Celkan T - Search Results

1

Investigation of (epi)genotype causes and follow-up manifestations in the patients with classical and atypical phenotype of Beckwith-Wiedemann spectrum.

Tüysüz B, Güneş N, Geyik F, Yeşil G, Celkan T, Vural M. Tüysüz B, et al. Among authors: celkan t. Am J Med Genet A. 2021 Jun;185(6):1721-1731. doi: 10.1002/ajmg.a.62158. Epub 2021 Mar 11. Am J Med Genet A. 2021. PMID: 33704912

2

Neurofibromatosis type 1: Expanded variant spectrum with multiplex ligation-dependent probe amplification and genotype-phenotype correlation in 138 Turkish patients.

Güneş N, Yeşil G, Geyik F, Kasap B, Celkan T, Kebudi R, Tüysüz B. Güneş N, et al. Among authors: celkan t. Ann Hum Genet. 2021 Sep;85(5):155-165. doi: 10.1111/ahg.12422. Epub 2021 Apr 20. Ann Hum Genet. 2021. PMID: 33877690

3

Clinical and Molecular Characterization of Fanconi Anemia Patients in Turkey.

Toksoy G, Uludağ Alkaya D, Bagirova G, Avcı Ş, Aghayev A, Günes N, Altunoğlu U, Alanay Y, Başaran S, Berkay EG, Karaman B, Celkan TT, Apak H, Kayserili H, Tüysüz B, Uyguner ZO. Toksoy G, et al. Among authors: celkan tt. Mol Syndromol. 2020 Nov;11(4):183-196. doi: 10.1159/000509838. Epub 2020 Sep 23. Mol Syndromol. 2020. PMID: 33224012 Free PMC article.

4

Macrocephaly-capillary malformation syndrome in a newborn with tetralogy of fallot and sagittal sinus thrombosis.

Ercan TE, Oztunc F, Celkan T, Bor M, Kizilkilic O, Vural M, Perk Y, Islak C, Tuysuz B. Ercan TE, et al. Among authors: celkan t. J Child Neurol. 2013 Jan;28(1):115-9. doi: 10.1177/0883073812439346. Epub 2012 Mar 25. J Child Neurol. 2013. PMID: 22451530

5

Thiamine-responsive megaloblastic anemia: early diagnosis may be effective in preventing deafness.

Onal H, Bariş S, Ozdil M, Yeşil G, Altun G, Ozyilmaz I, Aydin A, Celkan T. Onal H, et al. Among authors: celkan t. Turk J Pediatr. 2009 May-Jun;51(3):301-4. Turk J Pediatr. 2009. PMID: 19817279

6

Use of hyperbaric oxygen therapy of purpura fulminans in an extremely low birth weight preterm: A case report.

Yılmaz A, Kaya N, Meriç R, Bayramli Z, Öroğlu B, Celkan TT, Vural M, Perk Y. Yılmaz A, et al. Among authors: celkan tt. J Neonatal Perinatal Med. 2023;16(2):339-342. doi: 10.3233/NPM-200428. J Neonatal Perinatal Med. 2023. PMID: 32741781

7

Clinical course of pediatric large vascular anomalies located in the extremities.

Oktay BK, Kaçar AG, Özel SÇ, Ocak S, Celkan T. Oktay BK, et al. Among authors: celkan t. Turk Arch Pediatr. 2021 May 1;56(3):213-218. doi: 10.5152/TurkArchPediatr.2021.20089. eCollection 2021. Turk Arch Pediatr. 2021. PMID: 34104911 Free PMC article.

8

Pediatric Stroke: A Single-Center Experience.

Söbü E, Özdemir N, Uysal S, Buyru N, Celkan T. Söbü E, et al. Among authors: celkan t. J Pediatr Hematol Oncol. 2019 Oct;41(7):519-524. doi: 10.1097/MPH.0000000000001539. J Pediatr Hematol Oncol. 2019. PMID: 31259821

9

Comparison of outcomes of children with acute lymphoblastic leukemia treated with BMF protocol across 2 decades.

Sunamak EÇ, Özdemir N, Koka A, Yantiri L, Apak H, Celkan T. Sunamak EÇ, et al. Among authors: celkan t. Pediatr Hematol Oncol. 2021 Mar;38(2):134-146. doi: 10.1080/08880018.2020.1825573. Epub 2020 Nov 10. Pediatr Hematol Oncol. 2021. PMID: 33170046

10

Zinc finger protein 384 (ZNF384) impact on childhood mixed phenotype acute leukemia and B-cell precursor acute lymphoblastic leukemia.

Sudutan T, Erbilgin Y, Hatirnaz Ng O, Karaman S, Karakas Z, Kucukcankurt F, Celkan T, Timur C, Ozdemir GN, Hacısalihoglu S, Gelen SA, Sayitoğlu M. Sudutan T, et al. Among authors: celkan t. Leuk Lymphoma. 2022 Dec;63(12):2931-2939. doi: 10.1080/10428194.2022.2095630. Epub 2022 Aug 3. Leuk Lymphoma. 2022. PMID: 35921545

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