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Akademisyen

FATİH SÜHEYL EZGÜ

PROFESÖR

GAZİ 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 183
  • Proje 0
  • Kitap 23
  • Bildiri 232
  • Patent 0
  • Sanatsal 0
Scopus (SJR) Q1 52 Q2 57 Q3 25 Q4 13
WoS (JCR) Q1 19 Q2 41 Q3 38 Q4 45
TR Index 13 makale

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

Üst %1 makale 4
Üst %10 makale 12
Ort. yüzdelik 62.7%
Üst %1 payı 2.7%
Üst %10 payı 8.1%

Makaleler

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

Dizin filtreleri

Toplam 183 yayın

Scopus (SJR)
Q1 52 Q2 57 Q3 25 Q4 13
WoS (JCR)
Q1 19 Q2 41 Q3 38 Q4 45
TR Index
13 makale

Makale listesi

  1. 2026 Gene Therapies: Any Merit in Nephrology? Giornale Italiano di Nefrologia DOI 10.69097/42-05-2025-06 YÖKSİS SJR Q3 OpenAlex 36.3%
  2. 2025 The Role of Genetics in Congenital Heart Disease-Associated Pulmonary Arterial Hypertension Pediatric Cardiology DOI 10.1007/s00246-025-03847-z YÖKSİS SJR Q2 JCR Q3 OpenAlex 66.3%
  3. 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%
  4. 2025 Rapidly progressive late-oset X-linked adrenoleukodystrophy with a novel mutation. JCEM Case Reports DOI 10.1210/jcemcr/luae218.003 YÖKSİS SJR Q4 OpenAlex 0.8%
  5. 2025 Mucopolysaccharidosis or Skeletal Dysplasia?: Important Clinical and Radiologic Clues for Differential Diagnosis of Based on Difficult Cases Journal of Clinical Research in Pediatric Endocrinology DOI 10.4274/jcrpe.galenos.2025.2025-8-11 YÖKSİS TR Index SJR Q2 JCR Q2 OpenAlex 35.8%
  6. 2025 Markers of Inflammation and Autoinflammation in Patients With Gaucher Disease: A Single-Center Observational Study Clinical Pediatrics DOI 10.1177/00099228251392699 YÖKSİS SJR Q3 JCR Q4 OpenAlex 73.0%
  7. 2024 Comprehensive evaluation of patients with primary hyperoxaluria type 1: A nationwide study Nephrology DOI 10.1111/nep.14273 YÖKSİS SJR Q1 JCR Q3 OpenAlex 83.1%
  8. 2024 Intestinal microbiota composition of children with glycogen storage Type I patients European Journal of Clinical Nutrition DOI 10.1038/s41430-024-01412-0 YÖKSİS SJR Q1 JCR Q2 OpenAlex 73.2%
  9. 2024 Endocrinological and metabolic profile of Gaucher disease patients treated with enzyme replacement therapy Journal of Pediatric Endocrinology and Metabolism DOI 10.1515/jpem-2023-0504 YÖKSİS SJR Q2 JCR Q3 OpenAlex 68.0%
  10. 2024 Glycogen storage disorder types IX: the mutation spectrum and ethnic distribution Orphanet Journal of Rare Diseases DOI 10.1186/s13023-024-03488-0 YÖKSİS OpenAlex üst %10 OpenAlex 90.1%
  11. 2024 Advances in Immune Tolerance Induction in Enzyme Replacement Therapy Pediatric Drugs DOI 10.1007/s40272-024-00627-9 YÖKSİS SJR Q1 JCR Q1 OpenAlex 85.2%
  12. 2024 Giant thymic cyst overclouding the diagnosis of fibrodysplasia ossificans progressiva: an inconvenient coincidence Rheumatology DOI 10.1093/rheumatology/kead591 YÖKSİS SJR Q1 JCR Q1 OpenAlex 25.6%
  13. 2024 Association between CLOCK gene polymorphisms with circadian rhythm, chrononutrition, dietary intake, and metabolic parameters in adolescents Frontiers in Public Health DOI 10.3389/fpubh.2024.1435460 YÖKSİS SJR Q1 JCR Q1 OpenAlex 72.3%
  14. 2024 Mucopolysaccharidosis type VII (Sly syndrome) - What do we know? Molecular Genetics and Metabolism DOI 10.1016/j.ymgme.2024.108145 YÖKSİS SJR Q2 JCR Q2 OpenAlex üst %10 OpenAlex 90.7%
  15. 2024 New perspectives for the treatment and follow-up of glycogen storage disease type V: DL-3-hydroxybutyric acid with modified Atkins diet and quadriceps femoris shear wave elastography Journal of Pediatric Endocrinology and Metabolism DOI 10.1515/jpem-2024-0284 YÖKSİS SJR Q2 JCR Q3 OpenAlex 59.4%
  16. 2024 Pterin Profiling in Serum, Dried Blood Spot, and Urine Samples Using LC-MS/MS in Patients with Inherited Hyperphenylalaninemia Molecular Syndromology DOI 10.1159/000535853 YÖKSİS SJR Q3 JCR Q4 OpenAlex 80.8%
  17. 2023 Expert-opinion-based guidance for the care of children with lysosomal storage diseases during the COVID-19 pandemic: An experience-based Turkey perspective. Frontiers in public health DOI 10.3389/fpubh.2023.1092895 YÖKSİS OpenAlex 1.0%
  18. 2023 Long-Term Experience with Anaphylaxis and Desensitization to Alglucosidase Alfa in Pompe Disease International Archives of Allergy and Immunology DOI 10.1159/000528343 YÖKSİS SJR Q2 JCR Q3 OpenAlex 83.3%
  19. 2023 Endocrinological, immunological and metabolic features of patients with Fabry disease under therapy J Pediatr Endocrinol Metab DOI 10.1515/jpem-2023-0105 YÖKSİS SJR Q2 JCR Q3 OpenAlex 44.3%
  20. 2023 A possibly new autoinflammatory disease due to compound heterozygous phosphomevalonate kinase gene mutation JOINT BONE SPINE DOI 10.1016/j.jbspin.2022.105490 YÖKSİS SJR Q2 JCR Q1 OpenAlex 71.1%

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