Kasap-Demir B - Search Results

1

Secondary pseudohypoaldosteronism caused by urinary tract infection associated with urinary tract anomalies: case reports.

Torun-Bayram M, Soylu A, Kasap-Demir B, Alaygut D, Türkmen M, Kavukçu S. Torun-Bayram M, et al. Turk J Pediatr. 2012 Jan-Feb;54(1):67-70. Turk J Pediatr. 2012. PMID: 22397047

2

An 11-year-old child with autosomal dominant polycystic kidney disease who presented with nephrolithiasis.

Firinci F, Soylu A, Kasap Demir B, Turkmen M, Kavukcu S. Firinci F, et al. Case Rep Med. 2012;2012:428749. doi: 10.1155/2012/428749. Epub 2012 Apr 11. Case Rep Med. 2012. PMID: 22567016 Free PMC article.

3

Cyclosporine causes no hearing defect in paediatric patients with nephrotic syndrome.

Kasap-Demir B, Özmen D, Kırkım G, Doğan E, Soylu A, Şerbetçioğlu B, Kavukçu S. Kasap-Demir B, et al. Int J Audiol. 2017 Sep;56(9):701-705. doi: 10.1080/14992027.2017.1329556. Epub 2017 May 25. Int J Audiol. 2017. PMID: 28541783

4

Can a hand radiograph indicate a special diagnosis in a child with chronic kidney disease? Questions.

Soyaltın E, Kasap-Demir B, Alparslan C, Arslansoyu-Çamlar S, Öncel EP, Kırbıyık Ö, Alaygut D, Yavaşcan Ö, Türe G, Mutlubaş F. Soyaltın E, et al. Pediatr Nephrol. 2018 May;33(5):799-800. doi: 10.1007/s00467-017-3740-2. Epub 2017 Jul 12. Pediatr Nephrol. 2018. PMID: 28702761 No abstract available.

5

Can a hand radiograph indicate a special diagnosis in a child with chronic kidney disease? Answers.

Soyaltın E, Kasap-Demir B, Alparslan C, Arslansoyu-Çamlar S, Öncel EP, Kırbıyık Ö, Alaygut D, Yavaşcan Ö, Türe G, Mutlubaş F. Soyaltın E, et al. Pediatr Nephrol. 2018 May;33(5):801-803. doi: 10.1007/s00467-017-3742-0. Epub 2017 Jul 24. Pediatr Nephrol. 2018. PMID: 28741273 No abstract available.

6

Successful Management of a Rare Cause of Hemolytic Uremic Syndrome With Eculizumab in a Child.

Alparslan C, Yavaşcan Ö, Kasap Demir B, Atmiş B, Karabay Bayazit A, Leblebisatan G, Öncel EP, Alaygut D, Mutlubaş F, Aksu N. Alparslan C, et al. J Pediatr Hematol Oncol. 2018 Jul;40(5):401-404. doi: 10.1097/MPH.0000000000001121. J Pediatr Hematol Oncol. 2018. PMID: 29578925

7

A novel homozygous W99G mutation in CLDN-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in Turkish siblings.

Alparslan C, Öncel EP, Akbay S, Alaygut D, Mutlubaş F, Tatlı M, Konrad M, Yavaşcan Ö, Kasap-Demir B. Alparslan C, et al. Turk J Pediatr. 2018;60(1):76-80. doi: 10.24953/turkjped.2018.01.011. Turk J Pediatr. 2018. PMID: 30102483 Free article.

8

A rare cause of neonatal hypertension: Congenital mesoblastic nephroma.

Soyaltın E, Alaygut D, Alparslan C, Özdemir T, Çamlar SA, Mutlubaş F, Kasap-Demir B, Yavaşcan Ö. Soyaltın E, et al. Turk J Pediatr. 2018;60(2):198-200. doi: 10.24953/turkjped.2018.02.014. Turk J Pediatr. 2018. PMID: 30325129 Free article.

9

A Child Diagnosed With Treatment-Resistant Polyarteritis Nodosa: Can the Clinical Diagnosis Be Different?

Alaygut D, Alparslan C, Öncel EP, Mutlubaş F, Özdemir T, Yavaşcan Ö, Kasap Demir B. Alaygut D, et al. Arch Rheumatol. 2019 Apr 22;34(3):338-342. doi: 10.5606/ArchRheumatol.2019.7075. eCollection 2019 Sep. Arch Rheumatol. 2019. PMID: 31598601 Free PMC article.

10

Anuria in neonatal intensive care: Questions.

Özdemir-Şimşek Ö, Arslansoyu-Çamlar S, Üstün H, İngenç İN, Erfidan G, Soyaltın E, Akar M, Alaygut D, Mutlubaş F, Engür D, Öncel MY, Kasap-Demir B. Özdemir-Şimşek Ö, et al. Pediatr Nephrol. 2020 Dec;35(12):2259-2260. doi: 10.1007/s00467-020-04580-w. Epub 2020 May 25. Pediatr Nephrol. 2020. PMID: 32451730 No abstract available.

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