Keser I - Search Results

1

MEFV gene mutations in Turkish children with juvenile idiopathic arthritis.

Comak E, Dogan CS, Akman S, Koyun M, Gokceoglu AU, Keser I. Comak E, et al. Among authors: keser i. Eur J Pediatr. 2013 Aug;172(8):1061-7. doi: 10.1007/s00431-013-2003-x. Epub 2013 Apr 16. Eur J Pediatr. 2013. PMID: 23588594

2

Clinical evaluation of R202Q alteration of MEFV genes in Turkish children.

Comak E, Akman S, Koyun M, Dogan CS, Gokceoglu AU, Arikan Y, Keser I. Comak E, et al. Among authors: keser i. Clin Rheumatol. 2014 Dec;33(12):1765-71. doi: 10.1007/s10067-014-2602-6. Epub 2014 Apr 10. Clin Rheumatol. 2014. PMID: 24718488

3

The association between intragenic SNP haplotypes and mutations of the beta globin gene in a Turkish population.

Bilgen T, Arikan Y, Canatan D, Yeşilipek A, Keser I. Bilgen T, et al. Among authors: keser i. Blood Cells Mol Dis. 2011 Mar 15;46(3):226-9. doi: 10.1016/j.bcmd.2011.01.004. Epub 2011 Feb 18. Blood Cells Mol Dis. 2011. PMID: 21333566

4

Combination of Hb Knossos [Cod 27 (G-T)] and IVSII-745 (C-G) in a Turkish patient with beta-thalassemia major.

Keser I, Manguoglu E, Kayisli O, Yesilipek A, Luleci G. Keser I, et al. Genet Test. 2007 Fall;11(3):228-30. doi: 10.1089/gte.2006.0521. Genet Test. 2007. PMID: 17949282

5

Subtelomeric rearrangements of dysmorphic children with idiopathic mental retardation reveal 8 different chromosomal anomalies.

Mihçi E, Ozcan M, Berker-Karaüzüm S, Keser I, Taçoy S, Hapsolat S, Lüleci G. Mihçi E, et al. Among authors: keser i. Turk J Pediatr. 2009 Sep-Oct;51(5):453-9. Turk J Pediatr. 2009. PMID: 20112600

6

combination of IVS2.849 A-G witH IVS1.1 G-A: a mutation of beta-globin gene in a Turkish beta-thalessemia major patient.

Manguoğlu E, Sargin CF, Nal N, Keser I, Küpesiz A, Yeşilipek A, Lüleci G. Manguoğlu E, et al. Among authors: keser i. Pediatr Hematol Oncol. 2005 Jun;22(4):291-5. doi: 10.1080/08880010590935185. Pediatr Hematol Oncol. 2005. PMID: 16020116

7

Insertion/deletion polymorphism and serum activity of the angiotensin-converting enzyme in Turkish patients with obstructive sleep apnea syndrome.

Ogus C, Ket S, Bilgen T, Keser I, Cilli A, Gocmen AY, Tosun O, Gumuslu S. Ogus C, et al. Among authors: keser i. Biochem Genet. 2010 Jun;48(5-6):516-23. doi: 10.1007/s10528-010-9335-2. Epub 2010 Feb 25. Biochem Genet. 2010. PMID: 20182789

8

Gap-PCR Screening for Common Large Deletional Mutations of β-Globin Gene Cluster Revealed a Higher Prevalence of the Turkish Inversion/Deletion (δβ)0 Mutation in Antalya.

Bilgen T, Altıok Clark Ö, Öztürk Z, Yeşilipek MA, Keser İ. Bilgen T, et al. Among authors: keser i. Turk J Haematol. 2016 Jun 5;33(2):107-11. doi: 10.4274/tjh.2014.0242. Epub 2015 Aug 6. Turk J Haematol. 2016. PMID: 26377447 Free PMC article.

9

Relationship between SP1 polymorphism and osteoporosis in beta-thalassemia major patients.

Guzeloglu-Kayisli O, Cetin Z, Keser I, Ozturk Z, Tuncer T, Canatan D, Luleci G. Guzeloglu-Kayisli O, et al. Among authors: keser i. Pediatr Int. 2008 Aug;50(4):474-6. doi: 10.1111/j.1442-200X.2008.02609.x. Pediatr Int. 2008. PMID: 19143970

10

The effect of CYP1A2 gene polymorphisms on Theophylline metabolism and chronic obstructive pulmonary disease in Turkish patients.

Uslu A, Ogus C, Ozdemir T, Bilgen T, Tosun O, Keser I. Uslu A, et al. Among authors: keser i. BMB Rep. 2010 Aug;43(8):530-4. doi: 10.5483/bmbrep.2010.43.8.530. BMB Rep. 2010. PMID: 20797314 Free article. Clinical Trial.

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