Aysun Çaltık Yılmaz

ORCID: 0000-0003-0774-4419
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About
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Research Areas
  • Pediatric Urology and Nephrology Studies
  • Complement system in diseases
  • Renal Diseases and Glomerulopathies
  • Kidney Stones and Urolithiasis Treatments
  • Renal Transplantation Outcomes and Treatments
  • Pharmacological Effects and Toxicity Studies
  • Neonatal Health and Biochemistry
  • Biomedical Research and Pathophysiology
  • Blood groups and transfusion
  • Ion Transport and Channel Regulation
  • Urinary Bladder and Prostate Research
  • Metabolism and Genetic Disorders
  • Hormonal Regulation and Hypertension
  • Urinary Tract Infections Management
  • Adenosine and Purinergic Signaling
  • Electrolyte and hormonal disorders
  • Organ Transplantation Techniques and Outcomes
  • COVID-19 Clinical Research Studies
  • Vascular anomalies and interventions
  • Vasculitis and related conditions
  • Dialysis and Renal Disease Management
  • Urological Disorders and Treatments
  • Inflammatory Biomarkers in Disease Prognosis
  • Bacillus and Francisella bacterial research
  • Animal Virus Infections Studies

Başkent University
1997-2024

Memorial Ankara Hospital
2023-2024

Istanbul University
2024

Istanbul University-Cerrahpaşa
2024

Başkent University Hospital
2020-2023

S.B. Keçiören Eğitim ve Araştırma Hastanesi
2014-2020

Erzincan Binali Yıldırım University
2019

Chest Diseases Hospital
2015

Boston Children's Hospital
2014

Fowl adenovirus-4 is a causative agent of hydropericardium hepatitis syndrome (HHS) in chickens and has been frequently reported from many countries. adenoviruses cause severe disease mortality broiler layer breeders Azerbaijan. Therefore, this study, pathological lesions the dissemination fowl into visceral organs infected birds were investigated as well molecular characterisation detected strains. For this, liver, heart spleen 20 necropsied originated breeder flock embeded on FTA cards...

10.1186/s12917-024-04081-0 article EN cc-by BMC Veterinary Research 2024-06-07

To investigate the demographic, clinical and laboratory data of children with idiopathic nephrotic syndrome (INS), to determine prognostic factors that affect outcome patients.Medical charts 372 patients diagnosed have INS followed up at least 5 years between January 1990 December 2008 were evaluated, respectively. After initial findings documented, therapeutic protocols, prognosis investigated.299 (80.4%) steroid responsive 73 (19.6%) not. Focal segmental glomerulosclerosis (FSGS) was...

10.3109/0886022x.2015.1010940 article EN Renal Failure 2015-02-17

Abstract Liddle syndrome (LS) is a familial disease characterized by early onset hypertension (HT). Although regarded as rare, its incidence may be greater than expected because the classical findings of hypokalemic metabolic alkalosis with suppressed renin and aldosterone levels are not consistently present. Herein, we present case an adolescent boy maternal relatives who were followed up misdiagnosis essential HT for long duration. Clinical diagnosis LS was confirmed on genetic analysis....

10.1111/ped.12985 article EN Pediatrics International 2016-06-21

Objective: To investigate Blastocystis’ etiologic role and association with gastrointestinal symptomatology in acute chronic urticaria patients to identify Blastocystis subtypes responsible for urticaria.Methods: The study included healthy individuals that presented our polyclinic between June 2015 May 2017. participants were assigned into Group I (137 patients), subdivided (72) (65), Π (129 control individuals). presence was investigated by native-Lugol examination, trichrome staining, PCR...

10.4103/1995-7645.269905 article EN Asian Pacific Journal of Tropical Medicine 2019-01-01

We described the case of a 36-year-old Turkish female with an extralobar pulmonary sequestration who suffered from chest and back pain for five years without any evidence infection. A X-ray showed area opacity behind cardiac silhouette in lower left hemithorax. CT scan thorax intravenous contrast 9 x 7 cm size ovoid mass necrosis lobe. It revealed two aortic branches directed toward opacity. She subsequently underwent surgery anomalous tissue was removed by excision. The patient diagnosed...

10.4081/monaldi.2013.98 article EN cc-by-nc Monaldi Archives for Chest Disease 2015-11-25

Late antibody-mediated rejection triggered by donor-specific antibodies is a leading cause of kidney allograft failure. Effective treatment options for late are limited in renal transplant recipients. Here, we report 2 pediatric cases severe resistant to conventional immunosuppressive therapy who were successfully treated with eculizumab. Two patients fulfilled the diagnostic criteria (positive antibodies, elevated mean fluorescence index, acute and/or chronic morphological lesions...

10.6002/ect.pediatricsymp2022.o15 article EN Experimental and Clinical Transplantation 2022-05-01

Hydropericardium hepatitis syndrome (HHS) caused by fowl adenovirus-4 have been frequently reported in commercial chickens from several countries causing significant economical losses. In Azerbaijan, adenovirus infections broiler and layer breeders flocks cause severe disease mortality. Here we investigated the pathological lesions dissemination of into visceral organs infected birds. Tissue samples containing liver, heart spleen 20 necropsied were collected on FTA cards presence was...

10.20944/preprints202304.0236.v1 preprint EN 2023-04-12

Literature supports the protective role of mineralocorticoid antagonist (MRA) against renal injury induced by aldosterone in kidney transplant recipients. However, there is limited data available regarding safety and efficacy MRAs pediatric patients. Therefore, we aimed to investigate effect long-term eplerenone administration children with chronic allograft nephropathy (CAN).Twenty-six biopsy-proven CAN, an estimated glomerular filtration rate (eGFR ) > 40 mL/min per 1.73 m2 a significant...

10.1111/petr.14557 article EN Pediatric Transplantation 2023-06-07

Sonuç: Öğrencilerin öncelikle gerçek anlamda bir cinsel eğitime, beraberinde AIDS ve diğer yolla bulaşan hastalıklar ile ilgili sağlıklı bilgilendirme çalışmalarına ihtiyaçları

10.4274/jcp.62207 article TR Güncel Pediatri 2014-04-01

Objective: Congenital nephrogenic diabetes insipidus (CNDI) is a rare inherited disorder characterized by renal insensitivity to arginine vasopressin (AVP).In the majority of cases, CNDI caused mutations in receptor 2 (AVPR2) gene.Our objective report novel mutation AVPR2 gene causing 6-year-old boy, presenting with growth failure and dull normal cognitive functions.Methods: The proband was third off-spring non-consanguineous parents had polyuria (4.3 L/day), polydipsia (5 L/day).The...

10.4274/jcrpe.0097 article EN cc-by-nc-nd Journal of Clinical Research in Pediatric Endocrinology 2018-07-10

Background: The prognostic factors, the outcome and most favorable treatment regimen are not entirely known for children with membranoproliferative glomerulonephritis (MPGN). MPGN is a rarely observed disease more prevalent in adolescents, so we aimed to review clinical histological properties, treatments of our patients who were diagnosed as MPGN. Methods: Fifty-one – selected from biopsy records Dr. Sami Ulus Maternity Children's Hospital Pediatric Nephrology Department January 1999 2011....

10.3109/0886022x.2014.929843 article EN Renal Failure 2014-07-28

In patients with chronic renal failure (CRF) on regular dialysis treatment, limboconjunctival degeneration and calcifications are common. The mechanisms of ectopic conjunctival corneal calcification remain largely speculative. aim the present work was to study tear calcium levels in failure, which could alter excretion patterns, examine whether level fluid is more diagnostic importance than static blood.Tear were measured 25 compared 14 normal subjects. Conjunctival deposits graded by Porter...

10.1177/112067219700700211 article EN European Journal of Ophthalmology 1997-04-01

An eight-year old boy who was healthy previously had a history of use trimethoprime-sulphametoxsazole (TPM-SMX) because diarrhea ten days before presentation. He hospitalized painful swelling occured in the legs under this treatment, he fever and joint pain for last five days. In his personal history, there no pathology except frequent aphtous ulcers mouth it learned that familial any hereditary or rheumatic disease.

10.5152/tpa.2014.1707 article EN Türk Pediatri Arşivi 2014-05-23

Accepted : 24.12.2012 strains, mainly O157, and has a good prognosis (2, 3). Atypical HUS or diarrhea (-) may be idiopathic, familial due to variety of conditions such as therapeutic drug usage (ovulation inhibitors, immunosuppressive agents), various diseases (malignancies, systemic lupus erythematosus), pregnancy infections (4, 5). It can occur at any age including newborns it frequently recurrent course poor renal (1, 4,

10.5262/tndt.2013.1002.18 article EN Turkish Nephrology Dialysis Transplantation 2013-05-10

Abstract Background Patients with nephrotic syndrome (NS) are at a higher risk of developing invasive pneumococcal disease (IPD). Pneumococcal carriage studies helpful tools for detecting potentially infectious serotypes and guiding immunization efforts. nasopharyngeal colonization is common, IPD can easily occur in an immunosuppressed state. Limited information available regarding the frequency individuals NS. The aim this study was to evaluate serotype distribution children Methods...

10.1007/s00467-024-06423-4 article EN cc-by Pediatric Nephrology 2024-06-05

Background/Objectives: Eculizumab is a first-line treatment for atypical hemolytic uremic syndrome (aHUS), and patients undergoing eculizumab therapy may become more susceptible to infection caused by Neisseria meningitidis (Nm). While meningococcal vaccination required therapy, there limited knowledge about carriage in children with aHUS. We aimed evaluate (1) the prevalence of Nm carriage, (2) serogroup distribution, (3) immunization status Methods: The Meningo-aHUS study prospective,...

10.3390/children11101164 article EN cc-by Children 2024-09-25
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