Ozkilic AC - Search Results

1

The investigation of GSTT1, GSTM1 and SOD polymorphism in bladder cancer patients.

Cengiz M, Ozaydin A, Ozkilic AC, Dedekarginoglu G. Cengiz M, et al. Among authors: ozkilic ac. Int Urol Nephrol. 2007;39(4):1043-8. doi: 10.1007/s11255-007-9179-9. Epub 2007 Mar 6. Int Urol Nephrol. 2007. PMID: 17340208

2

The role of N-acetylcysteine treatment on anti-oxidative status in patients with type II diabetes mellitus.

Ozkilic AC, Cengiz M, Ozaydin A, Cobanoglu A, Kanigur G. Ozkilic AC, et al. J Basic Clin Physiol Pharmacol. 2006;17(4):245-54. doi: 10.1515/jbcpp.2006.17.4.245. J Basic Clin Physiol Pharmacol. 2006. PMID: 17338280

3

The effects of vigabatrin on rat liver antioxidant status.

Cengiz M, Yüksel A, Ozaydin A, Ozkiliç A, Cetinel O, Seven M. Cengiz M, et al. Drug Metabol Drug Interact. 2005;21(2):109-15. doi: 10.1515/dmdi.2005.21.2.109. Drug Metabol Drug Interact. 2005. PMID: 16355976

4

T102C polymorphism of serotonin-2A receptor gene in Turkish schizophrenia patients: Association with cognitive impairment and soft neurological signs.

Özçetin A, Poyraz BÇ, Poyraz CA, Bozhüyük E, Bolat N, Balcioğlu İ, Özkiliç AÇ, Genç ZS, Cengiz M. Özçetin A, et al. Among authors: ozkilic ac. Indian J Psychiatry. 2014 Oct;56(4):359-64. doi: 10.4103/0019-5545.146528. Indian J Psychiatry. 2014. PMID: 25568476 Free PMC article.

5

Dysmorphic face in two siblings with infantile neuroaxonal dystrophy.

Seven M, Ozkiliç A, Yüksel A. Seven M, et al. Genet Couns. 2002;13(4):465-73. Genet Couns. 2002. PMID: 12558119

6

A variant of Cenani-Lenz type syndactyly.

Seven M, Yüksel A, Ozkiliç A, Elçioğlu N. Seven M, et al. Genet Couns. 2000;11(1):41-7. Genet Couns. 2000. PMID: 10756427

7

A case of symbrachydactyly with oligodactyly.

Seven M, Yuksel A, Ozkilic A. Seven M, et al. Genet Couns. 2001;12(1):77-83. Genet Couns. 2001. PMID: 11332981

8

A case of acampomelic campomelic dysplasia.

Ozkilic A, Seven M, Yuksel A. Ozkilic A, et al. Genet Couns. 2002;13(1):23-8. Genet Couns. 2002. PMID: 12017234

9

Joubert syndrome co-existing with partial Xp trisomy: review of the literature.

Güven GS, Fenerci EY, Deviren A, Ozkiliç A, Yüksel A, Hacihanefioğlu S. Güven GS, et al. Genet Couns. 2004;15(3):321-8. Genet Couns. 2004. PMID: 15517825 Review.

10

Trisomy 9p syndrome in two brothers: with new clinical findings and review of the literature.

Hacihanefioğlu S, Güven GS, Deviren A, Silahtaroğlu AN, Yosunvkaya Fenerci E, Ozkiliç A, Yüksel A. Hacihanefioğlu S, et al. Genet Couns. 2002;13(1):41-8. Genet Couns. 2002. PMID: 12017237 Review.

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