Travaux scientifiques

Prof. Dr. Erkin Serdaroğlu

193 publications. La source de l’information est indiquée à côté de chaque publication.

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  1. Effect of the timing of dialysis initiation on left ventricular hypertrophy and ınflammation in pediatric patients

    Pediatric Nephrology, 2017

    Source : ORCID

  2. FIBROMUSCULAR DYSPLASIA-A RARE CAUSE OF RENOVASCULAR HYPERTENSION

    PEDIATRIC NEPHROLOGY, 2017

    Source : ORCID

  3. HENOCH-SCHONLEIN PURPURA WITH POLYNEU ROPATHYA CASE REPORT

    PEDIATRIC NEPHROLOGY, 2017

    Source : ORCID

  4. IGA NEPHROPATHY AND IGG4 RELATED ORBITAL DISEASE: A CHILD CASE

    PEDIATRIC NEPHROLOGY, 2017

    Source : ORCID

  5. IMPACT OF HEMOGLOBIN VARIABILITY ON OUTCOME PARAMETERS IN PEDIATRIC DIALYSIS PATIENTS

    PEDIATRIC NEPHROLOGY, 2017

    Source : ORCID

  6. Incidence and causes of urolithiasis in children between 0-2 years

    Minerva Urologica E Nefrologica, 2017

    DOI 10.23736/s0393-2249.16.02675-8 PMID 27625318 10 citations (Europe PMC) Source : ORCID

  7. Incidence and causes of urolithiasis in children between 0-2 years.

    Minerva urologica e nefrologica= The Italian journal of urology and nephrology, 2017

    Source : ORCID

  8. Peritoneal dialysis access revision in children: causes, interventions, and outcomes

    Clinical Journal of the American Society of Nephrology, 2017

    DOI 10.2215/cjn.05270516 PMID 27899416 41 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

  9. Yenidoğanda İdrar Yolu Enfeksiyonları

    Türkiye Çocuk Hastalıkları Dergisi, 2017

    DOI 10.12956/tjpd.2017.288 12 citations (OpenAlex) Texte intégral en libre accèsSource : ORCID

  10. MP554RELATIONSHIP BETWEEN INTRAPERITONEAL PRESSURE AND PULMONARY FUNCTION TESTS IN CHILDREN TREATED WITH CAPD

    Nephrology Dialysis Transplantation, 2017

    DOI 10.1093/ndt/gfx176.mp554 Texte intégral en libre accèsSource : OpenAlex

  11. A Rare Cause of Seizure: Gitelman Syndrome

    Journal of Neuroscience and Neuropsychology, 2017

    DOI 10.18875/2577-7890.1.105 Texte intégral en libre accèsSource : OpenAlex

  12. The experience of canakinumab in renal amyloidosis secondary to Familial Mediterranean fever

    Molecular and Cellular Pediatrics, 2016

    DOI 10.1186/s40348-016-0058-2 PMID 27590627 25 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

  13. Clinical characteristics and follow-up results of the children with unilateral renal agenesis and hypoplasia

    Izmir Dr Behcet Uz Cocuk Hastanesi Dergisi, 2016

    DOI 10.5222/buchd.2016.185 1 citation (OpenAlex) Texte intégral en libre accèsSource : ORCID

  14. THE ASSESSMENT OF PROTHROMBOTIC POTENTIAL USING THROMBIN GENERATION ASSAY IN PATIENTS WITH NEPHROTIC SYNDROME IN CHILDHOOD

    THROMBOSIS RESEARCH, 2016

    Source : ORCID

  15. Temiz Aralıklı Kateterizasyon

    Turkiye Klinikleri Journal of Pediatric Surgery Special Topics, 2016

    Source : ORCID

  16. Temiz Aralıklı Kateterizasyon

    Turkiye Klinikleri Pediatric Surgery - Special Topics, 2016

    Source : OpenAlex

  17. Clinical characteristics and follow-up results of the children with unilateral renal agenesis and hypoplasia.

    İzmir Dr. Behçet Uz Çocuk Hastanesi Dergisi, 2016

    Source : OpenAlex

  18. RESULTS OF TURKISH MULTICENTRIC NATIONAL CYSTINOSIS REGISTRY

    DSpace - FIRAT (Fırat University), 2015

    Texte intégral en libre accèsSource : OpenAlex

  19. RESULTS OF TURKISH MULTICENTRIC NATIONAL CYSTINOSIS REGISTRY

    Bursa Uludag University - AVESIS, 2015

    Source : OpenAlex

  20. Thrombotic Microangiopathy with Complement Factor H Gene Mutations Unassociated with Atypical Hemolytic Uremic Syndrome

    Turkish Journal of Hematology, 2015

    DOI 10.4274/tjh.2015.0084 PMID 26376595 1 citation (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

  21. A case of thrombotic microangiopathy with CFH gene alterations that are not associated with atypical hemolytic uremic syndrome

    Journal of Thrombosis and Haemostasis, 2015

    Source : ORCID

  22. Defects of CRB2 cause steroid-resistant nephrotic syndrome

    The American Journal of Human Genetics, 2015

    DOI 10.1016/j.ajhg.2014.11.014 PMID 25557779 86 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

  23. Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome

    Nature genetics, 2015

    DOI 10.1038/ng.3512 PMID 26878725 174 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

  24. Rare Cause of Pediatric Urolithiasis: Xanthinuria

    Haseki Tip Bulteni, 2015

    DOI 10.4274/haseki.2304 Texte intégral en libre accèsSource : ORCID

  25. THEEFFECT OF DIALYSIS INITIATION TIMING ON LEFT VENTRICULAR HYPERTROPHY AND INFLAMMATION IN PEDIATRIC PATIENTS

    PEDIATRIC NEPHROLOGY, 2015

    Source : ORCID

  26. Tüberoskleroz kompleksinde renal tutulum

    Dicle Tıp Dergisi, 2015

    DOI 10.5798/diclemedj.0921.2015.01.0532 1 citation (OpenAlex) Texte intégral en libre accèsSource : ORCID

  27. Tüberoskleroz kompleksinde renal tutulum/Kidney involvement in tuberous sclerosis complex

    Dicle Tip Dergisi, 2015

    Source : ORCID

  28. Çocuklarda Ürolitiyazisin Nadir Nedeni: Ksantinüri

    Medical Bulletin of Haseki/Haseki Tip Bulteni, 2015

    Source : ORCID

  29. Renal Dysfunction in Pediatric Thalassemia Major Patients and Evaluation of Urine NGAL Levels in Thalassemia

    Blood, 2014

    DOI 10.1182/blood.v124.21.4049.4049 5 citations (OpenAlex) Source : OpenAlex

  30. Adequate 25-hydroxyvitamin D Levels Are Associated With Less Proteinuria And Attenuate Renal Failure Progression In Children With Chronic Kidney Disease

    Pediatric Nephrology, 2014

    Source : ORCID

  31. Association of mannose binding lectin codon 54 polymorphism with predisposition to Henoch--Schönlein purpura in childhood

    International journal of rheumatic diseases, 2014

    DOI 10.1111/1756-185x.12321 PMID 24576294 3 citations (Europe PMC) Source : ORCID

  32. Clinical and radiological course of simple renal cysts in children

    Urology, 2014

    DOI 10.1016/j.urology.2013.08.055 PMID 24188862 17 citations (Europe PMC) Source : ORCID

  33. Early Results of Endoscopic Treatment of Vesicoureteral Reflux with Polyacrylate Polyalcohol Copolymer

    Urologia Internationalis, 2014

    DOI 10.1159/000354879 PMID 24335079 3 citations (Europe PMC) Source : ORCID

  34. Evaluation of left atrial functions in children with chronic renal failure

    Anadulu Kardiyoloji Dergisi: AKD, 2014

    DOI 10.5152/akd.2014.4675 PMID 24598444 3 citations (Europe PMC) Source : ORCID

  35. Renal Agenesis And Hypoplasia In Humans Are Not Associated Glial Cell Line-derived Neurotrophic Factor

    PEDIATRIC NEPHROLOGY, 2014

    Source : ORCID

  36. Risk Factors For Loss Of Residual Diuresis In Children On Chronic Peritoneal Dialysis

    PEDIATRIC NEPHROLOGY, 2014

    Source : ORCID

  37. Front & Back Matter

    Urologia Internationalis, 2014

    DOI 10.1159/000360902 Source : OpenAlex

  38. Pediatrik Hastalarda Dializ Tedavisine Erken veya Geç Başlamanın Sol Ventrikül Hipertrofisi veya İnflamasyona Etkisi Var Mı

    AYBU AVESIS, 2014

    Source : OpenAlex

  39. Association between RAS gene polymorphisms (ACE I/D, AGT M235T) and Henoch-Schonlein purpura in a Turkish population

    Disease Markers, 2013

    DOI 10.3233/dma-120946 Source : ORCID

  40. Association between RAS gene polymorphisms (ACE I/D, AGT M235T) and Henoch-Schönlein purpura in a Turkish population

    Disease markers, 2013

    DOI 10.1155/2013/624757 PMID 23151617 10 citations (OpenAlex) Texte intégral en libre accèsSource : ORCID

  41. Impact of PD Prescription on Fluid and Blood Pressure Control in Children Undergoing Automated Peritoneal Dialysis

    PEDIATRIC NEPHROLOGY, 2013

    Source : ORCID

  42. Involution of multicystic dysplastic kidney: is it predictable?

    Journal of pediatric urology, 2013

    DOI 10.1016/j.jpurol.2012.04.014 PMID 22687342 11 citations (Europe PMC) Source : ORCID

  43. RENAL AGENESIS AND HYOPLASIA IN HUMANS ARE NOT ASSOCIATED GLIAL CELL LINE-DERIVED NEUROTROPHIC FACTOR

    Çanakkale Onsekiz Mart University AVESIS, 2013

    Source : ORCID

  44. 1036 Gracile Syndrome in a Turkish Newborn Infant Caused by a Homozygous Mutation (P99L) in Complex Iii Assembly Factor BCS1L

    Archives of Disease in Childhood, 2012

    DOI 10.1136/archdischild-2012-302724.1036 Texte intégral en libre accèsSource : ORCID

  45. An evaluation of childhood infection related nephrectomies and the prevalence of xanthogranulomatous pyelonephritis

    Journal of Dr. Behcet Uz Children's Hospital, 2011

    DOI 10.5222/buchd.2011.075 Source : ORCID

  46. Cardiac geometry in children receiving chronic peritoneal dialysis: findings from the International Pediatric Peritoneal Dialysis Network (IPPN) registry

    Clinical Journal of the American Society of Nephrology, 2011

    DOI 10.2215/cjn.05990710 PMID 21737855 62 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

  47. Causes of death and predictors of survival in pediatric PD: Insights from the International Pediatric PD Network (IPPN) registry

    PEDIATRIC NEPHROLOGY, 2011

    Source : ORCID

  48. Dr. Behçet Uz Çocuk Hastanesi patoloji laboratuarında 2009-2010 yıllarında incelenen böbrek biyopsilerinin klinik ve histopatolojik profili

    2011

    Source : ORCID

  49. Pediatrik olgularda enfeksiyonla ilişkili nefrektomilerin irdelenmesi ve ksantogranülomatöz pyelonefrit prevalansı

    İzmir Dr. Behçet Uz Çocuk Hastanesi Dergisi, 2011

    Source : ORCID

  50. The clinic and histopathological profile of the renal biopsies evaluated between 2009-2010 at the Pathology Department of Dr. Behçet Uz Children's Hospital.

    İzmir Dr. Behçet Uz Çocuk Hastanesi Dergisi, 2011

    DOI 10.5222/buchd.2011.051 2 citations (OpenAlex) Source : ORCID