Search Results - "Guven, Sercin"

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  1. 1

    Assessment of the oral health status of children with chronic kidney disease by Sezer, Berkant, Kaya, Remziye, Kodaman Dokumacıgil, Nur, Sıddıkoğlu, Duygu, Güven, Serçin, Yıldız, Nurdan, Alpay, Harika, Kargül, Betül

    “…Background There are various oral symptoms related to the disease and its management in individuals with chronic kidney disease (CKD). The aim of the study was…”
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    Journal Article
  2. 2

    Clinical Predictors of Steroid Resistance in Childhood Nephrotic Syndrome by Cicek, Neslihan, Yıldız, Nurdan, Guven, Sercin, Kaya, Mehtap, Gokce, Ibrahim, Alpay, Harika

    Published in Clinical pediatrics (01-10-2024)
    “…We aimed to evaluate the clinical parameters, histopathological findings of nephrotic syndrome (NS) patients, and independent factors predicting steroid…”
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  3. 3

    Collapsing Glomerulopathy in a Patient with a TRPC6 Mutation Presenting as Rapidly Progressive Glomerulonephritis: A Case Report and Review of the Literature by Gokce, Ibrahim, Kaya, Mehtap, Cicek, Neslihan, Guven, Sercin, Ercetin, Yigit, Yildiz, Nurdan, Kaya, Handan, Alpay, Harika

    “…Collapsing glomerulopathy (CG) is a proliferative disease characterized by segmental or global wrinkling of the glomerular basement membrane and the formation…”
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  4. 4

    A case of granulomatosis of polyangiitis presenting with COVID-19 infection: False-positivity or co-existence? by KAYA, Mehtap, GOKCE, Ibrahim, GUVEN, Sercin, PUL, Serim, ALPAY, Harika

    Published in Marmara Medical Journal (29-09-2023)
    “…Coronavirus disease 2019 (COVID-19) was declared a global pandemic and a public health emergency worldwide in March 2020. COVID-19 presents with non-specific…”
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  5. 5

    Pediatric crush-related acute kidney injury and risk factors: a single center experience by Taner, Sevgin, Ozdemir, Ulas, Kandemir Gulmez, Tugba, Güven, Sercin, Cicek, Neslihan, Kelesoglu, Emre, Arslan, Ilknur, Celik, Umit

    Published in Journal of nephrology (31-08-2024)
    “…Crush injury, the most important trauma complication encountered in earthquake victims, occurs as a result of prolonged compression of muscle mass. Crush…”
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  6. 6

    Clinical and genetic characterization of children with cubilin variants by Cicek, Neslihan, Alpay, Harika, Guven, Sercin, Alavanda, Ceren, Türkkan, Özde Nisa, Pul, Serim, Demirci, Ece, Yıldız, Nurdan, Ata, Pınar, Gokce, Ibrahim

    Published in Pediatric nephrology (Berlin, West) (01-04-2023)
    “…Background Cubilin is one of the receptor proteins responsible for reabsorption of albumin in proximal tubules and is encoded by the CUBN gene. We aimed to…”
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    Is renal abscess still a problem? by SAK, Mehtap, GOKCE, Ibrahim, CICEK, Neslihan, GUVEN, Sercin, ERGELEN, Rabia, YILDIZ, Nurdan, ALPAY, Harika

    Published in Marmara Medical Journal (01-01-2021)
    “…Renal abscess, the accumulation of infected fluid in the kidney, is a rare condition seen in children as well as adults. It leads to long term hospital…”
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    Differential diagnosis of classical Bartter syndrome and Gitelman syndrome: Do we need genetic analysis? by GUVEN, Sercin, GOKCE, Ibrahim, ALAVANDA, Ceren, CICEK, Neslihan, BODUR DEMIRCI, Ece, SAK, Mehtap, PUL, Serim, TURKKAN, Ozde Nisa, YILDIZ, Nurdan, ATA, Pinar, ALPAY, Harika

    Published in Marmara Medical Journal (01-01-2021)
    “…Objective: Classical Bartter syndrome (cBS) and Gitelman syndrome (GS) are genotypically distinct, but there is a phenotypic overlapamong these two diseases,…”
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    Catastrophic antiphospholipid syndrome accompanied by complement regulatory gene mutation by Pul, Serim, Gökçe, İbrahim, Bodur, Ece Demirci, Güven, Serçin, Çiçek, Neslihan, Sak, Mehtap, Türkkan, Özde Nisa, Filinte, Deniz, Pehlivanoğlu, Cemile, Sözeri, Betül, Alpay, Harika

    Published in The Turkish journal of pediatrics (01-03-2023)
    “…Antiphospholipid syndrome (APS), particularly the catastrophic antiphospholipid syndrome (CAPS), is one of the rare causes of thrombotic microangiopathy (TMA)…”
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  13. 13

    Phenotypic and genotypic characteristics of children with Bartter syndrome by Güven, Serçin, Ata, Pınar, Yıldız, Nurdan, Türkkan, Özde Nisa, Pul, Serim, Sak, Mehtap, Demirci, Ece Bodur, Çiçek, Neslihan, Alavanda, Ceren, Gökçe, İbrahim, Alpay, Harika

    Published in Turkish journal of pediatrics (01-09-2022)
    “…Introduction. Bartter syndrome (BS) is a group of autosomal-recessive tubular disorders and it is classified into five genetic subtypes. BS can also be…”
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  14. 14

    Magnesium and Anti-phosphate Treatment with Bisphosphonates for Generalised Arterial Calcification of Infancy: A Case Report by Dursun, Fatma, Atasoy Öztürk, Tülay, Güven, Serçin, Kırmızıbekmez, Heves, Seymen Karabulut, Gülcan, Kalın, Sevinç, Sözeri, Betül

    “…Generalized arterial calcification of infancy (GACI) is a rare autosomal-recessive disorder, characterized by calcification of the internal elastic lamina,…”
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  15. 15

    Changes in Bacterial Resistance Patterns of Pediatric Urinary Tract Infections and Rationale for Empirical Antibiotic Therapy by Gökçe, İbrahim, Çiçek, Neslihan, Güven, Serçin, Altuntaş, Ülger, Bıyıklı, Neşe, Yıldız, Nurdan, Alpay, Harika

    Published in Balkan medical journal (01-09-2017)
    “…The causative agent spectrum and resistance patterns of urinary tract infections in children are affected by many factors. To demonstrate antibiotic resistance…”
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  16. 16

    Molecular Aspects of Distal Kidney Tubular Acidosis in Children, Its Long-Term Outcome, and Relationship with Hyperammonemia by Güven, Serçin, Gökçe, İbrahim, Alavanda, Ceren, Öztürk Hişmi, Burcu, Çiçek, Neslihan, Bodur Demirci, Ece, Sak, Mehtap, Yıldız, Nurdan, Ata, Pınar, Alpay, Harika

    Published in Turkish archives of pediatrics (01-07-2022)
    “…OBJECTIVEWe aimed to present the characteristics, genetic analysis results, long-term progno- sis of our patients with distal kidney tubular acidosis, and the…”
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  17. 17

    Salt wasting in two neonates with posterior urethral valves: secondary pseudohypoaldosteronism by ALTUNTAŞ, Ülger, GÖKCE, İbrahim, TUĞTEPE, Halil, BENZER, Meryem, GÜVEN, Serçin, YILDIZ, Nurdan, ALPAY, Harika

    Published in Marmara Medical Journal (01-01-2017)
    “…Sekonder psödohipoaldosteronizm (PHA), böbrek tübüllerininaldosterona duyarsızlığı ile karakterize, hiperkalemi, hiponatremi ve metabolik asidoz ile kendini…”
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    The utility of biomarkers to predict steroid response in idiopathic nephrotic syndrome by Çiçek, Neslihan, Gökçe, İbrahim, Güven, Serçin, Yaman, Ali, Alpay, Harika

    Published in Marmara Medical Journal (30-10-2024)
    “…Objective: The most common form of nephrotic syndrome (NS) is minimal change disease (MCD) in children and focal segmental glomerulosclerosis (FSGS) following…”
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    Diagnostic Pitfalls of a Newborn with Congenital Nephrogenic Diabetes Insipidus by Güran, Ömer, Güven, Serçin, Kırmızıbekmez, Heves, Akgün Doğan, Özlem, Karadeniz Bilgin, Leyla

    “…Congenital nephrogenic diabetes insipidus (NDI) is a rare cause of hypernatremia in newborns. Central diabetes insipidus (CDI) is the main differential…”
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