Ağbaş A - Search Results

1

A novel homozygous missense variant in TBC1D31 in a consanguineous family with congenital anomalies of the kidney and urinary tract (CAKUT).

Saygılı S, Koşukcu C, Baştuğ T, Doğan ÖA, Yılmaz EK, Kalyoncu AU, Ağbaş A, Canpolat N, Çalışkan S, Ozaltin F. Saygılı S, et al. Among authors: agbas a. Clin Genet. 2023 Dec;104(6):679-685. doi: 10.1111/cge.14406. Epub 2023 Jul 19. Clin Genet. 2023. PMID: 37468454

2

Congenital erythropoietic porphyria.

Kürkçüoğlu M, Tunç B, Ağbaş A. Kürkçüoğlu M, et al. Among authors: agbas a. Turk J Pediatr. 1985 Jan-Mar;27(1):39-44. Turk J Pediatr. 1985. PMID: 3984055 No abstract available.

3

Cardiovascular alterations do exist in children with stage-2 chronic kidney disease.

Taşdemir M, Eroğlu AG, Canpolat N, Konukoğlu D, Ağbaş A, Sevim MD, Çalışkan S, Sever L. Taşdemir M, et al. Among authors: agbas a. Clin Exp Nephrol. 2016 Dec;20(6):926-933. doi: 10.1007/s10157-016-1234-3. Epub 2016 Jan 28. Clin Exp Nephrol. 2016. PMID: 26822545

4

Cobalamin C defect-hemolytic uremic syndrome caused by new mutation in MMACHC.

Adrovic A, Canpolat N, Caliskan S, Sever L, Kıykım E, Agbas A, Baumgartner MR. Adrovic A, et al. Among authors: agbas a. Pediatr Int. 2016 Aug;58(8):763-5. doi: 10.1111/ped.12953. Epub 2016 Jun 21. Pediatr Int. 2016. PMID: 27324188

5

Sjögren's syndrome associated with systemic lupus erythematosus.

Taşdemir M, Hasan C, Ağbaş A, Kasapçopur Ö, Canpolat N, Sever L, Çalışkan S. Taşdemir M, et al. Among authors: agbas a. Turk Pediatri Ars. 2016 Sep 1;51(3):166-168. doi: 10.5152/TurkPediatriArs.2016.2001. eCollection 2016 Sep. Turk Pediatri Ars. 2016. PMID: 27738403 Free PMC article.

6

Hemodiafiltration is associated with reduced inflammation, oxidative stress and improved endothelial risk profile compared to high-flux hemodialysis in children.

Ağbaş A, Canpolat N, Çalışkan S, Yılmaz A, Ekmekçi H, Mayes M, Aitkenhead H, Schaefer F, Sever L, Shroff R. Ağbaş A, et al. PLoS One. 2018 Jun 18;13(6):e0198320. doi: 10.1371/journal.pone.0198320. eCollection 2018. PLoS One. 2018. PMID: 29912924 Free PMC article. Clinical Trial.

7

Leptin and ghrelin in chronic kidney disease: their associations with protein-energy wasting.

Canpolat N, Sever L, Agbas A, Tasdemir M, Oruc C, Ekmekci OB, Caliskan S. Canpolat N, et al. Among authors: agbas a. Pediatr Nephrol. 2018 Nov;33(11):2113-2122. doi: 10.1007/s00467-018-4002-7. Epub 2018 Jul 6. Pediatr Nephrol. 2018. PMID: 29980850

8

The Relationship between the Waist Circumference and Increased Carotid Intima Thickness in Obese Children.

Sönmez HE, Canpolat N, Ağbaş A, Taşdemir M, Ekmekçi ÖB, Alikaşifoğlu M, Sever L, Çalışkan S. Sönmez HE, et al. Among authors: agbas a. Child Obes. 2019 Oct;15(7):468-475. doi: 10.1089/chi.2019.0022. Epub 2019 Jun 27. Child Obes. 2019. PMID: 31246513

9

The Frequency of Familial Congenital Anomalies of the Kidney and Urinary Tract: Should We Screen Asymptomatic First-Degree Relatives Using Urinary Tract Ultrasonography?

Suman Gök E, Ayvacı A, Ağbaş A, Adaletli İ, Canpolat N, Sever L, Çalışkan S. Suman Gök E, et al. Among authors: agbas a. Nephron. 2020;144(4):170-175. doi: 10.1159/000505402. Epub 2020 Jan 7. Nephron. 2020. PMID: 31910412

10

COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndrome.

Ozdemir G, Gulhan B, Atayar E, Saygılı S, Soylemezoglu O, Ozcakar ZB, Eroglu FK, Candan C, Demir BK, Soylu A, Yüksel S, Alpay H, Agbas A, Duzova A, Hayran M, Ozaltin F, Topaloglu R. Ozdemir G, et al. Among authors: agbas a. Pediatr Nephrol. 2020 Oct;35(10):1941-1952. doi: 10.1007/s00467-020-04574-8. Epub 2020 May 11. Pediatr Nephrol. 2020. PMID: 32394188

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