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akaturk Academic measurement

Academician profile · PROFESÖR

ALİ DURSUN

HACETTEPE ÜNİVERSİTESİ

  • TIP FAKÜLTESİ
  • DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
Articles YÖKSİS 109
Projects 1
Books 3
Proceedings 166
Patents 1
Artistic 1
Scopus (SJR)
Q1 27 Q2 30 Q3 16 Q4 3
WoS (JCR)
Q1 17 Q2 20 Q3 24 Q4 15
TR Index 13 articles

Scopus (SJR)

Q1 27 Q2 30 Q3 16 Q4 3

WoS (JCR)

Q1 17 Q2 20 Q3 24 Q4 15

TR Index

13 articles

109 publications total

Articles

  1. 2025 Comparison of Ketogenesis and Ketolysis Defects: A Retrospective Single-Center Study of 30 Patients TURKISH ARCHIVES OF PEDIATRICS DOI 10.5152/TurkArchPediatr.2025.25156
  2. 2025 Endoplasmic reticulum stress pathways and cellular death mechanisms in patients with phenylketonuria MOLECULAR BIOLOGY REPORTS DOI 10.1007/s11033-025-10681-2
  3. 2025 Clinical and laboratory characteristics of propionic acidemia in a Turkish cohort JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM DOI 10.1515/jpem-2024-0366
  4. 2025 Metabolomics and Lipidomics Explore Phenotype-Specific Molecular Signatures for Phenylketonuria INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES DOI 10.3390/ijms26157171
  5. 2025 Phenotypic diversity in NAXE mutations NEUROLOGICAL SCIENCES DOI 10.1007/s10072-025-08006-z
  6. 2025 High prevalence of low bone mineral density in young adults with phenylketonuria POSTGRADUATE MEDICINE DOI 10.1080/00325481.2024.2444873
  7. 2025 Comprehensive analysis of 1103 infants referred to a single center due to positive newborn screening test for phenylketonuria TURKISH JOURNAL OF PEDIATRICS DOI 10.24953/turkjpediatr.2025.5263
  8. 2024 Long-term clinical evaluation of patients with alpha-mannosidosis – A multicenter study European Journal of Medical Genetics DOI 10.1016/j.ejmg.2024.104927
  9. 2024 ELFN1 is a new extracellular matrix (ECM)-associated protein Life Sciences DOI 10.1016/j.lfs.2024.122900
  10. 2024 High prevalence of low bone mineral density in young adults with phenylketonuria Postgraduate Medicine DOI 10.1080/00325481.2024.2444873
  11. 2024 A transposase-derived gene required for human brain development bioRxiv DOI 10.1101/2023.04.28.538770
  12. 2024 Exploring metabolic alterations in PYCR2 deficiency: Unveiling pathways and clinical presentations of hypomyelinating leukodystrophy 10 American Journal of Medical Genetics Part A DOI 10.1002/ajmg.a.63645
  13. 2024 Blood Phenylalanine Levels in Patients with Phenylketonuria from Europe between 2012 and 2018: Is It a Changing Landscape? Nutrients DOI 10.3390/nu16132064
  14. 2024 Longitudinal Dietary Intake Data in Patients with Phenylketonuria from Europe: The Impact of Age and Phenylketonuria Severity Nutrients DOI https://pubmed.ncbi.nlm.nih.gov/39275225/
  15. 2024 From Shadows to Diagnosis: Unraveling L-2 Hydroxyglutaric Aciduria in Adulthood ARCHIVES OF EPILEPSY DOI 10.4274/ArchEpilepsy.2024.24114
  16. 2024 Long-term clinical evaluation of patients with alpha-mannosidosis - A multicenter study EUROPEAN JOURNAL OF MEDICAL GENETICS DOI 10.1016/j.ejmg.2024.104927
  17. 2024 ELFN1 is a new extracellular matrix (ECM)-associated protein LIFE SCIENCES DOI 10.1016/j.lfs.2024.122900
  18. 2023 COVID-19 in inherited metabolic disorders: Clinical features and risk factors for disease severity Molecular Genetics and Metabolism DOI 10.1016/j.ymgme.2023.107607
  19. 2023 Predictors of eventual requirement of phenylalanine-restricted diet in young infants with phenylalanine hydroxylase deficiency initially managed with sapropterin monotherapy Elsevier BV DOI 10.1016/j.ymgme.2023.107706
  20. 2022 Single Institutional Experience with GM1 Gangliosidosis: Clinical and Laboratory Results of 14 Patients BALKAN MEDICAL JOURNAL DOI 10.4274/balkanmedj.galenos.2022.2022-3-75

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