Evaluation of monocyte to high-density lipoprotein cholesterol ratio in the presence and severity of metabolic syndrome AU Uslu, Y Sekin, G Tarhan, N Canakcı, M Gunduz, M Karagulle Clinical and Applied Thrombosis/Hemostasis 24 (5), 828-833, 2018 | 66 | 2018 |
Depression and anxiety among parents of phenylketonuria children M Gunduz, N Arslan, O Unal, S Cakar, P Kuyum, SF Bulbul Neurosciences Journal 20 (4), 350-356, 2015 | 59 | 2015 |
Assessment of nutritional status in children with cancer and effectiveness of oral nutritional supplements D Gürlek Gökçebay, S Emir, T Bayhan, HA Demir, M Gunduz, B Tunc Pediatric hematology and oncology 32 (6), 423-432, 2015 | 54 | 2015 |
The impact of phenylketonuria on PKU patients’ quality of life: using of the phenylketonuria-quality of life (PKU-QOL) questionnaires IM Alptekin, N Koc, M Gunduz, FP Cakiroglu Clinical nutrition ESPEN 27, 79-85, 2018 | 27 | 2018 |
Severe renal tubulopathy in a newborn due to BCS1L gene mutation: effects of different treatment modalities on the clinical course F Ezgu, S Senaca, M Gunduz, L Tumer, A Hasanoglu, U Tiras, R Unsal, ... Gene 528 (2), 364-366, 2013 | 23 | 2013 |
The implementation of neonatal peritoneal dialysis in a clinical setting S Unal, L Bilgin, M Gunduz, N Uncu, MN Azili, T Tiryaki The Journal of Maternal-Fetal & Neonatal Medicine 25 (10), 2111-2114, 2012 | 23 | 2012 |
IgE-mediated hypersensitivity and desensitisation with recombinant enzymes in Pompe disease and type I and type VI mucopolysaccharidosis M Capanoglu, E Dibek Misirlioglu, D Azkur, E Vezir, H Guvenir, M Gunduz, ... International archives of allergy and immunology 169 (3), 198-202, 2016 | 21 | 2016 |
Utility of peritoneal dialysis in neonates affected by inborn errors of metabolism L Bilgin, S Unal, M Gunduz, N Uncu, T Tiryaki Journal of Paediatrics and Child Health 50 (7), 531-535, 2014 | 20 | 2014 |
Preeclampsia disrupts the normal physiology of leptin T Gursoy, D Aliefendioğlu, AT Aslan, M Gunduz, A Haberal, M Senes, ... American journal of perinatology 19 (06), 303-310, 2002 | 18 | 2002 |
Identification of three novel mutations in fourteen patients with citrullinemia type 1 E Kose, O Unal, S Bulbul, M Gunduz, J Häberle, N Arslan Clinical biochemistry 50 (12), 686-689, 2017 | 15 | 2017 |
Management of hypersensitivity reactions to enzyme replacement therapy in children with lysosomal storage diseases IT Yagmur, OU Uzun, AK Yavas, IK Celik, M Toyran, M Gunduz, E Civelek, ... Annals of Allergy, Asthma & Immunology 125 (4), 460-467, 2020 | 14 | 2020 |
Incidence and risk factors for hepatic sinusoidal obstruction syndrome after allogeneic hematopoietic stem cell transplantation: A retrospective multicenter study of Turkish … N Soyer, M Gunduz, E Tekgunduz, B Deveci, H Ozdogu, HH Sahin, ... Transfusion and Apheresis Science 59 (4), 102827, 2020 | 14 | 2020 |
Alkaptonuria in Turkey: Clinical and molecular characteristics of 66 patients PT Kisa, M Gunduz, S Dorum, OU Uzun, NE Cakar, GK Yildirim, S Erdol, ... European journal of medical genetics 64 (5), 104197, 2021 | 12 | 2021 |
Postoperative pain management for circumcision; Comparison of frequently used methods C Munevveroglu, M Gunduz Pakistan Journal of Medical Sciences 36 (2), 91, 2020 | 12 | 2020 |
Prediction of gestational week in Kivircik ewes using fetal ultrasound measurements. MC Gunduz, O Turna, M Ucmak, S Apaydin, G Kasikci, B Ekiz, NI Gezer | 12 | 2010 |
Pediatric flexible bronchoscopy in the intensive care unit: A multicenter study E Atag, F Unal, H Yazan, S Girit, ZS Uyan, AP Ergenekon, E Yayla, ... Pediatric Pulmonology 56 (9), 2925-2931, 2021 | 11 | 2021 |
Clinical and molecular characteristics and time of diagnosis of patients with classical galactosemia in an unscreened population in Turkey P Teke Kisa, M Kose, O Unal, E Er, BO Hismi, FS Bulbul, E Kose, ... Journal of Pediatric Endocrinology and Metabolism 32 (7), 675-681, 2019 | 11 | 2019 |
Cystic anastomosing hemangioma of the ovary: a case report with immunohistochemical and ultrastructural analysis M Gunduz, O Hurdogan, S Onder, E Yavuz International Journal of Surgical Pathology 27 (4), 437-440, 2019 | 11 | 2019 |
Recurrence of carbamoyl phosphate synthetase 1 (CPS1) deficiency in Turkish patients: characterization of a founder mutation by use of recombinant CPS1 from insect cells expression L Hu, C Diez-Fernandez, V Ruefenacht, BÖ Hismi, Ö Ünal, E Soyucen, ... Molecular genetics and metabolism 113 (4), 267-273, 2014 | 11 | 2014 |
Survival in rhino-orbito-cerebral mucormycosis: An international, multicenter ID-IRI study Y Cag, H Erdem, M Gunduz, S Komur, H Ankarali, S Ural, M Tasbakan, ... European journal of internal medicine 100, 56-61, 2022 | 10 | 2022 |