Karaman S - Search Results

1

Increased Iron Deficiency and Iron Deficiency Anemia in Children with Zinc Deficiency.

Ergul AB, Turanoglu C, Karakukcu C, Karaman S, Torun YA. Ergul AB, et al. Among authors: karaman s. Eurasian J Med. 2018 Feb;50(1):34-37. doi: 10.5152/eurasianjmed.2017.17237. Epub 2018 Feb 1. Eurasian J Med. 2018. PMID: 29531489 Free PMC article.

2

An analysis of children with brucellosis associated with haemophagocytic lymphohistiocytosis.

Karaman K, Akbayram S, Kaba S, Karaman S, Garipardiç M, Aydin I, Öner AF. Karaman K, et al. Among authors: karaman s. Infez Med. 2016 Jun 1;24(2):123-30. Infez Med. 2016. PMID: 27367321 Free article.

3

Is Low-level Laser Therapy a Candidate to Be a Good Alternative in the Treatment of Mucositis in Childhood Leukemia?

Karaman K, Sarica A, Tunc SK, Karaman S. Karaman K, et al. Among authors: karaman s. J Pediatr Hematol Oncol. 2022 Jan 1;44(1):e199-e203. doi: 10.1097/MPH.0000000000002306. J Pediatr Hematol Oncol. 2022. PMID: 34986132 Clinical Trial.

4

Triosephosphate Isomerase Deficiency: E105D Mutation in Unrelated Patients and Review of the Literature.

Selamioğlu A, Karaca M, Balcı MC, Körbeyli HK, Durmuş A, Yıldız EP, Karaman S, Gökçay GF. Selamioğlu A, et al. Among authors: karaman s. Mol Syndromol. 2023 Jun;14(3):231-238. doi: 10.1159/000528192. Epub 2023 Jan 19. Mol Syndromol. 2023. PMID: 37323194 Free PMC article.

5

Seroprevalence of hepatitis a and associated factors among 1-15 year old children in Eastern Turkey.

Karaman S, Karaman K, Kızılyıldız BS, Ceylan N, Kaba S, Parlak M, Beger B, Ceylan A. Karaman S, et al. Among authors: karaman k. Int J Clin Exp Med. 2015 Oct 15;8(10):19394-9. eCollection 2015. Int J Clin Exp Med. 2015. PMID: 26770581 Free PMC article.

6

Indicator of early kidney injury in adolescents with polycystic ovary syndrome: Can urine NGAL level be?

Karaman S, Sabancıoğulları E, Karaman E, Başaranoğlu M, Çetin M, Karaman K. Karaman S, et al. Among authors: karaman k, karaman e. Gynecol Endocrinol. 2021 Feb;37(2):117-120. doi: 10.1080/09513590.2020.1787377. Epub 2020 Jul 1. Gynecol Endocrinol. 2021. PMID: 32608277 Free article.

7

Wiskott-Aldrich syndrome: Two case reports with a novel mutation.

Kamuran K, Çetin M, Geylan H, Karaman S, Demir N, Yurekturk E, Yavuz İ, Yavuz G, Tuncer O. Kamuran K, et al. Among authors: karaman s. Pediatr Hematol Oncol. 2017 Aug;34(5):286-291. doi: 10.1080/08880018.2017.1397072. Epub 2017 Dec 4. Pediatr Hematol Oncol. 2017. PMID: 29200320

8

Novel Frameshift Autosomal Recessive Loss-of-Function Mutation in SMARCD2 Encoding a Chromatin Remodeling Factor Mediates Granulopoiesis.

Yucel E, Karakus IS, Krolo A, Kiykim A, Heredia RJ, Tamay Z, Cipe FE, Karakoc-Aydiner E, Ozen A, Karaman S, Boztug K, Baris S. Yucel E, et al. Among authors: karaman s. J Clin Immunol. 2021 Jan;41(1):59-65. doi: 10.1007/s10875-020-00878-4. Epub 2020 Oct 6. J Clin Immunol. 2021. PMID: 33025377 Review.

9

Donor age and long-term culture affect differentiation and proliferation of human bone marrow mesenchymal stem cells.

Zaim M, Karaman S, Cetin G, Isik S. Zaim M, et al. Among authors: karaman s. Ann Hematol. 2012 Aug;91(8):1175-86. doi: 10.1007/s00277-012-1438-x. Epub 2012 Mar 8. Ann Hematol. 2012. PMID: 22395436

10

Identification of three novel pathogenic ITGA2B and one novel pathogenic ITGB3 mutations in patients with hereditary Glanzmann's thrombasthenia living in Eastern Turkey.

Karaman K, Yürektürk E, Geylan H, Yaşar AŞ, Karaman S, Aymelek HS, Çetin M, Oner AF. Karaman K, et al. Among authors: karaman s. Platelets. 2021 Feb 17;32(2):238-242. doi: 10.1080/09537104.2020.1732331. Epub 2020 Feb 22. Platelets. 2021. PMID: 32089034 Free article.

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