Akademisyen
EBRU CANDA
DOÇENT
EGE 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 79
- Proje 0
- Kitap 7
- Bildiri 97
- Patent 0
- Sanatsal 0
Scopus (SJR)
Q1
17
Q2
20
Q3
29
Q4
2
WoS (JCR)
Q1
8
Q2
16
Q3
17
Q4
26
TR Index
27
makale
Alan+yıl+tür normalize OpenAlex yüzdelik — Clarivate ESI / SciVal değildir.
Üst %1 makale
0
Üst %10 makale
1
Ort. yüzdelik
98.2%
Üst %1 payı
0.0%
Üst %10 payı
100.0%
Makaleler
YÖKSİS ve OpenAlex kaynak ayrımıyla makaleler; quartile ve TR Index ile daraltabilirsiniz.
Makale listesi
- 2025 Rapid lipid-lowering response in two cases of autosomal recessive hypercholesterolemia YÖKSİS SJR Q1 JCR Q1
- 2025 Real-World Experience from Türkiye: Genetic and Therapeutic Insights in Pediatric Heterozygous Familial Hypercholesterolemia YÖKSİS TR Index SJR Q2 JCR Q2
- 2025 Insights into skeletal involvement in adult Gaucher disease: a single-center experience YÖKSİS SJR Q2 JCR Q3
- 2025 EVALUATION OF EXPERIENCED CLINICAL EVENTS IN POMPE DISEASE BASED ON REAL-LIFE DATA YÖKSİS SJR Q2 JCR Q3
- 2025 Simultaneous Determination of Lyso-Gb1 and Lyso-Gb3 in Plasma Using Salt-Assisted Liquid-Liquid Extraction Combined with LC-MS/MS YÖKSİS SJR Q1 JCR Q2
- 2025 Mucolipidosis type II and III: clinical spectrum, genetic landscape, and longitudinal outcomes in a pediatric cohort with six novel mutations YÖKSİS SJR Q3 JCR Q3
- 2025 Orofacial manifestations in mucopolysaccharidoses: a comprehensive clinical and radiographic evaluation of 35 pediatric cases YÖKSİS SJR Q1 JCR Q2
- 2025 DHCR24-Related Desmosterolosis in the First Reported Turkish Patient: Expanding the Genotypic and Phenotypic Spectrum. Journal of Clinical Lipidology YÖKSİS SJR Q1 JCR Q1
- 2025 Severe Hypercholesterolemia in a Pediatric Cohort: Familial Homozygous and Autosomal Recessive Hypercholesterolemia YÖKSİS SJR Q1 JCR Q1
- 2025 Long-Term Outcomes of Chenodeoxycholic Acid Therapy for Cerebrotendinous Xanthomatosis: A Nationwide Study on Prognostic Factors and Treatment Response YÖKSİS SJR Q1 JCR Q2
- 2025 Genotype-Phenotype Correlations and Shifting Diagnosis Age in Turkish Mucopolysaccharidosis Type II Patients: A Multicenter Retrospective Study YÖKSİS SJR Q2 JCR Q1
- 2025 A novel SLC44A gene variant in a patient with neonatal cholestasis and liver failure YÖKSİS SJR Q3 JCR Q4
- 2025 Nutritional management and geno-phenotyping of clinical nutrition in patients with glycogen storage diseases type VI and IX YÖKSİS SJR Q1 JCR Q2
- 2025 Next generation sequencing in children with isolated congenital cataract YÖKSİS SJR Q2 JCR Q3
- 2025 A retrospective study on neuropsychiatric presentations of mucopolysaccharidoses YÖKSİS TR Index
- 2025 Cardiac involvement as a gateway to the diagnosis of inherited metabolic disorders: A 16-year pediatric experience from a tertiary metabolic center YÖKSİS TR Index
- 2025 Effect of large neutral amino acids treatment on blood phenylalanine, tyrosine, and tryptophan levels in adolescent and young adult PKU patients YÖKSİS JCR Q4
- 2024 Clinical, biochemical, and molecular insights into Cerebrotendinous Xanthomatosis: A nationwide study of 100 Turkish individuals YÖKSİS SJR Q2 JCR Q2 OpenAlex üst %10 OpenAlex 98.2%
- 2024 Long‐term personalized high‐protein, high‐fat diet in pediatric patients with glycogen storage disease type IIIa: Evaluation of myopathy, metabolic control, physical activity, growth, and dietary compliance YÖKSİS SJR Q1 JCR Q2
- 2024 Long-term clinical outcomes and management of hypertriglyceridemia in children with Apo-CII deficiency YÖKSİS SJR Q1 JCR Q1