Yayınlar (Son 5 yıldaki yayınlar sıralanmıştır)
- Özen MA, Taşdemir M, Aygün MS, Necef I, Aydın E, Bilge I, Eroğlu E. Is there a unique symptom in lower urinary tract dysfunction in children? Low Urin Tract Symptoms. 2020 Nov 2. doi: 10.1111/luts.12363. Epub ahead of print. PMID: 33137854.
- Pınarbaşı AS, Dursun I, Gokce I, Çomak E, Saygılı S, Bayram MT, Donmez O, Melek E, Tekcan D, Çiçek N, Yılmaz D, Tabel Y, Yıldırım ZY, Bahat E, Koyun M, Soylu A, Canpolat N, Aksu B, Çelakıl ME, Taşdemir M, Benzer M, Özçelik G, Bakkaloğlu SA, Düşünsel R. Predictors of poor kidney outcome in children with C3 glomerulopathy. Pediatr Nephrol. 2020 Oct 31. doi: 10.1007/s00467-020-04799-7. Epub ahead of print. PMID: 33130981.
- Taşdemir M, Erginöz E, Gayret ÖB, Bilge I. Ambulatory arterial stiffness index is increased in obese children. Turk J Pediatr. 2020;62(2):259-266. doi: 10.24953/turkjped.2020.02.012. PMID: 32419418.
- Borzych-Duzalka D, Shroff R, Ariceta G, Yap YC, Paglialonga F, Xu H, Kang HG, Thumfart J, Aysun KB, Stefanidis CJ, Fila M, Sever L, Vondrak K, Szabo AJ, Szczepanska M, Ranchin B, Holtta T, Zaloszyc A, Bilge I, Warady BA, Schaefer F, Schmitt CP. Vascular Access Choice, Complications, and Outcomes in Children on Maintenance Hemodialysis: Findings From the International Pediatric Hemodialysis Network (IPHN) Registry. Am J Kidney Dis. 2019 Aug;74(2):193-202
- Schaefer F, Benner L, Borzych-Dużałka D, Zaritsky J, Xu H, Rees L, Antonio ZL, Serdaroglu E, Hooman N, Patel H, Sever L, Vondrak K, Flynn J, Rébori A, Wong W, Hölttä T, Yildirim ZY, Ranchin B, Grenda R, Testa S, Drożdz D, Szabo AJ, Eid L, Basu B, Vitkevic R, Wong C, Pottoore SJ, Müller D, Dusunsel R, Celedon CG, Fila M, Sartz L, Sander A, Warady BA; International Pediatric Peritoneal Dialysis Network (IPPN) Registry. Global Variation of Nutritional Status in Children Undergoing Chronic Peritoneal Dialysis: A Longitudinal Study of the International Pediatric Peritoneal Dialysis Network. Sci Rep. 2019 Mar 20;9(1):4886.
- Mutlu GY, Taşdemir M, Kızılkan NU, Güran T, Hatun Ş, Kayserili H, Bilge I. 2019. A rare cause of chronic hyponatremia in an infant: Questions. Pediatr Nephrol, doi: 10.1007/s00467-019-04335-2
- Mutlu GY, Taşdemir M, Kızılkan NU, Güran T, Hatun Ş, Kayserili H, Bilge I. 2019. A rare cause of chronic hyponatremia in an infant: Answers. Pediatr Nephrol, doi: 10.1007/s00467-019-04337-0
- Taşdemir M, Yılmaz S, Baba ZF, Bilge I. 2019. Comments on the letter of Galland et al. on “A rare cause of AA amyloidosis and end-stage kidney failure.” Pediatric Nephrol, doi: 10.1007/s00467-019-04277-9
- Taşdemir M, Yılmaz S, Baba ZF, Bilge I. 2018. A rare cause of AA amyloidosis and end-stage kidney failure: Questions. Pediatr Nephrol, doi: 10.1007/s00467-018-4152-7.
- Taşdemir M, Yılmaz S, Baba ZF, Bilge I. 2018. A rare cause of AA amyloidosis and end-stage kidney failure: Answers. Pediatr Nephrol, doi: 10.1007/s00467-018-4153-6.
- Yildirim Yuruk Z, Pehlivanoglu C, Yilmaz A, Coban A, Aksu B, Emre S, Bilge I, Ince Z, Kavas U, Erden G, Sirin A: Peritoneal dialysis in infants: Single Center Experience. J Child 2018.92485
- Sönmez HE, Canpolat N, Ağbaş A, Taşdemir M, Ekmekçi ÖB, Alikaşifoğlu M, Sever L, and Çalışkan S. 2019. Childhood Obesity, doi: 10.1089/chi.2019.0022.
- Özen MA, Mutluer T, Necef I, Shabsog M, Taşdemir M, Bilge I, Eroğlu E. 2019. The overlooked association between lower urinary tract dysfunction and psychiatric disorders: a short screening test for clinical practice. J Pediatr Urol, doi: 10.1016/j.jpurol.2019.03.025.
- Yurt A, Göknar N, Akıncı N, Yıldırım ZY, Taşdemir M, Benzer M, Gökçe İ, Candan C, Küçük N, Uzuner S, Özçelik G, Demirkol D, Sever L, Çalışkan S. 2018. Outbreak of Shiga Toxin-producing Escherichia coli-associated Hemolytic Uremic Syndrome in Istanbul in 2015: Outcome and Experience with Eculizumab. Pediatr Nephrol, doi: 10.1007/s00467-0184033-0.
- Bostan Gayret Ö, Taşdemir M, Erol M, Nacaroğlu HT, Zengi O, Yiğit Ö. 2018. Are there any new reliable markers to detect renal injury in obese children? Biomarkers in obese children. Renal Failure, 40(1), 416-422., doi: 10.1080/0886022X.2018.1489284
- Ozen MA, Tasdemir M, Gündoğdu G, Bilge I, Büyükünal C, Eroğlu E. 2018. Does Voiding Cystourethrogram Exclude Posterior Urethral Valves in Late Presenting Cases? J Ped Surgery, doi: 10.1055/s-00381672146.
- Bakkaloğlu SA, Kandur Y, Akcaboy M, Serdaroğlu E, Noyan A, Parmaksız G, Bayazıt AK, Sever L, Taşdemir M, Özlü SG, Özçelik G, Dursun İ, Alparslan C. 2018. Time-averaged hemoglobin values, not hemoglobin cycling, have an impact on outcomes in pediatric dialysis patients. Pediatric Nephrol, 33(11), doi: 10.1007/s00467-018-4013-4,
- Canpolat N, Sever L, Ağbaş A, Taşdemir M, Oruç , Ekmekci OB, Caliskan S. 2018. Leptin and ghrelin in chronic kidney disease: their associations with protein-energy wasting. Pediatr Nephrol, https://doi.org/10.1007/s00467-018-4002-7
- Taşdemir M, Fuçucuoğlu D, Küçük SH, Erol M, Yiğit Ö, Bilge I. 2018. Urinary biomarkers in the early detection and follow-up of tubular injury in childhood urolithiasis. Clin Exp Nephrol, 22(1):133-141. doi: 10.1007/s10157-017-1436-3.
- Özen MA, Gündoğdu G, Taşdemir M, Eroğlu E. 2017. Complication of newborn circumcision: Meatal stenosis or meatal web? J Pediatr Urol, 13(6):617.e1-617.e4. doi: 10.1016/j.jpurol.2017.05.007.
- Rosti RO, Sotak BN, Bielas SL, Bhat G, Silhavy JL, Aslanger AD, Altunoglu U, Bilge I, Tasdemir M, Yzaguirrem AD, Musaev D, Infante S, Thuong W, Marin-Valencia I, Nelson SF, Kayserili H, Gleeson JG. 2017. Homozygous mutation in NUP107 leads to microcephaly with steroid-resistant nephrotic condition similar to Galloway-Mowat syndrome. J Med Genet, 54(6):399-403. doi: 10.1136/jmedgenet-2016-104237.
- Demirkol D, Şık G, Topal N, Çıtak A, Zeybek Ç, Tüten A, Bilge I. Continuous Venovenous Hemodiafiltration in the Treatment of Maple Syrup Urine Disease. Blood Purif. 2016;42(1):27-32. doi: 10.1159/000443783. Epub 2016 Mar 22. PubMed PMID: 26998605.
- Küçükemre-Aydın B, Öğrendil-Yanar Ö, Bilge I, Baş F, Poyrazoğlu Ş, Yılmaz A, Emre S, Bundak R, Saka N, Darendeliler F. An easily missed diagnosis: 17-alpha-hydroxylase/17,20-lyase deficiency. Turk J Pediatr. 2015 May-Jun;57(3):277-81. PubMed PMID: 26701948.
- Erol M, Yigit O, Tasdemir M, Bostan Gayret O, Buke O, Gunes A, Hamilcikan S, Kasapcopur O. 2016. Potential of Serum and Urinary Matrix Metalloproteinase-9 Levels for the Early Detection of Renal Involvement in Children With Henoch-Schönlein Purpura. Iran J Pediatr, Jun 5;26(4):e6129.
- Taşdemir M, Eroğlu AG, Canpolat N, Konukoğlu D, Ağbaş A, Sevim MD, Çalışkan S, Sever L. 2016. Cardiovascular alterations do exist in children with stage-2 chronic kidney disease. Clin Exp Nephrol, Dec;20(6):926-933.
- Ha IS, Yap HK, Munarriz RL, Zambrano PH, Flynn JT, Bilge I, Szczepanska M, Lai WM, Antonio ZL, Gulati A, Hooman N, van Hoeck K, Higuita LM, Verrina E, Klaus G, Fischbach M, Riyami MA, Sahpazova E, Sander A, Warady BA, Schaefer F; International Pediatric Peritoneal Dialysis Network Registry. Risk factors for loss of residual renal function in children treated with chronic peritoneal dialysis. Kidney Int. 2015 Sep;88(3):605-13. doi: 10.1038/ki.2015.108. Epub 2015 Apr 15. PubMed PMID: 25874598; PubMed Central PMCID: PMC4558567.
- Candan C, Canpolat N, Gökalp S, Yıldız N, Turhan P, Taşdemir M, Sever L, Çalışkan S. Subclinical cardiovascular disease and its association with risk factors in children with steroid-resistant nephrotic syndrome. Pediatr Nephrol. 2014 Jan;29(1):95-102. doi: 10.1007/s00467-013-2608-3.