Search

Your search keyword '"Tekcan, Demet"' showing total 133 results
Start Over Author "Tekcan, Demet"
133 results on '"Tekcan, Demet"'

1. Complement gene mutations in children with C3 glomerulopathy: do they affect the response to mycophenolate mofetil?

Author

Günay, Neslihan, Dursun, İsmail, Gökçe, İbrahim, Akbalık Kara, Mehtap, Tekcan, Demet, Çiçek, Neslihan, Torun Bayram, Meral, Koyun, Mustafa, Dinçel, Nida, Dursun, Hasan, Saygılı, Seha, Yürük Yıldırım, Zeynep Nagehan, Yüksel, Selçuk, Dönmez, Osman, Yel, Sibel, Demircioğlu Kılıç, Beltinge, Aydoğ, Özlem, Atmış, Bahriye, Çaltık Yılmaz, Aysun, Bakkaloğlu, Sevcan A., Aytaç, Mehmet Baha, Taşdemir, Mehmet, Kasap Demir, Belde, Soylu, Alper, Çomak, Elif, Kantar Özşahin, Aslı, Kaçar, Alper, Canpolat, Nur, Yılmaz, Alev, Girişgen, İlknur, Akkoyunlu, Kadirye Betül, Alpay, Harika, and Poyrazoğlu, Hakan M.

Published
2024
Full Text
View/download PDF

2. Urine soluble TLR4 levels may contribute to predict urinary tract infection in children: the UTILISE Study

Author

Aksu, Bagdagul, Afonso, Alberto Caldas, Akil, Ipek, Alpay, Harika, Atmis, Bahriye, Aydog, Ozlem, Bayazıt, Aysun Karabay, Bayram, Meral Torun, Bilge, Ilmay, Bulut, Ipek Kaplan, Buyukkaragoz, Bahar, Comak, Elif, Demir, Belde Kasap, Dincel, Nida, Donmez, Osman, Durmus, Mehmet Akif, Dursun, Hasan, Dusunsel, Ruhan, Duzova, Ali, Ertan, Pelin, Gedikbasi, Asuman, Goknar, Nilufer, Guven, Sercin, Hacihamdioglu, Duygu, Jankauskiene, Augustina, Kalyoncu, Mukaddes, Kavukcu, Salih, Kenan, Bahriye Uzun, Kucuk, Nuran, Kural, Bahar, Litwin, Mieczysław, Montini, Giovanni, Morello, William, Obrycki, Lukasz, Omer, Beyhan, Oner, Huseyin Adil, Ozdemir, Ebru Misirli, Ozkayin, Nese, Paripovic, Dusan, Pehlivanoglu, Cemile, Saygili, Seha, Schaefer, Franz, Schaefer, Susanne, Sonmez, Ferah, Tabel, Yilmaz, Tas, Nesrin, Tasdemir, Mehmet, Teixeira, Ana, Tekcan, Demet, Topaloglu, Rezan, Tulpar, Sebahat, Turkkan, Ozde Nisa, Uysal, Berfin, Uysalol, Metin, Vitkevic, Renata, Yavuz, Sevgi, Yel, Sibel, Yildirim, Tarik, Yildirim, Zeynep Yuruk, Yildiz, Nurdan, Yuksel, Selcuk, Yurtseven, Eray, and Yilmaz, Alev

Published
2024
Full Text
View/download PDF

4. Urinary HSP70 improves diagnostic accuracy for urinary tract infection in children: UTILISE study

Author

Yilmaz, Alev, Afonso, Alberto Caldas, Akil, Ipek, Aksu, Bagdagul, Alpay, Harika, Atmis, Bahriye, Aydog, Ozlem, Bayazıt, Aysun Karabay, Bayram, Meral Torun, Bilge, Ilmay, Bulut, Ipek Kaplan, Buyukkaragoz, Bahar, Comak, Elif, Demir, Belde Kasap, Dincel, Nida, Donmez, Osman, Durmus, Mehmet Akif, Dursun, Hasan, Dusunsel, Ruhan, Duzova, Ali, Ertan, Pelin, Gedikbasi, Asuman, Goknar, Nilufer, Guven, Sercin, Hacihamdioglu, Duygu, Jankauskiene, Augustina, Kalyoncu, Mukaddes, Kavukcu, Salih, Kenan, Bahriye Uzun, Kucuk, Nuran, Kural, Bahar, Litwin, Mieczysław, Montini, Giovanni, Morello, William, Nayir, Ahmet, Obrycki, Lukasz, Omer, Beyhan, Ozdemir, Ebru Misirli, Ozkayin, Nese, Paripovic, Dusan, Pehlivanoglu, Cemile, Saygili, Seha, Schaefer, Susanne, Sonmez, Ferah, Tabel, Yilmaz, Tas, Nesrin, Tasdemir, Mehmet, Teixeira, Ana, Tekcan, Demet, Tulpar, Sebahat, Turkkan, Ozde Nisa, Uysal, Berfin, Uysalol, Metin, Vaiciuniene, Daiva, Yavuz, Sevgi, Yel, Sibel, Yildirim, Tarik, Yildirim, Zeynep Yuruk, Yildiz, Nurdan, Yuksel, Selcuk, Yurtseven, Eray, Schaefer, Franz, and Topaloglu, Rezan

Published
2023
Full Text
View/download PDF

6. Hypogammaglobulinemia in a Child with Clericuzio-Type Poikiloderma with Neutropenia.

Author

Tekcan, Demet, Kulhas Celik, Ilknur, Comert, Meltem, and Artac, Hasibe

Abstract

Introduction: Poikiloderma with neutropenia (PN) is a rare autosomal recessive hereditary disease caused by biallelic mutations of the USB1 gene. It is characterized by poikiloderma, chronic noncyclic neutropenia, and recurrent sinopulmonary infections with bronchiectasis. Here we report a case with homozygous c.531delA mutation in USB1 gene. Case: An 15-month-old boy was admitted to our clinic with skin hyperpigmentation, growth retardation, and recurrent lower respiratory tract infections. The medical history revealed that he was hospitalized 6 times due to pneumonia since the age of 3 months. His physical examination showed facial dysmorphism with triangular face, depressed nasal bridge, and frontal bossing. He also had poikiloderma in the whole body. Skin biopsy was performed and showed only hyperkeratosis. His weight and height were below the 3 percentile. He is the first child of his consangenius parents. In the laboratuary findings; he has mild neutropenia (1,100/mm3), hypogammaglobulinemia (serum IgG: 351 mg/dL, IgA: 17 mg/dL, IgM: 20 mg/dL) and, peripheral lymphocyte subset analysis was normal. Neutropenia was also observed in previous examinations (980-560-840/mm3). Immunoglobulin replacement therapy and antibiotic prophylaxis were started. Exome sequence analysis showed the presence of known homozygous variant (c.351delA) in USB1 gene. Conclusion: Poikiloderma with neutropenia mainly affects the myeloid lineage. Unlike other patients in the literature, we observed hypogammaglobulinemia in addition to neutropenia in our patient. This case illustrated that it is important to monitor serum immunoglobulin levels in symptomatic patients with recurrent infections. [ABSTRACT FROM AUTHOR]

Published
2024
Full Text
View/download PDF

7. Macroscopic hematuria, facing an uncommon disease: Answers

Author

Nalcacioglu, Hulya, Tekcan, Demet, Meydan, Bilge Can, Onal, Hulya Gozde, and Aydog, Ozlem

Subjects
Children -- Diseases, Glomerulonephritis -- Diagnosis -- Care and treatment, Hematuria -- Causes of, Health
Abstract

Author(s): Hulya Nalcacioglu [sup.1] , Demet Tekcan [sup.1] , Bilge Can Meydan [sup.2] , Hulya Gozde Onal [sup.1] , Ozlem Aydog [sup.1] Author Affiliations: (1) grid.411049.9, 0000 0004 0574 2310, [...]

Published
2022
Full Text
View/download PDF

8. Predictors of poor kidney outcome in children with C3 glomerulopathy

Author

Pinarbasi, Ayse Seda, Dursun, Ismail, Gokce, Ibrahim, Çomak, Elif, Saygili, Seha, Bayram, Meral Torun, Donmez, Osman, Melek, Engin, Tekcan, Demet, Cicek, Neslihan, Yilmaz, Dilek, Tabel, Yilmaz, Yildirim, Zeynep Y., Bahat, Elif, Koyun, Mustafa, Soylu, Alper, and Canpolat, Nur

Subjects
Chronic kidney failure -- Risk factors, Glomerulonephritis -- Prognosis -- Complications and side effects, Pediatric research, Health
Abstract

Background C3 glomerulopathy (C3G) is characterized by heterogeneous clinical presentation, outcome, and predominant C3 accumulation in glomeruli without significant IgG. There is scarce outcome data regarding childhood C3G. We describe clinical and pathological features, treatment and outcomes, and risk factors for progression to chronic kidney disease stage 5 (CKD5) in the largest pediatric series with biopsy-proven C3G. Methods Sixty pediatric patients with C3G from 21 referral centers in Turkey were included in this retrospective study. Patients were categorized according to CKD stage at last visit as CKD5 or non-CKD5. Demographic data, clinicopathologic findings, treatment, and outcome data were compared and possible risk factors for CKD5 progression determined using Cox proportional hazards model. Results Mean age at diagnosis was 10.6 ± 3.0 years and follow-up time 48.3 ± 36.3 months. Almost half the patients had gross hematuria and hypertension at diagnosis. Nephritic-nephrotic syndrome was the commonest presenting feature (41.6%) and 1/5 of patients presented with nephrotic syndrome. Membranoproliferative glomerulonephritis was the leading injury pattern, while 40 patients had only C3 staining. Patients with DDD had significantly lower baseline serum albumin compared with C3GN. Eighteen patients received eculizumab. Clinical remission was achieved in 68.3%. At last follow-up, 10 patients (16.6%) developed CKD5: they had lower baseline eGFR and albumin and higher frequency of nephrotic syndrome and dialysis requirement than non-CKD5 patients. Lower serum albumin and eGFR at diagnosis were independent predictors for CKD5 development. Conclusions Children with C3G who have impaired kidney function and hypoalbuminemia at diagnosis should be carefully monitored for risk of progression to CKD5. Graphical abstract, Author(s): Ayse Seda Pinarbasi [sup.1] , Ismail Dursun [sup.1] , Ibrahim Gokce [sup.2] , Elif Çomak [sup.3] , Seha Saygili [sup.4] , Meral Torun Bayram [sup.5] , Osman Donmez [sup.6] [...]

Published
2021
Full Text
View/download PDF

9. Predictors of poor kidney outcome in children with C3 glomerulopathy

Author

Pınarbaşı, Ayşe Seda, Dursun, Ismail, Gokce, Ibrahim, Çomak, Elif, Saygılı, Seha, Bayram, Meral Torun, Donmez, Osman, Melek, Engin, Tekcan, Demet, Çiçek, Neslihan, Yılmaz, Dilek, Tabel, Yılmaz, Yıldırım, Zeynep Y., Bahat, Elif, Koyun, Mustafa, Soylu, Alper, Canpolat, Nur, Aksu, Bağdagül, Çelakıl, Mehtap Ezel, Taşdemir, Mehmet, Benzer, Meryem, Özçelik, Gül, Bakkaloğlu, Sevcan A., and Düşünsel, Ruhan

Published
2021
Full Text
View/download PDF

10. Purine Nucleoside Phosphorylase Deficiency Presenting with Neurological Involvement: A Case Report of Two Siblings.

Author

TEKCAN, Demet, CELIK, Ilknur KULHAS, TARRANT, Teresa K., HERSFIELD, Michael S., and ARTAC, Hasibe

Subjects
*THERAPEUTIC use of immunoglobulins, *NUCLEOSIDES, *PHYSICAL diagnosis, *HEMATOPOIETIC stem cell transplantation, *T cells, *IMMUNOLOGICAL deficiency syndromes, *LYMPHOPENIA, *BLOOD collection, *TREATMENT effectiveness, *NEUROLOGICAL disorders, *DEVELOPMENTAL disabilities, *GLYCOSIDES, *TRANSFERASES, *GENOMES, *SEQUENCE analysis, *CHILDREN
Abstract

Purine nucleoside phosphorylase (PNP) deficiency is a rare immunodeficiency syndrome generally characterized by profound T cell deficiency and variable B cell function. More than half of PNP-deficient patients present with neurological dysfunction, with manifestations such as mental and motor retardation, spasticity, hypertonia, ataxia, and behavioral disturbances. Here, we report two siblings diagnosed with PNP deficiency in early infancy. Our patients had developmental delays, and their immunological findings indicated T-B+NK+ leaky/atypical severe combined immune deficiency. The patients are being treated with regular intravenous immunoglobulin replacement, as well as trimethoprim-sulfomethoxazole and fluconazole, for prophylaxis in preparation for transplantation. These cases draw attention to the possibility of primary immune deficiency in patients with recurrent infections and lymphopenia. In addition, PNP deficiency should be kept in mind in the presence of developmental delay, low uric acid levels, and lymphopenia. [ABSTRACT FROM AUTHOR]

Published
2024
Full Text
View/download PDF

11. The relationship between urine heat shock protein 70 and congenital anomalies of the kidney and urinary tract: UTILISE study

Author

Aksu, Bagdagul, primary, Afonso, Alberto Caldas, additional, Akil, Ipek, additional, Alpay, Harika, additional, Atmis, Bahriye, additional, Aydog, Ozlem, additional, Bakkaloglu, Sevcan, additional, Bayazıt, Aysun Karabay, additional, Bayram, Meral Torun, additional, Bilge, Ilmay, additional, Bulut, Ipek Kaplan, additional, Cetinkaya, Ayse Pinar Goksu, additional, Comak, Elif, additional, Demir, Belde Kasap, additional, Dincel, Nida, additional, Donmez, Osman, additional, Durmus, Mehmet Akif, additional, Dursun, Hasan, additional, Dusunsel, Ruhan, additional, Duzova, Ali, additional, Ertan, Pelin, additional, Gedikbasi, Asuman, additional, Goknar, Nilufer, additional, Guven, Sercin, additional, Hacihamdioglu, Duygu, additional, Jankauskiene, Augustina, additional, Kalyoncu, Mukaddes, additional, Kavukcu, Salih, additional, Kenan, Bahriye Uzun, additional, Kucuk, Nuran, additional, Kural, Bahar, additional, Litwin, Mieczysław, additional, Montini, Giovanni, additional, Morello, William, additional, Obrycki, Lukasz, additional, Omer, Beyhan, additional, Misirli Ozdemir, Ebru, additional, Ozkayin, Nese, additional, Paripovic, Dusan, additional, Pehlivanoglu, Cemile, additional, Saygili, Seha, additional, Schaefer, Franz, additional, Schaefer, Susanne, additional, Sonmez, Ferah, additional, Tabel, Yilmaz, additional, Tas, Nesrin, additional, Tasdemir, Mehmet, additional, Teixeira, Ana, additional, Tekcan, Demet, additional, Topaloglu, Rezan, additional, Tulpar, Sebahat, additional, Turkkan, Ozde Nisa, additional, Uysal, Berfin, additional, Uysalol, Metin, additional, Vitkevic, Renata, additional, Yavuz, Sevgi, additional, Yel, Sibel, additional, Yildirim, Tarik, additional, Yildirim, Zeynep Yuruk, additional, Yildiz, Nurdan, additional, Yuksel, Selcuk, additional, Yurtseven, Eray, additional, and Yilmaz, Alev, additional

Published
2024
Full Text
View/download PDF

15. Urine soluble TLR4 levels may contribute to predict urinary tract infection in children: the UTILISE Study

Author

Aksu, Bagdagul, primary, Afonso, Alberto Caldas, additional, Akil, Ipek, additional, Alpay, Harika, additional, Atmis, Bahriye, additional, Aydog, Ozlem, additional, Bayazıt, Aysun Karabay, additional, Bayram, Meral Torun, additional, Bilge, Ilmay, additional, Bulut, Ipek Kaplan, additional, Buyukkaragoz, Bahar, additional, Comak, Elif, additional, Demir, Belde Kasap, additional, Dincel, Nida, additional, Donmez, Osman, additional, Durmus, Mehmet Akif, additional, Dursun, Hasan, additional, Dusunsel, Ruhan, additional, Duzova, Ali, additional, Ertan, Pelin, additional, Gedikbasi, Asuman, additional, Goknar, Nilufer, additional, Guven, Sercin, additional, Hacihamdioglu, Duygu, additional, Jankauskiene, Augustina, additional, Kalyoncu, Mukaddes, additional, Kavukcu, Salih, additional, Kenan, Bahriye Uzun, additional, Kucuk, Nuran, additional, Kural, Bahar, additional, Litwin, Mieczysław, additional, Montini, Giovanni, additional, Morello, William, additional, Obrycki, Lukasz, additional, Omer, Beyhan, additional, Oner, Huseyin Adil, additional, Ozdemir, Ebru Misirli, additional, Ozkayin, Nese, additional, Paripovic, Dusan, additional, Pehlivanoglu, Cemile, additional, Saygili, Seha, additional, Schaefer, Franz, additional, Schaefer, Susanne, additional, Sonmez, Ferah, additional, Tabel, Yilmaz, additional, Tas, Nesrin, additional, Tasdemir, Mehmet, additional, Teixeira, Ana, additional, Tekcan, Demet, additional, Topaloglu, Rezan, additional, Tulpar, Sebahat, additional, Turkkan, Ozde Nisa, additional, Uysal, Berfin, additional, Uysalol, Metin, additional, Vitkevic, Renata, additional, Yavuz, Sevgi, additional, Yel, Sibel, additional, Yildirim, Tarik, additional, Yildirim, Zeynep Yuruk, additional, Yildiz, Nurdan, additional, Yuksel, Selcuk, additional, Yurtseven, Eray, additional, and Yilmaz, Alev, additional

Published
2023
Full Text
View/download PDF

18. Macroscopic hematuria, facing an uncommon disease: Questions

Author

Nalcacioglu, Hulya, Tekcan, Demet, Meydan, Bilge Can, Onal, Hulya Gozde, and Aydog, Ozlem

Subjects
Hematuria -- Diagnosis -- Demographic aspects -- Risk factors, Kidney diseases -- Diagnosis -- Demographic aspects -- Risk factors, Health
Abstract

Author(s): Hulya Nalcacioglu [sup.1] , Demet Tekcan [sup.1] , Bilge Can Meydan [sup.2] , Hulya Gozde Onal [sup.1] , Ozlem Aydog [sup.1] Author Affiliations: (1) grid.411049.9, 0000 0004 0574 2310, [...]

Published
2022
Full Text
View/download PDF

19. Urinary HSP70 improves diagnostic accuracy for urinary tract infection in children: UTILISE study

Author

Yilmaz, Alev, primary, Afonso, Alberto Caldas, additional, Akil, Ipek, additional, Aksu, Bagdagul, additional, Alpay, Harika, additional, Atmis, Bahriye, additional, Aydog, Ozlem, additional, Bayazıt, Aysun Karabay, additional, Bayram, Meral Torun, additional, Bilge, Ilmay, additional, Bulut, Ipek Kaplan, additional, Buyukkaragoz, Bahar, additional, Comak, Elif, additional, Demir, Belde Kasap, additional, Dincel, Nida, additional, Donmez, Osman, additional, Durmus, Mehmet Akif, additional, Dursun, Hasan, additional, Dusunsel, Ruhan, additional, Duzova, Ali, additional, Ertan, Pelin, additional, Gedikbasi, Asuman, additional, Goknar, Nilufer, additional, Guven, Sercin, additional, Hacihamdioglu, Duygu, additional, Jankauskiene, Augustina, additional, Kalyoncu, Mukaddes, additional, Kavukcu, Salih, additional, Kenan, Bahriye Uzun, additional, Kucuk, Nuran, additional, Kural, Bahar, additional, Litwin, Mieczysław, additional, Montini, Giovanni, additional, Morello, William, additional, Nayir, Ahmet, additional, Obrycki, Lukasz, additional, Omer, Beyhan, additional, Ozdemir, Ebru Misirli, additional, Ozkayin, Nese, additional, Paripovic, Dusan, additional, Pehlivanoglu, Cemile, additional, Saygili, Seha, additional, Schaefer, Susanne, additional, Sonmez, Ferah, additional, Tabel, Yilmaz, additional, Tas, Nesrin, additional, Tasdemir, Mehmet, additional, Teixeira, Ana, additional, Tekcan, Demet, additional, Tulpar, Sebahat, additional, Turkkan, Ozde Nisa, additional, Uysal, Berfin, additional, Uysalol, Metin, additional, Vaiciuniene, Daiva, additional, Yavuz, Sevgi, additional, Yel, Sibel, additional, Yildirim, Tarik, additional, Yildirim, Zeynep Yuruk, additional, Yildiz, Nurdan, additional, Yuksel, Selcuk, additional, Yurtseven, Eray, additional, Schaefer, Franz, additional, and Topaloglu, Rezan, additional

Published
2022
Full Text
View/download PDF

21. Eculizumab therapy in a patient with dense-deposit disease associated with partial lipodystropy

Author

Ozkaya, Ozan, Nalcacioglu, Hulya, Tekcan, Demet, Genc, Gurkan, Meydan, Bilge Can, Ozdemir, B. Handan, and Baysal, M. Kemal

Subjects
Health
Abstract

Background Dense deposit disease (DDD) (also known as membranoproliferative glomerulonephritis type II) in childhood is a rare glomerulonephritis with frequent progression to end-stage renal disease (ESRD) and a high recurrence after kidney transplantation. The pathophysiologic basis of DDD is associated with the uncontrolled systemic activation of the alternative pathway (AP) of the complement cascade. Case-diagnosis/treatment A 14-year-old girl presented with edema and nephrotic range proteinuria. Blood tests showed hypoalbuminemia, nephrotic range proteinuria, normal renal function, and a low C3 level. Renal biopsy confirmed the diagnosis of crescentic DDD. Complement analysis revealed strong AP activation (low C3), positive C3 nephritic factor (C3NeF), and a decreased complement factor H (CFH) levels with CFH polymorphisms. Therapy with eculizumab was considered after the failure of corticosteroid and plasmapheresis to modulate the ongoing massive proteinuria and persistence of low serum C3 levels. There was a marked clinical and biochemical response following the administration of eculizumab. Conclusions Our case emphasizes the efficacy of eculizumab in the management of crescentic DDD in a patient with a normal renal function, in a short follow-up period. Considering previously reported cases, it appears that eculizumab represents a promising new approach which may prevent progression to ESRD in a subset of patients with DDD., Author(s): Ozan Ozkaya [sup.1], Hulya Nalcacioglu [sup.1], Demet Tekcan [sup.1], Gurkan Genc [sup.1], Bilge Can Meydan [sup.2], B. Handan Ozdemir [sup.3], M. Kemal Baysal [sup.4], Hasan Tahsin Keceligil [sup.5] Author [...]

Published
2014
Full Text
View/download PDF

28. Predictors of poor kidney outcome in children with C3 glomerulopathy

Author

Pınarbaşı, Ayşe Seda, primary, Dursun, Ismail, additional, Gokce, Ibrahim, additional, Çomak, Elif, additional, Saygılı, Seha, additional, Bayram, Meral Torun, additional, Donmez, Osman, additional, Melek, Engin, additional, Tekcan, Demet, additional, Çiçek, Neslihan, additional, Yılmaz, Dilek, additional, Tabel, Yılmaz, additional, Yıldırım, Zeynep Y., additional, Bahat, Elif, additional, Koyun, Mustafa, additional, Soylu, Alper, additional, Canpolat, Nur, additional, Aksu, Bağdagül, additional, Çelakıl, Mehtap Ezel, additional, Taşdemir, Mehmet, additional, Benzer, Meryem, additional, Özçelik, Gül, additional, Bakkaloğlu, Sevcan A., additional, and Düşünsel, Ruhan, additional

Published
2020
Full Text
View/download PDF

32. Çocukluk Çağı İdiyopatik Nefrotik Sendromunda Mikofenolat-Mofetil Etkinliği

Author

MUTLUBAŞ, FATMA, KAVUKÇU, SALİH, BİLGE, ILMAY, TEKCAN, DEMET, KALYONCU, MUKADDES, EKİM, MESİHA, AKİL, İPEK, YÜKSEL, SELÇUK, KAPLAN BULUT, İPEK, Anarat, Ali, TABEL, YILMAZ, GÖKÇE, İBRAHİM, ERTAN, PELİN, DÜŞÜNSEL, RUHAN, TORUN BAYRAM, MERAL, YILMAZ, ALEV, UZUN KENAN, BAHRİYE, KARABAY BAYAZIT, AYSUN, GÜRGÖZE, METİN KAYA, DURSUN, İSMAİL, BAKKALOĞLU EZGÜ, SEVCAN AZİME, ATMIŞ, BAHRİYE, KARA, ASLIHAN, SOYALTIN, EREN, and YEL, SİBEL

Published
2019

33. Çocukluk çağında idiyopatik nefrotik sendromunda mikofenolat-mofetil etkinliği

Author

BİLGE, İLMAY, KARA, ASLIHAN, TEKCAN, DEMET, ATMIŞ, BAHRİYE, BAKKALOĞLU EZGÜ, SEVCAN AZİME, DURSUN, İSMAİL, GÜRGÖZE, METİN KAYA, KARABAY BAYAZIT, AYSUN, SERDAROĞLU, ERKİN, UZUN KENAN, BAHRİYE, YILMAZ, ALEV, KALYONCU, MUKADDES, EKİM, MESİHA, ÖZUNAN, İPEK, YÜKSEL, SELÇUK, KAPLAN BULUT, İPEK, ANARAT, ALİ, TABEL, YILMAZ, GÖKÇE, İBRAHİM, DÜŞÜNSEL, RUHAN, KAVUKÇU, SALİH, TORUN BAYRAM, MERAL, MUTLUBAŞ, FATMA, YEL, SİBEL, and SOYALTIN, EREN

Published
2019

34. Çocukluk Çağı İdiopatik Nefrotik Sendromunda Mikofenolat-Mofetil Etkinliği

Author

TORUN BAYRAM, MERAL, KAVUKÇU, SALİH, DÜŞÜNSEL, RUHAN, ERTAN, PELİN, GÖKÇE, İBRAHİM, TABEL, YILMAZ, ANARAT, ALİ, KAPLAN BULUT, İPEK, YÜKSEL, SELÇUK, AKİL, İPEK, EKİM, MESİHA, KALYONCU, MUKADDES, BİLGE, İLMAY, YILMAZ, ALEV, UZUN KENAN, BAHRİYE, SERDAROĞLU, ERKİN, KARABAY BAYAZIT, AYSUN, GÜRGÖZE, METİN KAYA, DURSUN, İSMAİL, BAKKALOĞLU EZGÜ, SEVCAN AZİME, ATMIŞ, BAHRİYE, TEKCAN, DEMET, KARA, ASLIHAN, SOYALTIN, EREN, YEL, SİBEL, and MUTLUBAŞ, FATMA

Published
2019

35. Clinical course of C3 glomerulopathy in Turkish children: a multicenter study

Author

Dursun, Ismail, Pinarbasi, Ayse Seda, Gokce, Ibrahim, Comak, Elif, Seha Kamil Saygili, Bayram, Meral Torun, Donmez, Osman, Melek, Engin, Tekcan, Demet, Yilmaz, Dilek, Ezgu, Sevcan Azime Bakkaloglu, Tabel, Yilmaz, Yildirim, Zeynep Y., Bahat, Elif, Koyun, Mustafa, Soylu, Alper, Cahskan, Salim, Yavas, Bagdagul, Celakil, Mehtap Ezel, Tasdemir, Mustafa, Benzer, Meryem, Ozcelik, Gul, and Dusunsel, Ruhan

Published
2018

36. Autosomal-dominant polycystic kidney disease in children: preliminary results of a Turkısh national, multicenter study

Author

BİRCAN, ZELAL, KASAP DEMİR, BELDE, BEK, KENAN, DURSUN, İSMAİL, ALPAY, HARİKA, AÇIKGÖZ, YONCA, YAZILITAŞ, FATMA, YÜRÜK YILDIRIM, ZEYNEP NAGEHAN, GÖKÇE, İBRAHİM, YILMAZ, DİLEK, TULPAR, SABAHAT, IŞIK, GÜNEŞ, ERTAN, PELİN, AĞBAŞ, AYŞE, AYDOĞ, ÖZLEM, MUTLUBAŞ, FATMA, TEKCAN, DEMET, ÇİÇEK DENİZ, NESLİHAN, KARABAY BAYAZIT, AYSUN, SOYALTIN, EREN, ÇELAKIL, MEHTAP, SOYLU, ALPER, TORUN BAYRAM, MERAL, NALÇACIOĞLU, HÜLYA, and BAHAT ÖZDOĞAN, ELİF

Published
2018

37. AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY DISEASE IN CHILDREN: PRELIMINARY RESULTS OF A TURKISH NATIONAL, MULTICENTER STUDY

Author

Ozdogan, Elif Bahat, Hulya Nalcacioglu, Alpay, Harika, Dursun, Ismail, Bek, Kenan, Demir, Belde Kasap, Tekcan, Demet, Acikgoz, Yonca, Melek, Engin, Yazilitas, Fatma, Bayram, Meral Torun, Yildirim, Zeynep Yuruk, Gokce, Ibrahim, Yilmaz, Dilek, Tulpar, Sebahat, Isik, Gunes, Ertan, Pelin, Agbas, Ayse, Aydog, Ozlem, Mutlubas, Fatma, Bircan, Zelal, Cicek, Neslihan, Bayazit, Aysun Karabay, Soylu, Alper, Soyaltin, Eren, Celakil, Mehtap Ezel, and Yildiz, Nurdan

Published
2018

38. A single center study of the patients with cystinuria

Author

Tekcan, Demet, Aydog, Ozlem, Genc, Gurkan, Kendirci, Nergis, Hulya Nalcacioglu, Ozkaya, Ozan, İstinye Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Özkaya, Ozan, Ozan Özkaya / AAO-2136-2020, Ozan Özkaya / 7003365098, and Ondokuz Mayıs Üniversitesi

Abstract

be partially treated with bicarbonate, bone marrow transplantation or possibly gene therapy. WOS:000443998400506 Q1

Published
2018

39. The Evaluation of Left Ventricular Functions in Children With Steroid-Sensitive Nephrotic Syndrome

Author

Hulya Nalcacioglu, Ozkaya, Ozan, Kafali, Candas, Tekcan, Demet, Baysal, Kemal, Ondokuz Mayıs Üniversitesi, İstinye Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Özkaya, Ozan, Ozan Özkaya / AAO-2136-2020, and Ozan Özkaya / 7003365098

Abstract

Nephrotic syndrome has been associated with increased risk of cardiovascular diseases (CVD), which may be attributable to the hypoalbuminemia, dyslipidemia, hypercoagulopathy or inflammatory activation. In childhood minimal change disease is less prone to CVD because of the transient nature of the metabolic abnormalities and steroid exposure. The aim of the present study was to evaluate the presence of cardiac systolic and diastolic dysfunction in pediatric patients with steroid – sensitive nephrotic syndrome (SSNS). WOS:000443998400393 Q1

Published
2018

43. Acoustic Radiation Force Impulse Quantification in the Evaluation of Renal Parenchyma Elasticity in Pediatric Patients With Chronic Kidney Disease

Author

Bilgici, Meltem Ceyhan, Bekci, Tumay, Genc, Gurkan, Tekcan, Demet, Tomak, Leman, Zonguldak Bülent Ecevit Üniversitesi, and OMÜ

Subjects
elastography, pediatrics, ultrasound, acoustic radiation force impulse, chronic kidney disease
Abstract

WOS: 000406344700003, PubMed: 28390141, Objectives-To evaluate renal parenchymal elasticity with acoustic radiation force impulse imaging in pediatric patients with chronic kidney disease (CKD) and compare with healthy volunteers. Methods-Thirty-eight healthy volunteers and 30 pediatric CKD patients were enrolled in this prospective study. The shear wave velocity (SW) values of both kidneys in CKD patients and healthy volunteers were evaluated. Results-The mean SW in healthy volunteers was 2.2160.34 m/s, whereas the same value was 1.81 +/- 0.49, 1.72 +/- 0.63, 1.66 +/- 0.29, 1.48 +/- 0.37, and 1.23 +/- 0.27 for stages 1, 2, 3, 4, and 5 in CKD patients, respectively. The SW was significantly lower for each stage in the CKD patients compared with healthy volunteers. Acoustic radiation force impulse could not predict the different stages of CKD, with the exception of stage 5. The cut-off value for predicting CKD was 1.81 m/s; at this threshold, sensitivity was 76.5% and specificity was 92.1% (area under the curve = 0.870 [95% confidence interval: 0.750-0.990]; P < .001). Interobserver agreement expressed as intraclass coefficient correlation was 0.65 (95% confidence interval: 0.34 to 0.83; P < .001). Conclusions-Acoustic radiation force impulse may be a potentially useful tool in detecting CKD in pediatric patients.

Published
2017

Catalog

Books, media, physical & digital resources
See catalog results