Aysel Taktak

ORCID: 0000-0001-7724-9160
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Research Areas
  • Renal Diseases and Glomerulopathies
  • Pediatric Urology and Nephrology Studies
  • Nephrotoxicity and Medicinal Plants
  • Vasculitis and related conditions
  • Kidney Stones and Urolithiasis Treatments
  • Congenital Heart Disease Studies
  • Renal and Vascular Pathologies
  • Complement system in diseases
  • Inflammasome and immune disorders
  • Parvovirus B19 Infection Studies
  • Urticaria and Related Conditions
  • Genetic and Kidney Cyst Diseases
  • Pharmacological Effects and Toxicity Studies
  • Polyomavirus and related diseases
  • Seismic Imaging and Inversion Techniques
  • Vascular anomalies and interventions
  • Cystic Fibrosis Research Advances
  • Salivary Gland Disorders and Functions
  • Herpesvirus Infections and Treatments
  • Pregnancy and Medication Impact
  • Gout, Hyperuricemia, Uric Acid
  • Autoimmune and Inflammatory Disorders Research
  • Cerebral Venous Sinus Thrombosis
  • Selenium in Biological Systems
  • Urinary and Genital Oncology Studies

Diyarbakır Gazi Yaşargil Eğitim ve Araştırma Hastanesi
2022

Mustafa Kemal University
2020-2021

Selçuk Üniversitesi Tıp Fakültesi Hastanesi
2021

Sağlık Bilimleri Üniversitesi
2021

Marmara University
2020

Ministry of Health
2013-2017

Dr Sami Ulus Çocuk Sağlığı ve Hastalıkları Eğitim ve Araştırma Hastanesi
2017

Hitit Üniversitesi Çorum Eğitim ve Araştırma Hastanesi
2017

Ankara University
2016

Ankara Onkoloji Eğitim ve Araştırma Hastanesi
2015

Objectives. The aim of this report was to evaluate and discuss treatment pediatric familial Mediterranean fever (FMF) patients with anti-interleukin1 (IL-1) agents. Methods. Refractory or colchicine unresponsive FMF described as severe frequent attacks and/or having high acute phase reactance levels despite a maximum dose (2 mg/day). Disease course, adverse effects, duration follow-up, protocols, responses the therapies were discussed. Results. Eight (6 male, 2 female) refractory identified....

10.3109/14397595.2014.987437 article EN Modern Rheumatology 2014-12-22

The aim of this report is to evaluate the plasma exchange as a choice for management life-threating gastrointestinal system (GIS) involvement in Henoch-Schönlein purpura (HSP) when refractory conventional therapies.We retrospectively reviewed medical records HSP patients who had therapy due massive GIS involvement. We reported age, gender, initial presentation, etiological or triggering factors and disease course. Treatment modalities, side effects their outcomes were noted.We 7 cases...

10.1186/1546-0096-12-s1-p357 article EN cc-by Pediatric Rheumatology 2014-09-01

The term nutcracker syndrome (NS) refers to the compression of left renal vein between aorta and superior mesenteric artery (SMA) causing venous hypertension.The symptoms vary from asymptomatic hematuria severe pelvic congestion.The purpose this study is evaluate clinical characteristics patients with NS correlation laboratory findings Doppler sonographic measurements.Sixty-three were evaluated (19 boys 44 girls) since January 2004 2014.The mean age was 12.21 ± 3.21 years (range...

10.5546/aap.2017.eng.165 article EN Archivos Argentinos de Pediatria 2017-02-13

Abstract Hemophagocytic lymphohistiocytosis ( HLH ) is a fatal, hyper‐inflammatory syndrome that characterized by untimely activation of macrophages, and manifests as cytopenia, organ dysfunction, coagulopathy. Secondary can be associated with infection, drugs, malignancy, transplantation, mostly triggered infection. Herein, we report the case patient H enoch– S chönlein purpura HSP who developed severe secondary to V aricella zoster

10.1111/ped.12523 article EN Pediatrics International 2015-04-01

Cytomegalovirus (CMV) infections are mostly seen in immunocompromised patients. However, unusual manifestations or complications of acquired CMV immunocompetent patients rarely reported. CMV-related hemorrhagic cystitis is extremely rare but should be considered even We present a case 3-year-old boy with intermittent, terminal gross hematuria lasting for 1 month. There was no history genitourinary trauma stone disease. Urine analysis revealed eumorphic red blood cells and proteinuria....

10.3109/0886022x.2014.926757 article EN Renal Failure 2014-06-16

Abstract Proteinuria has been shown to be an important and potentially treatable risk factor for graft loss. The aim of this study was evaluate prevalence, etiology, outcome proteinuria during the follow‐up children with renal transplantation. We retrospectively reviewed files transplanted between 2006 2016 in our center. All patients were interpreted respect demographic data clinical laboratory features including information about proteinuria. Chi‐square test Mann‐Whitney U used analysis....

10.1111/petr.13068 article EN Pediatric Transplantation 2017-10-09

Presentación de casos clínicos RESUMENLa púrpura Schönlein-Henoch (PSH) es la vasculitis más frecuente en los niños.Los procesos vasculíticos pueden afectar el pulmón.Si bien hemorragia alveolar difusa puede considerarse una las manifestaciones PSH, no un cuadro frecuente.En este artículo presentamos caso niña 10 años con nefritis por PSH que sufrió pulmonar.La paciente recibió tratamiento satisfactorio metilprednisolona intravenosa.La

10.5546/aap.2016.e366 article ES Archivos Argentinos de Pediatria 2016-09-08

The objective of this study is to determine the clinical features unilateral multicystic dysplastic kidney (MCDK) patients.The demographic, clinical, laboratory, and radiologic MCDK patients at Diyarbakır Children’s Hospital Gazi Yaşargil Training Research between January 2008-June 2019 were retrospectively evaluated.A total 111 [59 (53.2%) male 52(46.8%) female] with followed for a mean period 41.89 ± 32.03 months. was located on left right sides in 46 (41.4%) 65 (58.6%) children,...

10.3906/sag-2011-175 article EN TURKISH JOURNAL OF MEDICAL SCIENCES 2021-01-29

Thrombotic microangiopathy (TM), especially thrombotic thrombocytopenic purpura (TTP) is described in systemic lupus erythematosus (SLE) as a severe hematological involvement. However hemolytic uremic syndrome (HUS) seen less frequently SLE, particularly an initial presentation. Here we present 15-year old boy presenting with gross hematuria, decreased urinary output and petechial lesions. He was diagnosed atypical HUS according to the classical triad of TM, along observation...

10.24953/turkjped.2016.02.018 article EN The Turkish Journal of Pediatrics 2016-04-25

Sjogren’s syndrome (SS) is a systemic autoimmune disease that presents with inflammation of lacrimal and salivary glands accompanied by extraglanduler complications. The spectrum extends from sicca symptoms to involvement.In childhood, SS an extremely rare disorder (1).Here we present girl who was first presented cutaneous lesions.

10.1186/1546-0096-12-s1-p290 article EN cc-by Pediatric Rheumatology 2014-09-01

Amaç: İdiyopatik nefrotik sendrom (İNS) çocuklarda en sık görülen glomerüler hastalık olup, %80’i steroide duyarlıdır. Steroide duyarlı (SDNS) hastalarının yaklaşık yarısı steroid bağımlı sendromudur (SBNS). Bu çalışmanın amacı ilk atağında başvuran SDNS hastalarında, bağımlılığını tedavi öncesi öngörebilecek risk faktörlerini belirlemektir. Gereç ve Yöntem: Çocuk Nefroloji Kliniğimize Eylül 2016-Eylül 2018 tarihleri arasında atak İNS ile tedavisine yanıtlı hastalar geriye dönük olarak...

10.26650/jchild.2020.3.807529 article TR cc-by-nc Çocuk Dergisi / Journal of Child 2020-12-28

Amaç: Bu çalışmanın amacı idiyopatik epilepsi tanılı çocuklarda anti epileptik tedavi kesimi sonrası nöbet tekrarına etki eden risk faktörlerini değerlendirmektir.

10.12956/tchd.773401 article TR Turkish Journal of Pediatric Disease 2021-01-20

Objective: Acute tubulointerstitial nephritis (aTIN) is a rare cause of acute renal injury in children. The incidence cases linked to insensible use energy drinks has increased recent years. In thıs study, we aimed examine patients with aTIN connected drink detail our own patients.Methods: this the files (aTIN pediatric nephrology clinic were retrospectively screened.Results: 32 included study (F/M: 22/10). Mean age was 12±4.3 years (9-17). most common causes etiology drugs (18; 56.2%) and...

10.17944/mkutfd.941866 article EN cc-by Mustafa Kemal Üniversitesi Tıp Dergisi 2021-08-19

ÖzKistik böbrek hastalıkları, kalıtımsal hastalıkları içinde en sık görülen grup olup, her biri farklı etiyoloji, patogenez, klinik prezentasyon ve prognoza sahiptir

10.4274/jcp.40427 article TR Güncel Pediatri 2015-04-01

Henoch-Schönlein purpura (HSP) is the most common vasculitis in children.Vasculitic processes can involve lung.Although diffuse alveolar hemorrhage may be seen as one of manifestation HSP, it not a frequent presentation.Here we reported case 10-year-old girl with HSP nephritis who developed pulmonary hemorrhage.The patient was treated successfully intravenous methylprednisolone.A review literature revealed that young age good prognostic sign and immunosuppressive drugs supportive management...

10.5546/aap.2016.eng.e366 article EN Archivos Argentinos de Pediatria 2016-09-08
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