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Dilek Güneş
Dilek Güneş
İstanbul Üniversitesi İstanbul Tıp Fakültesi
Verified email at istanbul.edu.tr
Title
Cited by
Cited by
Year
Primary coenzyme Q10 Deficiency-6 (COQ10D6): Two siblings with variable expressivity of the renal phenotype
ZY Yildirim, G Toksoy, O Uyguner, A Nayir, S Yavuz, U Altunoglu, ...
European Journal of Medical Genetics 63 (1), 103621, 2020
192020
Predictive factors of drug-resistant epilepsy in children presenting under 2 years of age: experience of a tertiary center in Turkey
EP Yildiz, D Gunes, G Bektas, T Aksu Uzunhan, B Tatli, M Caliskan, ...
Acta Neurologica Belgica 118, 71-75, 2018
192018
GEBELİK DÖNEMİNDE VE İKİ FARKLI YAŞTA KARDEŞ EMZİRME: OLGU SUNUMLARI
E Devecioğlu, DK Güneş, B Kural, T Eren, G Gökçay
Journal of Istanbul Faculty of Medicine 77 (4), 60-63, 2015
92015
Farber disease: A clinical diagnosis
B Ekici, D Kürkçü, M Çalışkan
Journal of pediatric neurosciences 7 (2), 154-155, 2012
82012
Breastfeeding during pregnancy and tandem nursing
E Devecioglu, D Kurkcu, B Kural, T Eren, E Gokcay
JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI 77 (4), 2014
52014
Clinical and bi-genomic DNA findings of patients suspected to have mitochondrial diseases
A Gedikbasi, G Toksoy, M Karaca, C Gulec, MC Balci, D Gunes, S Gunes, ...
Frontiers in Genetics 14, 1191159, 2023
12023
Clinical, biochemical, and molecular insights into Cerebrotendinous Xanthomatosis: A nationwide study of 100 Turkish individuals
T Zubarioglu, E Kıykım, E Köse, FT Eminoğlu, PT Kısa, MC Balcı, I Özer, ...
Molecular genetics and metabolism 142 (2), 108493, 2024
2024
YENİDOĞAN DÖNEMİ ENDOKRİN HASTALIKLAR
YK HASPOLAT, S ERTUĞRUL, T AKÇAY
2020
PRIMARY COENZYME Q10 DEFICIENCY-6 (COQ10D6): CASE REPORT
ZY Yildirim, A Nayir, O Uyguner, G Toksoy, S Yavuz, U Altunoglu, ...
PEDIATRIC NEPHROLOGY 32 (9), 1763-1763, 2017
2017
Geç Tip Beta Laktam Allerjisinde Tanısal Testlerin Önemi: Olgu Sunumu.
D Özçeker, D Kürkçü, Ö Umur, AG Gençay, Z Tamay, N Güler
Asthma Allergy Immunology/Astim Allerji Immunoloji 14 (2), 2016
2016
The Importance of Diagnostic Tests in Delayed Type Beta-Lactam Allergy: A Case Report
D Ozceker, D Kurkcu, O Umur, A Gencay, Z Tamay, N Guler
ASIM ALLERJI IMMUNOLOJI 14 (2), 2016
2016
Clinical and bi-genomic DNA findings of patients suspected to have mitochondrial diseases
G TOKSOY, B KARAMAN, M KARACA, AD ASLANGER, Ç GÜLEÇ, ...
İNFANTİL TİP POMPE HASTALIĞI ULUSAL KONSENSUS ÇALIŞMASI
E Aktaşoğlu, A İNCİ, İ OKUR, G BİBEROĞLU, R ÖKTEM, F EZGÜ, ...
L2-Hydroxyglutaric Aciduria: Clinical and Biochemical Evaluation of 33 Patients from a Single Center
N BAYRAKTAR ELTUTAN, S GÜNEŞ, D Güneş, M BALCI, M DEMİRKOL, ...
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