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akaturk Akademik ölçüm

Akademisyen profili · PROFESÖR

FATİH ÖZALTIN

HACETTEPE ÜNİVERSİTESİ

  • TIP FAKÜLTESİ
  • DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
Makale YÖKSİS 200
Proje 1
Kitap 9
Bildiri 18
Patent 1
Sanatsal 1
Scopus (SJR)
Q1 108 Q2 45 Q3 26 Q4 1
WoS (JCR)
Q1 93 Q2 26 Q3 28 Q4 33
TR Index 18 makale

Scopus (SJR)

Q1 108 Q2 45 Q3 26 Q4 1

WoS (JCR)

Q1 93 Q2 26 Q3 28 Q4 33

TR Index

18 makale

Toplam 200 yayın

Makaleler

  1. 2025 Comprehensive analysis of pediatric urolithiasis in a tertiary care center and insights into demographics, risk factors, and management outcomes Journal of Pediatric Urology DOI 10.1016/j.jpurol.2025.03.006
  2. 2025 A Novel NUP85 Variant Expanding the Phenotypic Spectrum of NUP85‐Associated Steroid‐Resistant Nephrotic Syndrome Clinical Genetics DOI 10.1111/cge.14703
  3. 2025 Anti-nephrin autoantibodies in steroid-resistant nephrotic syndrome may inform treatment strategy Kidney International DOI 10.1016/j.kint.2025.01.019
  4. 2025 Efficacy of Calcineurin Inhibition in Children With Steroid-Resistant Nephrotic Syndrome Kidney International Reports DOI 10.1016/j.ekir.2025.07.037
  5. 2025 The clinical characteristics of patients with congenital nephrotic syndrome secondary to NPHS1 mutation: Is nephrectomy still a therapeutic option for selected cases? Pediatric Nephrology DOI 10.1007/s00467-025-06774-6
  6. 2025 Response to: Nephrectomy for congenital nephrotic syndrome: unanswered questions Pediatric Nephrology DOI 10.1007/s00467-025-06831-0
  7. 2025 COVID-19 in Children with Chronic Kidney Disease; Does it Differ Much? Klinische Pädiatrie DOI 10.1055/a-2207-3153
  8. 2024 Short Bowel Syndrome Is Not a Contraindication for Kidney Transplantation Pediatric Transplantation DOI 10.1111/petr.14889
  9. 2024 Acute kidney injury in children with moderate-severe COVID-19 and multisystem inflammatory syndrome in children: a referral center experience Pediatric Nephrology DOI 10.1007/s00467-023-06125-3
  10. 2024 Steroid-Resistant Nephrotic Syndrome due to NPHS2 Variants Is Not Associated With Posttransplant Recurrence Kidney International Reports DOI 10.1016/j.ekir.2024.01.005
  11. 2024 Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT) Kidney International DOI 10.1016/j.kint.2023.11.032
  12. 2024 Adolescence-onset atypical hemolytic uremic syndrome: is it different from infant-onset? Clinical and Experimental Nephrology DOI 10.1007/s10157-024-02505-7
  13. 2024 Calcineurin inhibitor‐related hyperkalemia is caused by hyporeninemic hypoaldosteronism and fludrocortisone is an effective treatment: Report of a case series and review of the literature Pediatric Transplantation DOI 10.1111/petr.14778
  14. 2024 The Clinical and Mutational Spectrum of 69 Turkish Children with Autosomal Recessive or Autosomal Dominant Polycystic Kidney Disease: A Multicenter Retrospective Cohort Study S. Karger AG DOI 10.1159/000528258
  15. 2024 Omic Studies on In Vitro Cystinosis Model: siRNA-Mediated CTNS Gene Silencing in HK-2 Cells Laboratory Investigation DOI 10.1016/j.labinv.2023.100287
  16. 2024 Variable phenotype and genotype of pediatric patients with HNF1B nephropathy Clinical Nephrology DOI 10.5414/CN111310
  17. 2024 Management of pediatric hemolytic uremic syndrome The Turkish Journal of Pediatrics DOI 10.24953/turkjped.2023.596
  18. 2023 A rare cause of nephrotic syndrome—sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literature Springer Science and Business Media LLC DOI 10.1007/s00467-022-05656-5
  19. 2023 Metabolomic Analyses to Identify Candidate Biomarkers of Cystinosis Int J Mol Sci DOI 10.3390/ijms24032603
  20. 2023 Long-term kidney follow-up after pediatric acute kidney support therapy for children less than 15 kg Springer Science and Business Media LLC DOI 10.1007/s00467-023-06013-w

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