Bilimsel çalışmalar

Prof. Dr. Erkin Serdaroğlu

193 yayın. Her yayının yanında bilginin kaynağı yazar.

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  1. Etiologp of Hematuria in Childhood

    The Journal of Tepecik Education and Research Hospital, 2005

    DOI 10.5222/terh.2005.98624 Açık erişimli tam metinKaynak: ORCID

  2. Correlative value of magnetic resonance imaging for neurodevelopmental outcome in periventricular leukomalacia

    Developmental Medicine & Child Neurology, 2004

    DOI 10.1017/s0012162204001264 PMID 15540633 56 atıf (OpenAlex) Kaynak: OpenAlex

  3. Alterations in circadian and ultradian cardiovascular rhythms in children with chronic renal failure

    American Journal of Hypertension, 2004

    Kaynak: ORCID

  4. Children with chronic renal failure have blunted and delayed rhythms of blood pressure and heart rate

    Journal of Hypertension, 2004

    Kaynak: ORCID

  5. HDR (hypoparathyroidism, sensorineural deafness, renal dysplasia) syndrome presenting with hypocalcemia-induced generalized psoriasis

    Journal of Pediatric Endocrinology and Metabolism, 2004

    DOI 10.1515/jpem.2004.17.7.1031 PMID 15301053 11 atıf (OpenAlex) Kaynak: ORCID

  6. Is ACE gene polymorphism a risk factor for renal scarring with low-grade reflux?

    Pediatric Nephrology, 2004

    DOI 10.1007/s00467-004-1486-0 PMID 15138870 17 atıf (Europe PMC) Kaynak: ORCID

  7. Bir olgu nedeniyle klasik ksantinüri

    2003

    Kaynak: OpenAlex

  8. Classical Xanthinuria: A Case Report

    eArsiv - Adu (Adnan Menderes University), 2003

    Açık erişimli tam metinKaynak: OpenAlex

  9. A novel missense mutation of the bilirubin UDP-glucuronosyltransferase gene in a Turkish patient with Crigler-Najjar syndrome type 1

    Journal of pediatric gastroenterology and nutrition, 2003

    DOI 10.1097/00005176-200311000-00024 PMID 14581810 6 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID

  10. Ace Gene Polymorphism And Renal Scarring In Children With Vesicoureteral Reflux

    Nephrology Dialysis Transplantation, 2003

    Kaynak: ORCID

  11. An elevated hemidiaphragm 3 months after internal jugular vein hemodialysis catheter placement

    Seminars in dialysis, 2003

    DOI 10.1046/j.1525-139x.2003.16054.x PMID 12753693 14 atıf (OpenAlex) Kaynak: ORCID

  12. Metabolic Etiology In Pediatric Urolithiasis

    Nephrology Dialysis Transplantation, 2003

    Kaynak: ORCID

  13. Podocin (nphs2) Gene Mutation In Turkish Children With Steroid Resistant Nephrotic Syndrome

    Nephrology Dialysis Transplantation, 2003

    Kaynak: ORCID

  14. Normal Gamma Glutamil Transferaz Düzeyleri İleSeyreden Bir İntrahepatik Kolestaz Formu:Byler Sendromu

    Turkiye Klinikleri Journal of Pediatrics, 2002

    Kaynak: OpenAlex

  15. Matür yenidoğanlarda sepsisde mikroorganizmaların dağılımı

    AYBU AVESIS, 2002

    Kaynak: OpenAlex

  16. Çocuk Hemodiyaliz Olgularında Hemodiyaliz Sırasında Oluşan Akut Komplikasyonlar

    Turkiye Klinikleri Journal of Pediatrics, 2002

    Kaynak: OpenAlex

  17. A FORM OF INTRAHEPATIC CHOLESTASIS CHARACTERIZED BY NORMALGAMMA GLUTAMYL TRANSFERASE LEVELS: BYLER SYNDROME

    Turkiye Klinikleri Journal of Pediatrics, 2002

    Kaynak: ORCID

  18. ACUTE COMPLICATIONS DURING HAEMODIALYSIS IN PEDIATRIC PATIENTS

    Turkiye Klinikleri Journal of Pediatrics, 2002

    Kaynak: ORCID

  19. Griscelli sendromu: bir olgu sunumu

    2002

    Kaynak: ORCID

  20. Quantification Of Hypercalcuria With Urine Calcium-osmolality Ratio In Children

    Nephrology Dialysis Transplantation, 2002

    Kaynak: ORCID

  21. Urine Protein-osmolality Ratio For Quantification Of Proteinuria In Children

    Nephrology Dialysis Transplantation, 2002

    Kaynak: ORCID

  22. Griscelli Syndrome: A Case Report

    eArsiv - Adu (Adnan Menderes University), 2002

    Açık erişimli tam metinKaynak: ORCID

  23. High-Dose Intravenous Immunoglobulin Treatment in Intractable Childhood Epilepsy

    Turkish Journal of Medical Sciences, 2000

    Kaynak: ORCID

  24. Konjenital dev melanositik nevüs zemininde gelişen bir pediatrik nodüler malign melanom olgusu

    eArsiv - Adu (Adnan Menderes University), 2000

    Açık erişimli tam metinKaynak: ORCID

  25. Lamotrigine Treatment in Childhood Drug-Resistant Epilepsy

    Turkish Journal of Medical Sciences, 2000

    Kaynak: ORCID

  26. Niemann-Pick disease type C

    COCUK SAGLIGI VE HASTALIKARI DERGISI, 2000

    Kaynak: ORCID

  27. ay-15 yaş arası çocuklarda demir eksikliği anemisi sıklığı

    Ege Pediatri Bülteni, 2000

    Kaynak: ORCID

  28. Akut ve stabil KOAH olgular> nda oksidatif stres

    Solunum, 1999

    Kaynak: ORCID

  29. High dose intravenous immunoglobulin treatment in intractable childhood epilepsy

    Epilepsia, 1999

    Kaynak: ORCID

  30. Histopathologic and immunohistochemical analyses of Hodgkin's disease and the correlation with Epstein-Barr virus

    Turkish Journal of Cancer, 1999

    Kaynak: ORCID

  31. Lamotrigine treatment in childhood drug registant epilepsy

    Epilepsia, 1999

    Kaynak: ORCID

  32. Lamotrigine treatment in childhood drug registant epilepsy.

    EPILEPSIA, 1999

    Kaynak: ORCID

  33. Veno-occlusive disease of the liver after chemotherapy for acute lymphoblastic leukemia: a case report

    Turkish Journal of Cancer, 1999

    Kaynak: ORCID

  34. Bartter Benzeri Sendromlar:Bartter ve Gitelman Sendromu Olguları

    Turkiye Klinikleri Journal of Pediatrics, 1999

    Kaynak: OpenAlex

  35. Proliferating cell nuclear antigen and its prognostic significance in childhood Hodgkin’s disease: preliminary study

    Turkish Journal of Cancer, 1998

    Kaynak: ORCID

  36. Interval Between Symptom Onset and Diagnosis (Lag time) of Pediatric Tumors

    Turkiye Klinikleri Journal of Pediatrics, 1997

    Kaynak: ORCID

  37. Pediatrik Tümörlerde Tanıda Gecikme Süresi

    Turkiye Klinikleri Journal of Pediatrics, 1997

    Kaynak: ORCID

  38. Salmonella infeksiyonlu 127 olgunun değerlendirilmesi

    İnfeks. Derg, 1996

    Kaynak: ORCID

  39. A Case Of Pediatric Noduler Malign Melanoma Developed On Basis Of The Congenital Giant Melanocytic Nevus

    Kaynak: ORCID

  40. Atipik Hemolitik Üremik Sendrom ile İlişkili Olmayan Kompleman Faktör H Gen Mutasyonları Gösteren Trombotik Mikroanjiopati

    Kaynak: ORCID

  41. Tek taraflı renal agenezi ve hipoplazili çocukların klinik özellikleri ve izlem sonuçları

    Kaynak: ORCID

  42. Urea Cycle Disorders In Neonates: 6 Cases Report

    Kaynak: ORCID

  43. Çocukluk Yaş Grubunda Hematüri Etiyolojisi

    İzmir Tepecik Eğitim ve Araştırma Hastanesi Dergisi

    Kaynak: ORCID