TR Index JCR Q4
  15. 2025 Developmental and Cognitive Outcomes in 342 Patients With Different Types of Hyperphenylalaninemia SiSli Etfal Hastanesi Tip Bulteni / The Medical Bulletin of Sisli Hospital DOI 10.14744/SEMB.2025.09471 YÖKSİS TR Index JCR Q3
  16. 2025 Sistinozis Hastalarında İskelet Sağlığının Değerlendirilmesi: Çukurova Üniversitesi Deneyimi Ankara Eğitim ve Araştırma Hastanesi Tıp Dergisi DOI 10.20492/aeahtd.1615823 YÖKSİS TR Index
  17. 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
  18. 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
  19. 2024 Two new patients with acromesomelic dysplasia, PRKG2 type-identification and characterization of the first missense variant. European journal of human genetics : EJHG DOI 10.1038/s41431-023-01472-z YÖKSİS SJR Q1 JCR Q1
  20. 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

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